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Shwab EK, Pathak GA, Harvey J, Belloy ME, Fischer CE, Lutz MW, Scholz SW, Cook N,
                                          Reid DM, Chen J, Guan DX, Oliveira F, Sinclair LI, Imo U, Creese B, Chiba-Falek O,
                                          Neuropsychiatric Syndromes Professional Interest Area Multiomics Work Group (2025)
                                          Leveraging multiomic approaches to elucidate mechanisms of heterogeneity in Alzheimer’s
                                          disease: Neuropsychiatric symptoms, co-pathologies, and sex differences. Alzheimer’s
                                          & Dementia, 21(8), e70549. PMID: 40823789; PMCID: PMC12359071; DOI: 10.1002/alz.70549. 
                                        
                                     
                                 
                                  
                                 
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Gershon E, Xia C, Alliey-Rodriguez N, Tamminga C, Keshavan M, Pearlson G, Keedy S,
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Benca-Bachman CE, Bubier J, Syed RA, Romero Villela PN, Palmer RHC (2023) Polygenic
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Odintsova VV, Hagenbeek FA, van der Laan CM, van de Weijer S, Boomsma DI (2023) Genetics
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Liu H, Li G, Sturgis EM, Shete S, Dahlstrom KR, Du M, Amos CI, Christiani DC, Lazarus
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Mathews C, de Leeuw C, Goudriaan A, Smit A, Yu D, Scharf J, Verheijen M, Posthuma
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Orihara S, Goto A, Taguri M (2022) Instrumental variable estimation of causal effects
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Luo X, Guo X, Luo X, Tan Y, Zhang P, Yang K, Xie T, Shi J, Zhang Y, Xu J, Zuo L, Li
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Donvito G, Muldoon PP, Jackson KJ, Ahmad U, Zaveri NT, McIntosh JM, Chen X, Lichtman
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Shete S, Liu H, Wang J, Yu R, Sturgis EM, Li G, Dahlstrom KR, Liu Z, Amos CI, Wei
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Sadeh N, Spielberg JM, Logue MW, Hayes JP, Wolf EJ, McGlinchey RE, Milberg WP, Schichman
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Wang K, Chen X, Ward SC, Liu Y, Ouedraogo Y, Xu C, Cederbaum AI, Lu Y (2019) CYP2A6
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Xiang B, Yang BZ, Zhou H, Kranzler H, Gelernter J (2019) GWAS and network analysis
                                          of co-occurring nicotine and alcohol dependence identifies significantly associated
                                          alleles and network. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 180(1), 3-11. PMID: 30488612; PMCID: PMC6918694; DOI: 10.1002/ajmg.b.32692. 
                                        
                                    
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Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B,
                                          Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M,
                                          Miron K, Lu C, Wang T, Samler K, Wang X, Costain G, Hoang N, Pellecchia G, Wei J,
                                          Patel RV, Thiruvahindrapuram B, Roifman M, Merico D, Goodale T, Drmic I, Speevak M,
                                          Howe JL, Yuen RKC, Buchanan JA, Vorstman JAS, Marshall CR, Wintle RF, Rosenberg DR,
                                          Hanna GL, Woodbury-Smith M, Cytrynbaum C, Zwaigenbaum L, Elsabbagh M, Flanagan J,
                                          Fernandez BA, Carter MT, Szatmari P, Roberts W, Lerch J, Liu X, Nicolson R, Georgiades
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Cabana-Dominguez J, Arenas C, Cormand B, Fernandez-Castillo N (2018) MiR-9, miR-153
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Liu D, Zhang H (2018) Residuals and Diagnostics for Ordinal Regression Models: A Surrogate
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Pineda-Cirera L, Cabana-Dominguez J, Roncero C, Cozar M, Grau-Lopez L, Abad AC, Martinez-Luna
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Rabinowitz JA, Musci RJ, Milam AJ, Benke K, Uhl GR, Sisto DY, Ialongo NS, Maher BS
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Sulovari A, Liu Z, Zhu Z, Li D (2018) Genome-wide meta-analysis of copy number variations
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Zhang H, Liu D, Zhao J, Bi X (2018) Modeling Hybrid Traits for Comorbidity and Genetic
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Jensen KP, Smith AH, Herman AI, Farrer LA, Kranzler HR, Sofuoglu M, Gelernter J (2017)
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Liu D, Zhang H (2018) Residuals and Diagnostics for Ordinal Regression Models: A Surrogate
                                          Approach. Journal of the American Statistical Association, 113(522), 845-854. PMID: 30220754; PMCID: PMC6133273; DOI: 10.1080/01621459.2017.1292915. 
                                        
                                    
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Martinez-Rivera A, Hao J, Tropea TF, Giordano TP, Kosovsky M, Rice RC, Lee A, Huganir
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Melroy-Greif WE, Simonson MA, Corley RP, Lutz SM, Hokanson JE, Ehringer MA (2017)
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Polimanti R, Zhang H, Smith AH, Zhao H, Farrer LA, Kranzler HR, Gelernter J (2017)
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Wang J, Talluri R, Shete S (2017) Selection of X-chromosome Inactivation Model. Cancer Informatics, 16, 1176935117747272. PMID: 29308008; PMCID: PMC5751921; DOI: 10.1177/1176935117747272. 
                                        
