Lambertus Klei


Ontology type: schema:Person     


Person Info

NAME

Lambertus

SURNAME

Klei

Publications in SciGraph latest 50 shown

  • 2018-07 An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders in NATURE GENETICS
  • 2018-05 An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder in NATURE GENETICS
  • 2018-04 Genetic risk for schizophrenia and psychosis in Alzheimer disease in MOLECULAR PSYCHIATRY
  • 2017-07 Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders in NATURE GENETICS
  • 2016-11 Gene expression elucidates functional impact of polygenic risk for schizophrenia in NATURE NEUROSCIENCE
  • 2015-12 The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment in NATURE COMMUNICATIONS
  • 2015-02 Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways in NATURE NEUROSCIENCE
  • 2014-12 Rare deleterious mutations of the gene EFR3A in autism spectrum disorders in MOLECULAR AUTISM
  • 2014-12 The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism in NATURE COMMUNICATIONS
  • 2014-12 DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics in MOLECULAR AUTISM
  • 2014-11 Synaptic, transcriptional and chromatin genes disrupted in autism in NATURE
  • 2014-08 Most genetic risk for autism resides with common variation in NATURE GENETICS
  • 2013-09 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs in NATURE GENETICS
  • 2012-12 Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis in NATURE GENETICS
  • 2012-12 Genome-wide association study of Alzheimer's disease with psychotic symptoms in MOLECULAR PSYCHIATRY
  • 2012-12 Common genetic variants, acting additively, are a major source of risk for autism in MOLECULAR AUTISM
  • 2012-04 Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis in GENES & IMMUNITY
  • 2011-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy in NATURE GENETICS
  • 2011-04 Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men in OSTEOPOROSIS INTERNATIONAL
  • 2010-07 Functional impact of global rare copy number variation in autism spectrum disorders in NATURE
  • 2009-06 Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study in NATURE GENETICS
  • 2009-05 Autism genome-wide copy number variation reveals ubiquitin and neuronal genes in NATURE
  • 2009-02 Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study in NATURE GENETICS
  • 2007-07 Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation in HUMAN GENETICS
  • 2007-06 Testing for association based on excess allele sharing in a sample of related cases and controls in HUMAN GENETICS
  • 2007-03 Mapping autism risk loci using genetic linkage and chromosomal rearrangements in NATURE GENETICS
  • 2005-08 Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia in HUMAN GENETICS
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