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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

artículo científico publicado en 2010

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2009

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

artículo científico publicado en 2005

Neutrophil Recruitment and Barrier Impairment in Celiac Disease: A Genomic Study

article published in 2007

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