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List of works by Stefanie Heilmann-Heimbach

192 MicroRNAs and their regulatory interactions in the human hair follicle

scholarly article by L.M. Hochfeld published in September 2016

257 Is EBF1 a negative regulator of WNT10A in the development of androgenetic alopecia?

scholarly article by L.M. Hochfeld published in October 2017

268 Male-pattern baldness and its association with coronary heart disease

scholarly article by Stefanie Heilmann-Heimbach published in October 2017

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders

scientific article

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. ⬇️

scientific article published on 03 October 2016

Adverse genomic alterations and stemness features are induced by field cancerization in the microenvironment of hepatocellular carcinomas

scientific article published on 15 March 2017

Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment

scientific article

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

scientific article published on 04 July 2016

Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

article

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations

scientific article published on 12 June 2017

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer

scientific article published on 29 December 2016

Association of age-of-onset groups with GWAS significant schizophrenia and bipolar disorder loci in Romanian bipolar I patients

scientific article published on 10 November 2015

Associations between SNPs and immune-related circulating proteins in schizophrenia.

scientific article published on 3 October 2017

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

scientific article published on 2 March 2016

Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate

scientific article published on 19 September 2017

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

scientific article

Comparative 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

scientific article published in 2022

DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning

scientific article published on 03 February 2020

Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia.

scientific article published on 06 April 2016

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

scientific article published in February 2022

Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis

scientific article published on 4 April 2013

Epigenome-wide association study of alcohol use disorder in five brain regions

scientific article published on 13 November 2021

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

scientific article published in July 2017

Evidence for a polygenic contribution to androgenetic alopecia

article

Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs

scientific article

Fine mapping of the human AR/EDA2R locus in androgenetic alopecia

scientific article published on 01 March 2010

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

scientific article

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

scientific article

Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2.

scientific article published on 6 January 2016

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

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 association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy

scientific article

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

scientific article

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia ⬇️

scientific article published on 9 April 2018

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 borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

scientific article published on 20 June 2017

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 of pathological gambling

scientific article published on 14 June 2016

Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci

scientific article published on 22 January 2015

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

scientific article published on 26 October 2011

Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment

scientific article

Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.

scientific article published on 16 June 2016

Hormonal regulation in male androgenetic alopecia-Sex hormones and beyond: Evidence from recent genetic studies

scientific article published on 17 June 2020

Hunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?

scientific article published on 4 February 2016

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

scientific article published on 27 April 2017

ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development

scientific article published on 08 February 2017

Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata

scientific article published on 22 October 2014

Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease

scientific article published on 11 December 2014

Investigation of SHANK3 in schizophrenia

scientific article

Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss

scientific article published on 19 December 2013

Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

scientific article published on 16 July 2013

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

scientific article published on 20 June 2014

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

scientific article

Linkage and Association Analysis Identifies TRAF1 Influencing Common Carotid Intima-Media Thickness

scientific article published on 8 November 2016

Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles

scientific article published on 10 November 2020

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

scientific article

Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

scientific article

Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.

scientific article published on 29 January 2014

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum

scientific article published on 06 May 2022

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

scientific article

No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia ⬇️

scientific article published on July 1, 2013

Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample

scientific article published on 02 March 2018

O100 : The hepatic microenvironment induces a CSC phenotype and determines the prognosis of HCC patients

PLD3 in non-familial Alzheimer's disease

scientific article published in April 2015

Prediction of male-pattern baldness from genotypes

scientific article published on 28 October 2015

Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function

scientific article

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

scientific article

SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients

article

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

scientific article

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

scientific article

Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

scientific article

Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness

scientific article published in December 2011

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

scientific article published on February 2017

The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer

scientific article

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