about
Rare variant testing of imputed data: an analysis pipeline typified.Quick, "imputation-free" meta-analysis with proxy-SNPsSUCLG2 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.A one-degree-of-freedom test for supra-multiplicativity of SNP effectsNovel genetic matching methods for handling population stratification in genome-wide association studies.Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample.Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.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.METAINTER: meta-analysis of multiple regression models in genome-wide association studies.PLD3 in non-familial Alzheimer's disease.Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss.The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients.Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss.Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identified.Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss.Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss.Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans.Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its EtiologyIntegrated Genome-Wide Pathway Association Analysis with INTERSNPThe exhaustive genomic scan approach, with an application to rare-variant association analysis
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description
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Dmitriy Drichel
@ast
Dmitriy Drichel
@en
Dmitriy Drichel
@es
Dmitriy Drichel
@nl
type
label
Dmitriy Drichel
@ast
Dmitriy Drichel
@en
Dmitriy Drichel
@es
Dmitriy Drichel
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prefLabel
Dmitriy Drichel
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Dmitriy Drichel
@en
Dmitriy Drichel
@es
Dmitriy Drichel
@nl
P106
P31
P496
0000-0001-5978-3458