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Andrey A. Shabalin, Ph.D. - Publications

Affiliations: 
2010 Statistics University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Statistics, Bioinformatics Biology
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40/76 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Guintivano J, Shabalin AA, Chan RF, Rubinow DR, Sullivan PF, Meltzer-Brody S, Aberg KA, van den Oord EJCG. Test-statistic inflation in methylome-wide association studies. Epigenetics. 1-4. PMID 32425094 DOI: 10.1080/15592294.2020.1758382  0.305
2019 Clark SL, Hattab MW, Chan RF, Shabalin AA, Han LKM, Zhao M, Smit JH, Jansen R, Milaneschi Y, Xie LY, van Grootheest G, Penninx BWJH, Aberg KA, van den Oord EJCG. A methylation study of long-term depression risk. Molecular Psychiatry. PMID 31501512 DOI: 10.1038/S41380-019-0516-Z  0.35
2019 Chan RF, Shabalin AA, Montano C, Hannon E, Hultman CM, Fallin MD, Feinberg AP, Mill J, van den Oord EJCG, Aberg KA. Independent Methylome-Wide Association Studies of Schizophrenia Detect Consistent Case-Control Differences. Schizophrenia Bulletin. PMID 31165892 DOI: 10.1093/Schbul/Sbz056  0.343
2019 Anderson J, Shabalin A, Shade J, Bakian A, Adkins D, Callor WB, Christensen E, DiBlasi E, Gray D, Hayward C, Porteous D, Edwards A, Li Q, Coon H, Docherty A. SA91A GENOME-WIDE ASSOCIATION STUDY OF COMPLETED SUICIDE IN UTAH European Neuropsychopharmacology. 29: S1238. DOI: 10.1016/J.Euroneuro.2018.08.313  0.301
2019 DiBlasi E, Li Q, Anderson J, Callor WB, Christensen E, Jerominski L, Sargent R, Gray D, Camp N, Shabalin A, Docherty A, Coon H. 66Analyses Of Disease-Associated And Likely Functional Variants From Psycharray Implicate Genes Involved In Risk For Completed Suicide European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.073  0.331
2019 McClay J, Shabalin A. SEQUENCE MOTIF AND PROTEIN DOMAIN ENRICHMENT ANALYSIS OF PSYCHIATRIC GWAS FINDINGS European Neuropsychopharmacology. 29: S943. DOI: 10.1016/J.Euroneuro.2017.08.289  0.35
2019 Aberg K, Dean B, Shabalin A, Zhao M, Chan R, Hattab M, van Grootheest G, Han L, Aghajani M, Milaneschi Y, Jansen R, Xie L, Clark S, Penninx B, van den Oord E. METHYLOME-WIDE ASSOCIATION STUDIES FOR MAJOR DEPRESSIVE DISORDER IN BLOOD OVERLAP WITH METHYLATION RESULTS FROM BRAIN AND LARGE-SCALE GWAS European Neuropsychopharmacology. 29: S807-S808. DOI: 10.1016/J.Euroneuro.2017.08.048  0.362
2019 Clark S, Hattab M, Shabalin A, Han L, Chan R, Zhao M, Smit J, Jansen R, Milaneschi Y, Xie L, van Grootheest G, Penninx B, Aberg K, van den Oord E. PREDICTING THE FUTURE DISEASE STATUS OF DEPRESSED PATIENTS FROM DNA METHYLATION PATTERNS IN BLOOD European Neuropsychopharmacology. 29: S793-S794. DOI: 10.1016/J.Euroneuro.2017.08.025  0.309
2018 Coon H, Darlington TM, DiBlasi E, Callor WB, Ferris E, Fraser A, Yu Z, William N, Das SC, Crowell SE, Chen D, Anderson JS, Klein M, Jerominski L, Cannon D, ... Shabalin A, et al. Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. Molecular Psychiatry. PMID 30353169 DOI: 10.1038/S41380-018-0282-3  0.329
2018 Aberg KA, Dean B, Shabalin AA, Chan RF, Han LKM, Zhao M, van Grootheest G, Xie LY, Milaneschi Y, Clark SL, Turecki G, Penninx BWJH, van den Oord EJCG. Methylome-wide association findings for major depressive disorder overlap in blood and brain and replicate in independent brain samples. Molecular Psychiatry. PMID 30242228 DOI: 10.1038/S41380-018-0247-6  0.33
2018 Aberg KA, Shabalin AA, Chan RF, Zhao M, Kumar G, van Grootheest G, Clark SL, Xie LY, Milaneschi Y, Penninx BWJH, van den Oord EJCG. Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder. Translational Psychiatry. 8: 162. PMID 30135428 DOI: 10.1038/S41398-018-0205-8  0.381
2018 Xia H, Jahr FM, Kim NK, Xie L, Shabalin AA, Bryois J, Sweet DH, Kronfol MM, Palasuberniam P, McRae M, Riley BP, Sullivan PF, van den Oord EJ, McClay JL. Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk. Human Molecular Genetics. PMID 29905862 DOI: 10.1093/Hmg/Ddy222  0.373
2018 Docherty AR, Fonseca-Pedrero E, Debbané M, Chan RCK, Linscott RJ, Jonas KG, Cicero DC, Green MJ, Simms LJ, Mason O, Watson D, Ettinger U, Waszczuk M, Rapp A, Grant P, ... ... Shabalin AA, et al. Enhancing Psychosis-Spectrum Nosology Through an International Data Sharing Initiative. Schizophrenia Bulletin. PMID 29788473 DOI: 10.1093/Schbul/Sby059  0.338
2018 Shabalin AA, Hattab MW, Clark SL, Chan RF, Kumar G, Aberg KA, van den Oord EJCG, Birol I. RaMWAS: Fast Methylome-Wide Association Study Pipeline for Enrichment Platforms. Bioinformatics (Oxford, England). PMID 29447401 DOI: 10.1093/Bioinformatics/Bty069  0.354
2018 Aberg KA, Chan RF, Xie L, Shabalin AA, van den Oord EJCG. Methyl-CpG-Binding Domain Sequencing: MBD-seq. Methods in Molecular Biology (Clifton, N.J.). 1708: 171-189. PMID 29224145 DOI: 10.1007/978-1-4939-7481-8_10  0.307
2017 Palowitch J, Shabalin A, Zhou YH, Nobel AB, Wright FA. Estimation of cis-eQTL effect sizes using a log of linear model. Biometrics. PMID 29073327 DOI: 10.1111/Biom.12810  0.633
2017 Li G, Shabalin AA, Rusyn I, Wright FA, Nobel AB. An empirical Bayes approach for multiple tissue eQTL analysis. Biostatistics (Oxford, England). PMID 29029013 DOI: 10.1093/Biostatistics/Kxx048  0.66
2017 Aberg KA, Chan RF, Shabalin AA, Zhao M, Turecki G, Heine Staunstrup N, Starnawska A, Mors O, Xie LY, van den Oord EJCG. A MBD-seq protocol for large-scale methylome-wide studies with (very) low amounts of DNA. Epigenetics. 0. PMID 28703682 DOI: 10.1080/15592294.2017.1335849  0.33
2017 Chan RF, Shabalin AA, Xie LY, Adkins DE, Zhao M, Turecki G, Clark SL, Aberg KA, van den Oord EJ. Enrichment methods provide a feasible approach to comprehensive and adequately powered investigations of the brain methylome. Nucleic Acids Research. PMID 28334972 DOI: 10.1093/Nar/Gkx143  0.335
2017 Clark SL, Adkins DE, Kumar G, Aberg KA, Nerella S, Xie L, Collins AL, Crowley JJ, Quackenbush CR, Hilliard CE, Shabalin AA, Vrieze SI, Peterson RE, Copeland WE, Silberg JL, et al. Deep sequencing of 71 candidate genes to characterize variation associated with alcohol dependence. Alcoholism, Clinical and Experimental Research. PMID 28196272 DOI: 10.1111/Acer.13352  0.32
2017 Hattab MW, Shabalin AA, Clark SL, Zhao M, Kumar G, Chan RF, Xie LY, Jansen R, Han LK, Magnusson PK, van Grootheest G, Hultman CM, Penninx BW, Aberg KA, van den Oord EJ. Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies. Genome Biology. 18: 24. PMID 28137292 DOI: 10.1186/S13059-017-1148-8  0.324
2015 McClay JL, Shabalin AA, Dozmorov MG, Adkins DE, Kumar G, Nerella S, Clark SL, Bergen SE, Hultman CM, Magnusson PK, Sullivan PF, Aberg KA, van den Oord EJ. High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction. Genome Biology. 16: 291. PMID 26699738 DOI: 10.1186/S13059-015-0842-7  0.337
2015 Sudmant PH, Rausch T, Gardner EJ, Handsaker RE, Abyzov A, Huddleston J, Zhang Y, Ye K, Jun G, Hsi-Yang Fritz M, Konkel MK, Malhotra A, Stütz AM, Shi X, Paolo Casale F, ... ... Shabalin AA, et al. An integrated map of structural variation in 2,504 human genomes. Nature. 526: 75-81. PMID 26432246 DOI: 10.1038/Nature15394  0.386
2015 Clark SL, McClay JL, Adkins DE, Aberg KA, Kumar G, Nerella S, Xie L, Collins AL, Crowley JJ, Quakenbush CR, Hillard CE, Gao G, Shabalin AA, Peterson RE, Copeland WE, et al. Deep Sequencing of Three Loci Implicated in Large-Scale Genome-Wide Association Study Smoking Meta-Analyses. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. PMID 26283763 DOI: 10.1093/Ntr/Ntv166  0.335
2015 Shabalin AA, Aberg KA, van den Oord EJ. Candidate gene methylation studies are at high risk of erroneous conclusions. Epigenomics. 7: 13-5. PMID 25687462 DOI: 10.2217/Epi.14.70  0.338
2015 Kumar G, Clark SL, McClay JL, Shabalin AA, Adkins DE, Xie L, Chan R, Nerella S, Kim Y, Sullivan PF, Hultman CM, Magnusson PK, Aberg KA, van den Oord EJ. Refinement of schizophrenia GWAS loci using methylome-wide association data. Human Genetics. 134: 77-87. PMID 25284466 DOI: 10.1007/S00439-014-1494-5  0.392
2015 Ardlie KG, DeLuca DS, Segrè AV, Sullivan TJ, Young TR, Gelfand ET, Trowbridge CA, Maller JB, Tukiainen T, Lek M, Ward LD, Kheradpour P, Iriarte B, Meng Y, Palmer CD, ... ... Shabalin AA, et al. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans Science. 348: 648-660. DOI: 10.1126/science.1262110  0.619
2014 Gatti DM, Svenson KL, Shabalin A, Wu LY, Valdar W, Simecek P, Goodwin N, Cheng R, Pomp D, Palmer A, Chesler EJ, Broman KW, Churchill GA. Quantitative trait locus mapping methods for diversity outbred mice. G3 (Bethesda, Md.). 4: 1623-33. PMID 25237114 DOI: 10.1534/G3.114.013748  0.326
2014 Wright FA, Sullivan PF, Brooks AI, Zou F, Sun W, Xia K, Madar V, Jansen R, Chung W, Zhou YH, Abdellaoui A, Batista S, Butler C, Chen G, Chen TH, ... ... Shabalin A, et al. Heritability and genomics of gene expression in peripheral blood. Nature Genetics. 46: 430-7. PMID 24728292 DOI: 10.1038/Ng.2951  0.426
2013 Ramasamy A, Trabzuni D, Gibbs JR, Dillman A, Hernandez DG, Arepalli S, Walker R, Smith C, Ilori GP, Shabalin AA, Li Y, Singleton AB, Cookson MR, Hardy J, et al. Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies. Nucleic Acids Research. 41: e88. PMID 23435227 DOI: 10.1093/Nar/Gkt069  0.364
2013 Shabalin AA, Nobel AB. Reconstruction of a low-rank matrix in the presence of Gaussian noise Journal of Multivariate Analysis. 118: 67-76. DOI: 10.1016/J.Jmva.2013.03.005  0.573
2012 Shabalin AA. Matrix eQTL: ultra fast eQTL analysis via large matrix operations. Bioinformatics (Oxford, England). 28: 1353-8. PMID 22492648 DOI: 10.1093/Bioinformatics/Bts163  0.387
2012 Wright FA, Shabalin AA, Rusyn I. Computational tools for discovery and interpretation of expression quantitative trait loci. Pharmacogenomics. 13: 343-52. PMID 22304583 DOI: 10.2217/Pgs.11.185  0.37
2012 Xia K, Shabalin AA, Huang S, Madar V, Zhou YH, Wang W, Zou F, Sun W, Sullivan PF, Wright FA. seeQTL: a searchable database for human eQTLs. Bioinformatics (Oxford, England). 28: 451-2. PMID 22171328 DOI: 10.1093/Bioinformatics/Btr678  0.325
2012 Weigman VJ, Chao HH, Shabalin AA, He X, Parker JS, Nordgard SH, Grushko T, Huo D, Nwachukwu C, Nobel A, Kristensen VN, Børresen-Dale AL, Olopade OI, Perou CM. Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival. Breast Cancer Research and Treatment. 133: 865-80. PMID 22048815 DOI: 10.1007/S10549-011-1846-Y  0.623
2010 Gatti DM, Zhao N, Chesler EJ, Bradford BU, Shabalin AA, Yordanova R, Lu L, Rusyn I. Sex-specific gene expression in the BXD mouse liver. Physiological Genomics. 42: 456-68. PMID 20551147 DOI: 10.1152/Physiolgenomics.00110.2009  0.383
2009 Lickwar CR, Rao B, Shabalin AA, Nobel AB, Strahl BD, Lieb JD. The Set2/Rpd3S pathway suppresses cryptic transcription without regard to gene length or transcription frequency. Plos One. 4: e4886. PMID 19295910 DOI: 10.1371/Journal.Pone.0004886  0.615
2009 Gatti DM, Shabalin AA, Lam TC, Wright FA, Rusyn I, Nobel AB. FastMap: fast eQTL mapping in homozygous populations. Bioinformatics (Oxford, England). 25: 482-9. PMID 19091771 DOI: 10.1093/Bioinformatics/Btn648  0.627
2009 Shabalin AA, Weigman VJ, Perou CM, Nobel AB. Finding large average submatrices in high dimensional data Annals of Applied Statistics. 3: 985-1012. DOI: 10.1214/09-Aoas239  0.628
2008 Shabalin AA, Tjelmeland H, Fan C, Perou CM, Nobel AB. Merging two gene-expression studies via cross-platform normalization. Bioinformatics (Oxford, England). 24: 1154-60. PMID 18325927 DOI: 10.1093/Bioinformatics/Btn083  0.634
Low-probability matches (unlikely to be authored by this person)
2023 Han S, DiBlasi E, Monson ET, Shabalin A, Ferris E, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crockett DK, Li QS, Willour V, Bakian AV, et al. Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes. Molecular Psychiatry. PMID 37794117 DOI: 10.1038/s41380-023-02282-x  0.295
2019 Chan RF, Turecki G, Shabalin AA, Guintivano J, Zhao M, Xie LY, van Grootheest G, Kaminsky ZA, Dean B, Penninx BWJH, Aberg KA, van den Oord EJCG. Cell Type-Specific Methylome-wide Association Studies Implicate Neurotrophin and Innate Immune Signaling in Major Depressive Disorder. Biological Psychiatry. PMID 31889537 DOI: 10.1016/J.Biopsych.2019.10.014  0.292
2018 Han LKM, Aghajani M, Clark SL, Chan RF, Hattab MW, Shabalin AA, Zhao M, Kumar G, Xie LY, Jansen R, Milaneschi Y, Dean B, Aberg KA, van den Oord EJCG, Penninx BWJH. Epigenetic Aging in Major Depressive Disorder. The American Journal of Psychiatry. appiajp201817060595. PMID 29656664 DOI: 10.1176/Appi.Ajp.2018.17060595  0.281
2018 Han L, Aghajani M, Clark S, Hattab M, Shabalin A, Zhao M, Kumar G, Chan R, Xie L, Jansen R, Milaneschi Y, Aberg K, Oord EVd, Penninx B. Accelerated biological aging in major depressive disorder: capturing aging patterns in DNA methylation with machine learning methods European Neuropsychopharmacology. 28. DOI: 10.1016/J.Euroneuro.2017.12.119  0.277
