A list of publications indexed in Journal Citation Reports and other scientific issues related to the group.

  •  2021
    • Gómez-Carballa, Alberto and Barral-Arca, Ruth and Cebey-López, Miriam and Bello, Xabier and Pardo-Seco, Jacobo and Martinón-Torres, Federico and Salas, Antonio (2021). Identification of a Minimal 3-Transcript Signature to Differentiate Viral from Bacterial Infection from Best Genome-Wide Host RNA Biomarkers: A Multi-Cohort Analysis. International Journal of Molecular Sciences; 22(6):3148. https://doi.org/10.3390/ijms22063148
    • Pardo-Seco J, Dacosta AI, Rivero-Calle I, Martinón-Torres F Broset E, Pardo-Seco J, Kanno AI, Aguilo N, Dacosta AI, Rivero-Calle I, Gonzalo-Asensio J, Locht C, Leite LCC, Martin C, Martinón-Torres F. (2021). BCG vaccination improves DTaP immune responses in mice and is associated with lower pertussis incidence in ecological epidemiological studies.. EBioMedicine; 65(1):103254. https://doi.org/10.1016/j.ebiom.2021.103254
    • Pischedda S, O'Connor D, Fairfax BP, Salas A, Martinon-Torres F, Pollard AJ and Trück J. (2021). Changes in epigenetic profiles throughout early childhood and their relationship to the response to pneumococcal vaccination.. Clinical Epigenetics; 13(1):29. https://doi.org/10.1186/s13148-021-01012-w
    • Alberto Gómez-Carballa, Ruth Barral-Arca, Miriam Cebey-López, Maria José Currás-Tuala, Sara Pischedda, José Gómez-Rial, Dominic Habgood-Coote, Jethro A Herberg, Myrsini Kaforou, Federico Martinón-Torres, Antonio Salas (2021). Host Transcriptomic Response Following Administration of Rotavirus Vaccine in Infants' Mimics Wild Type Infection.. Frontiers in Inmunology; 11(1):3517. https://doi.org/10.3389/fimmu.2020.580219
    • Jacobo Pardo-Seco, Alberto Gómez-Carballa, Xabier Bello, Federico Martinón-Torres, Antonio Salas (2021). Pitfalls of barcodes in the study of worldwide SARS-CoV-2 variation and phylodynamics. Zoological Research; 1(42):87-93. https://doi.org/10.24272/j.issn.2095-8137.2020.364
  •  2020
    • Wildenbeest JG, Zuurbier RP, Korsten K, van Houten MA, Billard MN, Derksen-Lazet N, Snape MD, Drysdale SB, Robinson H, Pollard AJ, Heikkinen T, Cunningham S, Leach A, Martinón-Torres F, Rodríguez-Tenreiro Sánchez C, Gómez-Carballa A, Bont LJ; RESCEU Investigators (2020). Respiratory Syncytial Virus Consortium in Europe (RESCEU) Birth Cohort Study: Defining the Burden of Infant Respiratory Syncytial Virus Disease in Europe. The Journal of Infectious Diseases; 222(Supplement 7):S606–S612. https://doi.org/10.1093/infdis/jiaa310
    • Roy P Zuurbier, Louis J Bont, Annefleur C Langedijk, Mirjam Hamer, Koos Korsten, Simon B Drysdale, Matthew D Snape, Hannah Robinson, Andrew J Pollard, Federico Martinón-Torres, Carmen Rodríguez-Tenreiro Sánchez, Alberto Gómez-Carballa, Ana Isabel Dacosta-Urbieta, Terho Heikkinen, Steve Cunningham, Marlies A van Houten, Joanne G Wildenbeest (2020). Low Sensitivity of BinaxNOW RSV in Infants. The Journal of Infectious Diseases; 222(Supplement 7):S640–S647. https://doi.org/10.1093/infdis/jiaa050
    • Gómez-Carballa, Alberto, Bello, Xabier, Jacobo Pardo-Seco, María Luisa Pérez del Molino, Federico Martinón-Torres and Antonio Salas (2020). Phylogeography of SARS-CoV-2 pandemic in Spain: a story of multiple introductions, micro-geographic stratification, founder effects, and super-spreaders. Zoological Research; 41(6):605-620. https://doi.org/10.24272/j.issn.2095-8137.2020.217

    • Laura Argiz, Sonsoles Infante, Adrianna Machinena, Mariona Pascal, Luis Echeverria, Simona Barni, Teresa Garriga-Baraut, Stefania Arasi, Jose Domingo Moure, Alberto Gomez-Carballa, Federico Martinon-Torres, Robert J. Boyle, Marta Vazquez-Ortiz (2020). Reactions on re-exposure following negative and inconclusive follow-up food challenges in children with acute FPIES. The Journal of Allergy and Clinical Immunology; 8(9):3228-3231.e3. https://doi.org/10.1016/j.jaip.2020.05.040
    • Cebey-López, Miriam and Salas, Antonio (2020). Recognising the asymptomatic enemy. The Lancet Infectious Diseases; 21(3):305-306. https://doi.org/10.1016/S1473-3099(20)30587-9
    • Gómez-Rial Jose, Currás-Tuala Maria José, Rivero-Calle Irene, Gómez-Carballa Alberto, Cebey-López Miriam, Rodríguez-Tenreiro Carmen, Dacosta-Urbieta Ana, Rivero-Velasco Carmen, Rodríguez-Núñez Nuria, Trastoy-Pena Rocio, Rodríguez-García Javier, Salas Antonio, Martinón-Torres Federico (2020). Increased serum levels of sCD14 and sCD163 indicate a preponderant role for monocytes in COVID-19 immunopathology. Frontiers in Immunology. https://doi.org/10.3389/fimmu.2020.560381
    • Ana Dacosta-Urbieta, Irene Rivero-Calle , Jacobo Pardo-Seco, Lorenzo Redondo-Collazo, Antonio Salas , Jose Gómez-Rial, Federico Martinón-Torres (2020). Seroprevalence of SARS-CoV-2 Among Pediatric Healthcare Workers in Spain. Frontiers in Pediatrics; 8(1):547. https://doi.org/10.3389/fped.2020.00547
    • Alberto Gómez-Carballa, Xabier Bello, Jacobo Pardo-Seco, Federico Martinón-Torres and Antonio Salas (2020). Mapping genome variation of SARS-CoV-2 worldwide highlights the impact of COVID-19 super-spreaders. Genome Research; 30(10):1434-1448. https://doi.org/10.1101/gr.266221.120
    • Irene Rivero-Calle, Jose Gómez-Rial, Louis Bont, Bradford D. Gessner, Melvin Kohn, Ron Dagan, Daniel C. Payne, Laia Bruni, Andrew J. Pollard, Adolfo García-Sastre, Denise L. Faustman, Albert Osterhaus, Robb Butler, Francisco Giménez Sánchez, Francisco Álvarez, Myrsini Kaforou, Xabier Bello and Federico Martinón-Torres (2020). TIPICO X: report of the 10th interactive infectious disease workshop on infectious diseases and vaccines. Human Vaccines & Immunotherapeutics; 0(0):1-14. https://doi.org/10.1080/21645515.2020.1788301
    • Gómez-Rial J, Rivero-Calle I, Salas A, Martinón-Torres F (2020). Role of Monocytes/Macrophages in Covid-19 Pathogenesis: Implications for Therapy. Infection and Drug Resistance; 13:2485-2493. https://doi.org/10.2147/IDR.S258639
    • Barral-Arca R, Gómez-Carballa A, Cebey-López M, Currás-Tuala MJ, Pischedda S, Viz-Lasheras S, Bello S, Martinón-Torres F, Salas A (2020). RNA-Seq data-mining allows the discovery of two long non-coding RNA biomarkers of viral infection in humans. International Journal of Molecular Sciences; 21(8):2748. http://doi.org/10.3390/ijms21082748

    • Barral-Arca R, Gómez-Carballa A, Cebey-López M, Bello X, Martinón-Torres F, Salas A (2020). A Meta-Analysis of Multiple Whole Blood Gene Expression Data Unveils a Diagnostic Host-Response Transcript Signature for Respiratory Syncytial Virus. International Journal of Molecular Sciences; 21(5):1831. https://doi.org/10.3390/ijms21051831

    • Salas A, Schönherr S, Bandelt H-J, Gómez-Carballa A, Weissensteiner H (2020). Extraordinary claims require extraordinary evidence in asserted mtDNA biparental inheritance. Forensic Sci Int Genet; in press. https://doi.org/10.1016/j.fsigen.2020.102274

    • Bermúdez de León M, León-Cachón RBR, Silva-Ramírez B, González-Ríos RN, Escobedo-Guajardo B, Leyva-Parra R, Tovar-Cisneros B, González-González E, Alvarado-Díaz A, Vázquez-Monsiváis O, Mata-Tijerina V, Puente-Lugo L, Álvarez- Galván E, Currás-Tuala MJ, Aguado-Barrera M, Castorena-Torres F, Alcocer-González JM, Elizondo G, Salinas-Martínez AM (2020). Association study of genetic polymorphisms in proteins involved in oseltamivir transport, metabolism, and interactions with adverse reactions in Mexican patients with acute respiratory diseases. The Pharmacogenomics Journal; 20(4):613-620. https://doi.org/10.1038/s41397-020-0151-8
    • Carvalho GC, Freire-Aradas A, Fondevila M, Santos C, Salas A, Henao J, Isaza C, Beltrán L, Nogueira SV, Castillo A, Ibarra A, Moreno CF, Söchtig J, Ruiz Y, Barreto G, Rondon F, Zabala W, Borjas L, Carracedo A, Phillips C (2020). PIMA: A population informative multiplex for the Americas. Forensic science international. Genetics; 44:102200. http://doi.org/10.1016/j.fsigen.2019.102200
  •  2019
    • Rivero-Calle I, Pardo-Seco J, Raguindin PF, Alvez F, Gómez-Rial J, Salas A, Martinón-Sanchez J, Martinón-Torres F (2019). Routine infant vaccination of pneumococcal conjugate vaccines has decreased pneumonia across all age groups in Northern Spain. Human Vaccines & Immunotherapeutics. http://doi.org/10.1080/21645515.2019.1690884
    • Jacobo Pardo-Seco, Alberto Gómez-Carballa, Xabier Bello, Federico Martinón-Torres, Antonio Salas (2019). Biogeographical informativeness of Y-STR haplotypes. Science Bulletin; 64(19):1381-1384. https://doi.org/10.1016/j.scib.2019.07.025
    • Gómez-Carballa A, Cebey-López M, Pardo-Seco J, Barral-Arca R, Rivero-Calle I, Pischedda S, Gómez-Rial J, Barros F, Martinón-Torres F, Salas A (2019). A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children. Scientific reports; 9:11780. http://doi.org/10.1038/s41598-019-48162-9
    • Ceres Fernández-Rozadilla, Miriam Álvarez-Barona, Esther Schamschula, Sahra Bodo, Anael Lopez-Novo, Andrés Dacal, Consuelo Calviño-Costas, Ángel Lancho, Jorge Amigo, Xabier Bello, José Manuel Cameselle-Teijeiro, Ángel Carracedo, Chrystelle Colas, Martine Muleris, Katharina Wimmer, Clara Ruiz-Ponte (2019). Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum. Cancers; 11(8):1081. https://doi.org/10.3390/cancers11081081
    • Martinón-Torres F, Bosch X, Rappuoli R, Ladhani S, Redondo E, Vesikari T, García-Sastre A, Rivero-Calle I, Gómez-Rial J, Salas A, Martín C, Finn A, Butler R (2019). TIPICO IX: report of the 9th interactive infectious disease workshop on infectious diseases and vaccines. Human Vaccines & Immunotherapeutics; 15:2405-2415. http://doi.org/10.1080/21645515.2019.1609823
    • Salas A, Pardo-Seco J, Cebey-López M, Gómez-Rial J, Pischedda S, Barral-Arca R, Justicia-Grande A, Rivero-Calle I, Vilar J, Martinón-Torres F (2019). Impact of rotavirus vaccination on childhood hospitalizations for seizures: Heterologous or unforeseen direct vaccine effects?. Vaccine; 37:3362-3368. http://doi.org/10.1016/j.vaccine.2019.04.086
    • Esperón-Moldes US, Pardo-Seco J, Montalván-Suárez M, Fachal L, Ginarte M, Rodríguez-Pazos L, Gómez-Carballa A, Moscoso F, Ugalde-Noritz N, Ordóñez-Ugalde A, Tettamanti-Miranda D, Ruiz JC, Salas A, Vega A (2019). Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population. Scientific Reports; 9. http://doi.org/10.1038/s41598-019-43133-6
    • Borghini L, Png E, Binder A, Wright VJ, Pinnock E, Hazelzet J, Emonts M, Schlapbach LJ, Anderson S, Secka F, Salas A, Fink C, Carrol ED, Pollard AJ, Coin LJ, Kuijpers TW, Martinon-Torres F, Zenz W, Levin M, Hibberd ML, Davila S, EUCLIDS consortium (2019). Identification of regulatory variants associated with genetic susceptibility to meningococcal disease. Scientific reports; 9:6966. http://doi.org/10.1038/s41598-019-43292-6
    • Gómez-Rial J, Sánchez-Batán S, Rivero-Calle I, Pardo-Seco J, Salas A, Martinón-Torres F (2019). Further considerations on rotavirus vaccination and seizure-related hospitalization rates. Infection and drug resistance; 12:989-991. http://doi.org/10.2147/IDR.S208756
    • Barral-Arca R, Pardo-Seco J, Bello X, Martinón-Torres F, Salas A (2019). Ancestry patterns inferred from massive RNA-seq data. RNA; 25:857-868. http://doi.org/10.1261/rna.070052.118
    • Salas A, Schönherr S, Bandelt H, Gómez-Carballa A, Weissensteiner H (2019). Extraordinary claims require extraordinary evidence in the case of asserted mtDNA biparental inheritance. http://doi.org/10.1101/585752
    • Salas A (2019). The natural selection that shapes our genomes. Forensic science international. Genetics; 39:57-60. http://doi.org/10.1016/j.fsigen.2018.12.003
    • González-Fortes G, Tassi F, Trucchi E, Henneberger K, Díez-Del-Molino D, Schroeder H, Barroso-Ruíz C, Barroso-Medina C, Grandal-d\'Anglade A, Salas A, Fabregas VR, Vaquero M, Alonso S, Lozano M, Fernández-Rodríguez C, Manica A, Hofreiter M, Barbujani G (2019). A western route of prehistoric human migration from Africa into the Iberian Peninsula. Proceedings. Biological sciences; 286:20182288. http://doi.org/10.1098/rspb.2018.2288
  •  2018
    • Vinner L, de Barros D, Chan J, Spence JP, Allentoft ME, Vimala T, Racimo F, Pinotti T, Rasmussen S, Margaryan A, Iraeta-Orbegozo M, Mylopotamitaki D, Wooller M, Bataille C, Becerra-Valdivia L, Chivall D, Comeskey D, Devièse T, Grayson DK, George L, Harry H, Alexandersen V, Primeau C, Erlandson J, Rodrigues-Carvalho C, Reis S, Cybulski J, Vullo C, Morello F, Vilar M, Wells S, Gregersen K, Hansen-Kasper L, Lynnerup N, Mirazón-Lahr M, Kjær K, Strauss A, Alfonso-Durruty M, Salas A, Schroeder H, Higham T, Malhi RS, Rasic JT, Souza L, Santos FR, Malaspinas A, Sikora M, Nielsen R, Song YS, Meltzer DJ, Willerslev E (2018). Early human dispersals within the Americas. Science; 362:eaav2621. http://doi.org/10.1126/science.aav2621
    • Gómez-Rial J, Sánchez BS, Rivero-Calle I, Pardo-Seco J, Martinón-Martínez J, Salas A, Martinón-Torres F (2018). Rotavirus infection beyond the gut. Infection and Drug Resistance; Volume 12:55-64. http://doi.org/10.2147/idr.s186404
    • Salas A, Catelli L, Pardo-Seco J, Gómez-Carballa A, Martinón-Torres F, Roberto-Barcena J, Vullo C (2018). Y-chromosome Peruvian origin of the 500-year-old Inca child mummy sacrificed in Cerro Aconcagua (Argentina). Science Bulletin; 63:1457-1459. http://doi.org/10.1016/j.scib.2018.08.009

