Author details

Full Name

Andrey A Shabalin

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37310323	General . specific vulnerabilities: polygenic risk scores and higher-order psychopathology dimensions in the Adolescent Brain Cognitive Development (ABCD) Study.		2023
36253440	Genome-wide association study meta-analysis of suicide death and suicidal behavior.	Molecular Psychiatry	2023
37591353	Examining the relationship between genetic risk for depression and youth episodic stress exposure.		2023
36893177	Polygenic risk scores for asthma and allergic disease associate with COVID-19 severity in 9/11 responders.		2023
35212135	Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide.	Am J Med Genet B Neuropsychiatr Genet	2022
36307804	Polygenic association of glomerular filtration rate decline in world trade center responders.	BMC Nephrol	2022
35378236	Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms.	J Am Acad Child Adolesc Psychiatry	2022
35689615	TwinEQTL: ultrafast and powerful association analysis for eQTL and GWAS in twin studies.	Genetics	2022
35614386	Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs.	BMC Genomics	2022
35545664	Unique and joint associations of polygenic risk for major depression and opioid use disorder with endogenous opioid system function.		2022
34799694	The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders.	Mol Psychiatry	2022
34559220	Suicide and Psychosis: Results From a Population-Based Cohort of Suicide Death (N = 4380).	Schizophr Bull	2022
34821019	Exploring the genetic overlap of suicide-related behaviors and substance use disorders.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2021
34234108	Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach.	Transl Psychiatry	2021
34042246	Rare protein-coding variants implicate genes involved in risk of suicide death.	Am J Med Genet B Neuropsychiatr Genet	2021
34330890	Genetic association study of childhood aggression across raters, instruments, and age.	Transl Psychiatry	2021
31165892	Independent Methylome-Wide Association Studies of Schizophrenia Detect Consistent Case-Control Differences.	Schizophr Bull	2020
32425094	Test-statistic inflation in methylome-wide association studies.	Epigenetics	2020
31889537	Cell Type-Specific Methylome-wide Association Studies Implicate Neurotrophin and Innate Immune Signaling in Major Depressive Disorder.	Biol Psychiatry	2020
32221549	Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland.	Schizophr Bull	2020
30353169	Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide.	Molecular Psychiatry	2020
30242228	Methylome-wide association findings for major depressive disorder overlap in blood and brain and replicate in independent brain samples.	Mol Psychiatry	2020
31501512	A methylation study of long-term depression risk.	Molecular Psychiatry	2020
30339992	Polygenic risk scoring and prediction of mental health outcomes.		2019
29788473	Enhancing Psychosis-Spectrum Nosology Through an International Data Sharing Initiative.	Schizophr Bull	2018
29029013	An empirical Bayes approach for multiple tissue eQTL analysis.	Biostatistics	2018
29905862	Building a schizophrenia genetic network: transcription factor 4 regulates genes involved in neuronal development and schizophrenia risk.	Hum Mol Genet	2018
30135428	Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder.	Translational Psychiatry	2018
30320886	A Whole Methylome Study of Ethanol Exposure in Brain and Blood: An Exploration of the Utility of Peripheral Blood as Proxy Tissue for Brain in Alcohol Methylation Studies.	Alcohol Clin Exp Res	2018
29447401	RaMWAS: fast methylome-wide association study pipeline for enrichment platforms.		2018
29224145	Methyl-CpG-Binding Domain Sequencing: MBD-seq.	Methods in Molecular Biology	2018
29656664	Epigenetic Aging in Major Depressive Disorder.	American Journal of Psychiatry	2018
29073327	Estimation of cis-eQTL effect sizes using a log of linear model.	Biometrics	2018
28137292	Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies.	Genome Biol	2017
28334972	Enrichment methods provide a feasible approach to comprehensive and adequately powered investigations of the brain methylome.	Nucleic Acids Res	2017
28703682	A MBD-seq protocol for large-scale methylome-wide studies with (very) low amounts of DNA.	Epigenetics	2017
28196272	Deep Sequencing of 71 Candidate Genes to Characterize Variation Associated with Alcohol Dependence.	Alcohol Clin Exp Res	2017
26283763	Deep Sequencing of Three Loci Implicated in Large-Scale Genome-Wide Association Study Smoking Meta-Analyses.	Nicotine Tob Res	2016
26656881	A Whole Methylome CpG-SNP Association Study of Psychosis in Blood and Brain Tissue.	Schizophr Bull	2016
26146898	Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use.	Alcohol Clin Exp Res	2015
25284466	Refinement of schizophrenia GWAS loci using methylome-wide association data.	Hum Genet	2015
25687462	Candidate gene methylation studies are at high risk of erroneous conclusions.	Epigenomics	2015
26432246	An integrated map of structural variation in 2,504 human genomes.	Nature	2015
26699738	High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction.	Genome Biol	2015
24728292	Heritability and genomics of gene expression in peripheral blood.	Nat Genet	2014
25237114	Quantitative trait locus mapping methods for diversity outbred mice.	G3 (Bethesda)	2014
23435227	Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies.	Nucleic Acids Res	2013
22171328	seeQTL: a searchable database for human eQTLs.	Bioinformatics	2012
22304583	Computational tools for discovery and interpretation of expression quantitative trait loci.	Pharmacogenomics	2012
22492648	Matrix eQTL: ultra fast eQTL analysis via large matrix operations.		2012