Lista de obras - 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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2022

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

artículo científico publicado en 2020

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

artículo científico publicado en 2016

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

artículo científico publicado en 2022

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

artículo científico publicado en 2013

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

artículo científico publicado en 2021

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

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2019

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

artículo científico publicado en 2016

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

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2018

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

artículo científico

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 of pathological gambling

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2016

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

artículo científico publicado en 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?

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Investigation of SHANK3 in schizophrenia

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

artículo científico publicado en 2017

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?

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2022

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

PLD3 in non-familial Alzheimer's disease

artículo científico publicado en 2015

Prediction of male-pattern baldness from genotypes

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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 ⬇️

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Lista de obras de Stefanie Heilmann-Heimbach

192 MicroRNAs and their regulatory interactions in the human hair follicle

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

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

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

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

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

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

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Evidence for a polygenic contribution to androgenetic alopecia

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

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

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

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

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

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

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

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

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

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

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

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

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

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

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

Genome-wide association study of pathological gambling

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

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

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

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

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

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

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

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

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

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

Investigation of SHANK3 in schizophrenia

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

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

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

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

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

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

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

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?

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

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

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

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

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

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

PLD3 in non-familial Alzheimer's disease

Prediction of male-pattern baldness from genotypes

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

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

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

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

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

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

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

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

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