    • Gómez-Carballa A, Pardo-Seco J, Brandini S, Achilli A, Perego UA, Coble MD, Diegoli TM, Álvarez-Iglesias V, Martinón-Torres F, Olivieri A, Torroni A, Salas A (2018). The peopling of South America and the trans-Andean gene flow of the first settlers. Genome research; 28:767-779. http://doi.org/10.1101/gr.234674.118
    • Martinón-Torres F, Salas A, Rivero-Calle I, Cebey-López M, Pardo-Seco J, Herberg JA, Boeddha NP, Klobassa DS, Secka F, Paulus S, Schlapbach LJ, Driessen GJ, Anderson ST, Emonts M, Zenz W, Carrol ED, Levin M, EUCLIDS Consortium (2018). Life-threatening infections in children in Europe (the EUCLIDS Project): a prospective cohort study. The Lancet. Child & adolescent health; 2:404-414. http://doi.org/10.1016/S2352-4642(18)30113-5
    • Barral-Arca R, Pardo-Seco J, Martinón-Torres F, Salas A (2018). A 2-transcript host cell signature distinguishes viral from bacterial diarrhea and it is influenced by the severity of symptoms. Scientific reports; 8:8043. http://doi.org/10.1038/s41598-018-26239-1
    • Salas A, Pardo-Seco J, Barral-Arca R, Cebey-López M, Gómez-Carballa A, Rivero-Calle I, Pischedda S, Currás-Tuala M, Amigo J, Gómez-Rial J, Martinón-Torres F, GENDRES Network (2018). Whole Exome Sequencing identifies new host genomic susceptibility factors in empyema caused by streptococcus pneumoniae in children: A pilot study. Genes; 9:240. http://doi.org/10.3390/genes9050240
    • Gómez-Rial J, Rivero-Calle I, Rodríguez-Tenreiro C, Redondo-Collazo L, Gómez-Carballa A, Pardo-Seco J, Salas A, Martinón-Torres F (2018). Rotavirus intestinal infection induces an oral mucosa cytokine response. PloS one; 13:e0195314. http://doi.org/10.1371/journal.pone.0195314
    • Schroeder H, Sikora M, Gopalakrishnan S, Cassidy LM, Maisano-Delser P, Sandoval-Velasco M, Schraiber JG, Rasmussen S, Homburger JR, Ávila-Arcos MC, Allentoft ME, Renaud G, Gómez-Carballa A, Laffoon JE, Carr RS, Schaffer WC, Day JS, Hoogland M, Salas A, Bustamante CD, Nielsen R, Bradley DG, Hofman CL, Willerslev E (2018). Origins and genetic legacies of the Caribbean Taino. Proceedings of the National Academy of Sciences of the United States of America; 115:2341-2346. http://doi.org/10.1073/pnas.1716839115

    • Toscanini U, Gaviria A, Pardo-Seco J, Gómez-Carballa A, Moscoso F, Vela M, Cobos S, Lupero A, Martinón-Torres F, Carabajo-Marcillo A, Yunga-León R, Ugalde-Noritz N, Ordoñez-Ugalde A, Salas A (2018). The geographic mosaic of Ecuadorian Y-chromosome ancestry. Forensic science international. Genetics; 33:59-65. http://doi.org/10.1016/j.fsigen.2017.11.011
    • Brandini S, Bergamaschi P, Cerna MF, Gandini F, Bastaroli F, Bertolini E, Cereda C, Ferretti L, Gómez-Carballa A, Battaglia V, Salas A, Semino O, Achilli A, Olivieri A, Torroni A (2018). The Paleo-Indian Entry into South America According to Mitogenomes. Molecular biology and evolution; 35:299-311. http://doi.org/10.1093/molbev/msx267

    • Jorge Amigo, Ramón Rama-Garda, Xabier Bello, Beatriz Sobrino, Jesús de Blas, María Martín-Ortega, Theodore C. Jessop, Ángel Carracedo, María Isabel García Loza, Eduardo Domínguez (2018). tagFinder: A Novel Tag Analysis Methodology That Enables Detection of Molecules from DNA-Encoded Chemical Libraries. SLAS DISCOVERY: Advancing the Science of Drug Discovery; 23(5):397-404. https://doi.org/10.1177/2472555217753840
  •  2017
    • Salas A, Pardo-Seco J, Cebey-López M, Gómez-Carballa A, Obando-Pacheco P, Rivero-Calle I, Currás-Tuala M, Amigo J, Gómez-Rial J, Martinón-Torres F, GENDRES network (2017). Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus Disease. Scientific reports; 7:15888. http://doi.org/10.1038/s41598-017-15752-4
    • Fortes-Lima C, Gessain A, Ruiz-Linares A, Bortolini M, Migot-Nabias F, Bellis G, Restrepo-Berta N, Rojas W, Avendaño-Tamayo E, Bedoya G, Orlando L, Salas A, Helgason A, Gilbert MT, Sikora M, Schroeder H, Dugoujon J (2017). Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname. American journal of human genetics; 101:725-736. http://doi.org/10.1016/j.ajhg.2017.09.021
    • Pischedda S, Barral-Arca R, Gómez-Carballa A, Pardo-Seco J, Álvarez-Iglesias V, Martinón-Torres F, Vullo C, Salas A (2017). Phylogeographic and genome-wide investigations of Vietnam ethnic groups reveal signatures of complex historical demographic movements. Scientific reports; 7:12630. http://doi.org/10.1038/s41598-017-12813-6
    • Aung T, Ozaki M, Lee-Mei C, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, Haripriya A, Williams SE, Astakhov YS, Orr AC, Burdon KP, Nakano S, Mori K, Abu-Amero K, Hauser M, Li Z, Prakadeeswari G, Cherecheanu-Alina P, Kang JH, Nelson S, Hayashi K, Manabe S, Kazama S, Zarnowski T, Inoue K, Irkec M, Coca-Prados M, Sugiyama K, Järvelä I, Schlottmann P, Lamari H, Nilgün Y, Bikbov M, Cha-Soon C, Yamashiro K, Zenteno JC, Jonas JB, Kumar RS, Perera SA, Kobakhidze N, George R, Vijaya L, Do T, Edward DP, de Juan M, Pakravan M, Moghimi S, Ideta R, Bach-Holm D, Kappelgaard P, Wirostko B, Thomas S, Gaston D, Bedard K, Greer WL, Yang Z, Chen X, Huang L, Sang J, Jia H, Jia L, Qiao C, Zhang H, Liu X, Zhao B, Wang Y, Xu L, Leruez S, Reynier P, Chichua G, Tabagari S, Uebe S, Zenkel M, Berner D, Mossböck G, Weisschuh N, Hoja U, Welge-Luessen U, Mardin C, Founti P, Chatzikyriakidou A, Pappas T, Anastasopoulos E, Lambropoulos A, Ghosh A, Shetty R, Porporato N, Saravanan V, Venkatesh R, Shivkumar C, Kalpana N, Sarangapani S, Kanavi MR, Beni-Afsaneh N, Yazdani S, Lashay A, Naderifar H, Khatibi N, Fea A, Lavia C, Dallorto L, Rolle T, Frezzotti P, Paoli D, Salvi E, Manunta P, Mori Y, Miyata K, Higashide T, Chihara E, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Aihara M, Inatani M, Miyake M, Gotoh N, Matsuda F, Yoshimura N, Ikeda Y, Ueno M, Sotozono C, Jeoung-Jin W, Sagong M, Park-Kyu H, Ahn J, Cruz-Aguilar M, Ezzouhairi SM, Rafei A, Chong-Yaan F, Ng-Xiao Y, Goh-Shuang R, Chen Y, Khan-Muhammad I, Olawoye OO, Ashaye AO, Ugbede I, Onakoya A, Kizor-Akaraiwe N, Teekhasaenee C, Suwan Y, Supakontanasan W, Okeke S, Uche NJ, Asimadu I, Ayub H, Akhtar F, Kosior-Jarecka E, Lukasik U, Lischinsky I, Castro V, Grossmann-Rodolfo P, Sunaric-Megevand G, Roy S, Dervan E, Silke E, Rao A, Sahay P, Fornero P, Cuello O, Sivori D, Zompa T, Mills RA, Souzeau E, Mitchell P, Wang-Jie J, Hewitt AW, Coote M, Crowston JG, Astakhov SY, Akopov EL, Emelyanov A, Vysochinskaya V, Kazakbaeva G, Fayzrakhmanov R, Al-Obeidan SA, Owaidhah O, Aljasim-Leyla A, Chowbay B, Foo-Jia N, Soh RQ, Sim-Kar S, Xie Z, Mok-Shi Q, Soo-Hui M, Chen-Xiao Y, Heng-Khai K, Husain R, Ho S, Hillmer AM, Cheng C, Escudero-Domínguez FA, González-Sarmiento R, Martinon-Torres F, Salas A, Pathanapitoon K, Hansapinyo L, Wanichwecharugruang B, Kitnarong N, Sakuntabhai A, Nguyn HX, Nguyn TV, Zenz W, Binder A, Klobassa DS, Hibberd ML, Davila S, Herms S, Nöthen MM, Moebus S, Rautenbach RM, Ziskind A, Carmichael TR, Ramsay M, Álvarez L, García M, González-Iglesias H, Rodríguez-Calvo PP, Fernández-Vega-Cueto L, Oguz C, Tamcelik N, Atalay E, Batu B, Aktas D, Kasım B, Coleman AL, Liu Y, Challa P, Herndon L, Kuchtey RW, Kuchtey J, Curtin K, Chaya CJ, Crandall A, Zangwill LM, Wong-Tien Y, Nakano M, Kinoshita S, den HA, Vesti E, Fingert JH, Lee RK, Sit AJ, Shingleton BJ, Wang N, Cusi D, Qamar R, Kraft P, Pericak-Vance MA, Raychaudhuri S, Heegaard S, Kivelä T, Reis A, Kruse FE, Weinreb RN, Pasquale LR, Haines JL, Thorsteinsdottir U, Jonasson F, Milea D, Ritch R, Kubota T, Tashiro K, Vithana EN, Micheal S, Topouzis F, Craig JE, Dubina M, Sundaresan P, Stefansson K, Wiggs JL, Pasutto F, Khor-Chiea C (2017). Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature genetics; 49:993-1004. http://doi.org/10.1038/ng.3875
    • Gómez-Rial J, Talavero-González C, Rodríguez-Tenreiro C, Vilanova-Trillo L, Gómez-Carballa A, Rivero-Calle I, Justicia-Grande A, Pardo-Seco J, Redondo-Collazo L, Salas A, Martinón-Torres F (2017). Salivary epidermal growth factor correlates with hospitalization length in rotavirus infection. BMC infectious diseases; 17:370. http://doi.org/10.1186/s12879-017-2463-0
    • Heinz T, Pala M, Gómez-Carballa A, Richards MB, Salas A (2017). Updating the African human mitochondrial DNA tree: Relevance to forensic and population genetics. Forensic science international. Genetics; 27:156-159. http://doi.org/10.1016/j.fsigen.2016.12.016
  •  2016
    • Salas A, Martinón-Torres F, Gómez-Carballa A (2016). ‘Infertile’ studies on mitochondrial DNA variation in asthenozoospermic Tunisian men. Biochemistry and Biophysics Reports; 8:114-119. http://doi.org/10.1016/j.bbrep.2016.08.002
    • Pardo-Seco J, Llull C, Berardi G, Gómez A, Andreatta F, Martinón-Torres F, Toscanini U, Salas A (2016). Genomic continuity of Argentinean Mennonites. Scientific reports; 6:36392. http://doi.org/10.1038/srep36392
    • Martinón-Torres F, Png E, Khor-Chiea C, Davila S, Wright VJ, Sim-Kar S, Vega A, Fachal L, Inwald D, Nadel S, Carrol ED, Martinón-Torres N, Alonso-Sonia M, Carracedo A, Morteruel E, López-Bayón J, Torre-Andrés C, Monge-Cristina C, de Aguilar P, Torné-Elisabeth E, Martínez-Padilla MC, Levin M, Hibberd ML, Salas A, ESIGEM network, ESPID meningococcal consortium – UK, EUCLIDS consortium members - Imperial College London (www.euclids-project.eu) (2016). Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies. Scientific reports; 6:35842. http://doi.org/10.1038/srep35842
    • Salas A, Marco-Puche G, Triviño JC, Gómez-Carballa A, Cebey-López M, Rivero-Calle I, Vilanova-Trillo L, Rodríguez-Tenreiro C, Gómez-Rial J, Martinón-Torres F (2016). Strong down-regulation of glycophorin genes: A host defense mechanism against rotavirus infection. Infection, genetics and evolution; 44:403-411. http://doi.org/10.1016/j.meegid.2016.07.044
    • Herberg JA, Kaforou M, Wright VJ, Shailes H, Eleftherohorinou H, Hoggart CJ, Cebey-López M, Carter MJ, Janes VA, Gormley S, Shimizu C, Tremoulet AH, Barendregt AM, Salas A, Kanegaye J, Pollard AJ, Faust SN, Patel S, Kuijpers T, Martinón-Torres F, Burns JC, Coin LJ, Levin M, for the IRIS Consortium (2016). Diagnostic test accuracy of a 2-transcript host RNA signature for discriminating bacterial vs viral infection in febrile children. JAMA; 316:835. http://doi.org/10.1001/jama.2016.11236

