82 Publications (Page 2 of 4)
2014
A statistical framework for testing the causal effects of fetal drive
Liu, NianjunLiu, NianjunArcher, EdwardArcher, EdwardSrinivasasainagendra, VinodhSrinivasasainagendra, VinodhAllison, David B and Allison, David B
Frontiers in genetics, vol. 5, pp. 464, 2014-00-00. | Journal Article
 
A unified GMDR method for detecting gene-gene interactions in family and unrelated samples with application to nicotine dependence.
Chen, Guo-BoChen, Guo-BoLiu, NianjunLiu, NianjunKlimentidis, Yann CKlimentidis, YannZhu, XiaofengZhu, XiaofengZhi, DeguiZhi, DeguiWang, XujingWang, XujingLou, Xiang-Yang and Lou, Xiang-Yang
Human genetics, vol. 133, (no. 2), pp. 139-50, 2014/Feb. | Journal Article
 
Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.
Yan, QiYan, QiTiwari, Hemant KTiwari, Hemant K.Yi, NengjunYi, NengjunLin, Wan YuLin, Wan YuGao, GuiminGao, GuiminLou, Xiang-YangLou, Xiang-YangCui, XiangqinCui, XiangqinLiu, Nianjun and Liu, Nianjun
Genetic epidemiology, vol. 38, (no. 5), pp. 447-456, July 2014. | Journal Article
 
Multivariate Dimensionality Reduction Approaches to Identify Gene-Gene and Gene-Environment Interactions Underlying Multiple Complex Traits
Xu, Hai-MingXu, Hai-MingXu, Hai-MingSun, Xi-WeiSun, Xi-WeiSun, Xi-WeiQi, TingQi, TingQi, TingLin, Wan-YuLin, Wan YuLin, Wan YuLiu, NianjunLiu, NianjunLiu, NianjunLou, Xiang-YangLou, Xiang-Yang and Lou, Xiang-Yang
PloS one, vol. 9, (no. 9), pp. e108103, 2014-00-00. | Journal Article
 
Rare variant association testing by adaptive combination of P-values.
Lin, Wan YuLin, Wan YuLou, Xiang-YangLou, Xiang-YangGao, GuiminGao, GuiminLiu, Nianjun and Liu, Nianjun
PloS one, vol. 9, (no. 1), pp. e85728, 2014. | Journal Article
2013
A Rapid Association Test Procedure Robust under Different Genetic Models Accounting for Population Stratification
Chen, WenanChen, SamArcher, Kellie JLiu, NianjunLi, QizhaiZhao, ZhongmingSun, Shumei and Gao, Guimin
Human Heredity, vol. 75, (no. 1), pp. 23-33, May 2013. | Journal Article
 
