Publications

Cited over 4,400 times, h-index 24, i10-index 37. Every entry links to the article at its original journal. Complete and current lists: ORCID 0000-0002-4417-1018 | Google Scholar | PubMed. * denotes corresponding author.

2026

  1. M Corpas*, H Guio, S Fatumo (2026). Agentic genomics: from pipeline automation to autonomous validation. Cell Genomics, 101305.
  2. M Corpas*, A Iacoangeli, M Bourdenx, M Aldraimli, N Skene, S Fatumo, H Guio (2026). Trustworthy agentic genomics through versioned skill libraries. bioRxiv.
  3. M Corpas*, A Iacoangeli (2026). Benchmarking large language models for extracting biobank-derived insights into health and disease. PLOS Computational Biology 22(4): e1014224.
  4. M Corpas*, O Ojewunmi, H Guio, S Fatumo (2026). Electronic health record-linked biobank expansion reveals global health inequities. Annual Review of Biomedical Data Science.
  5. V Soriano, JM Ramos, L Gallego, et al., M Corpas, et al., H Blasco-Fontecilla (2026). Hospitalizations in adolescents with autism spectrum disorder are rising in Spain. Child and Adolescent Psychiatry and Mental Health.
  6. AB Kamiza, T Chikowore, G Chen, et al., M Corpas, et al., S Fatumo (2026). KidneyGenAfrica: multi-cohort genome-wide association study and polygenic prediction of kidney function in 110,000 Africans. Nature Communications.

2025

  1. M Corpas*, H Guio, C Lopez-Correa, S Fatumo (2025). Why genomic diversity should not be framed by census alone. Nature Genetics.
  2. H Guio, C Sanchez, V Borda, et al., M Corpas, et al., E Tarazona-Santos (2025). The Peruvian Genome Project: expanding the global pool of genome diversity from South America. Frontiers in Genetics.
  3. V Soriano, JM Ramos, M Faraco, et al., M Corpas, et al., H Blasco-Fontecilla (2025). Hospitalizations in adolescents with anorexia nervosa in Spain over two decades. Journal of Eating Disorders.
  4. E González-Fraile, V Soriano, JM Ramos, et al., M Corpas, et al., H Blasco-Fontecilla (2025). Two decades of hospital admissions for adolescents with depression in Spain. Journal of Affective Disorders.
  5. H Blasco-Fontecilla, JM Ramos, MI López-Ibor, et al., M Corpas, et al., V Soriano (2025). Rising rate of hospitalizations in adolescents with attention deficit hyperactive disorder in Spain. Journal of Attention Disorders 29(6): 411-422.
  6. M Corpas*, M Pius, M Poburennaya, H Guio, M Dwek, S Nagaraj, C Lopez-Correa, A Popejoy, S Fatumo (2025). Bridging genomics’ greatest challenge: the diversity gap. Cell Genomics 5(1): 100724.

2024

  1. M Corpas*, V Soriano, T Perucho, JS Rincón-Redondo, M Pérez-Alonso, JAG Ranea, C de Mendoza, F Morán (2024). Playing catching up: proceedings of the 1st Spanish conference on genomic medicine. AIDS Reviews 26(3): 130-140.
  2. V Soriano, JM Ramos, MI López-Ibor, et al., M Corpas, et al., H Blasco-Fontecilla (2024). Hospital admissions in adolescents with mental disorders in Spain over the last two decades: a mental health crisis? European Child & Adolescent Psychiatry 34(3): 1125-1134.
  3. V Soriano, JM Ramos, MI López-Ibor, et al., M Corpas, et al., H Blasco-Fontecilla (2024). Trends in suicidal behavior among hospitalized adolescents in Spain over two decades. Journal of Affective Disorders 363: 106-111.
  4. R Santos, V Moreno-Torres, I Pintos, O Corral, C de Mendoza, V Soriano, M Corpas* (2024). Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients. GigaByte.
  5. SR Samarasinghe, SB Lee, M Corpas, S Fatumo, HJ Guchelaar, SH Nagaraj* (2024). Mapping the pharmacogenetic landscape in a Ugandan population: implications for personalized medicine in an underrepresented population. Clinical Pharmacology & Therapeutics 116(4): 980-995.
  6. M Corpas, MK Siddiqui, O Soremekun, R Mathur, D Gill, S Fatumo* (2024). Addressing ancestry and sex bias in pharmacogenomics. Annual Review of Pharmacology and Toxicology 64: 53-64.

