List of works - Joachim Hallmayer

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

scientific journal article

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

scientific article published on 14 October 2011

Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak

scientific article

Common variants in P2RY11 are associated with narcolepsy

scientific article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

Erratum: Common variants in P2RY11 are associated with narcolepsy

scholarly article published in Nature Genetics

Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus

scholarly article published in Nature Genetics

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

scientific article published on 15 July 2010

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

scientific article

Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic

scientific journal article

Head circumferences in twins with and without Autism Spectrum Disorders

scientific article published on September 2013

ImmunoChip study implicates antigen presentation to T cells in narcolepsy

scientific article

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

scientific journal article

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

scientific article

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

scientific article

Narcolepsy is strongly associated with the T-cell receptor alpha locus

scientific article

Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

scientific article

Prenatal and perinatal risk factors in a twin study of autism spectrum disorders

scientific article

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

scientific article

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

scientific article

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

scientific article

Using fMRI connectivity to define a treatment-resistant form of post-traumatic stress disorder

scientific article published on 01 April 2019

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome

scientific article

Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

scientific article

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

scientific article published on 6 March 2017

List of works by Joachim Hallmayer

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

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak

Common variants in P2RY11 are associated with narcolepsy

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Erratum: Common variants in P2RY11 are associated with narcolepsy

Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus

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

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

Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic

Head circumferences in twins with and without Autism Spectrum Disorders

ImmunoChip study implicates antigen presentation to T cells in narcolepsy

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

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

Narcolepsy is strongly associated with the T-cell receptor alpha locus

Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

Prenatal and perinatal risk factors in a twin study of autism spectrum disorders

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

Using fMRI connectivity to define a treatment-resistant form of post-traumatic stress disorder

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome

Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder