about
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesG protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthStrong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer.Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinA genome-wide association study in 574 schizophrenia trios using DNA poolingA genome-wide association study for late-onset Alzheimer's disease using DNA poolingGenetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaGenome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26Susceptibility variants for male-pattern baldness on chromosome 20p11.Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness.Detection of chromosomal breakpoints in patients with developmental delay and speech disordersHigh-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer.Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataThe DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity.Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors.Patient-specific driver gene prediction and risk assessment through integrated network analysis of cancer omics profiles.Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry.Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers.The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function.Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing.Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its EtiologyLoss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic DiseaseGenomic landscape of lung adenocarcinoma in East AsiansMethionine is a metabolic dependency of tumor-initiating cellsPublisher Correction: Methionine is a metabolic dependency of tumor-initiating cellsLinking Cancer Stem Cell Plasticity to Therapeutic Resistance-Mechanism and Novel Therapeutic Strategies in Esophageal Cancer
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Axel M Hillmer
@ast
Axel M Hillmer
@en
Axel M Hillmer
@es
Axel M Hillmer
@nl
Axel M Hillmer
@sl
type
label
Axel M Hillmer
@ast
Axel M Hillmer
@en
Axel M Hillmer
@es
Axel M Hillmer
@nl
Axel M Hillmer
@sl
altLabel
Axel Hillmer
@en
prefLabel
Axel M Hillmer
@ast
Axel M Hillmer
@en
Axel M Hillmer
@es
Axel M Hillmer
@nl
Axel M Hillmer
@sl
P1053
B-7485-2015
N-2927-2014
P106
P21
P31
P3829
P496
0000-0002-3381-7266