Author details

Full Name

Anuar Konkashbaev

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36797672	Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.	BMC Genomics	2023
35383711	Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.	Pharmacogenet Genomics	2022
30827500	GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.	Am J Hum Genet	2019
29955180	Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.	Nat Genet	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
26856248	Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.	Pharmacogenomics J	2017
28729732	Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping.	Sci Rep	2017
25158072	Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.	Am J Psychiatry	2015
25818895	SCAN database: facilitating integrative analyses of cytosine modification and expression QTL.	Database (Oxford)	2015
26126966	Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group.	Leukemia	2015
24980783	Establishment of CYP2D6 reference samples by multiple validated genotyping platforms.	Pharmacogenomics J	2014
24549002	Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.	Clin Pharmacol Ther	2014
23243203	Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.	J Natl Cancer Inst	2013
22889924	Genome-wide association study of Tourette's syndrome.	Mol Psychiatry	2013
22889921	Genome-wide association study of obsessive-compulsive disorder.	Mol Psychiatry	2013
24204291	Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.	PLoS Genet	2013
23755828	Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.	Lancet	2013
21647700	Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.	Diabetologia	2011
20598280	Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.	Am J Hum Genet	2010
20040764	The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution.	Blood	2010
19933162	SCAN: SNP and copy number annotation.	Bioinformatics	2010
18192023	Recursive trace line method for detecting myelinated bundles: a comparison study with pyramidal cell arrays.	Journal of Neuroscience Methods	2008
17846124	Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.	Diabetes	2007
17282753	Automated recursive segmentation of large neocortical images using standard deviation as termination criteria.	Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings	2005