2018 Anderson JS, Shade J, DiBlasi E, Shabalin AA, Docherty AR. Polygenic risk scoring and prediction of mental health outcomes. Current Opinion in Psychology. 27: 77-81. PMID 30339992 DOI: 10.1016/J.Copsyc.2018.09.002  0.276
2018 Clark SL, Costin BN, Chan RF, Johnson AW, Xie L, Jurmain JL, Kumar G, Shabalin AA, Pandey AK, Aberg KA, Miles MF, van den Oord E. 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. Alcoholism, Clinical and Experimental Research. PMID 30320886 DOI: 10.1111/Acer.13905  0.272
2019 Docherty A, Shabalin A, DiBlasi E, Bacanu S, Coon H. 69 GENOME-WIDE ANALYSIS OF SUICIDE DEATH AND POLYGENIC PREDICTION OF PREMORBID CLINICAL DIAGNOSES European Neuropsychopharmacology. 29: S98. DOI: 10.1016/J.Euroneuro.2019.07.210  0.269
2015 Clark SL, Aberg KA, Nerella S, Kumar G, McClay JL, Chen W, Xie LY, Harada A, Shabalin AA, Gao G, Bergen SE, Hultman CM, Magnusson PK, Sullivan PF, van den Oord EJ. Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use. Alcoholism, Clinical and Experimental Research. PMID 26146898 DOI: 10.1111/Acer.12790  0.267
2020 Docherty AR, Shabalin AA, Adkins DE, Mann F, Krueger RF, Bacanu SA, Campbell A, Hayward C, Porteous DJ, McIntosh AM, Kendler KS. Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland. Schizophrenia Bulletin. PMID 32221549 DOI: 10.1093/Schbul/Sbaa042  0.263
2019 Coon H, Shabalin A, DiBlasi E, Keeshin B, Bakian A, Ferris E, Callor WB, Velinder M, Pedersen B, Christensen E, Quinlan A, Marth G, Li Q, Gray D, Docherty A. T61SUICIDE DEATHS SELECTED FOR GENETIC RISK: POLYGENIC RISK SCORE CHARACTERISTICS AND HIGH-IMPACT SEQUENCE VARIANTS European Neuropsychopharmacology. 29: S248. DOI: 10.1016/J.Euroneuro.2019.08.260  0.26
2024 Nievergelt CM, Maihofer AX, Atkinson EG, Chen CY, Choi KW, Coleman JRI, Daskalakis NP, Duncan LE, Polimanti R, Aaronson C, Amstadter AB, Andersen SB, Andreassen OA, Arbisi PA, Ashley-Koch AE, ... ... Shabalin A, et al. Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics. PMID 38637617 DOI: 10.1038/s41588-024-01707-9  0.23
2019 Han L, Aghajani M, Clark S, Chan R, Hattab M, Shabalin A, Zhao M, Kumar G, Xie LY, Jansen R, Milaneschi Y, Dean B, Aberg K, Oord EVd, Penninx B. S.14.08 Epigenetic aging in major depressive disorder European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.11.951  0.228
2022 Xia K, Shabalin AA, Yin Z, Chung W, Sullivan PF, Wright FA, Styner M, Gilmore JH, Santelli RC, Zou F. TwinEQTL: Ultra Fast and Powerful Association Analysis for eQTL and GWAS in Twin Studies. Genetics. PMID 35689615 DOI: 10.1093/genetics/iyac088  0.227
2021 DiBlasi E, Shabalin AA, Monson ET, Keeshin BR, Bakian AV, Kirby AV, Ferris E, Chen D, William N, Gaj E, Klein M, Jerominski L, Callor WB, Christensen E, Smith KR, et al. Rare protein-coding variants implicate genes involved in risk of suicide death. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34042246 DOI: 10.1002/ajmg.b.32861  0.226
2023 Docherty AR, Mullins N, Ashley-Koch AE, Qin X, Coleman JRI, Shabalin A, Kang J, Murnyak B, Wendt F, Adams M, Campos AI, DiBlasi E, Fullerton JM, Kranzler HR, Bakian AV, et al. GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. The American Journal of Psychiatry. 180: 723-738. PMID 37777856 DOI: 10.1176/appi.ajp.21121266  0.223
