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Lista de obras de Stefan Herms

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

artículo científico publicado en 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

artículo científico publicado en 2012

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

artículo científico publicado en 2010

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

artículo científico publicado en 2002

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

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

artículo científico publicado en 2011

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

artículo científico publicado en 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.

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

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.

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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

artículo científico publicado en 2016

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

artículo científico publicado en 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.

artículo científico publicado en 2009

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico

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

artículo científico publicado en 2013

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.

artículo científico publicado en 2010

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2009

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

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

artículo científico publicado en 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2009

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

artículo científico publicado en 2017

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

artículo científico publicado en 2022

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

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Investigation of the role of TCF4 rare sequence variants in schizophrenia

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

artículo científico publicado en 2016

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

artículo científico publicado en 2010

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

artículo científico publicado en 2017

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

artículo científico publicado en 2009

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.

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Shared genetic etiology between alcohol dependence and major depressive disorder.

artículo científico publicado en 2018

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

artículo científico publicado en 2020

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

artículo científico publicado en 2011

Small molecules enable highly efficient neuronal conversion of human fibroblasts

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Strong association of variants around FOXE1 and orofacial clefting.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

artículo científico publicado en 2008

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

artículo científico publicado en 2014

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

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2010

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

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

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2009

VEGF Gene Haplotypes Are Associated With Sarcoidosis

article

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

artículo científico publicado en 2010

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

artículo científico publicado en 2009

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

artículo científico publicado en 2014

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