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Bertram Müller‐Myhsok

32 works· latest 2022· 6 institutionscluster: provisionalORCID 0000-0002-0719-101X

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Citations4,365

Works here32

Most cited in this library

Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder2013 · 548 citations
Predictors of developmental dyslexia in European orthographies with varying complexity2012 · 450 citations
Cognitive mechanisms underlying reading and spelling development in five European orthographies2013 · 415 citations
Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks2009 · 294 citations
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores2019 · 269 citations

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Works

32 shown

Discovery of 42 genome-wide significant loci associated with dyslexia

Nature Genetics·2022·99 authors·Open access

141citations

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Proceedings of the National Academy of Sciences·2022·94 authors·Open access

133citations

Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning

Neuropsychopharmacology·2021·30 authors·Open access

54citations

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

Molecular Psychiatry·2020·49 authors·Open access

121citations

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

American Journal of Psychiatry·2019·92 authors·review·Open access

269citations

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Translational Psychiatry·2019·45 authors·Open access

105citations

Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence

Journal of Child Psychology and Psychiatry·2017·16 authors·Open access

104citations

Genetic variants in RBFOX3 are associated with sleep latency

European Journal of Human Genetics·2016·74 authors·Open access

39citations

Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome‐wide association and polygenic scoring study

American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2014·30 authors·Open access

128citations

Cognitive mechanisms underlying reading and spelling development in five European orthographies

Learning and Instruction·2013·30 authors·Open access

415citations

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

European Journal of Human Genetics·2013·40 authors·Open access

67citations

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

Proceedings of the National Academy of Sciences·2013·14 authors·Open access

548citations

Predictors of developmental dyslexia in European orthographies with varying complexity

Journal of Child Psychology and Psychiatry·2012·38 authors·Open access

450citations

Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia

PLoS ONE·2012·7 authors·Open access

67citations

Imaging genetics of FOXP2 in dyslexia

European Journal of Human Genetics·2011·12 authors·Open access

52citations

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2010·16 authors

29citations

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies

Molecular Psychiatry·2010·39 authors·Open access

182citations

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

American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2009·13 authors

41citations

A Hypomorphic Vasopressin Allele Prevents Anxiety-Related Behavior

PLoS ONE·2009·17 authors·Open access

73citations

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

Psychiatric Genetics·2009·13 authors

70citations

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

Journal of Neural Transmission·2008·12 authors·Open access

41citations

Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15

European Child & Adolescent Psychiatry·1999·8 authors

51citations

Evidence for Linkage of Spelling Disability to Chromosome 15

The American Journal of Human Genetics·1998·8 authors·Open access

171citations