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Author Details

Stefanie Heilmann-Heimbach
Institute of Human Genetics, University Hospital of Bonn & University of Bonn
2010
135
34
PMIDPaper TitleJournal TitlePublished Year
38036661Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients.Psychopharmacology (Berl)2024
37985413The first genome-wide association study in the Argentinian and Chilean populations identifies shared genetics with Europeans in Alzheimer's disease.Alzheimers Dement2024
36319675Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.Eur J Hum Genet2023
37486023Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.Ann Neurol2023
37737258Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss.Nat Commun2023
37777856GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.Am J Psychiatry2023
37643212Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by <i>HLA-DRB1*04</i> subtypes.Proc Natl Acad Sci U S A2023
37671665Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.Br J Dermatol2023
37195665Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease.JAMA Netw Open2023
36652833Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders.Schizophr Res2023
36674414Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.Int J Mol Sci2023
36895094Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer's disease within a cognitive reserve framework.Alzheimers Dement2023
36336714Genetic prediction of male pattern baldness based on large independent datasets.Eur J Hum Genet2023
32758327Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.Psychol Med2022
35379992New insights into the genetic etiology of Alzheimer's disease and related dementias.Nat Genet2022
35639372Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.JAMA Neurol2022
35523767Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum.Transl Psychiatry2022
36066633Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.Acta Neuropathol2022
36238604Genome-wide association study in patients with posterior urethral valves.Front Pediatr2022
35923707Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes.Front Genet2022
36352089A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.Commun Biol2022
36351892Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles.Transl Psychiatry2022
36121467The serotonin receptor 3E variant is a risk factor for female IBS-D.J Mol Med (Berl)2022
35098976Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and Diet.J Prev Alzheimers Dis2022
35119146Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia.Exp Dermatol2022
35305013A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels.J Clin Endocrinol Metab2022
35199045First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>.HGG Adv2022
34528480MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.J Dent Res2022
34817932Acquired Resistance to Antiangiogenic Therapies in Hepatocellular Carcinoma Is Mediated by Yes-Associated Protein 1 Activation and Transient Expansion of Stem-Like Cancer Cells.Hepatol Commun2022
34775485Epigenome-wide association study of alcohol use disorder in five brain regions.Neuropsychopharmacology2022
34656040Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients.J Affect Disord2022
33431802Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families.Transl Psychiatry2021
33590662"The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20â¿¿years after assessment.Am J Med Genet B Neuropsychiatr Genet2021
34901950Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID-19.Skin Health Dis2021
34674705Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients.BMC Med Genomics2021
34556731Polygenic risk for obsessive-compulsive disorder (OCD) predicts brain response during working memory task in OCD, unaffected relatives, and healthy controls.Sci Rep2021
34789355Interplay between the Genetics of Personality Traits, severe Psychiatric Disorders, and COVID-19 Host Genetics in the Susceptibility to SARS-CoV-2 Infection - ADDENDUM.BJPsych Open2021
34659794Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection.BJPsych Open2021
34506541Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness.PLoS One2021
34127797Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning.Neuropsychopharmacology2021
34015192Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2.J Dtsch Dermatol Ges2021
31712721Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.Mol Psychiatry2021
31712720Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.Mol Psychiatry2021
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
32451266Replication of a hippocampus specific effect of the tescalcin regulating variant rs7294919 on gray matter structure.Eur Neuropsychopharmacol2020
32012148DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning.PLoS Comput Biol2020
33167971Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles.BMC Dermatol2020
32946134Hormonal regulation in male androgenetic alopecia-Sex hormones and beyond: Evidence from recent genetic studies.Exp Dermatol2020
32918782Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo.Cell Prolif2020
32617075Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells.Mediators Inflamm2020
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Collaborators

Institute of Human Genetics, University Hospital Bonn
Co-authored papers 87
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Co-authored papers 34
Central Institute of Mental Health, University of Mannheim
Co-authored papers 32
Central Institute of Mental Health, Heidelberg University
Co-authored papers 27
University of Duisburg-Essen
Co-authored papers 26
University of Bonn, School of Medicine & University Hospital Bonn.
Co-authored papers 24
Central Institute of Mental Health, Heidelberg University
Co-authored papers 24
Institute of Human Genetics, University of Bonn
Co-authored papers 23
Co-authored papers 19
University Hospital Bonn
Co-authored papers 18
Central Institute of Mental Health, Heidelberg University
Co-authored papers 17
Central Institute of Mental Health, University of Heidelberg
Co-authored papers 14
Max Planck Institute of Psychiatry
Co-authored papers 14
University Hospital Basel and University of Basel
Co-authored papers 13
Oslo University Hospital & Institute of Clinical Medicine, University of Oslo
Co-authored papers 12
Co-authored papers 11
SUNY Upstate Medical University
Co-authored papers 11
Institute of Human Genetics, University of Bonn
Co-authored papers 10
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 9
Heidelberg University
Co-authored papers 9
Philipps University of Marburg
Co-authored papers 9
Co-authored papers 9
Co-authored papers 9
Institute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital
Co-authored papers 8
Institute of Psychiatric Phenomics and Genomics (IPPG), University Hospital
Co-authored papers 8
Co-authored papers 7
Oslo University Hospital
Co-authored papers 7
University of Oxford
Co-authored papers 7
University Hospital Munster, University of Munster
Co-authored papers 7
Co-authored papers 7