2023

  1. M Corpas*, S Fatumo (2023). Generalisation of genomic findings and applications of polygenic risk scores. BMC Medical Genomics 16(1): 175.
  2. AB Kamiza, SM Touré, F Zhou, et al., M Corpas, et al., S Fatumo (2023). Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Nature Communications 14(1): 5403.
  3. N Skantharajah, S Baichoo, TF Boughtwood, et al., J Kumuthini, M Corpas* (2023). Equity, diversity and inclusion at the Global Alliance for Genomics and Health. Cell Genomics 3(10): 100386.
  4. M Corpas*, C de Mendoza, V Moreno-Torres, et al., O Corral, V Soriano (2023). Genetic signature detected in T cell receptors from patients with severe COVID-19. iScience 26(10): 107735.
  5. CF Wright, P Campbell, RY Eberhardt, et al., HV Firth and the DDD Consortium (2023). Genomic diagnosis of rare pediatric disease in the United Kingdom and Ireland. New England Journal of Medicine 388(17): 1559-1571.
  6. V Moreno-Torres, C de Mendoza, M Martínez-Urbistondo, et al., M Corpas, V Soriano (2023). Predictors of in-hospital mortality in HIV-infected patients with COVID-19. QJM: An International Journal of Medicine.

2022

  1. I Pintos, V Moreno-Torres, F Ibánez-Estéllez, et al., M Corpas, O Corral, V Soriano, C de Mendoza (2022). Is SARS-CoV-2 the only cause of long-COVID? AIDS Reviews.
  2. S Fatumo*, A Kamiza, S Toure, et al., M Corpas, et al., T Chikowore (2022). Transferability of genetic risk scores in African populations. Nature Medicine 28(6): 1163-1166.
  3. M Corpas*, K Megy, A Metastasio, E Lehmann (2022). Implementation of individualised polygenic risk score analysis: a test case of a family of four. BMC Medical Genomics.

2021

  1. M Corpas*, S Beck, GG Glusman, M Shabani (2021). Editorial: personal genomes: accessing, sharing, and interpretation. Frontiers in Genetics 12: 687584.
  2. M Corpas*, K Megy, V Mistry, A Metastasio, E Lehmann (2021). Whole genome interpretation for a family of five. Frontiers in Genetics 12: 535123.

2018

  1. S Beck*, AM Berner, G Bignell, et al., M Corpas, et al., J Wood (2018). Personal Genome Project UK (PGP-UK): a research and citizen science hybrid project in support of personalized medicine. BMC Medical Genomics 11(1): 108.
  2. A Bueno, R Rodríguez-López, A Reyes-Palomares, E Rojano, M Corpas, J Nevado, P Lapunzina, F Sánchez-Jiménez, JAG Ranea* (2018). Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases. European Journal of Human Genetics 26(10): 1451.
  3. A Thorogood*, J Bobe, B Prainsack, et al., M Corpas, et al., E Kleiderman (2018). APPLaUD: access for patients and participants to individual level uninterpreted genomic data. Human Genomics 12(1): 7.
  4. M Corpas*, NV Kovalevskaya, FGG Nielsen (2018). A FAIR guide for data providers to maximise sharing of human genomic data. PLOS Computational Biology 14(3): e1005873.

2017

  1. M Tamiru, S Natsume, H Takagi, et al., M Corpas, et al., R Terauchi (2017). Genome sequencing of the staple food crop white Guinea yam enables the development of a molecular marker for sex determination. BMC Biology 15(1): 86.
  2. RC Jiménez*, M Kuzak, M Alhamdoosh, et al., M Corpas, et al., S Crouch (2017). Four simple recommendations to encourage best practices in research software. F1000Research 6: 876.
  3. C Horro, M Cook, TK Attwood, MD Brazas, JM Hancock, P Palagi, M Corpas, R Jimenez* (2017). BioCIDER: a contextualisation InDEx for biological resources discovery. Bioinformatics 33(16): 2607-2608.
  4. MV Schneider, TK Attwood, M Corpas, et al., G Rustici (2017). GOBLET standards committee: best practices and standards in bioinformatics and biocuration. F1000Research 6.

2016

  1. H Artaza, N Chue Hong, M Corpas*, et al., T Van Parys (2016). Top 10 metrics for life science software good practices. F1000Research 5: 2000.
  2. A Reyes-Palomares, A Bueno, F Sanchez-Jimenez, MA Medina, M Corpas, JAG Ranea* (2016). Systematic identification of phenotypically enriched loci using a patient network of genomic disorders. BMC Genomics 17: 232.

2015

  1. M Corpas*, W Valdivia-Granda, N Torres, et al., PN Robinson (2015). Crowdsourced direct-to-consumer genomic analysis of a family quartet. BMC Genomics 16: 910.
  2. G Yachdav, T Goldberg, S Wilzbach, et al., B Rost, M Corpas* (2015). Anatomy of BioJS, an open source community for the life sciences. eLife 4: e07009.
  3. G Rallapalli, Fraxinus Players, DGO Saunders, et al., M Corpas, et al., D MacLean (2015). Lessons from Fraxinus, a crowd-sourced citizen science game in genomics. eLife 4: e07460.
  4. F Psomopoulos*, AM Duarte*, C Blanchet, AM Bonvin, M Corpas, et al., SB Suhr (2015). Future opportunities and trends for e-infrastructures and life sciences. Frontiers in Genetics 6: 197.
  5. TK Attwood, E Bongcam-Rudloff, ME Brazas, M Corpas, et al., The GOBLET Consortium (2015). GOBLET: the Global Organisation for Bioinformatics Learning, Education and Training. PLOS Computational Biology 11(4): e1004143.
  6. A Budd*, M Corpas*, MD Brazas*, FC Fuller*, et al., N Blomberg (2015). A quick guide for building a successful bioinformatics community. PLOS Computational Biology 11(2): e1003972.
  7. A Budd*, H Dinkel, M Corpas, et al., NT Wood (2015). Ten simple rules for organizing an unconference. PLOS Computational Biology 11(1): e1003905.