2019 Waszczuk M, Docherty A, Shabalin A, Michelini G, Perlman G, Kuan PF, Klein D, Kotov R. T59POLYGENIC RISK TO DEVELOPMENTAL TRAJECTORIES OF HIERARCHICALLY-ORGANIZED INTERNALIZING PSYCHOPATHOLOGY European Neuropsychopharmacology. 29: S247. DOI: 10.1016/J.Euroneuro.2019.08.258  0.222
2021 Ip HF, van der Laan CM, Krapohl EML, Brikell I, Sánchez-Mora C, Nolte IM, St Pourcain B, Bolhuis K, Palviainen T, Zafarmand H, Colodro-Conde L, Gordon S, Zayats T, Aliev F, Jiang C, ... ... Shabalin AA, et al. Genetic association study of childhood aggression across raters, instruments, and age. Translational Psychiatry. 11: 413. PMID 34330890 DOI: 10.1038/s41398-021-01480-x  0.218
2018 Han L, Verhoeven J, Aghajani M, Clark S, Hattab M, Shabalin A, Zhao M, Kumar G, Chan R, Xie LY, Milaneschi Y, Jansen R, Aberg K, Oord Evd, Penninx B. 41. Telomere Length, Epigenetic Aging and Depression in the Netherlands Study of Depression and Anxiety (NESDA) Biological Psychiatry. 83. DOI: 10.1016/J.Biopsych.2018.02.058  0.212
2022 Merrill CB, Montgomery AB, Pabon MA, Shabalin AA, Rodan AR, Rothenfluh A. Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs. Bmc Genomics. 23: 399. PMID 35614386 DOI: 10.1186/s12864-022-08637-y  0.191
2023 Nievergelt CM, Maihofer AX, Atkinson EG, Chen CY, Choi KW, Coleman JR, Daskalakis NP, Duncan LE, Polimanti R, Aaronson C, Amstadter AB, Andersen SB, Andreassen OA, Arbisi PA, Ashley-Koch AE, ... ... Shabalin A, et al. Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disorders. Medrxiv : the Preprint Server For Health Sciences. PMID 37693460 DOI: 10.1101/2023.08.31.23294915  0.187
2019 Waszczuk M, Kuan PF, Docherty A, Shabalin A, Bromet E, Luft B, Kotov R. S13POLYGENIC PREDICTION OF PTSD TRAJECTORIES IN 9/11 RESPONDERS European Neuropsychopharmacology. 29: S120. DOI: 10.1016/J.Euroneuro.2019.08.014  0.181
2021 Alkelai A, Greenbaum L, Docherty AR, Shabalin AA, Povysil G, Malakar A, Hughes D, Delaney SL, Peabody EP, McNamara J, Gelfman S, Baugh EH, Zoghbi AW, Harms MB, Hwang HS, et al. The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders. Molecular Psychiatry. PMID 34799694 DOI: 10.1038/s41380-021-01383-9  0.163
2022 Li QS, Shabalin AA, DiBlasi E, Gopal S, Canuso CM, Palotie A, Drevets WC, Docherty AR, Coon H. Genome-wide association study meta-analysis of suicide death and suicidal behavior. Molecular Psychiatry. PMID 36253440 DOI: 10.1038/s41380-022-01828-9  0.158
2020 Docherty AR, Shabalin AA, DiBlasi E, Monson E, Mullins N, Adkins DE, Bacanu SA, Bakian AV, Crowell S, Chen D, Darlington TM, Callor WB, Christensen ED, Gray D, Keeshin B, et al. Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents. The American Journal of Psychiatry. 177: 917-927. PMID 32998551 DOI: 10.1176/appi.ajp.2020.19101025  0.15
2021 Colbert SMC, Hatoum AS, Shabalin A, Li QS, Coon H, Nelson EC, Agrawal A, Docherty AR, Johnson EC. Exploring the genetic overlap of suicide-related behaviors and substance use disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34821019 DOI: 10.1002/ajmg.b.32880  0.141
