Center-Authored Papers

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Cade BE, Chen H, Stilp AM, Gleason KJ, Sofer T, Ancoli-Israel S, Arens R, Bell GI, Below JE, Bjonnes AC et al..  2016.  Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.. American journal of respiratory and critical care medicine. Abstract
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He Q, Cai T, Liu Y, Zhao N, Harmon QE, Almli LM, Binder EB, Engel SM, Ressler KJ, Conneely KN et al..  2016.  Prioritizing individual genetic variants after kernel machine testing using variable selection.. Genetic epidemiology. 40(8):722-731. Abstract
He KY, Wang H, Cade BE, Nandakumar P, Giri A, Ware EB, Haessler J, Liang J, Smith JA, Franceschini N et al..  2017.  Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.. PLoS genetics. 13(3):e1006678. Abstract
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Li Y, Prentice RL, Lin X.  2008.  Semiparametric Maximum Likelihood Estimation in Normal Transformation Models for Bivariate Survival Data.. Biometrika. 95(4):947-960. Abstract
Lin X, Lee S, Wu MC, Wang C, Chen H, Li Z, Lin X.  2016.  Test for rare variants by environment interactions in sequencing association studies.. Biometrics. 72(1):156-164. Abstract
Liu C-Y, Stucker I, Chen C, Goodman GE, McHugh MK, D'Amelio AM, Etzel CJ, Li S, Lin X, Christiani DC.  2015.  Genome-wide gene-asbestos exposure interaction association study identifies a common susceptibility variant on 22q13.31 associated with lung cancer risk.. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 24(10):1564-1573. Abstract