    • Barral-Arca R, Pischedda S, Gómez-Carballa A, Pastoriza A, Mosquera-Miguel A, López-Soto M, Martinón-Torres F, Álvarez-Iglesias V, Salas A (2016). Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula. PloS one; 11:e0159735. http://doi.org/10.1371/journal.pone.0159735
    • Weissensteiner H, Pacher D, Kloss-Brandstätter A, Forer L, Specht G, Bandelt H, Kronenberg F, Salas A, Schönherr S (2016). HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing. Nucleic acids research; 44:W58-63. http://doi.org/10.1093/nar/gkw233

    • Justicia-Grande AJ, Pardo-Seco J, Cebey-López M, Vilanova-Trillo L, Gómez-Carballa A, Rivero-Calle I, Puente-Puig M, Curros-Novo C, Gómez-Rial J, Salas A, Redondo-Collazo L, Rodríguez-Tenreiro C, Martinón-Torres F, Respiratory Syncytial Virus network (ReSVinet) (2016). Development and Validation of a New Clinical Scale for Infants with Acute Respiratory Infection: The ReSVinet Scale. PloS one; 11:e0157665. http://doi.org/10.1371/journal.pone.0157665
    • Toscanini U, Brisighelli F, Llull C, Berardi G, Gómez A, Andreatta F, Pardo-Seco J, Gómez-Carballa A, Martinón-Torres F, Álvarez-Iglesias V, Salas A (2016). Charting the Y-chromosome ancestry of present-day Argentinean Mennonites. Journal of human genetics; 61:507-13. http://doi.org/10.1038/jhg.2016.3
    • Mauricio Esguerra, Alexey Siretskiy, Xabier Bello, Jessica Sallander, Hugo Gutiérrez-de-Terán (2016). GPCR-ModSim: A comprehensive web based solution for modeling G-protein coupled receptors. Nucleic Acids Research; 44(1):455–462. https://doi.org/10.1093/nar/gkw403
    • Cebey-López M, Herberg J, Pardo-Seco J, Gómez-Carballa A, Martinón-Torres N, Salas A, Justicia A, Rivero-Calle I, Sumner E, Fink C, Martinón-Torres F, GENDRES network (2016). Does Viral Co-Infection Influence the Severity of Acute Respiratory Infection in Children?. PloS one; 11:e0152481. http://doi.org/10.1371/journal.pone.0152481
    • Pardo-Seco J, Heinz T, Taboada-Echalar P, Martinón-Torres F, Salas A (2016). Mapping the genomic mosaic of two 'Afro-Bolivians' from the isolated Yungas valleys. BMC Genomics; 17:207. http://doi.org/10.1186/s12864-016-2520-x
    • Antonio Figueras, Diego Robledo, André Corvelo, Miguel Hermida, Patricia Pereiro, Juan A Rubiolo, Jéssica Gómez-Garrido, Laia Carreté, Xabier Bello, Marta Gut, Ivo Glynne-Gut, Marina Marcet-Houben, Gabriel Forn-Cuní, Beatriz Galán, José Luis García, José Luis Abal-Fabeiro, Belen G. Pardo, Xoana Taboada, Carlos Fernández, Anna Vlasova, Antonio Hermoso-Pulido, Roderic Guigó, José Antonio Álvarez-Dios, Antonio Gómez-Tato, Ana Viñas, Xulio Maside, Toni Gabaldón, Beatriz Novoa, Carmen Bouza, Tyler Alioto, Paulino Martínez (2016). Whole genome sequencing of turbot (Scophthalmus maximus; Pleuronectiformes): a fish adapted to demersal life. DNA research; 23(3):181–192. https://doi.org/10.1093/dnares/dsw007
    • Cebey-López M, Pardo-Seco J, Gómez-Carballa A, Martinón-Torres N, Rivero-Calle I, Justicia A, Redondo L, Martínez-Padilla MC, Giménez-Sánchez F, Salas A, Martinón-Torres F, GENDRES Network (2016). Role of Vitamin D in Hospitalized Children With Lower Tract Acute Respiratory Infections. Journal of pediatric gastroenterology and nutrition; 62:479-85. http://doi.org/10.1097/MPG.0000000000001003
    • Toscanini U, Brisighelli F, Moreno F, Pantoja-Astudillo JA, Morales-Eugenia A, Bustos P, Pardo-Seco J, Salas A (2016). Analysis of Y-chromosome STRs in Chile confirms an extensive introgression of European male lineages in urban populations. Forensic science international. Genetics; 21:76-80. http://doi.org/10.1016/j.fsigen.2015.12.005
    • Coia V, Cipollini G, Anagnostou P, Maixner F, Battaggia C, Brisighelli F, Gómez-Carballa A, Destro BG, Salas A, Zink A (2016). Whole mitochondrial DNA sequencing in Alpine populations and the genetic history of the Neolithic Tyrolean Iceman. Scientific reports; 6:18932. http://doi.org/10.1038/srep18932

    • Gómez-Carballa A, Moreno F, Álvarez-Iglesias V, Martinón-Torres F, García-Magariños M, Pantoja-Astudillo JA, Aguirre-Morales E, Bustos P, Salas A (2016). Revealing latitudinal patterns of mitochondrial DNA diversity in Chileans. Forensic science international. Genetics; 20:81-88. http://doi.org/10.1016/j.fsigen.2015.10.002
    • Martinez-Cadenas C, Blanco-Verea A, Hernando B, Brion M, Carracedo A, Salas A, Capelli C (2016). The relationship between surname frequency and Y chromosome variation in Spain. European journal of human genetics : EJHG; 24:120-8. http://doi.org/10.1038/ejhg.2015.75

    • Toscanini U, Vullo C, Berardi G, Llull C, Borosky A, Gómez A, Pardo-Seco J, Salas A (2016). A comprehensive Y-STR portrait of Argentinean populations. Forensic science international. Genetics; 20:1-5. http://doi.org/10.1016/j.fsigen.2015.09.002
  •  2015
    • Manuel Vera, Xabier Bello, Jose-Antonio Álvarez-Dios, Belen G. Pardo, Laura Sánchez, Jens Carlsson, Jeanette E.L. Carlsson, Carolina Bartolomé, Xulio Maside, Paulino Martínez (2015). Screening of repetitive motifs inside the genome of the flat oyster (Ostrea edulis): Transposable elements and short tandem repeats. Marine Genomics; 24(1):335-341. https://doi.org/10.1016/j.margen.2015.08.006
    • Gómez-Carballa A, Catelli L, Pardo-Seco J, Martinón-Torres F, Roewer L, Vullo C, Salas A (2015). The complete mitogenome of a 500-year-old Inca child mummy. Scientific reports; 5:16462. http://doi.org/10.1038/srep16462
    • García-Magariños M, Egeland T, López-de-Ullibarri I, Hjort NL, Salas A (2015). A parametric approach to kinship hypothesis testing using identity-by-descent parameters. Statistical applications in genetics and molecular biology; 14:465-79. http://doi.org/10.1515/sagmb-2014-0080
    • Toscanini U, Moreno F, Pantoja-Astudillo JA, Morales-Eugenia A, Bustos P, Salas A (2015). A reference frequency database of 15 autosomal STRs in Chile. Forensic science international. Genetics; 19:35-36. http://doi.org/10.1016/j.fsigen.2015.05.016
    • Cebey-López M, Herberg J, Pardo-Seco J, Gómez-Carballa A, Martinón-Torres N, Salas A, Gormley S, Sumner E, Fink C, Martinón-Torres F, GENDRES network (2015). Viral Co-Infections in Pediatric Patients Hospitalized with Lower Tract Acute Respiratory Infections. PloS one; 10:e0136526. http://doi.org/10.1371/journal.pone.0136526
    • Gomes V, Pala M, Salas A, Álvarez-Iglesias V, Amorim A, Gómez-Carballa A, Carracedo A, Clarke DJ, Hill C, Mormina M, Shaw M, Dunne DW, Pereira R, Pereira V, Prata-Maria J, Sánchez-Diz P, Rito T, Soares P, Gusmão L, Richards MB (2015). Mosaic maternal ancestry in the Great Lakes region of East Africa. Human genetics; 134:1013-27. http://doi.org/10.1007/s00439-015-1583-0
    • Heinz T, Cárdenas JM, Álvarez-Iglesias V, Pardo-Seco J, Gómez-Carballa A, Santos C, Taboada-Echalar P, Martinón-Torres F, Salas A (2015). The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. PloS one; 10:e0134129. http://doi.org/10.1371/journal.pone.0134129
    • Pardo-Seco J, Cebey-López M, Martinón-Torres N, Salas A, Gómez-Rial J, Rodriguez-Tenreiro C, Martinón-Torres F (2015). Impact of Rotavirus Vaccination on Childhood Hospitalization for Seizures. The Pediatric infectious disease journal; 34:769-73. http://doi.org/10.1097/INF.0000000000000723
    • Salas A, Elson JL (2015). Mitochondrial DNA as a risk factor for false positives in case-control association studies. Journal of Genetics and Genomics; 42:169-72. http://doi.org/10.1016/j.jgg.2015.03.002
    • Tomás Gómez-Moracho, Carolina Bartolomé, Xabier Bello, R. Martín-Hernández, M. Higes, Xulio Maside (2015). Recent worldwide expansion of Nosema ceranae (Microsporidia) in Apis mellifera populations inferred from multilocus patterns of genetic variation. Infection, Genetics and Evolution; 31(1):87-94. https://doi.org/10.1016/j.meegid.2015.01.002
    • Schroeder H, Ávila-Arcos MC, Malaspinas A, Sandoval-Velasco M, Carpenter ML, Moreno-Mayar JV, Sikora M, Allentoft-Morten E, Samaniego JA, Haviser JB, Dee MW, Stafford TW, Salas A, Orlando L, Willerslev E, Bustamante CD, Gilbert MT (2015). Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean. Proceedings of the National Academy of Sciences of the United States of America; 112:3669-73. http://doi.org/10.1073/pnas.1421784112

