Ciencias de la Salud
Campo de conocimiento
![Foto de Ciencias de la Salud](/img/noimage.png)
![Foto de Wellcome Trust Sanger Institute](/img/noimage_org.png)
Wellcome Trust Sanger Institute
Cambridge, Reino UnidoPublicaciones en colaboración con investigadoras/es de Wellcome Trust Sanger Institute (13)
2023
2021
-
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
Nature Genetics, Vol. 53, Núm. 11, pp. 1543-1552
-
Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
2019
-
Molecular epidemiology of G12 rotavirus strains during eight consecutive epidemic seasons in the Basque Country (North of Spain), 2010–2018
Infection, Genetics and Evolution, Vol. 71, pp. 67-75
2015
-
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Nature Genetics, Vol. 47, Núm. 4, pp. 381-386
-
Identification of new SNPs in native South American populations by resequencing the y chromosome
Forensic Science International: Genetics, Vol. 15, pp. 111-114
-
The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades
Molecular Biology and Evolution, Vol. 32, Núm. 3, pp. 661-673
2014
-
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Forensic Science International: Genetics, Vol. 12, pp. 12-23
2012
2011
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Nature Genetics, Vol. 43, Núm. 12, pp. 1193-1201
2002
-
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia
Gene, Vol. 282, Núm. 1-2, pp. 87-94
-
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128