                                    
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Wang M, Huang J, Liu Y, Ma L, Potash JB, Han S (2017) COMBAT: A Combined Association
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Yang HC, Chen IC, Tsay YC, Li ZR, Chen CH, Hwu HG, Chen CH (2017) Using an Event-History
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Zollanvari A, Alterovitz G (2017) SNP by SNP by environment interaction network of
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Bidwell LC, Palmer RH, Brick L, McGeary JE, Knopik VS (2016) Genome-wide single nucleotide
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Clarke TK, Smith AH, Gelernter J, Kranzler HR, Farrer LA, Hall LS, Fernandez-Pujals
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Li M, Wei C, Wen Y, Wang T, Lu Q (2016) Detecting Gene-Gene Interactions Associated
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Melroy-Greif WE, Vadasz C, Kamens HM, McQueen MB, Corley RP, Stallings MC, Hopfer
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Palmer RH, Nugent NR, Brick LA, Bidwell CL, McGeary JE, Keller MC, Knopik VS (2016)
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Perry BL (2016) Gendering Genetics: Biological Contingencies in the Protective Effects
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Sadeh N, Wolf EJ, Logue MW, Lusk J, Hayes JP, McGlinchey RE, Milberg WP, Stone A,
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Sherva R, Wang Q, Kranzler H, Zhao H, Koesterer R, Herman A, Farrer LA, Gelernter
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Uddin M, Pellecchia G, Thiruvahindrapuram B, D’Abate L, Merico D, Chan A, Zarrei M,
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Zhao J, Zhang H (2016) Modeling Multiple Responses via Bootstrapping Margins with
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de Leeuw C, Goudriaan A, Smit AB, Yu D, Mathews CA, Scharf JM, Verheijen MH, Posthuma
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Derringer J, Corley RP, Haberstick BC, Young SE, Demmitt BA, Howrigan DP, Kirkpatrick
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Gelernter J, Kranzler HR, Sherva R, Almasy L, Herman AI, Koesterer R, Zhao H, Farrer
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Li D, Zhao H, Kranzler HR, Li MD, Jensen KP, Zayats T, Farrer LA, Gelernter J (2015)
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Muldoon PP, Chen J, Harenza JL, Abdullah RA, Sim-Selley LJ, Cravatt BF, Miles MF,
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Palmer RH, Brick L, Nugent NR, Bidwell LC, McGeary JE, Knopik VS, Keller MC (2015)
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Palmer RH, McGeary JE, Heath AC, Keller MC, Brick LA, Knopik VS (2015) Shared Additive
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Pan W, Chen YM, Wei P (2015) Testing for polygenic effects in genome-wide association
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Polimanti R, Yang C, Zhao H, Gelernter J (2015) Dissecting ancestry genomic background
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Repunte-Canonigo V, Herman M, Kawamura T, Kranzler HR, Sherva R, Gelernter J, Farrer
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Suchankova P, Yan J, Schwandt ML, Stangl BL, Caparelli EC, Momenan R, Jerlhag E, Engel
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Sun J, Kranzler HR, Bi J (2015) An Effective Method to Identify Heritable Components
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Talluri R, Shete S (2015) Evaluating methods for modeling epistasis networks with
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Wang KS, Zuo L, Pan Y, Xie C, Luo X (2015) Genetic variants in the CPNE5 gene are
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Xu K, Kranzler HR, Sherva R, Sartor CE, Almasy L, Koesterer R, Zhao H, Farrer LA,
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Zuo L, Saba L, Lin X, Tan Y, Wang K, Krystal JH, Tabakoff B, Luo X (2015) Significant
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Zuo L, Tan Y, Zhang X, Wang X, Krystal J, Tabakoff B, Zhong C, Luo X (2015) A New
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Zuo L, Wang T, Lin X, Wang J, Tan Y, Wang X, Yu X, Luo X (2015) Sex difference of
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Zuo L, Zhang CK, Sayward FG, Cheung KH, Wang K, Krystal JH, Zhao H, Luo X (2015) Gene-based
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Cao J, Liu X, Han S, Zhang CK, Liu Z, Li D (2014) Association of the HTR2A gene with
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Chen GB, Liu N, Klimentidis YC, Zhu X, Zhi D, Wang X, Lou XY (2014) A unified GMDR
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Feng Z (2014) A generalized quasi-likelihood scoring approach for simultaneously testing
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Gelernter J, Kranzler HR, Sherva R, Almasy L, Koesterer R, Smith AH, Anton R, Preuss
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Gelernter J, Kranzler HR, Sherva R, Koesterer R, Almasy L, Zhao H, Farrer LA (2014)
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Gelernter J, Sherva R, Koesterer R, Almasy L, Zhao H, Kranzler HR, Farrer L (2014)
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Hsieh TJ, Chang SH, Tai JJ (2014) A family-based robust multivariate association test
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Jiang Y, Li N, Zhang H (2014) Identifying Genetic Variants for Addiction via Propensity
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Li D, Sulovari A, Cheng C, Zhao H, Kranzler HR, Gelernter J (2014) Association of
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Li M, Gardiner JC, Breslau N, Anthony JC, Lu Q (2014) A non-parametric approach for
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Lobach I, Fan R, Manga P (2014) Genotype-based association models of complex diseases
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McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber
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                                          Bruun RD, Budman CL, Camarena B, Cath DC, Cavallini MC, Chouinard S, Coric V, Cullen
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                                          Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Lochner C, Lowe TL, Lyon
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                                          Nurmi E, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Reus VI,
                                          Richter MA, Riddle M, Robertson MM, Rosenberg D, Rouleau GA, Ruhrmann S, Sampaio AS,
                                          Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Tischfield JA, Vallada
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Muldoon PP, Jackson KJ, Perez E, Harenza JL, Molas S, Rais B, Anwar H, Zaveri NT,
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Song C, Zhang H (2014) TARV: tree-based analysis of rare variants identifying risk
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Taylor A, Wang KS (2014) Association between DPYSL2 gene polymorphisms and alcohol
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Wang J, Yu R, Shete S (2014) X-chromosome genetic association test accounting for
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Wang S, A DvdV, Xu Q, Seneviratne C, Pomerleau OF, Pomerleau CS, Payne TJ, Ma JZ,
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Yang J, Li MD (2014) Association and interaction analyses of 5-HT3 receptor and serotonin
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Yuan H, Dougherty JD (2014) Investigation of maternal genotype effects in autism by
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Zuo L, Lu L, Tan Y, Pan X, Cai Y, Wang X, Hong J, Zhong C, Wang F, Zhang XY, Vanderlinden
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Zuo L, Wang K, Wang G, Pan X, Zhang X, Zhang H, Luo X (2014) Common PTP4A1-PHF3-EYS
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Belsky DW, Moffitt TE, Baker TB, Biddle AK, Evans JP, Harrington H, Houts R, Meier
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Blaine S, Claus E, Harlaar N, Hutchison K (2013) TACR1 genotypes predict fMRI response
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Cui WY, Wang S, Yang J, Yi SG, Yoon D, Kim YJ, Payne TJ, Ma JZ, Park T, Li MD (2013)
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Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J,
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                                          of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic
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Du M, Prescott J, Cornelis MC, Hankinson SE, Giovannucci E, Kraft P, De Vivo I (2013)
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Guo X, Liu Z, Wang X, Zhang H (2013) Genetic association test for multiple traits
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Han S, Yang BZ, Kranzler HR, Liu X, Zhao H, Farrer LA, Boerwinkle E, Potash JB, Gelernter
                                          J (2013) Integrating GWASs and human protein interaction networks identifies a gene
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Liu Z, Guo X, Jiang Y, Zhang H (2013) NCK2 is significantly associated with opiates
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Lopes AM, Aston KI, Thompson E, Carvalho F, Gon�alves J, Huang N, Matthiesen R,
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                                          spermatogenic failure purges deleterious mutation load from the autosomes and both
                                          sex chromosomes, including the gene DMRT1. PLoS Genetics, 9(3), e1003349. PMID: 23555275; PMCID: PMC3605256; DOI: 10.1371/journal.pgen.1003349. 
                                        
