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List of works by Stefan Herms

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

scientific article published on 16 June 2014

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

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

scientific article

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

scientific article

A strobilurin fungicide enhances the resistance of tobacco against tobacco mosaic virus and Pseudomonas syringae pv tabaci

scientific article published in September 2002

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.

scientific article published on 31 May 2018

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

scientific article

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

scientific article

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

scientific article published on 31 August 2016

Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.

scientific article published on 9 November 2017

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

scientific article published on 16 March 2020

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

scientific article

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

scientific article published on 11 November 2019

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

scientific article published on 13 May 2008

Caspase recruitment domain 15 gene haplotypes in sarcoidosis

article

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

article

Commingling analysis of age-of-onset in bipolar I disorder and the morbid risk for major psychoses in first degree relatives of bipolar I probands

scientific article published on 9 July 2014

Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.

scientific article

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

scientific article

Copy number variants in German patients with schizophrenia

scientific article

Corrigendum to “Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue” [Brain Res. 1499 (2013) 136–144]

scholarly article by Katharina Pernhorst et al published March 2014 in Brain Research

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

scientific article

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Direct conversion of fibroblasts into stably expandable neural stem cells

scientific article

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

scientific article

Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia

scientific article

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder

article

Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate

scientific article published on 24 August 2012

Evidence for contribution of epigenetic mechanisms in the pathogenesis of systemic mast cell activation disease

article

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

article

Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate

scientific article published in April 2009

GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.

scientific article

Gene expression is stable in a complete CIB1 knockout keratinocyte model

scientific article published on 11 September 2020

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

scientific article

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

scientific article published on 17 July 2017

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

scientific article

Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.

scientific article

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

scientific article published on 21 January 2016

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

scientific article published on 24 September 2012

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

scientific article published in March 2011

Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

scientific article published on 30 September 2014

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar 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

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

scientific article

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

scientific article

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

scientific article

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

scientific article

Genome-wide association study identifies multiple susceptibility loci for glioma ⬇️

scientific article

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

scientific article

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

scientific article

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

article

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

scientific article published on 27 March 2017

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide association study on differentiated thyroid cancer

scientific journal article

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

scientific article (publication date: 11 March 2014)

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

scientific article

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

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

scientific article published on 18 October 2011

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

scientific article published in March 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

scientific article published on 8 August 2017

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

article

Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach

scientific article published on 17 September 2014

IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate

scientific article published in December 2009

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

scientific article

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

scientific article

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

scientific article

Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss

scientific article published in June 2012

Investigation of the role of TCF4 rare sequence variants in schizophrenia

scientific article published on 22 May 2015

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population

scientific article published in October 2008

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

scientific article

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

scientific article published on 8 April 2022

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

scientific article published on 11 August 2013

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

scientific article

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

scientific article published in February 2013

Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk

scientific article

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk

scientific article published on 16 July 2014

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

scientific article published on 17 June 2016

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients

scientific article published on 15 March 2010

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

scientific article

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

scientific article

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients

article published in 2009

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.

scientific article

Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis ⬇️

scientific article

Shared genetic etiology between alcohol dependence and major depressive disorder.

scientific article published in August 2018

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

scientific article published on 16 February 2020

Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

scientific article

Small molecules enable highly efficient neuronal conversion of human fibroblasts

scientific article

Stimulation of MMP-1 and CCL2 by NAMPT in PDL cells.

scientific article published on 22 August 2013

Strong association of variants around FOXE1 and orofacial clefting.

scientific article

Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array

scientific article published on 26 October 2015

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

scientific article

Susceptibility variants for male-pattern baldness on chromosome 20p11.

scientific article

Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome

scientific article

TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue

scientific article published on 22 May 2013

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

scientific article published on 04 May 2009

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

scientific article published on 19 July 2010

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

scientific article

The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in KitD816V systemic mastocytosis

scientific article published on May 2013

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scientific article published on 26 November 2018

Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent

scientific article

VEGF Gene Haplotypes Are Associated With Sarcoidosis

article

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

scientific article published in March 2010

Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples

scientific article

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

scientific article

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