Lista de obras - Dmitriy Drichel - Dominio Público Uruguay

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

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

artículo científico publicado en 2019

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

artículo científico publicado en 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

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

PLD3 in non-familial Alzheimer's disease

artículo científico publicado en 2015

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Rare variant testing of imputed data: an analysis pipeline typified

artículo científico publicado en 2014

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

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

artículo científico publicado en 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

artículo científico publicado en 2012

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

artículo científico publicado en 2020

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

artículo científico publicado en 2014

Lista de obras de Dmitriy Drichel

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

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 Etiology

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

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

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

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

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

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

Integrated Genome-Wide Pathway Association Analysis with INTERSNP

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

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

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

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

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

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

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

PLD3 in non-familial Alzheimer's disease

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

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

Rare variant testing of imputed data: an analysis pipeline typified

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

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

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

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