List of works - Lambertus Klei

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition

scientific article

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

scientific article

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

scientific article published on 06 June 2013

African Ancestry, SES, FEV1 And Asthma Exacerbations In Puerto Rican Children

African ancestry and lung function in Puerto Rican children

scientific article

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

scientific article published on 26 April 2018

Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.

scientific article published on 12 October 2016

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

scientific article

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men.

scientific article

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

scientific article published on July 2014

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

scientific article

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

scientific article

Common genetic variants, acting additively, are a major source of risk for autism

scientific article

Common risk variants identified in autism spectrum disorder

Consanguinity and increased risk for schizophrenia in Egypt

scientific article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees

scientific article published on 7 October 2011

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

scientific article

Discovering genetic ancestry using spectral graph theory

scientific article published in January 2010

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scholarly article published in Nature Genetics

Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure

scientific article

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation

scientific article published on 14 April 2007

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Heritability of morningness-eveningness and self-report sleep measures in a family-based sample of 521 hutterites

scientific article

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

scientific article

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men

scientific article

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

scientific article

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

scientific article

Joint evaluation of serum C-Reactive Protein levels and polygenic risk scores as risk factors for schizophrenia.

scientific article published on 21 December 2017

Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia

article

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

scientific article

Most genetic risk for autism resides with common variation ⬇️

scientific article

No association of psychosis in Alzheimer disease with neurodegenerative pathway genes ⬇️

scientific article published on November 18, 2010

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

scientific article published on 24 January 2008

Pleiotropy and principal components of heritability combine to increase power for association analysis

article

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects ⬇️

scientific article published on January 10, 2012

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients

scientific article

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

scientific article published on June 2013

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

scientific article

Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred

scientific article published on 31 May 2017

Semisoft clustering of single-cell data

article published in the Proceedings of the National Academy of Sciences of the United States of America

Synaptic, transcriptional and chromatin genes disrupted in autism

scientific article

Testing for association based on excess allele sharing in a sample of related cases and controls

scientific article published on 7 March 2007

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

scientific article

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families

scientific article

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scientific article

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies

scientific article

Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children

scientific article

List of works by Lambertus Klei

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

A genome-wide scan for common alleles affecting risk for autism

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

African Ancestry, SES, FEV1 And Asthma Exacerbations In Puerto Rican Children

African ancestry and lung function in Puerto Rican children

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men.

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Common genetic variants, acting additively, are a major source of risk for autism

Common risk variants identified in autism spectrum disorder

Consanguinity and increased risk for schizophrenia in Egypt

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

Discovering genetic ancestry using spectral graph theory

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure

Functional impact of global rare copy number variation in autism spectrum disorders

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Heritability of morningness-eveningness and self-report sleep measures in a family-based sample of 521 hutterites

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

Individual common variants exert weak effects on the risk for autism spectrum disorders

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Joint evaluation of serum C-Reactive Protein levels and polygenic risk scores as risk factors for schizophrenia.

Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Most genetic risk for autism resides with common variation ⬇️

No association of psychosis in Alzheimer disease with neurodegenerative pathway genes ⬇️

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

Pleiotropy and principal components of heritability combine to increase power for association analysis

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects ⬇️

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred

Semisoft clustering of single-cell data

Synaptic, transcriptional and chromatin genes disrupted in autism

Testing for association based on excess allele sharing in a sample of related cases and controls

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies

Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children