Publicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (27)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. A first update on mapping the human genetic architecture of COVID-19

    Nature

  2. Whole-genome sequencing reveals host factors underlying critical COVID-19

    Nature, Vol. 607, Núm. 7917, pp. 97-103

2016

  1. Primary distal renal tubular acidosis: Novel findings in patients studied by next-generation sequencing

    Pediatric Research, Vol. 79, Núm. 3, pp. 496-501

2015

  1. A 3′-UTR polymorphism in soluble epoxide hydrolase gene is associated with acute rejection in renal transplant recipients

    PLoS ONE, Vol. 10, Núm. 7

  2. ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: A Next Generation Sequencing approach

    Clinical Chemistry and Laboratory Medicine, Vol. 53, Núm. 10, pp. 1515-1519

  3. Association between the IL17RA rs4819554 polymorphism and reduced renal filtration rate in the Spanish RENASTUR cohort

    Human Immunology, Vol. 76, Núm. 2-3, pp. 75-78

  4. The donor ABCB1 (MDR-1) C3435T polymorphism is a determinant of the graft glomerular filtration rate among tacrolimus treated kidney transplanted patients

    Journal of Human Genetics, Vol. 60, Núm. 5, pp. 273-276

2014

  1. Soluble co-signaling molecules predict long-term graft outcome in kidney-transplanted patients

    PLoS ONE, Vol. 9, Núm. 12

2013

  1. A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort

    Gene, Vol. 527, Núm. 2, pp. 670-672

  2. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

    Molecular Psychiatry, Vol. 18, Núm. 4, pp. 461-470

2012

  1. Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus

    Molecular Genetics and Metabolism, Vol. 105, Núm. 3, pp. 525-527

2011

  1. APOE and Alzheimer disease: A major gene with semi-dominant inheritance

    Molecular Psychiatry, Vol. 16, Núm. 9, pp. 903-907

  2. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

    Nature Genetics, Vol. 43, Núm. 5, pp. 429-436

  3. Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations

    Neurobiology of Aging, Vol. 32, Núm. 4, pp. 756.e11-756.e15

  4. KCNQ1 gene variants and risk of new-onset diabetes in tacrolimus-treated renal-transplanted patients

    Clinical Transplantation, Vol. 25, Núm. 3

  5. Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

    Mitochondrion, Vol. 11, Núm. 1, pp. 176-181

2010

  1. Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy

    Biochemical and Biophysical Research Communications, Vol. 397, Núm. 3, pp. 576-579

  2. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: A meta-analysis study

    Journal of Alzheimer's Disease, Vol. 22, Núm. 1, pp. 247-255

2009

  1. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

    Nature Genetics, Vol. 41, Núm. 10, pp. 1094-1099