    • Gómez-Carballa A, Pardo-Seco J, Amigo J, Martinón-Torres F, Salas A (2015). Mitogenomes from The 1000 Genome Project reveal new Near Eastern features in present-day Tuscans. PloS one; 10:e0119242. http://doi.org/10.1371/journal.pone.0119242
    • Söchtig J, Álvarez-Iglesias V, Mosquera-Miguel A, Gelabert-Besada M, Gómez-Carballa A, Salas A (2015). Genomic insights on the ethno-history of the Maya and the \'Ladinos\' from Guatemala. BMC genomics; 16:131. http://doi.org/10.1186/s12864-015-1339-1
    • Cárdenas JM, Heinz T, Pardo-Seco J, Álvarez-Iglesias V, Taboada-Echalar P, Sánchez-Diz P, Carracedo A, Salas A (2015). The multiethnic ancestry of Bolivians as revealed by the analysis of Y-chromosome markers. Forensic science international. Genetics; 14:210-8. http://doi.org/10.1016/j.fsigen.2014.10.023
    • Fachal L, Mosquera-Miguel A, Pastor P, Ortega-Cubero S, Lorenzo E, Oterino-Durán A, Toriello M, Quintáns B, Camiña-Tato M, Sesar A, Vega A, Sobrido M, Salas A (2015). No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics; 168B:54-65. http://doi.org/10.1002/ajmg.b.32276
  •  2014
    • Parson W, Gusmão L, Morling N, Pokorak E, Prinz M, Salas A, DNA Commission of the International Society for Forensic Genetics (2014). DNA Commission of the International Society for Forensic Genetics: revised and extended guidelines for mitochondrial DNA typing. Forensic science international. Genetics; 13:134-42. http://doi.org/10.1016/j.fsigen.2014.07.010
    • Torrell H, Salas A, Abasolo N, Morén C, Garrabou G, Valero J, Alonso Y, Vilella E, Costas J, Martorell L (2014). Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics; 165B:607-17. http://doi.org/10.1002/ajmg.b.32264
    • Lazaridis I, Patterson N, Mittnik A, Renaud G, Mallick S, Kirsanow K, Sudmant PH, Schraiber JG, Castellano S, Lipson M, Berger B, Economou C, Bollongino R, Fu Q, Bos KI, Nordenfelt S, Li H, Prüfer K, Sawyer S, Posth C, Haak W, Hallgren F, Fornander E, Rohland N, Delsate D, Francken M, Guinet J, Wahl J, Ayodo G, Babiker HA, Bailliet G, Balanovska E, Balanovsky O, Barrantes R, Bedoya G, Ben-Ami H, Bene J, Berrada F, Bravi CM, Brisighelli F, Cali F, Churnosov M, Corach D, Damba L, Dryomov S, Dugoujon J, Fedorova SA, Gallego-Romero I, Gubina M, Hammer M, Henn BM, Hervig T, Hodoglugil U, Jha AR, Karachanak-Yankova S, Khusainova R, Khusnutdinova E, Kittles R, Kivisild T, Klitz W, Kučinskas V, Kushniarevich A, Laredj L, Litvinov S, Loukidis T, Mahley RW, Melegh B, Metspalu E, Molina J, Mountain J, Näkkäläjärvi K, Nesheva D, Nyambo T, Osipova L, Parik J, Platonov F, Posukh O, Romano V, Rothhammer F, Rudan I, Ruizbakiev R, Sahakyan H, Sajantila A, Salas A, Starikovskaya EB, Tarekegn A, Toncheva D, Turdikulova S, Uktveryte I, Utevska O, Vasquez R, Villena M, Voevoda M, Winkler CA, Yepiskoposyan L, Zalloua P, Zemunik T, Cooper A, Capelli C, Thomas MG, Ruiz-Linares A, Tishkoff SA, Singh L, Thangaraj K, Villems R, Comas D, Sukernik R, Metspalu M, Meyer M, Eichler EE, Burger J, Slatkin M, Pääbo S, Kelso J, Reich D, Krause J (2014). Ancient human genomes suggest three ancestral populations for present-day Europeans. Nature; 513:409-13. http://doi.org/10.1038/nature13673
    • Pardo-Seco J, Gómez-Carballa A, Amigo J, Martinón-Torres F, Salas A (2014). A genome-wide study of modern-day Tuscans: revisiting Herodotus's theory on the origin of the Etruscans. PloS one; 9:e105920. http://doi.org/10.1371/journal.pone.0105920
    • Salas A, García-Magariños M, Logan I, Bandelt H (2014). The saga of the many studies wrongly associating mitochondrial DNA with breast cancer. BMC Cancer; 14. http://doi.org/10.1186/1471-2407-14-659
    • Horacio Naveira, Xabier Bello, José Luis Abal-Fabeiro, Xulio Maside (2014). Evidence for the persistence of an active endogenous retrovirus (ERVE) in humans. Genetica; 142(5):451–460. https://doi.org/10.1007/s10709-014-9789-y
    • Purps J, Siegert S, Willuweit S, Nagy M, Alves C, Salazar R, Santos LH, Anslinger K, Bayer B, Ayub Q, Wei W, Xue Y, Tyler-Smith C, Bafalluy-Miriam B, Martínez-Jarreta B, Egyed B, Balitzki B, Tschumi S, Ballard D, Court-Denise S, Barrantes X, Bäßler G, Wiest T, Berger B, Niederstätter H, Parson W, Davis C, Budowle B, Burri H, Borer U, Koller C, Carvalho EF, Domingues PM, Chamoun-Wafaa T, Coble MD, Hill CR, Corach D, Caputo M, D\'Amato ME, Davison S, Decorte R, Ottoni C, Rickards O, Lu D, Jiang C, Dobosz T, Jonkisz A, Frank WE, Furac I, Gehrig C, Castella V, Grskovic B, Haas C, Wobst J, Hadzic G, Drobnic K, Honda K, Hou Y, Zhou D, Li Y, Hu S, Chen S, Immel U, Lessig R, Jakovski Z, Ilievska T, Klann AE, García-Cristina C, Kraaijenbrink T, Kondili A, Miniati P, Vouropoulou M, Kovacevic L, Marjanovic D, Lindner I, Mansour I, Al-Azem M, Andari-Ansar E, Marino M, Furfuro S, Locarno L, Martín P, Luque GM, Alonso A, Miranda-Luís S, Moreira H, Mizuno N, Iwashima Y, Silva R, Nastainczyk-Wulf M, Edelmann J, Kohl M, Nie S, Wang X, Cheng B, Núñez C, Pancorbo-Marian M, Olofsson JK, Morling N, Onofri V, Tagliabracci A, Pamjav H, Volgyi A, Barany G, Pawlowski R, Maciejewska A, Pelotti S, Pepinski W, Abreu-Glowacka M, Phillips C, Cárdenas J, Rey-Gonzalez D, Salas A, Brisighelli F, Capelli C, Toscanini U, Piccinini A, Piglionica M, Baldassarra SL, Ploski R, Konarzewska M, Jastrzebska E, Robino C, Sajantila A, Palo JU, Guevara E, Salvador J, Ungria-Maria C, Rodriguez-Jae J, Schmidt U, Schlauderer N, Saukko P, Schneider PM, Sirker M, Shin K, Skitsa I, Ampati A, Smith T, Calvit-Lina S, Stenzl V, Capal T, Tillmar A, Nilsson H, Turrina S, Verzeletti A, Cortellini V, Wetton JH, Gwynne GM, Jobling MA, Whittle MR, Sumita DR, Wolańska-Nowak P, Krawczak M, Nothnagel M, Roewer L (2014). A global analysis of Y-chromosomal haplotype diversity for 23 STR loci. Forensic science international. Genetics; 12:12-23. http://doi.org/10.1016/j.fsigen.2014.04.008
    • Marcheco-Teruel B, Parra EJ, Fuentes-Smith E, Salas A, Buttenschøn HN, Demontis D, Torres-Español M, Marín-Padrón LC, Gómez-Cabezas EJ, Alvarez-Iglesias V, Mosquera-Miguel A, Martínez-Fuentes A, Carracedo A, Børglum AD, Mors O (2014). Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers. PLoS genetics; 10:e1004488. http://doi.org/10.1371/journal.pgen.1004488
    • Pardo-Seco J, Martinón-Torres F, Salas A (2014). Evaluating the accuracy of AIM panels at quantifying genome ancestry. BMC genomics; 15:543. http://doi.org/10.1186/1471-2164-15-543
    • Fachal L, Gómez-Caamaño A, Álvarez-Iglesias V, Gómez-Carballa A, Calvo P, Salas A, Vega A (2014). No association between typical European mitochondrial variation and prostate cancer risk in a Spanish cohort. Journal of Human Genetics; 59:411-414. http://doi.org/10.1038/jhg.2014.46
    • Fachal L, Mosquera-Miguel A, Gómez-Caamaño A, Sánchez-García M, Calvo P, Lobato-Busto R, Salas A, Vega A (2014). Evaluating the role of mitochondrial DNA variation to the genetic predisposition to radiation-induced toxicity. Radiotherapy and Oncology; 111:199-205. http://doi.org/10.1016/j.radonc.2014.03.012
    • José Luis Abal-Fabeiro, Xulio Maside, José Llovo, Xabier Bello, María Torres, M. Treviño, L. Moldes, A. Muñoz, Ángel Carracedo, Carolina Bartolomé (2014). High-throughput genotyping assay for the large-scale genetic characterization of Cryptosporidium parasites from human and bovine samples. Parasitology; 141(4):491-500. https://doi.org/10.1017/S0031182013001807
  •  2013
    • Gómez-Carballa A, Pardo-Seco J, Fachal L, Vega A, Cebey M, Martinón-Torres N, Martinón-Torres F, Salas A (2013). Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. PloS one; 8:e75397. http://doi.org/10.1371/journal.pone.0075397
    • Pardo-Seco J, Amigo J, González-Manteiga W, Salas A (2013). A Generalized Model to Estimate the Statistical Power in Mitochondrial Disease Studies Involving 2×k Tables. PLoS ONE; 8:e73567. http://doi.org/10.1371/journal.pone.0073567
    • Newman SP, Deason ML, Pitsiladis YP, Salas A, Macaulay VA (2013). The West African Ethnicity of the Enslaved in Jamaica. Slavery & Abolition; 34:376-400. http://doi.org/10.1080/0144039x.2012.734054
    • Heinz T, Alvarez-Iglesias V, Pardo-Seco J, Taboada-Echalar P, Gómez-Carballa A, Torres-Balanza A, Rocabado O, Carracedo A, Vullo C, Salas A (2013). Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians. Forensic science international. Genetics; 7:537-42. http://doi.org/10.1016/j.fsigen.2013.05.012
    • José Luis Abal-Fabeiro, Xulio Maside, Xabier Bello, José Llovo, Carolina Bartolomé (2013). Multilocus patterns of genetic variation across Cryptosporidium species suggest balancing selection at the gp60 locus. Molecular Ecology; 22(18):4723-4732. https://doi.org/doi:10.1111/mec.12425
    • Mar Marzo, Xabier Bello, Marta Puig, Xulio Maside, Alfredo Ruiz (2013). Striking structural dynamism and nucleotide sequence variation of the transposon Galileo in the genome of Drosophila mojavensis. Mobile DNA; 4(1). https://doi.org/10.1186/1759-8753-4-6
    • Hugo Gutiérrez-de-Terán, Xabier Bello, David Rodríguez (2013). Characterization of the dynamic events of GPCRs by automated computational simulations. Biochemical Society Transactions; 41(1):205–212. https://doi.org/10.1042/BST20120287
    • Taboada-Echalar P, Alvarez-Iglesias V, Heinz T, Vidal-Bralo L, Gómez-Carballa A, Catelli L, Pardo-Seco J, Pastoriza A, Carracedo A, Torres-Balanza A, Rocabado O, Vullo C, Salas A (2013). The genetic legacy of the pre-colonial period in contemporary Bolivians. PloS one; 8:e58980. http://doi.org/10.1371/journal.pone.0058980
  •  2012
    • Brisighelli F, Blanco-Verea A, Boschi I, Garagnani P, Carracedo A, Capelli C, Salas A (2012). Patterns of Y-STR variation in Italy. Forensic science international. Genetics; 6:834-9. http://doi.org/10.1016/j.fsigen.2012.03.003
    • Salas A, Coble M, Desmyter S, Grzybowski T, Gusmão L, Hohoff C, Holland MM, Irwin JA, Kupiec T, Lee H, Ludes B, Lutz-Bonengel S, Melton T, Parsons TJ, Pfeiffer H, Prieto L, Tagliabracci A, Parson W (2012). A cautionary note on switching mitochondrial DNA reference sequences in forensic genetics. Forensic science international. Genetics; 6:e182-4. http://doi.org/10.1016/j.fsigen.2012.06.015
    • Bandelt H, Salas A (2012). Haplogrouping mitochondrial DNA sequences in Legal Medicine/Forensic Genetics. International journal of legal medicine; 126:901-16. http://doi.org/10.1007/s00414-012-0762-y
    • Reich D, Patterson N, Campbell D, Tandon A, Mazieres S, Ray N, Parra MV, Rojas W, Duque C, Mesa N, García LF, Triana O, Blair S, Maestre A, Dib JC, Bravi CM, Bailliet G, Corach D, Hünemeier T, Bortolini MC, Salzano FM, Petzl-Erler ML, Acuña-Alonzo V, Aguilar-Salinas C, Canizales-Quinteros S, Tusié-Luna T, Riba L, Rodríguez-Cruz M, Lopez-Alarcón M, Coral-Vazquez R, Canto-Cetina T, Silva-Zolezzi I, Fernandez-Lopez JC, Contreras AV, Jimenez-Sanchez G, Gómez-Vázquez MJ, Molina J, Carracedo A, Salas A, Gallo C, Poletti G, Witonsky DB, Alkorta-Aranburu G, Sukernik RI, Osipova L, Fedorova SA, Vasquez R, Villena M, Moreau C, Barrantes R, Pauls D, Excoffier L, Bedoya G, Rothhammer F, Dugoujon J, Larrouy G, Klitz W, Labuda D, Kidd J, Kidd K, Freimer NB, Price AL, Ruiz-Linares A (2012). Reconstructing Native American population history. Nature; 488:370-4. http://doi.org/10.1038/nature11258
    • Silbiger VN, Hirata MH, Luchessi AD, Genvigir-Fabiana D, Cerda A, Rodrigues AC, Willrich-Maria A, Arazi SS, Dorea EL, Bernik-Marcia M, Faludi AA, Bertolami MC, Santos C, Carracedo A, Salas A, Freire A, Lareu MV, Phillips C, Porras-Hurtado L, Fondevila M, Hirata-Rosario D (2012). Differentiation of African Components of Ancestry to Stratify Groups in a Case–Control Study of a Brazilian Urban Population. Genetic Testing and Molecular Biomarkers; 16:524-530. http://doi.org/10.1089/gtmb.2011.0267
    • Phillips C, García-Magariños M, Salas A, Carracedo A, Lareu MV (2012). SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?. Transfusion Medicine and Hemotherapy; 39:202-210. http://doi.org/10.1159/000338857
    • Lareu M, García-Magariños M, Phillips C, Quintela I, Carracedo A, Salas A (2012). Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data. Forensic Science International: Genetics; 6:350-353. http://doi.org/10.1016/j.fsigen.2011.07.011
    • Bodner M, Perego UA, Huber G, Fendt L, Röck AW, Zimmermann B, Olivieri A, Gómez-Carballa A, Lancioni H, Angerhofer N, Bobillo MC, Corach D, Woodward SR, Salas A, Achilli A, Torroni A, Bandelt H, Parson W (2012). Rapid coastal spread of First Americans: novel insights from South America's Southern Cone mitochondrial genomes. Genome research; 22:811-20. http://doi.org/10.1101/gr.131722.111
    • Cerezo M, Achilli A, Olivieri A, Perego UA, Gómez-Carballa A, Brisighelli F, Lancioni H, Woodward SR, López-Soto M, Carracedo A, Capelli C, Torroni A, Salas A (2012). Reconstructing ancient mitochondrial DNA links between Africa and Europe. Genome research; 22:821-6. http://doi.org/10.1101/gr.134452.111

