A. Konkashbaev

发表

The Genotype-Tissue Expression (GTEx) project

Ellen T. Gelfand, Bryan M. Gillard, Karna L. Robinson, 2013, Nature Genetics.

SCAN: SNP and copy number annotation

Wei Zhang, M. Eileen Dolan, Nancy J. Cox, 2010, Bioinform..

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

Jun S. Liu, Ellen T. Gelfand, Ayellet V. Segrè, 2015, Science.

Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping

N. Cox, E. Gamazon, A. Konkashbaev, 2017, Scientific Reports.

Genome-wide association study of obsessive-compulsive disorder

Y Wang, Dan J Stein, D V Conti, 2013, Molecular Psychiatry.

Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

Benjamin D. Greenberg, Ying Wang, Naomi R. Wray, 2013, PLoS genetics.

Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis

Dan J Stein, S. E. Stewart, R. Delorme, 2018, Molecular Psychiatry.

Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

Ayellet V. Segrè, M. McCarthy, Manolis Kellis, 2018, Nature Genetics.

Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.

Dan L Nicolae, Anna Tikhomirov, Nancy J Cox, 2010, American journal of human genetics.

Analysis of shared heritability in common disorders of the brain

Nick C Fox, Dan J Stein, Janice M. Fullerton, 2018, Science.

Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Ellen T. Gelfand, Ayellet V. Segrè, Casandra A. Trowbridge, 2016, Scientific Reports.

Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

Yusuke Nakamura, Dan M Roden, Matthew Oetjens, 2013, The Lancet.

Genome-wide association study of Tourette Syndrome

S. E. Stewart, A. Singleton, C. Sabatti, 2012, Molecular Psychiatry.

Genome-wide association study of obsessive-compulsive disorder

Dan J Stein, R. Delorme, M. Leboyer, 2013, Molecular Psychiatry.

Identification of Type 2 Diabetes Genes in Mexican Americans Through Genome-Wide Association Studies

Ying Sun, N. Cox, A. Konkashbaev, 2007, Diabetes.

Databases and ontologies SCAN : SNP and copy number annotation

D. Nicolae, E. Gamazon, A. Konkashbaev, 2009 .

Analysis of Genetically Determined Gene Expression Suggests Role of Inflammatory Processes in Etiology of Exfoliation Syndrome

E. Gamazon, A. Konkashbaev, U. Schlötzer-Schrehardt, 2020 .

Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension

Yusuke Nakamura, E. Gamazon, A. Konkashbaev, 2019, Pharmacogenetics and genomics.

Using an atlas of gene regulation across 44 human tissues to inform complex disease- 1 and trait-associated variation

M. McCarthy, Manolis Kellis, G. Getz, 2018 .

GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.

E. Knapik, E. Gamazon, A. Konkashbaev, 2019, American journal of human genetics.

Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.

E. Gamazon, H. Im, A. Konkashbaev, 2012, Journal of the National Cancer Institute.

Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Andrew B. Nobel, Fred A. Wright, Ivan Rusyn, 2015, Scientific Reports.

Integrating Cell-Based and Clinical Genome-Wide Studies to Identify Genetic Variants Contributing to Treatment Failure in Neuroblastoma Patients

E. Gamazon, H. Im, A. Konkashbaev, 2014, Clinical pharmacology and therapeutics.

Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome

E. Gamazon, A. Konkashbaev, U. Schlötzer-Schrehardt, 2020, bioRxiv.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

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.

A. Konkashbaev, R. Aster, K. Hansen, 2010, Blood.

Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines

Courtney E. French, D. Nickerson, S. Scherer, 2016, The Pharmacogenomics Journal.

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

D. Nicolae, E. Gamazon, A. Konkashbaev, 2011, Diabetologia.

SCAN database: facilitating integrative analyses of cytosine modification and expression QTL

Wei Zhang, Cong Liu, Xu Zhang, 2015, Database J. Biol. Databases Curation.

Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms

Yusuke Nakamura, Hae Kyung Im, Nancy J. Cox, 2014, The Pharmacogenomics Journal.

Erosion of melt layers developed during a plasma disruption

A. Konkashbaev, A. Hassanein, I. Konkashbaev, 1994 .

Ethnic Variation of TET2 SNP rs2454206 and Association with Clinical Outcome in Childhood AML: A Report from the Children’s Oncology Group

S. Raimondi, E. Gamazon, A. Konkashbaev, 2015, Leukemia.

Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping

E. Gamazon, A. Konkashbaev, E. Derks, 2017, Scientific Reports.

D. Nicolae, E. Gamazon, A. Konkashbaev, 2011 .

On Single-Array Genotype Calling Algorithms

Dan L. Nicolae, Anna Tikhomirov, Anuar Konkashbaev, 2008, 2008 International Conference on BioMedical Engineering and Informatics.

Transcriptome‐Wide Association Studies (TWAS): Methodologies, Applications, and Challenges

E. Gamazon, A. Konkashbaev, Dan Zhou, 2024, Current protocols.

Analysis of shared heritability in common disorders of the brain

Janice M. Fullerton, Thomas W. Mühleisen, C. Sudlow, 2018, Science.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

Melissa J. Green, R. Ophoff, E. Gamazon, 2013, Molecular Psychiatry.