                                    
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Pan Y, Luo X, Liu X, Wu LY, Zhang Q, Wang L, Wang W, Zuo L, Wang KS (2013) Genome-wide
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Pan Y, Wang KS, Wang L, Wu LY (2013) Common variants in HLA-DRA gene are associated
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Ray LA, Sehl M, Bujarski S, Hutchison K, Blaine S, Enoch MA (2013) The CRHR1 gene,
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Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon
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                                          Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez
                                          TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier
                                          E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun
                                          RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrio GB, Campbell DD, Cardona
                                          Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert
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Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans
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                                          F, Westenberg HG, Walitza S, Egberts K, Renner T, Miguel EC, Cappi C, Hounie AG, Conceicao
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Wang L, Liu X, Luo X, Zeng M, Zuo L, Wang KS (2013) Genetic variants in the fat mass-
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Wen Y, Schaid DJ, Lu Q (2013) A bivariate mann-whitney approach for unraveling genetic
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Zuo L, Saba L, Wang K, Zhang X, Krystal JH, Tabakoff B, Luo X (2013) Exome-wide association
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Zuo L, Wang K, Zhang X, Pan X, Wang G, Krystal JH, Zhang H, Luo X (2013) Sex chromosome-wide
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Zuo L, Wang K, Zhang XY, Krystal JH, Li CS, Zhang F, Zhang H, Luo X (2013) NKAIN1-SERINC2
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Zuo L, Wang K, Zhang XY, Pan X, Wang G, Tan Y, Zhong C, Krystal JH, State M, Zhang
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Zuo L, Wang KS, Zhang XY, Li CS, Zhang F, Wang X, Chen W, Gao G, Zhang H, Krystal
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Zuo L, Zhang H, Malison RT, Li CS, Zhang XY, Wang F, Lu L, Lu L, Wang X, Krystal JH,
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