    • Mosquera-Miguel A, Torrell H, Abasolo N, Arrojo M, Paz E, Ramos-Ríos R, Agra S, Páramo M, Brenlla J, Martínez S, Vilella E, Valero J, Gutiérrez-Zotes A, Martorell L, Costas J, Salas A (2012). No evidence that major mtDNA European haplogroups confer risk to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics; 159B:414-421. http://doi.org/10.1002/ajmg.b.32044
    • Deason ML, Salas A, Newman SP, Macaulay VA, St AM, Pitsiladis YP (2012). Interdisciplinary approach to the demography of Jamaica. BMC evolutionary biology; 12:24. http://doi.org/10.1186/1471-2148-12-24
    • David Rodríguez, Xabier Bello, Hugo Gutiérrez-de-Terán (2012). Molecular Modelling of G Protein-Coupled Receptors Through the Web. Molecular Informatics; 31(5):334-341. https://doi.org/doi:10.1002/minf.201100162
    • Marta Iglesias-Rey, Manuel Barreiro-de Acosta, Francisco Caamaño-Isorna, Isabel Vázquez-Rodríguez, Aurelio Lorenzo-González, Xabier Bello, J Enrique Domínguez-Muñoz (2012). Influence of alexithymia on health-related quality of life in inflammatory bowel disease: Are there any related factors?. Scandinavian Journal of Gastroenterology; 47(4):445-453. https://doi.org/10.3109/00365521.2012.654403
    • Amigo J, Salas A, Costas J (2012). GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications. Journal of Proteomics & Bioinformatics; 05. http://doi.org/10.4172/jpb.1000206
    • Bandelt H, Salas A (2012). Current Next Generation Sequencing technology may not meet forensic standards. Forensic Science International: Genetics; 6:143-145. http://doi.org/10.1016/j.fsigen.2011.04.004
    • Brisighelli F, Álvarez-Iglesias V, Fondevila M, Blanco-Verea A, Carracedo A, Pascali VL, Capelli C, Salas A (2012). Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage. PloS one; 7:e50794. http://doi.org/10.1371/journal.pone.0050794
    • Gandini F, Perego UA, Bodner M, Gómez-Carballa A, Corach D, Angerhofer N, Woodward SR, Semino O, Salas A, Parson W, Moraga M, Achilli A, Torroni A, Olivieri A (2012). Arrival of Paleo-Indians to the southern cone of South America: new clues from mitogenomes. PloS one; 7:e51311. http://doi.org/10.1371/journal.pone.0051311
    • Fachal L, Rodríguez-Pazos L, Ginarte M, Toribio J, Salas A, Vega A (2012). Multiple local and recent founder effects of TGM1 in Spanish families. PloS one; 7:e33580. http://doi.org/10.1371/journal.pone.0033580
    • Galanter-Joshua M, Fernandez-Lopez JC, Gignoux CR, Barnholtz-Sloan J, Fernandez-Rozadilla C, Via M, Hidalgo-Miranda A, Contreras AV, Figueroa-Laura U, Raska P, Jimenez-Sanchez G, Zolezzi-Irma S, Torres M, Ruiz-Ponte C, Ruiz Y, Salas A, Nguyen E, Eng C, Borjas L, Zabala W, Barreto G, González-Fernando R, Ibarra A, Taboada P, Porras L, Moreno F, Bigham A, Gutierrez G, Brutsaert T, León-Velarde F, Moore LG, Vargas E, Cruz M, Escobedo J, Rodriguez-Santana J, Rodriguez-Cintrón W, Chapela R, Ford JG, Bustamante C, Seminara D, Shriver M, Ziv E, Burchard-Esteban G, Haile R, Parra E, Carracedo A, LACE C (2012). Development of a panel of genome-wide ancestry informative markers to study admixture throughout the Americas. PLoS genetics; 8:e1002554. http://doi.org/10.1371/journal.pgen.1002554
    • Gómez-Carballa A, Ignacio-Veiga A, Alvarez-Iglesias V, Pastoriza-Mourelle A, Ruíz Y, Pineda L, Carracedo A, Salas A (2012). A melting pot of multicontinental mtDNA lineages in admixed Venezuelans. American journal of physical anthropology; 147:78-87. http://doi.org/10.1002/ajpa.21629
    • Gómez-Carballa A, Olivieri A, Behar DM, Achilli A, Torroni A, Salas A (2012). Genetic continuity in the Franco-Cantabrian region: new clues from autochthonous mitogenomes. PloS one; 7:e32851. http://doi.org/10.1371/journal.pone.0032851
    • Iglesias P, Salas A, Costoya JA (2012). The maintenance of mitochondrial genetic stability is crucial during the oncogenic process. Communicative & integrative biology; 5:34-8. http://doi.org/10.4161/cib.18160
    • Salas A, Elson JL (2012). Raising doubts about the pathogenicity of mitochondrial DNA mutation m.3308T>C in left ventricular hypertraveculation/noncompaction. Cardiology; 122:113-5. http://doi.org/10.1159/000339348
    • Toscanini U, Garcia-Magariños M, Berardi G, Egeland T, Raimondi E, Salas A (2012). Evaluating methods to correct for population stratification when estimating paternity indexes. PloS one; 7:e49832. http://doi.org/10.1371/journal.pone.0049832
  •  2011
    • Zhang A, Jia X, Bi R, Salas A, Li S, Xiao X, Wang P, Guo X, Kong Q, Zhang Q, Yao Y (2011). Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients. PLoS ONE; 6:e27750. http://doi.org/10.1371/journal.pone.0027750
    • Toscanini U, Gusmão L, Berardi G, Gomes V, Amorim A, Salas A, Raimondi E (2011). Male lineages in South American native groups: evidence of M19 traveling south. American journal of physical anthropology; 146:188-96. http://doi.org/10.1002/ajpa.21562
    • Catelli ML, Alvarez-Iglesias V, Gómez-Carballa A, Mosquera-Miguel A, Romanini C, Borosky A, Amigo J, Carracedo A, Vullo C, Salas A (2011). The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome. BMC genetics; 12:77. http://doi.org/10.1186/1471-2156-12-77
    • Martín-Guerrero I, Enjuanes A, Richter J, Ammerpohl O, Colomer D, Ardanaz M, Marco F, Salas A, Campo E, Siebert R, García-Orad A (2011). A putative “hepitype” in the ATM gene associated with chronic lymphocytic leukemia risk. Genes, Chromosomes and Cancer; 50:887-895. http://doi.org/10.1002/gcc.20912
    • Haworth A, Bertram L, Carrera P, Elson JL, Braastad CD, Cox DW, Cruts M, den DJ, Farrer MJ, Fink JK, Hamed SA, Houlden H, Johnson DR, Nuytemans K, Palau F, Robinson PN, Salas A, Schüle B, Sweeney MG, Woods MO, Amigo J, Sobrido M (2011). Call for participation in the neurogenetics consortium within the Human Variome Project. Neurogenetics; 12:169-73. http://doi.org/10.1007/s10048-011-0287-4
    • Cerezo M, Černý V, Carracedo A, Salas A (2011). New insights into the Lake Chad Basin population structure revealed by high-throughput genotyping of mitochondrial DNA coding SNPs. PloS one; 6:e18682. http://doi.org/10.1371/journal.pone.0018682
    • Amigo J, Salas A, Phillips C (2011). ENGINES: exploring single nucleotide variation in entire human genomes. BMC bioinformatics; 12:105. http://doi.org/10.1186/1471-2105-12-105

    • Gómez-Carballa A, Cerezo M, Balboa E, Heredia C, Castro-Feijóo L, Rica I, Barreiro J, Eirís J, Cabanas P, Martínez-Soto I, Fernández-Toral J, Castro-Gago M, Pombo M, Carracedo A, Barros F, Salas A (2011). Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromes. PloS one; 6:e18348. http://doi.org/10.1371/journal.pone.0018348
    • Álvarez-Iglesias V, Mosquera-Miguel A, Cuscó I, Carracedo A, Pérez-Jurado LA, Salas A (2011). Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder. BMC medical genetics; 12:50. http://doi.org/10.1186/1471-2350-12-50
    • Egeland T, Salas A (2011). A statistical framework for the interpretation of mtDNA mixtures: forensic and medical applications. PloS one; 6:e26723. http://doi.org/10.1371/journal.pone.0026723
    • Rodrigues AC, Purim SG, Silbiger VN, Willrich MA, Arazi SS, Luchessi AD, Hirata MH, Dorea EL, Santos C, Faludi AA, Bertolami MC, Salas A, Freire A, Lareu MV, Phillips C, Porras-Hurtado L, Fondevila M, Carracedo A (2011). Pharmacogenetics of OATP transporters reveals that SLCO1B1 c.388A>G variant is determinant of increased atorvastatin response. International journal of molecular sciences; 12:5815-27. http://doi.org/10.3390/ijms12095815
    • Seoane M, Mosquera-Miguel A, Gonzalez T, Fraga M, Salas A, Costoya JA (2011). The mitochondrial genome is a "genetic sanctuary" during the oncogenic process. PloS one; 6:e23327. http://doi.org/10.1371/journal.pone.0023327
  •  2010
    • Davila S, Wright VJ, Khor-Chiea C, Sim-Kar S, Binder A, Breunis WB, Inwald D, Nadel S, Betts H, Carrol ED, Hazelzet J, Emonts M, Lim-Chui C, Kuijpers TW, Martinon-Torres F, Salas A, Zenz W, Levin M, Hibberd ML, International Meningococcal Genetics Consortium (2010). Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. Nature Genetics; 42:772-6. http://doi.org/10.1038/ng.640
    • Perego UA, Angerhofer N, Pala M, Olivieri A, Lancioni H, Hooshiar-Kashani B, Carossa V, Ekins JE, Gómez-Carballa A, Huber G, Zimmermann B, Corach D, Babudri N, Panara F, Myres NM, Parson W, Semino O, Salas A, Woodward SR, Achilli A, Torroni A (2010). The initial peopling of the Americas: a growing number of founding mitochondrial genomes from Beringia. Genome research; 20:1174-9. http://doi.org/10.1101/gr.109231.110