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study
Perera, Minoli APerera, M.A.Perera, Minoli APerera, Minoli A.Perera, Minoli APerera, MinoliCavallari, Larisa H.Cavallari, Larisa HCavallari, Larisa HCavallari, Larisa HCavallari, L.H.Cavallari, Larisa HLimdi, NitaLimdi, Nita ALimdi, Nita ALimdi, Nita ALimdi, Nita A.Limdi, N.A.Gamazon, Eric RGamazon, Eric RGamazon, Eric RGamazon, Eric RGamazon, E.R.Gamazon, Eric R.Konkashbaev, AnuarKonkashbaev, A.Konkashbaev, AnuarKonkashbaev, AnuarKonkashbaev, AnuarKonkashbaev, AnuarDaneshjou, RoxanaDaneshjou, RoxanaDaneshjou, Roxana RDaneshjou, RoxanaDaneshjou, RoxanaDaneshjou, R.Pluzhnikov, AnnaPluzhnikov, AnnaPluzhnikov, AnnaPluzhnikov, AnnaPluzhnikov, A.Pluzhnikov, AnnaCrawford, Dana C.Crawford, Dana CCrawford, D.C.Crawford, Dana CCrawford, DanaCrawford, Dana CWang, JelaiWang, JelaiWang, JelaiWang, JelaiWang, JelaiWang, J.Liu, NianjunLiu, NianjunLiu, NianjunLiu, N.Liu, NianjunLiu, NianjunTatonetti, NicholasTatonetti, Nicholasal.Tatonetti, NicholasTatonetti, N.Tatonetti, NicholasBourgeois, S.Bourgeois, StephaneBourgeois, StephaneBourgeois, StephaneBourgeois, StephaneTakahashi, HarumiTakahashi, H.Takahashi, HarumiTakahashi, HarumiTakahashi, HarumiBradford, YukikoBradford, YukikoBradford, YukikoBradford, YukikoBradford, Y.Burkley, Benjamin MBurkley, Benjamin MBurkley, Benjamin MBurkley, B.M.Burkley, Benjamin MDesnick, Robert JDesnick, Robert JDesnick, R.J.Desnick, Robert JDesnick, Robert JHalperin, Jonathan LHalperin, J.L.Halperin, Jonathan LHalperin, Jonathan LHalperin, Jonathan LKhalifa, Sherief IKhalifa, S.I.Khalifa, Sherief IKhalifa, Sherief IKhalifa, Sherief ILangaee, Taimour YLangaee, Taimour YLangaee, Taimour YLangaee, T.Y.Langaee, Taimour YLubitz, Steven ALubitz, Steven ALubitz, Steven ALubitz, S.A.Lubitz, Steven ANutescu, Edith ANutescu, E.A.Nutescu, Edith ANutescu, Edith ANutescu, Edith AOetjens, MatthewOetjens, MatthewOetjens, MatthewOetjens, MatthewOetjens, M.Shahin, Mohamed HShahin, Mohamed HShahin, Mohamed HShahin, Mohamed HShahin, M.H.Patel, Shitalben RPatel, Shitalben RPatel, Shitalben RPatel, S.R.Patel, Shitalben RSagreiya, HershSagreiya, HershSagreiya, HershSagreiya, H.Sagreiya, HershTector, M.Tector, MatthewTector, MatthewTector, MatthewTector, MatthewWeck, Karen EWeck, K.E.Weck, Karen EWeck, Karen EWeck, Karen ERieder, Mark JRieder, M.J.Rieder, Mark JRieder, Mark JRieder, Mark JScott, Stuart AScott, StuartScott, Stuart AScott, Stuart AScott, S.A.Wu, Alan HWu, Alan HWu, Alan HWu, Alan HWu, A.H.B.Burmester, James KBurmester, James KBurmester, J.K.Burmester, James KBurmester, James KWadelius, MiaWadelius, M.Wadelius, MiaWadelius, MiaWadelius, MiaDeloukas, PanosDeloukas, P.Deloukas, PanosDeloukas, PanosDeloukas, PanosWagner, Michael JWagner, M.J.Wagner, Michael JWagner, Michael JWagner, Michael JMushiroda, TaiseiMushiroda, T.Mushiroda, TaiseiMushiroda, TaiseiMushiroda, TaiseiKubo, MichiakiKubo, MichiakiKubo, MichiakiKubo, M.Kubo, MichiakiRoden, Dan MRoden, Dan MRoden, D.M.Roden, Dan MRoden, Dan MCox, Nancy JCox, Nancy JCox, Nancy JCox, Nancy JCox, N.J.Altman, R.B.Altman, Russ BAltman, Russ BAltman, Russ BAltman, Russ BKlein, Teri EKlein, T.E.Klein, Teri EKlein, Teri EKlein, Teri ENakamura, YusukeNakamura, YusukeNakamura, Y.Nakamura, YusukeNakamura, YusukeJohnson, Julie AJohnson, J.A.Johnson, Julie AJohnson, Julie A and Johnson, Julie A
The Lancet, vol. 382, (no. 9894), pp. 790-6, Aug 31, 2013. | Journal Article
 
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.
Lin, Wan-YuLin, Wan YuLin, Wan YuYi, NengjunYi, NengjunYi, NengjunLou, Xiang-YangLou, Xiang-YangLou, Xiang-YangZhi, DeguiZhi, DeguiZhi, DeguiZhang, KuiZhang, KuiZhang, KuiGao, GuiminGao, GuiminGao, GuiminTiwari, Hemant KTiwari, Hemant KTiwari, Hemant K.Liu, NianjunLiu, Nianjun and Liu, Nianjun
Genetic epidemiology, vol. 37, (no. 6), pp. 560-70, 2013/Sep. | Journal Article
 
Long-Term Changes in Adiposity and Glycemic Control Are Associated With Past Adenovirus Infection
Lin, Wan YuWY, LinDubuisson, OlgaO, DubuissonRubicz, RohinaR, RubiczLiu, NianjunN, LiuAllison, David BDB, AllisonJE, CurranCurran, Joanne EAG, ComuzzieComuzzie, Anthony GBlangero, JohnJ, BlangeroLeach, Charles TCT, LeachGöring, HaraldH, GöringDhurandhar, Nikhil V and NV, Dhurandhar
Diabetes Care, vol. 36, (no. 3), pp. 701-707, Mar 2013. | Journal Article
 
