List of works - Bertram Müller-Myhsok

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

scientific article (publication date: 18 November 2004)

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

scientific article

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

scientific article

A mega-analysis of genome-wide association studies for major depressive disorder

scientific article

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

scientific article published on 26 April 2018

Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment

scientific article

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

scientific article

Common genetic variants influence human subcortical brain structures

scientific article

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

scientific article published in April 2013

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

scientific article

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

scientific article

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

scientific article

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Genome-wide association study of PR interval

scientific article

Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder

scientific article

Genome-wide meta-analysis identifies new susceptibility loci for migraine

scientific article

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

scientific article

Genome-wide association analysis identifies three new breast cancer susceptibility loci

scientific article published on 22 January 2012

Genome-wide association analysis identifies susceptibility loci for migraine without aura

scientific article

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

scientific article

A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression

scientific article published on September 2009

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

scientific article

Genome-wide association study reveals two new risk loci for bipolar disorder

scientific article (publication date: 11 March 2014)

Genome-wide association study identifies 30 loci associated with bipolar disorder.

scientific article

Polymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls

scientific article published in July 2008

Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks

scientific article (publication date: October 2009)

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

scientific article

Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression

scientific article

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

scientific article published on 27 July 2008

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder

scientific article published on 5 July 2006

Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies

scientific article

Predictors of developmental dyslexia in European orthographies with varying complexity

scientific article published on 10 December 2012

The neuronal transporter gene SLC6A15 confers risk to major depression

scientific article

Novel genetic loci underlying human intracranial volume identified through genome-wide association

scientific article (publication date: 3 October 2016)

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

scientific article published on 18 October 2011

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

scientific journal article

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

scientific article

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

scientific article

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients

scientific article

Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment

scientific article

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

scientific article

Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder

scientific article published on 01 June 2006

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

scientific article

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

article

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

scientific article published on 24 May 2016

Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.

scientific article

List of works by Bertram Müller-Myhsok

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

A mega-analysis of genome-wide association studies for major depressive disorder

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment

Identification of common variants associated with human hippocampal and intracranial volumes

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

Common genetic variants influence human subcortical brain structures

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

Analysis of shared heritability in common disorders of the brain

Genome-wide association study of PR interval

Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Genome-wide association study reveals two new risk loci for bipolar disorder

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Polymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls

Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder

Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies

Predictors of developmental dyslexia in European orthographies with varying complexity

The neuronal transporter gene SLC6A15 confers risk to major depression

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

Novel genetic loci associated with hippocampal volume

Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients

Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.