ELIECER
COTO GARCIA
Catedrático de Universidad
Universidad Autónoma de Madrid
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von Universidad Autónoma de Madrid (27)
2022
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A first update on mapping the human genetic architecture of COVID-19
Nature
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Whole-genome sequencing reveals host factors underlying critical COVID-19
Nature, Vol. 607, Núm. 7917, pp. 97-103
2016
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Primary distal renal tubular acidosis: Novel findings in patients studied by next-generation sequencing
Pediatric Research, Vol. 79, Núm. 3, pp. 496-501
2015
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A 3′-UTR polymorphism in soluble epoxide hydrolase gene is associated with acute rejection in renal transplant recipients
PLoS ONE, Vol. 10, Núm. 7
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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
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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
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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
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Soluble co-signaling molecules predict long-term graft outcome in kidney-transplanted patients
PLoS ONE, Vol. 9, Núm. 12
2013
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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
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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
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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
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APOE and Alzheimer disease: A major gene with semi-dominant inheritance
Molecular Psychiatry, Vol. 16, Núm. 9, pp. 903-907
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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
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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
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KCNQ1 gene variants and risk of new-onset diabetes in tacrolimus-treated renal-transplanted patients
Clinical Transplantation, Vol. 25, Núm. 3
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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
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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
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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
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Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Nature Genetics, Vol. 41, Núm. 10, pp. 1094-1099