about
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesSearch for new loci and low-frequency variants influencing glioma risk by exome-array analysisLarge-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Investigation of SHANK3 in schizophrenia.Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairmentFollow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility geneSUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociGenome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataMicrodeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?Genome-wide association study identifies multiple susceptibility loci for gliomaNo Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAsSupportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma.Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.Prediction of male-pattern baldness from genotypesAnalysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function.Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophreniaGenetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related CirrhosisHunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2.Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia.Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.Linkage and Association Analysis Identifies TRAF1 Influencing Common Carotid Intima-Media Thickness.Genome-wide association study of pathological gambling.Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment.Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.Association of age-of-onset groups with GWAS significant schizophrenia and bipolar disorder loci in Romanian bipolar I patients.Adverse genomic alterations and stemness features are induced by field cancerization in the microenvironment of hepatocellular carcinomas.Associations between SNPs and immune-related circulating proteins in schizophrenia.Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis.
P50
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P50
description
geneticus
@nl
hulumtuese
@sq
researcher
@en
հետազոտող
@hy
name
Stefanie Heilmann-Heimbach
@ast
Stefanie Heilmann-Heimbach
@de
Stefanie Heilmann-Heimbach
@en
Stefanie Heilmann-Heimbach
@es
Stefanie Heilmann-Heimbach
@nl
type
label
Stefanie Heilmann-Heimbach
@ast
Stefanie Heilmann-Heimbach
@de
Stefanie Heilmann-Heimbach
@en
Stefanie Heilmann-Heimbach
@es
Stefanie Heilmann-Heimbach
@nl
altLabel
Professor Stefanie Heilmann-Heimbach
@en
S Heilmann
@en
Stefanie Heilmann
@en
prefLabel
Stefanie Heilmann-Heimbach
@ast
Stefanie Heilmann-Heimbach
@de
Stefanie Heilmann-Heimbach
@en
Stefanie Heilmann-Heimbach
@es
Stefanie Heilmann-Heimbach
@nl
P1053
H-5942-2018
P106
P21
P31
P3829
P496
0000-0003-1057-465X