2014

  1. M Corpas*, RC Jimenez, E Bongcam-Rudloff, et al., TK Attwood (2014). The GOBLET training portal: a global repository of bioinformatics training materials, courses and trainers. Bioinformatics 31(1): 140-142.
  2. M Corpas* (2014). The BioJS article collection of open source components for biological data visualisation. F1000Research 3: 56.
  3. M Corpas*, RC Jimenez, SJ Carbon, et al., H Hermjakob* (2014). BioJS: an open source standard for biological visualisation, its status in 2014. F1000Research 3: 55.
  4. AS Thanki*, S Caim, M Corpas, RP Davey (2014). DNAContentViewer: a BioJS component to visualise GC/AT content. F1000Research 3: 54.
  5. AS Thanki*, RC Jimenez, GG Kaithakottil, M Corpas, RP Davey (2014). wigExplorer: a BioJS component to visualise wig data. F1000Research 3: 53.

2013

  1. RC Jimenez, JP Albar, J Bhak, et al., TK Attwood, M Corpas* (2013). iAnn: an event sharing platform for the life sciences. Bioinformatics 29(15): 1919-1921.
  2. J de Ridder, Y Bromberg, M Michaut, VP Satagopam, M Corpas, G Macintyre, T Alexandrov* (2013). The young PI buzz: learning from the organizers of the Junior Principal Investigator meeting at ISMB-ECCB 2013. PLOS Computational Biology 9(11): e1003350.
  3. M Corpas* (2013). Crowdsourcing the Corpasome. Source Code for Biology and Medicine 8: 13.
  4. RC Jimenez*, M Corpas (2013). Bioinformatics workflows and web services in systems biology made easy for experimentalists. Methods in Molecular Biology 1021: 299-310.
  5. J Gómez, LJ García, GA Salazar, et al., M Corpas, RC Jiménez* (2013). BioJS: an open source JavaScript framework for biological data visualization. Bioinformatics 29(8): 1103-1104.

2012

  1. M Corpas* (2012). A genome blogger manifesto. GigaScience 1: 15.
  2. GJ Swaminathan, E Bragin, EA Chatzimichali, M Corpas, AP Bevan, CF Wright, NP Carter, ME Hurles, HV Firth* (2012). DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders. Human Molecular Genetics 21(R1): R37-44.
  3. M Corpas*, S Fatumo, R Schneider (2012). How not to be a bioinformatician. Source Code for Biology and Medicine 7: 3.
  4. M Corpas*, E Bragin, S Clayton, P Bevan, HV Firth (2012). Interpretation of genomic copy number variants using DECIPHER. Current Protocols in Human Genetics 72: 8.14.1-8.14.17.
  5. M Corpas* (2012). A family experience of personal genomics. Journal of Genetic Counseling 21(3): 386-391.
  6. M Corpas* (2012). Spanish cuts: more economic damage. Nature 487(7405): 38.
  7. G Glusman, M Cariaso, RC Jimenez, D Swan, B Greshake, J Bhak, DW Logan, M Corpas* (2012). Low budget analysis of direct-to-consumer genomic testing familial data. F1000Research 1: 3.

2011

  1. RC Jimenez, GA Salazar, B Gel, P Bevan, J Dopazo, N Mulder, M Corpas* (2011). myKaryoView: a light-weight client for visualization of genomic data. PLOS ONE 6(10): e26345.
  2. M Corpas, S Doumbia, O Gascuel*, N Mulder (2011). Bamako 2009 conference on the bioinformatics of infectious diseases. Infection, Genetics and Evolution 11(4): 695-697.

2009

  1. HV Firth*, SM Richards, AP Bevan, S Clayton, M Corpas, D Rajan, S Van Vooren, Y Moreau, RM Pettett, NP Carter* (2009). DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. American Journal of Human Genetics 84(4): 524-533.

2008

  1. M Corpas, N Gehlenborg, SC Janga, PE Bourne* (2008). Ten simple rules for organizing a scientific meeting. PLOS Computational Biology 4(6): e1000080.
  2. F Reisinger, M Corpas, J Hancock, H Hermjakob, E Birney, P Kahlem* (2008). ENFIN: an integrative structure for systems biology. Lecture Notes in Computer Science (DILS) 5109: 132-143.

2007

  1. N Gehlenborg*, M Corpas, SC Janga (2007). Highlights from the Third International Society for Computational Biology Student Council Symposium. BMC Bioinformatics 8(Suppl 8): I1.

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