2021 Monson ET, Shabalin AA, Docherty AR, DiBlasi E, Bakian AV, Li QS, Gray D, Keeshin B, Crowell SE, Mullins N, Willour VL, Coon H. Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach. Translational Psychiatry. 11: 379. PMID 34234108 DOI: 10.1038/s41398-021-01500-w  0.136
2021 Docherty AR, Bakian AV, DiBlasi E, Shabalin AA, Chen D, Keeshin B, Monson E, Christensen ED, Li Q, Gray D, Coon H. Suicide and Psychosis: Results From a Population-Based Cohort of Suicide Death (N = 4380). Schizophrenia Bulletin. PMID 34559220 DOI: 10.1093/schbul/sbab113  0.133
2021 Waszczuk MA, Miao J, Docherty AR, Shabalin AA, Jonas KG, Michelini G, Kotov R. General . specific vulnerabilities: polygenic risk scores and higher-order psychopathology dimensions in the Adolescent Brain Cognitive Development (ABCD) Study. Psychological Medicine. 53: 1937-1946. PMID 37310323 DOI: 10.1017/S0033291721003639  0.132
2023 Waszczuk MA, Morozova O, Lhuillier E, Docherty AR, Shabalin AA, Yang X, Carr MA, Clouston SAP, Kotov R, Luft BJ. Polygenic risk scores for asthma and allergic disease associate with COVID-19 severity in 9/11 responders. Plos One. 18: e0282271. PMID 36893177 DOI: 10.1371/journal.pone.0282271  0.127
2022 Love T, Shabalin AA, Kember RL, Docherty AR, Zhou H, Koppelmans V, Gelernter J, Baker AK, Hartwell E, Dubroff J, Zubieta JK, Kranzler HR. Unique and joint associations of polygenic risk for major depression and opioid use disorder with endogenous opioid system function. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 35545664 DOI: 10.1038/s41386-022-01325-1  0.118
2022 Jami ES, Hammerschlag AR, Ip HF, Allegrini AG, Benyamin B, Border R, Diemer EW, Jiang C, Karhunen V, Lu Y, Lu Q, Mallard TT, Mishra PP, Nolte IM, Palviainen T, ... ... Shabalin AA, et al. Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms. Journal of the American Academy of Child and Adolescent Psychiatry. PMID 35378236 DOI: 10.1016/j.jaac.2021.11.035  0.113
2022 Coon H, Shabalin A, Bakian AV, DiBlasi E, Monson ET, Kirby A, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crowell SE, Gray D, Crockett DK, et al. Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 35212135 DOI: 10.1002/ajmg.b.32890  0.109
2022 Koraishy FM, Mann FD, Waszczuk MA, Kuan PF, Jonas K, Yang X, Docherty A, Shabalin A, Clouston S, Kotov R, Luft B. Polygenic association of glomerular filtration rate decline in world trade center responders. Bmc Nephrology. 23: 347. PMID 36307804 DOI: 10.1186/s12882-022-02967-5  0.103
2021 Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, et al. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological Psychiatry. PMID 34861974 DOI: 10.1016/j.biopsych.2021.05.029  0.1
2023 Harrison TJ, Docherty AR, Finsaas MC, Kotov R, Shabalin AA, Waszczuk MA, Katz BA, Davila J, Klein DN. Examining the relationship between genetic risk for depression and youth episodic stress exposure. Journal of Affective Disorders. 340: 649-657. PMID 37591353 DOI: 10.1016/j.jad.2023.08.088  0.1
2020 Waszczuk MA, Docherty AR, Shabalin AA, Miao J, Yang X, Kuan PF, Bromet E, Kotov R, Luft BJ. Polygenic prediction of PTSD trajectories in 9/11 responders. Psychological Medicine. 1-9. PMID 33092657 DOI: 10.1017/S0033291720003839  0.088
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