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List of works by Dmitriy Drichel

A one-degree-of-freedom test for supra-multiplicativity of SNP effects

scientific article

Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans.

scientific article

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

article

Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample

scientific article

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

scientific article published on 16 January 2016

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

scientific article published on 03 November 2020

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Identification and characterization of two functional variants in the human longevity gene FOXO3.

scientific article published on 12 December 2017

Integrated Genome-Wide Pathway Association Analysis with INTERSNP

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 male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss

scientific article published in June 2012

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

scientific article published on 20 June 2014

Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss

scientific article published on 4 August 2011

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

scientific article published on 27 November 2015

METAINTER: meta-analysis of multiple regression models in genome-wide association studies

scientific article published on 23 September 2014

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

scientific article

Novel genetic matching methods for handling population stratification in genome-wide association studies

scientific article published on 14 March 2015

PLD3 in non-familial Alzheimer's disease

scientific article published in April 2015

Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3.

scientific article published on 17 January 2018

Quick, "imputation-free" meta-analysis with proxy-SNPs

scientific article

Rare variant testing of imputed data: an analysis pipeline typified

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

Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss

scientific article published on 5 November 2012

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

scientific article published in May 2012

The exhaustive genomic scan approach, with an application to rare-variant association analysis

scientific article published on 15 May 2020

The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients

scientific article published in April 2014

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