    • Pereira L, Cerný V, Cerezo M, Silva NM, Hájek M, Vasíková A, Kujanová M, Brdicka R, Salas A (2010). Linking the sub-Saharan and West Eurasian gene pools: maternal and paternal heritage of the Tuareg nomads from the African Sahel. European journal of human genetics : EJHG; 18:915-23. http://doi.org/10.1038/ejhg.2010.21
    • Salas A, Amigo J (2010). A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups. PloS one; 5:e10218. http://doi.org/10.1371/journal.pone.0010218
    • Toscanini U, Salas A, García-Magariños M, Gusmão L, Raimondi E (2010). Population stratification in Argentina strongly influences likelihood ratio estimates in paternity testing as revealed by a simulation-based approach. International journal of legal medicine; 124:63-9. http://doi.org/10.1007/s00414-009-0359-2
  •  2009
    • Salas A, Fachal L, Marcos-Alonso S, Vega A, Martinón-Torres F, Grupo de investigación ESIGEM (Estudio Sobre la Influencia Genética en la Enfermedad Meningocócica) (2009). Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease. PloS one; 4:e8347. http://doi.org/10.1371/journal.pone.0008347
    • Yao Y, Salas A, Logan I, Bandelt H (2009). mtDNA data mining in GenBank needs surveying. American journal of human genetics; 85:929-33; author reply 933. http://doi.org/10.1016/j.ajhg.2009.10.023
    • Cerezo M, Bandelt H, Martín-Guerrero I, Ardanaz M, Vega A, Carracedo A, García-Orad A, Salas A (2009). High mitochondrial DNA stability in B-cell chronic lymphocytic leukemia. PloS one; 4:e7902. http://doi.org/10.1371/journal.pone.0007902
    • Cerezo M, Cerný V, Carracedo A, Salas A (2009). Applications of MALDI-TOF MS to large-scale human mtDNA population-based studies. Electrophoresis; 30:3665-73. http://doi.org/10.1002/elps.200900294
    • Salas A, Lovo-Gómez J, Alvarez-Iglesias V, Cerezo M, Lareu MV, Macaulay V, Richards MB, Carracedo A (2009). Mitochondrial echoes of first settlement and genetic continuity in El Salvador. PloS one; 4:e6882. http://doi.org/10.1371/journal.pone.0006882
    • Mosquera-Miguel A, Alvarez-Iglesias V, Cerezo M, Carracedo A, Salas A (2009). Testing the performance of mtSNP minisequencing in forensic samples. Forensic science international. Genetics; 3:261-4. http://doi.org/10.1016/j.fsigen.2009.04.006
    • Phillips C, Prieto L, Fondevila M, Salas A, Gómez-Tato A, Alvarez-Dios J, Alonso A, Blanco-Verea A, Brión M, Montesino M, Carracedo A, Lareu MV (2009). Ancestry analysis in the 11-M Madrid bomb attack investigation. PloS one; 4:e6583. http://doi.org/10.1371/journal.pone.0006583
    • Sandoval K, Buentello-Malo L, Peñaloza-Espinosa R, Avelino H, Salas A, Calafell F, Comas D (2009). Linguistic and maternal genetic diversity are not correlated in Native Mexicans. Human Genetics; 126:521-531. http://doi.org/10.1007/s00439-009-0693-y
    • Pala M, Achilli A, Olivieri A, Hooshiar-Kashani B, Perego UA, Sanna D, Metspalu E, Tambets K, Tamm E, Accetturo M, Carossa V, Lancioni H, Panara F, Zimmermann B, Huber G, Al-Zahery N, Brisighelli F, Woodward SR, Francalacci P, Parson W, Salas A, Behar DM, Villems R, Semino O, Bandelt H, Torroni A (2009). Mitochondrial haplogroup U5b3: a distant echo of the epipaleolithic in Italy and the legacy of the early Sardinians. American journal of human genetics; 84:814-21. http://doi.org/10.1016/j.ajhg.2009.05.004
    • Soares P, Ermini L, Thomson N, Mormina M, Rito T, Röhl A, Salas A, Oppenheimer S, Macaulay V, Richards MB (2009). Correcting for purifying selection: an improved human mitochondrial molecular clock. American journal of human genetics; 84:740-59. http://doi.org/10.1016/j.ajhg.2009.05.001
    • Brisighelli F, Capelli C, Alvarez-Iglesias V, Onofri V, Paoli G, Tofanelli S, Carracedo A, Pascali VL, Salas A (2009). The Etruscan timeline: a recent Anatolian connection. European journal of human genetics : EJHG; 17:693-6. http://doi.org/10.1038/ejhg.2008.224
    • García-Magariños M, López-de-Ullibarri I, Cao R, Salas A (2009). Evaluating the ability of tree-based methods and logistic regression for the detection of SNP-SNP interaction. Annals of human genetics; 73:360-9. http://doi.org/10.1111/j.1469-1809.2009.00511.x
    • Bandelt H, Salas A (2009). Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma. BMC cancer; 9:113. http://doi.org/10.1186/1471-2407-9-113
    • Patin E, Laval G, Barreiro LB, Salas A, Semino O, Santachiara-Benerecetti S, Kidd KK, Kidd JR, Hombert J, Gessain A, Froment A, Bahuchet S, Heyer E, Quintana-Murci L (2009). Inferring the demographic history of African farmers and pygmy hunter-gatherers using a multilocus resequencing data set. PLoS genetics; 5:e1000448. http://doi.org/10.1371/journal.pgen.1000448
    • Salas A, Marcos-Alonso S, Vega A, Fachal L, Martinón-Torres F, Grupo de Investigación ESIGEM (2009). La genómica al servicio de la pediatría en el estudio de la enfermedad multifactorial. Acta Pediátrica Española; 62:55-60. http://www.actapediatrica.com/index.php/secciones/revision/124-la-gen%C3%B3mica-al-servicio-de-la-pediatr%C3%ADa-en-el-estudio-de-la-enfermedad-multifactorial
    • Amigo J, Phillips C, Salas A, Carracedo A (2009). Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes. BMC bioinformatics; 10 Suppl 3:S5. http://doi.org/10.1186/1471-2105-10-S3-S5
    • Bandelt H, Yao Y, Bravi CM, Salas A, Kivisild T (2009). Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studies. Journal of human genetics; 54:174-81. http://doi.org/10.1038/jhg.2009.9
    • Carolina Bartolomé, Xabier Bello, Xulio Maside (2009). Widespread evidence for horizontal transfer of transposable elements across Drosophila genomes. Genome Biology; 10(2):R22. https://doi.org/10.1186/gb-2009-10-2-r22
    • Perego UA, Achilli A, Angerhofer N, Accetturo M, Pala M, Olivieri A, Hooshiar-Kashani B, Ritchie KH, Scozzari R, Kong Q, Myres NM, Salas A, Semino O, Bandelt H, Woodward SR, Torroni A (2009). Distinctive Paleo-Indian migration routes from Beringia marked by two rare mtDNA haplogroups. Current biology : CB; 19:1-8. http://doi.org/10.1016/j.cub.2008.11.058

    • Alvarez-Iglesias V, Mosquera-Miguel A, Cerezo M, Quintáns B, Zarrabeitia MT, Cuscó I, Lareu MV, García O, Pérez-Jurado L, Carracedo A, Salas A (2009). New population and phylogenetic features of the internal variation within mitochondrial DNA macro-haplogroup R0. PloS one; 4:e5112. http://doi.org/10.1371/journal.pone.0005112
    • Vega A, Salas A, Milne RL, Carracedo B, Ribas G, Ruibal A, de León A, González-Hernández A, Benítez J, Carracedo A (2009). Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study. Gynecologic oncology; 112:210-4. http://doi.org/10.1016/j.ygyno.2008.09.012
  •  2008
    • Phillips C, Rodriguez A, Mosquera-Miguel A, Fondevila M, Porras-Hurtado L, Rondon F, Salas A, Carracedo A (2008). D9S1120, a simple STR with a common Native American-specific allele: forensic optimization, locus characterization and allele frequency studies. Forensic science international. Genetics; 3:7-13. http://doi.org/10.1016/j.fsigen.2008.07.002
    • Bandelt H, Yao Y, Richards MB, Salas A (2008). The brave new era of human genetic testing. BioEssays : news and reviews in molecular, cellular and developmental biology; 30:1246-51. http://doi.org/10.1002/bies.20837
    • Amigo J, Salas A, Phillips C, Carracedo A (2008). SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access. BMC bioinformatics; 9:428. http://doi.org/10.1186/1471-2105-9-428
    • Bandelt H, Salas A, Taylor RW, Yao Y (2008). Exaggerated status of “novel” and “pathogenic” mtDNA sequence variants due to inadequate database searches. Human Mutation; 30:191-196. http://doi.org/10.1002/humu.20846
    • Toscanini U, Gusmão L, Berardi G, Amorim A, Carracedo A, Salas A, Raimondi E (2008). Y chromosome microsatellite genetic variation in two Native American populations from Argentina: population stratification and mutation data. Forensic science international. Genetics; 2:274-80. http://doi.org/10.1016/j.fsigen.2008.03.001
    • Kong Q, Salas A, Sun C, Fuku N, Tanaka M, Zhong L, Wang C, Yao Y, Bandelt H (2008). Distilling artificial recombinants from large sets of complete mtDNA genomes. PloS one; 3:e3016. http://doi.org/10.1371/journal.pone.0003016
    • Toscanini U, Salas A, Carracedo A, Berardi G, Amorim A, Gusmão L, Raimondi E (2008). A simulation-based approach to evaluate population stratification in Argentina. Forensic Science International: Genetics Supplement Series; 1:662-663. http://doi.org/10.1016/j.fsigss.2007.10.070
    • Mendizabal I, Sandoval K, Berniell-Lee G, Calafell F, Salas A, Martínez-Fuentes A, Comas D (2008). Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba. BMC evolutionary biology; 8:213. http://doi.org/10.1186/1471-2148-8-213
    • Yao Y, Kong Q, Salas A, Bandelt H (2008). Pseudomitochondrial genome haunts disease studies. Journal of Medical Genetics; 45:769-772. http://doi.org/10.1136/jmg.2008.059782
    • Brandstätter A, Zimmermann B, Wagner J, Göbel T, Röck AW, Salas A, Carracedo A, Parson W (2008). Timing and deciphering mitochondrial DNA macro-haplogroup R0 variability in Central Europe and Middle East. BMC evolutionary biology; 8:191. http://doi.org/10.1186/1471-2148-8-191
    • Bandelt H, Yao Y, Salas A (2008). The search of \'novel\' mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor. International journal of cardiology; 126:439-42. http://doi.org/10.1016/j.ijcard.2007.02.049
    • Fondevila M, Phillips C, Naveran N, Fernandez L, Cerezo M, Salas A, Carracedo A (2008). Case report: identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur. Forensic science international. Genetics; 2:212-8. http://doi.org/10.1016/j.fsigen.2008.02.005
    • Phillips C, Fondevila M, García-Magariños M, Rodriguez A, Salas A, Carracedo A (2008). Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic science international. Genetics; 2:198-204. http://doi.org/10.1016/j.fsigen.2008.02.002
    • Alvarez-Iglesias V, Barros F, Carracedo A, Salas A (2008). Minisequencing mitochondrial DNA pathogenic mutations. BMC medical genetics; 9:26. http://doi.org/10.1186/1471-2350-9-26
    • Egeland T, Salas A (2008). Statistical Evaluation of Haploid Genetic Evidence. The Open Forensic Science Journal; 1:4-11. http://doi.org/10.2174/1874402800801010004
    • Achilli A, Perego UA, Bravi CM, Coble MD, Kong Q, Woodward SR, Salas A, Torroni A, Bandelt H (2008). The phylogeny of the four pan-American MtDNA haplogroups: implications for evolutionary and disease studies. PloS one; 3:e1764. http://doi.org/10.1371/journal.pone.0001764
    • Prieto L, Alonso A, Alves C, Crespillo M, Montesino M, Picornell A, Brehm A, Ramírez J, Whittle M, Anjos M, Boschi I, Buj J, Cerezo M, Cardoso S, Cicarelli R, Comas D, Corach D, Doutremepuich C, Espinheira R, Fernández-Fernández I, Filippini S, Garcia-Hirschfeld J, González A, Heinrichs B, Hernández A, Leite F, Lizarazo R, López-Parra A, López-Soto M, Lorente J, Mechoso B, Navarro I, Pagano S, Pestano J, Puente J, Raimondi E, Rodríguez-Quesada A, Terra-Pinheiro M, Vidal-Rioja L, Vullo C, Salas A (2008). 2006 GEP-ISFG collaborative exercise on mtDNA: reflections about interpretation, artefacts, and DNA mixtures. Forensic Science International: Genetics; 2:126-133. http://doi.org/10.1016/j.fsigen.2007.10.010
    • Quintana-Murci L, Quach H, Harmant C, Luca F, Massonnet B, Patin E, Sica L, Mouguiama-Daouda P, Comas D, Tzur S, Balanovsky O, Kidd KK, Kidd JR, Hombert J, Gessain A, Verdu P, Froment A, Bahuchet S, Heyer E, Dausset J, Salas A, Behar DM (2008). Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers. Proceedings of the National Academy of Sciences of the United States of America; 105:1596-601. http://doi.org/10.1073/pnas.0711467105
    • Salas A, Álvarez-Iglesias V, Cerezo M, Mosquera A, Naverán N, Phillips C, Lareu MV, Carracedo A (2008). Chapter 29 Mitochondrial DNA: future challenges in forensic genetics. Handbook of Analytical Separations. http://doi.org/10.1016/s1567-7192(06)06033-5
    • Salas A, Vega A, Milne RL, García-Magariños M, Ruibal A, Benítez J, Carracedo A (2008). The ‘Pokemon’ (ZBTB7) Gene: No Evidence of Association with Sporadic Breast Cancer. Clinical medicine. Oncology; 2:CMO.S569. http://doi.org/10.4137/cmo.s569
    • Egeland T, Salas A (2008). Estimating haplotype frequency and coverage of databases. PloS one; 3:e3988. http://doi.org/10.1371/journal.pone.0003988
    • Parson W, Fendt L, Ballard D, Børsting C, Brinkmann B, Carracedo A, Carvalho M, Coble MD, Real-Francisco C, Desmyter S, Dupuy BM, Harrison C, Hohoff C, Just R, Krämer T, Morling N, Salas A, Schmitter H, Schneider PM, Sonntag M, Vallone PM, Brandstätter A (2008). Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: results of the 2006-2007 EDNAP collaborative exercise. Forensic science international. Genetics; 2:61-8. http://doi.org/10.1016/j.fsigen.2007.08.007
    • Salas A, Acosta A, Alvarez-Iglesias V, Cerezo M, Phillips C, Carracedo A (2008). The mtDNA ancestry of admixed Colombian populations. American journal of human biology : the official journal of the Human Biology Council; 20:584-91. http://doi.org/10.1002/ajhb.20783
    • Salas A, Alvarez-Iglesias V, Carracedo A (2008). Gender bias in the multiethnic genetic composition of central Argentina. Journal of human genetics; 53:662-74. http://doi.org/10.1007/s10038-008-0297-8
  •  2007
    • Phillips C, Salas A, Fondevila M, Gómez-Tato A, Alvarez-Dios J, Calaza M, de Cal M, Ballard D, Carracedo A, SNPforID C (2007). Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs. Forensic science international. Genetics; 1:273-80. http://doi.org/10.1016/j.fsigen.2007.06.008
    • Salas A, Carracedo A (2007). Studies of association in complex diseases: statistical problems related to the analysis of genetic polymorphisms. Revista clinica espanola; 207:563-5. http://doi.org/10.1157/13111575
    • Lovo-Gómez J, Salas A, Carracedo A (2007). Microsatellite autosomal genotyping data in four indigenous populations from El Salvador. Forensic science international; 170:86-91. http://doi.org/10.1016/j.forsciint.2006.05.031
    • Cerný V, Salas A, Hájek M, Zaloudková M, Brdicka R (2007). A bidirectional corridor in the Sahel-Sudan belt and the distinctive features of the Chad Basin populations: a history revealed by the mitochondrial DNA genome. Annals of human genetics; 71:433-52. http://doi.org/10.1111/j.1469-1809.2006.00339.x
    • Montesino M, Salas A, Crespillo M, Albarrán C, Alonso A, Alvarez-Iglesias V, Carvalho M, Corach D, Cruz C, di Lonardo A, Espinheira R, Filippini S, García-Hirschfeld J, Hernández A, Lima G, López-Soto M, Pagano S, Paredes M, Sala A, Sóñora S, Zurita A, Prieto L (2007). Analysis of body fluid mixtures by mtDNA sequencing: An inter-laboratory study of the GEP-ISFG working group. Forensic science international; 168:42-56. http://doi.org/10.1016/j.forsciint.2006.06.066
    • Salas A, Bandelt H, Macaulay V (2007). Phylogeographic investigations: the role of trees in forensic genetics. Forensic science international; 168:1-13. http://doi.org/10.1016/j.forsciint.2006.05.037
    • Bandelt H, Olivieri A, Bravi C, Yao Y, Torroni A, Salas A (2007). \'Distorted\' mitochondrial DNA sequences in schizophrenic patients. European journal of human genetics : EJHG; 15:400-2; author reply 402-4. http://doi.org/10.1038/sj.ejhg.5201781
    • Alvarez-Iglesias V, Carracedo A, Salas A (2007). Coding region mitochondrial DNA SNPs: targeting East Asian and Native American haplogroups. Forensic science international. Genetics; 1:44-55. http://doi.org/10.1016/j.fsigen.2006.09.001
    • Bandelt H, Yao Y, Salas A, Kivisild T, Bravi CM (2007). High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients. Biochemical and biophysical research communications; 352:283-91. http://doi.org/10.1016/j.bbrc.2006.10.131
    • Toscanini U, Gusmão L, Berardi G, Amorim A, Carracedo A, Salas A, Raimondi E (2007). Testing for genetic structure in different urban Argentinian populations. Forensic science international; 165:35-40. http://doi.org/10.1016/j.forsciint.2006.02.042
    • Brage A, Tomé S, García A, Carracedo A, Salas A (2007). Clinical and molecular characterization of Wilson disease in Spanish patients. Hepatology research : the official journal of the Japan Society of Hepatology; 37:18-26. http://doi.org/10.1111/j.1872-034X.2007.00010.x
  •  2006
    • Milne-Roger L, Ribas G, González-Neira A, Fagerholm R, Salas A, González E, Dopazo J, Nevanlinna H, Robledo M, Benítez J (2006). ERCC4Associated with Breast Cancer Risk: A Two-Stage Case-Control Study Using High-throughput Genotyping. Cancer Research; 66:9420-9427. http://doi.org/10.1158/0008-5472.can-06-1418
    • Crespillo M, Paredes MR, Prieto L, Montesino M, Salas A, Albarran C, V A, Amorin A, Berniell-Lee G, Brehm A, Carril JC, Corach D, Cuevas N, di Lonardo A, Doutremepuich C, Espinheira RM, Espinoza M, Gómez F, González A, Hernández A, Hidalgo M, Jimenez M, Leite-Fabio P, López AM, López-Soto M, Lorente JA, Pagano S, Palacio AM, Pestano JJ, Pinheiro MF, Raimondi E, Ramón M, Tovar F, Vidal-Rioja L, Vide MC, Whittle MR, Yunis JJ, Garcia-Hirschfel J (2006). Results of the 2003–2004 GEP-ISFG collaborative study on mitochondrial DNA: Focus on the mtDNA profile of a mixed semen-saliva stain. Forensic Science International; 160:157-167. http://doi.org/10.1016/j.forsciint.2005.09.005
    • Brandstätter A, Salas A, Niederstätter H, Gassner C, Carracedo A, Parson W (2006). Dissection of mitochondrial superhaplogroup H using coding region SNPs. Electrophoresis; 27:2541-50. http://doi.org/10.1002/elps.200500772
    • Kong Q, Bandelt H, Sun C, Yao Y, Salas A, Achilli A, Wang C, Zhong L, Zhu C, Wu S, Torroni A, Zhang Y (2006). Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations. Human molecular genetics; 15:2076-86. http://doi.org/10.1093/hmg/ddl130
    • Yao Y, Salas A, Bravi CM, Bandelt H (2006). A reappraisal of complete mtDNA variation in East Asian families with hearing impairment. Human genetics; 119:505-15. http://doi.org/10.1007/s00439-006-0154-9
    • Sanchez JJ, Phillips C, Børsting C, Balogh K, Bogus M, Fondevila M, Harrison CD, Musgrave-Brown E, Salas A, Syndercombe-Court D, Schneider PM, Carracedo A, Morling N (2006). A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis; 27:1713-24. http://doi.org/10.1002/elps.200500671
    • Álvarez-Iglesias V, Salas A, Cerezo M, Ramos-Luis E, Jaime J, Lareu M, Carracedo A (2006). Genotyping coding region mtDNA SNPs for Asian and Native American haplogroup assignation. International Congress Series; 1288:4-6. http://doi.org/10.1016/j.ics.2005.11.036
    • Toscanini U, Berardi G, Amorim A, Carracedo A, Salas A, Gusmão L, Raimondi E (2006). Forensic considerations on STR databases in Argentina. International Congress Series; 1288:337-339. http://doi.org/10.1016/j.ics.2005.09.168
    • Toscanini U, Gusmão L, Berardi G, Amorim A, Carracedo A, Salas A, Raimondi E (2006). Genetic variability of 17 Y chromosome STRs in two Native American populations from Argentina. International Congress Series; 1288:154-155. http://doi.org/10.1016/j.ics.2005.09.169
    • Salas A, Yao Y, Bandelt H (2006). Authors\' Reply. PLoS Medicine; 3:e166. http://doi.org/10.1371/journal.pmed.0030166
    • Fernández–Marmiesse A, Salas A, Vega A, Fernández–Lorenzo JR, Barreiro J, Carracedo A (2006). Mutation spectra ofABCC8 gene in Spanish patients with hyperinsulinism of infancy (HI). Human Mutation; 27:214-214. http://doi.org/10.1002/humu.9401
    • Bandelt H, Salas A, Bravi CM (2006). What is a \'novel\' mtDNA mutation--and does \'novelty\' really matter?. Journal of human genetics; 51:1073-82. http://doi.org/10.1007/s10038-006-0066-5
  •  2005
    • Ribas G, González-Neira A, Salas A, Milne RL, Vega A, Carracedo B, González E, Barroso E, Fernández LP, Yankilevich P, Robledo M, Carracedo A, Benítez J (2005). Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes. Human Genetics; 118:669-679. http://doi.org/10.1007/s00439-005-0094-9
    • Bandelt H, Kong Q, Parson W, Salas A (2005). More evidence for non-maternal inheritance of mitochondrial DNA?. Journal of medical genetics; 42:957-60. http://doi.org/10.1136/jmg.2005.033589
    • Salas A, Richards M, Lareu M, Sobrino B, Silva S, Matamoros M, Macaulay V, Carracedo A (2005). Shipwrecks and founder effects: divergent demographic histories reflected in Caribbean mtDNA. American journal of physical anthropology; 128:855-60. http://doi.org/10.1002/ajpa.20117
    • Salas A, Yao Y, Macaulay V, Vega A, Carracedo A, Bandelt H (2005). A critical reassessment of the role of mitochondria in tumorigenesis. PLoS medicine; 2:e296. http://doi.org/10.1371/journal.pmed.0020296
    • Salas A, Carracedo A, Richards M, Macaulay V (2005). Charting the ancestry of African Americans. American journal of human genetics; 77:676-80. http://doi.org/10.1086/491675
    • Salas A, Carracedo A, Macaulay V, Richards M, Bandelt H (2005). A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics. Biochemical and biophysical research communications; 335:891-9. http://doi.org/10.1016/j.bbrc.2005.07.161
    • Salas A, Phillips C, Carracedo A (2005). Ancestry vs physical traits: the search for ancestry informative markers (AIMs). International Journal of Legal Medicine; 120:188-189. http://doi.org/10.1007/s00414-005-0032-3
    • Beleza S, Gusmão L, Amorim A, Carracedo A, Salas A (2005). The genetic legacy of western Bantu migrations. Human genetics; 117:366-75. http://doi.org/10.1007/s00439-005-1290-3
    • Bandelt H, Achilli A, Kong Q, Salas A, Lutz-Bonengel S, Sun C, Zhang Y, Torroni A, Yao Y (2005). Low “penetrance” of phylogenetic knowledge in mitochondrial disease studies. Biochemical and Biophysical Research Communications; 333:122-130. http://doi.org/10.1016/j.bbrc.2005.04.055
    • Salas A, Vega A, Phillips C, Torres M, Quintela I, Carracedo A (2005). ZBTB7 HapMap in a worldwide population study. Breast Cancer Research; 7. http://doi.org/10.1186/bcr1110
    • Vega A, Salas A, Phillips C, Sobrino B, Carracedo B, Ruíz-Ponte C, Rodríguez-López R, Rivas G, Benítez J, Carracedo A (2005). Large-scale single nucleotide polymorphism analysis of candidates for low-penetrance breast cancer genes. Breast Cancer Research; 7. http://doi.org/10.1186/bcr1101
    • Costas J, Salas A, Phillips C, Carracedo A (2005). Human genome-wide screen of haplotype-like blocks of reduced diversity. Gene; 349:219-25. http://doi.org/10.1016/j.gene.2004.12.042
    • Salas A, Prieto L, Montesino M, Albarrán C, Arroyo E, Paredes-Herrera MR, di Lonardo A, Doutremepuich C, Fernández-Fernández I, de la Vega A, Alves C, López CM, López-Soto M, Lorente JA, Picornell A, Espinheira RM, Hernández A, Palacio AM, Espinoza M, Yunis JJ, Pérez-Lezaun A, Pestano JJ, Carril JC, Corach D, Alvarez-Iglesias V, Whittle MR, Brehm A, Gómez J (2005). Mitochondrial DNA error prophylaxis: assessing the causes of errors in the GEP\'02-03 proficiency testing trial. Forensic science international; 148:191-8. http://doi.org/10.1016/j.forsciint.2004.06.008
    • Salas A, Quintáns B, Alvarez-Iglesias V (2005). SNaPshot typing of mitochondrial DNA coding region variants. Methods in molecular biology (Clifton, N.J.); 297:197-208. http://doi.org/10.1385/1-59259-867-6:197
  •  2004
    • Salas A, Lutz-Bonengel S (2004). Artificial recombination in forensic mtDNA population databases. International journal of legal medicine; 118:267-73. http://doi.org/10.1007/s00414-004-0455-2
    • Plaza S, Salas A, Calafell F, Corte-Real F, Bertranpetit J, Carracedo A, Comas D (2004). Insights into the western Bantu dispersal: mtDNA lineage analysis in Angola. Human genetics; 115:439-47. http://doi.org/10.1007/s00439-004-1164-0
    • Bandelt H, Salas A, Bravi C (2004). Problems in FBI mtDNA database. Science (New York, N.Y.); 305:1402-4. http://doi.org/10.1126/science.305.5689.1402b
    • Egeland T, Salas A (2004). Inferring the most likely geographical origin of mtDNA sequence profiles. Annals of human genetics; 68:461-71. http://doi.org/10.1046/j.1529-8817.2004.00109.x
    • Lovo JS, Fondevila M, Salas A, Brión M, Lareu MV, Carracedo A (2004). Y-chromosome STR-haplotype typing in El Salvador. Forensic science international; 142:45-9. http://doi.org/10.1016/j.forsciint.2004.02.004
    • Brion M, Quintans B, Zarrabeitia M, Gonzalez-Neira A, Salas A, Lareu V, Tyler-Smith C, Carracedo A (2004). Micro-geographical differentiation in Northern Iberia revealed by Y-chromosomal DNA analysis. Gene; 329:17-25. http://doi.org/10.1016/j.gene.2003.12.035
    • Quintáns B, Alvarez-Iglesias V, Salas A, Phillips C, Carracedo A (2004). Typing of mitochondrial DNA coding region SNPs of forensic and anthropological interest using SNaPshot minisequencing. Forensic science international; 140:251-7. http://doi.org/10.1016/j.forsciint.2003.12.005
    • Salas A, Richards M, Lareu M, Scozzari R, Coppa A, Torroni A, Macaulay V, Carracedo A (2004). The African diaspora: mitochondrial DNA and the Atlantic slave trade. American journal of human genetics; 74:454-65. http://doi.org/10.1086/382194

    • Vega A, Salas A, Gamborino E, Sobrido MJ, Macaulay V, Carracedo A (2004). mtDNA mutations in tumors of the central nervous system reflect the neutral evolution of mtDNA in populations. Oncogene; 23:1314-20. http://doi.org/10.1038/sj.onc.1207214
    • Tully G, Bender K, Brignon E, Capelli C, Dimo-Simonin N, Eichmann C, Lambert C, Ludes B, Mevag B, Parson W, Pfeiffer H, Salas A, Staalstrom E (2004). Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts. Forensic science international; 140:1-11. http://doi.org/10.1016/S0379-0738(03)00181-6
    • Vigo E, Salas A, Pérez-Fernández R, Segura C (2004). Analysis of the vitamin D receptor Fokl polymorphism. Journal of endocrinological investigation; 27:158-62. http://doi.org/10.1007/bf03346261
    • Jaime JC, Fondevila M, Salas A, Lareu M, Carracedo A (2004). Nine autosomal STRs genotype profiles in a sample from Córdoba (Argentina). Forensic Science International; 139:81-83. http://doi.org/10.1016/j.forsciint.2003.07.005
    • Salas A, Renfrew C, Jones M (2004). The archaeogenetics of the dispersals of the Bantu-speaking people. McDonald Institute monographs. http://eprints.gla.ac.uk/33491/
  •  2003
    • Fondevila M, Jaime JC, Salas A, Lareu MV, Carracedo A (2003). Y-chromosome STR haplotypes in Córdoba (Argentina). Forensic Science International; 137:217-220. http://doi.org/10.1016/j.forsciint.2003.07.006
    • Paredes M, Galindo A, Bernal M, Avila S, Andrade D, Vergara C, Rincón M, Romero RE, Navarrete M, Cárdenas M, Ortega J, Suarez D, Cifuentes A, Salas A, Carracedo A (2003). Analysis of the CODIS autosomal STR loci in four main Colombian regions. Forensic science international; 137:67-73. http://doi.org/10.1016/s0379-0738(03)00271-8
    • Skitsa I, Salas A, Lareu M, Carracedo A (2003). STR-CODIS typing in Greece. Forensic Science International; 137:104-106. http://doi.org/10.1016/s0379-0738(03)00298-6
    • Brion M, Salas A, González-Neira A, Carracedo A (2003). Insights into Iberian population origins through the construction of highly informative Y-chromosome haplotypes using biallelic markers, STRs, and the MSY1 minisatellite. American journal of physical anthropology; 122:147-61. http://doi.org/10.1002/ajpa.10231
    • Prieto L, Montesino M, Salas A, Alonso A, Albarrán C, Alvarez S, Crespillo M, di Lonardo A, Doutremepuich C, Fernández-Fernández I, de la Vega A, Gusmão L, López CM, López-Soto M, Lorente JA, Malaghini M, Martínez CA, Modesti NM, Palacio AM, Paredes M, Pérez-Lezaun A, Pestano JJ, Puente J, Sala A, Vide M, Whittle MR, Yunis JJ, Gómez J, Spanish and Portuguese Working Group of the International Society of Forensic Genetics (2003). The 2000-2001 GEP-ISFG Collaborative Exercise on mtDNA: assessing the cause of unsuccessful mtDNA PCR amplification of hair shaft samples. Forensic science international; 134:46-53. http://doi.org/10.1016/s0379-0738(03)00095-1
    • Aler M, Salas A, Murcia E, Gisbert-Grifo M, Carracedo A (2003). Population study of eight novel Y-chromosome STRs (DYS460, DYS461, GATA-A10, GATA-C4, GATA-H4, DYS434, DYS437, DYS439) in a southeast Iberian population: looking for highly informative Y-chromosome haplotypes. International Journal of Legal Medicine; 117:127-131. http://doi.org/10.1007/s00414-002-0360-5
  •  2002
    • Bandelt H, Quintana-Murci L, Salas A, Macaulay V (2002). The fingerprint of phantom mutations in mitochondrial DNA data. American journal of human genetics; 71:1150-60. http://doi.org/10.1086/344397
    • Salas A, Richards M, Lareu M, Sobrino B, Sánchez-Diz P, Macaulay V, Carracedo A (2002). The making of the African mtDNA landscape. American journal of human genetics; 71:1082-111. http://doi.org/10.1086/344348
    • Pineda-Bernal L, Borjas-Fajardo L, Zabala W, Fernández E, Delgado W, Salas A, Sánchez-Diz P, Carracedo A (2002). Data for nine autosomal STRs markers (CSF1PO, D13S31, D16S539, D7S820, F13A01, FESFPS, TH01, vWA, TPOX) from Venezuela. Forensic science international; 125:277-8. http://doi.org/10.1016/s0379-0738(02)00004-x
    • Alonso A, Salas A, Albarrán C, Arroyo E, Castro A, Crespillo M, di Lonardo A, Lareu MV, Cubría-Carlos L, Soto-Manuel L, Lorente JA, Semper-Marta M, Palacio A, Paredes M, Pereira L, Lezaun-Anna P, Brito-José P, Sala A, Vide MC, Whittle M, Yunis JJ, Gómez J (2002). Results of the 1999-2000 collaborative exercise and proficiency testing program on mitochondrial DNA of the GEP-ISFG: an inter-laboratory study of the observed variability in the heteroplasmy level of hair from the same donor. Forensic science international; 125:1-7. http://doi.org/10.1016/s0379-0738(01)00602-8
    • Brión M, Cao R, Salas A, Carracedo A (2002). New method to measure minisatellite variant repeat variation in population genetic studies. American journal of human biology : the official journal of the Human Biology Council; 14:421-8. http://doi.org/10.1002/ajhb.10057
  •  2001
    • Salas A, Morling N, Carracedo A (2001). Fluorescent SSCP of overlapping fragments (FSSCP-OF): a highly sensitive method for the screening of mitochondrial DNA variation. Forensic science international; 124:97-103. http://doi.org/10.1016/s0379-0738(01)00574-6
    • Salas A, Carracedo A (2001). Autosomal STR genetic variation in negroid Chocó and Bogotá populations. International journal of legal medicine; 115:102-4. http://doi.org/10.1007/s004140100223
    • Vega A, Salas A, Costas J, Barros F, Carracedo A (2001). Length variability and interspersion patterns of the HRAS1 minisatellite: a new approach for the reconstruction of human population relationships. Annals of human genetics; 65:351-61. http://doi.org/10.1017/S0003480001008752
    • Aler M, Salas A, Sánchez-Diz P, Murcia E, Carracedo A, Gisbert M (2001). Y-chromosome STR haplotypes from a Western Mediterranean population sample. Forensic science international; 119:254-7. http://doi.org/10.1016/s0379-0738(00)00432-1
    • Aler M, Salas A, Gisbert M, Carracedo A (2001). Data for nine autosomal STRs markers from Valencia (East Mediterranean coast of the Iberian Peninsula). Forensic Science International; 116:37-39. http://doi.org/10.1016/s0379-0738(00)00345-5
    • Salas A, Carracedo A (2001). Heteroplasmy in mtDNA and the weight of evidence in forensic mtDNA analysis: a case report. International journal of legal medicine; 114:186-90. http://doi.org/10.1007/s004140000164
  •  2000
    • Salas A, Lareu V, Calafell F, Bertranpetit J, Carracedo A (2000). mtDNA hypervariable region II (HVII) sequences in human evolution studies. European journal of human genetics : EJHG; 8:964-74. http://doi.org/10.1038/sj.ejhg.5200563
    • Guillén M, Pestoni C, Salas A, Carracedo A (2000). Ethical-legal problems of DNA databases in criminal investigation. Journal of medical ethics; 26:266-71. http://doi.org/10.1136/jme.26.4.266
    • Barral S, Salas A, Carracedo A (2000). Sequence variation of two hypervariable short tandem repeats at the D22S683 and D6S477 loci. International journal of legal medicine; 113:146-9. http://doi.org/10.1007/s004140050286
  •  1998
    • Capeans C, Salas A, Piñeiro A, Sánchez-Salorio M, Carracedo A (1998). 160Thr mutation in the rhodopsin gene associated with retinitis pigmentosa. Human heredity; 48:237-40. http://doi.org/10.1159/000022809
    • Barral S, Salas A, Carracedo A (1998). Sequence variation of a variable short tandem repeat at the D18S535 locus. International journal of legal medicine; 111:337-9. http://doi.org/10.1007/s004140050185
    • Barral S, Salas A, Pestoni C, Carracedo A (1998). Sequence variation of a hypervariable short tandem repeat at the D1S1656 locus. International journal of legal medicine; 111:244-7. http://doi.org/10.1007/s004140050161
    • Salas A, Comas D, Bertranpetit J, Carracedo A (1998). mtDNA analysis of the Galician population: a genetic edge of European variation. European journal of human genetics : EJHG; 6:365-75. http://doi.org/10.1038/sj.ejhg.5200202
  •  1997
    • Carracedo A, Rodriguez-Calvo-Marı́a S, Pestoni C, Lareu MV, Bellas S, Salas A, Barros F (1997). Forensic DNA analysis in Europe: current situation and standardization efforts. Forensic Science International; 86:87-102. http://doi.org/10.1016/s0379-0738(97)02115-4
    • Barros F, Salas A, Carracedo A (1997). Rapid and enhanced detection of mitochondrial DNA variation using single-strand conformation analysis of superposed restriction enzyme fragments from polymerase chain reaction-amplified products. Electrophoresis; 18:52-4. http://doi.org/10.1002/elps.1150180110
  •  1996

International Society for Forensic Genetics (ISFG) award - 2009

The ISFG aims to promote scientific knowledge in the field of genetic markers as applied to forensic science.


This is mainly being achieved through regular meetings of either regional or international nature, our journal Forensic Science International: Genetics and the work of our expert DNA commissions. Click here to see the list of awardees of the ISFG.

A bit of history on the ISFG

The ISFG has been founded in Mainz, Germany by a group of dedicated blood group serologists in 1968 under the name of "Society for Forensic Haemogenetics" , to address the growing knowledge about polymorphic markers in human blood and their use in paternity testing as well as in forensic stain analysis. Since then, the society has grown rapidly, and has become an international society in the 1980's, carrying the acronym "ISFH". Due to the overwhelming success of DNA-based molecular genetic typing methods, the name was changed again in 1999 to include the more general term "genetics" instead of the original "haemogenetics", since DNA can be extracted from virtually all human tissues and body fluids carrying nucleated cells, resulting in the current name "ISFG".

Today, the society represents more than 1,200 members from over 60 countries from academic and government laboratories, as well as from private companies. Their expertise includes molecular genetics, blood group serology, mathematics and biostatistics, as well as legal matters ranging from criminal law to medical ethics. International congresses are held every two years, and further meetings are organized by the mostly language-based working groups, to address specific topics at the local level. Since 1989, the DNA Commission of the ISFG has published numerous recommendations addressing important topics to help establishing scientific standards in particular for new typing methods and genetic marker systems. Thus the society has adopted a pivotal role to take up the generally accepted scientific knowledge in the field of forensic genetics and condense it into specific guidelines with the overall aim to harmonize the important work derived from the studies of genetic markers in humans for the judicial system.

First International Zendal Awards

Zendal, the corporate brand of our group, draws together seven companies focused on research, development, manufacture and marketing of high added value products in the health sector.

Zendal awards

The International Zendal Awards aim to disseminate, promote and reward knowledge and research in the field of biotechnology worldwide.

Zendal’s mission is to contribute to the improvement of living conditions through research and development of medicines and vaccines for the prevention of diseases to human beings as well as animals. With this aim the group call the International Zendal Awards to divulge, dynamise and reward knowledge and research within the field of biotechnology worldwide.

Second edition of the Fernando del Castillo Martin Award

(Spanish Society of Pediatric Infectology) for the publication: Martinón-Torres F*, Salas A*, Rivero-Calle I*, Cebey-López M*, Pardo-Seco J*, Herberg JA*, Boeddha NP, Klobassa DS, Secka F, Paulus S, Schlapbach LJ, Driessen GJ, Anderson ST, Emonts M, Zenz W, Carrol ED, Levin M*, EUCLIDS Consortium (2018). Life-threatening infections in children in Europe (the EUCLIDS Project): a prospective cohort study. The Lancet. Child & adolescent health; 2:404-414. *Equal contribution


See Special issue: Host Infectomics in the Childhood; Editor: Antonio Salas

Despite the availability of new vaccines and antibacterial agents suppressing microbial pathogens, infectious diseases are among the leading cause of morbidity and mortality worldwide. While there are a number of studies dealing with infections in adults (mainly focused on some particular diseases, e.g., tuberculosis) and/or pathogens, less attention has been devoted to the pediatric age. To overcome this deficiency, several international consortia have emerged in the last decade aimed at investigating life-threatening infections affecting childhood.


‘Omic’ sciences are gaining growing attention in parallel with the development of new and cost-effective technologies, but also bioinformatic and mathematical solutions that allow dealing with big data from massive genotyping and sequencing technologies. The field of infectiology is one of the many in biomedicine that is benefiting from these new achievements, and in particular, the area studying host response to infection from different ‘omic’ perspectives, namely, host infectomics. Thus, there is now increasing evidence supporting that it is not only the pathogen that decides how and when to infect the host, but also the biological predisposition of the host to be infected by the pathogen. Most of the genomic studies published to date have focused their attention on genomics, first by exploring a few thousands of single nucleotide polymorphisms (SNPs) distributed throughout the whole genome in large case-control samples (e.g., population-based genome-wide association studies; GWAS), and more recently using parallel sequencing procedures (e.g., whole exome sequencing, WES). There are also interesting attempts in the terrain of transcriptomic, using microarrays and more recently RNAseq, to investigate the host genetic expression response to different infections and pathogens.

Other selected publications not indexed in Journal Citation Reports (JCR)

  • Richards M, Macaulay V, Hill C, Carracedo Á, Salas A. The archaeogenetics of the dispersals of the Bantu-speaking peoples. Editado por Martin Jones, McDonald Institute, University of Cambridge, Monographs: “Studies in honour of Colin Renfrew”. Chapter 6. 2004, ISBN/ISSN: 1–902937–25–2, ISSN: 1363–1349
  • Salas A, Brión M, Carracedo Á (2006) Genética Forense: los perfiles de ADN. Investigación y Ciencia (Scientific American) 353:34-35. Editorial: Prensa Científica, S. A. Barcelona (Spain). ISBN/ISSN: 0210-136X. [In Spanish]
Portada Investigacion y Ciencia
  • Salas A (2004) El ADN mitocondrial y su utilidad en Genética Forense”. El ADN y las nuevas técnicas científicas en la investigación policial. Revista Galega de Seguridade Pública 6:35-54. Editorial: Ed. Castellana [In Spanish]

Several metrics related to our research activity:


Academic Editor of peerJ.

PeerJ — the Journal of Life and Environmental Sciences is a peer-reviewed & Open Access journal publishing primary research and reviews in biology, life sciences, environmental sciences, and medicine.

Forensic Science International Genetics

Editorial board

Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of geneticsto human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.

International Journal of Molecular Science

Editorial board

IJMS is an international peer-reviewed open access journal providing an advanced forum for biochemistry, molecular and cell biology, molecular biophysics, molecular medicine, and all aspects of molecular research in chemistry, and is published semi-monthly online by MDPI.