Response to Comment on: Lin et al. Long-term changes in adiposity and glycemic control are associated with past adenovirus infection. Diabetes Care 2013;36:701-707.
Lin, Wan YuWY, LinDubuisson, OlgaO, DubuissonRubicz, RohinaR, RubiczLiu, NianjunN, LiuAllison, David BDB, AllisonJE, CurranCurran, Joanne EAG, ComuzzieComuzzie, Anthony GBlangero, JohnJ, BlangeroLeach, Charles TCT, LeachGöring, HaraldH, GöringDhurandhar, Nikhil V and NV, Dhurandhar
Diabetes care, vol. 36, (no. 9), pp. e162, 2013/Sep. | Journal Article
2012
A Generalized Sequential Bonferroni Procedure Using Smoothed Weights for Genome-Wide Association Studies Incorporating Information on Hardy-Weinberg Disequilibrium among Cases
Gao, GuiminKang, GuolianWang, JiexunChen, WenanQin, HuaizenJiang, BoLi, QizhaiSun, ChuanyuLiu, NianjunArcher, Kellie J and Allison, David B
Human Heredity, vol. 73, (no. 1), pp. 1-13, Mar 2012. | Journal Article
 
Genotype calling from next-generation sequencing data using haplotype information of reads.
Zhi, DeguiZhi, DeguiWu, JihuaWu, JihuaLiu, NianjunLiu, NianjunZhang, Kui and Zhang, Kui
Bioinformatics (Oxford, England), vol. 28, (no. 7), pp. 938-46, 2012/Apr/1. | Journal Article
 
Haplotype-based methods for detecting uncommon causal variants with common SNPs.
Lin, Wan YuLin, Wan-YuLin, Wan YuYi, NengjunYi, NengjunYi, NengjunZhi, DeguiZhi, DeguiZhi, DeguiZhang, KuiZhang, KuiZhang, KuiGao, GuiminGao, GuiminGao, GuiminTiwari, Hemant KTiwari, Hemant KTiwari, Hemant K.Liu, NianjunLiu, Nianjun and Liu, Nianjun
Genetic epidemiology, vol. 36, (no. 6), pp. 572-82, 2012/Sep. | Journal Article
 
Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness.
Lin, Wan Yu and Liu, Nianjun
Frontiers in genetics, vol. 3, pp. 107, 2012. | Journal Article
 
Similarity-Based Multimarker Association Tests for Continuous Traits
Lin, Wan YuLin, Wan-YuLin, Wan YuTiwari, Hemant KTiwari, Hemant KTiwari, Hemant K.Gao, GuiminGao, GuiminGao, GuiminZhang, KuiZhang, KuiZhang, KuiArcaroli, John JArcaroli, John JArcaroli, John J.Abraham, EdwardAbraham, EdwardAbraham, EdwardLiu, NianjunLiu, Nianjun and Liu, Nianjun
Annals of Human Genetics, vol. 76, (no. 3), pp. 260, 2012-05-00. | Journal Article
2011
Association between IL-32 genotypes and outcome in infection-associated acute lung injury.
Arcaroli, John JLiu, NianjunYi, Nengjun and Abraham, Edward
Critical care (London, England), vol. 15, (no. 3), pp. R138, 2011. | Journal Article
 
Controlling Population Structure in Human Genetic Association Studies with Samples of Unrelated Individuals.
Liu, NianjunZhao, HongyuPatki, AmitLimdi, Nita A and Allison, David B
Statistics and its interface, vol. 4, (no. 3), pp. 317-326, 2011. | Journal Article
 
Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data.
Chen, WenanChen, WenanGao, XiGao, XiWang, JiexunWang, JiexunSun, ChuanyuSun, ChuanyuWan, WenWan, WenZhi, DeguiZhi, DeguiLiu, NianjunLiu, NianjunChen, XiangningChen, XiangningGao, Guimin and Gao, Guimin
BMC proceedings, vol. 5 Suppl 9, pp. S86, 2011. | Journal Article
 
Evaluation of pooled association tests for rare variant identification.
Lin, Wan YuZhang, BoshaoYi, NengjunGao, Guimin and Liu, Nianjun
BMC proceedings, vol. 5 Suppl 9, pp. S118, 2011. | Journal Article
 
Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects.
Yi, NengjunLiu, NianjunZhi, Degui and Li, Jun
PLoS genetics, vol. 7, (no. 12), pp. e1002382, 2011/Dec. | Journal Article
 
Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate.
Zhang, BoshaoZhang, BoshaoZhi, DeguiZhi, DeguiZhang, KuiZhang, KuiGao, GuiminGao, GuiminLimdi, Nita NLimdi, Nita NLiu, Nianjun and Liu, Nianjun
Statistics and its interface, vol. 4, (no. 3), pp. 339-352, 2011. | Journal Article
2010
Warfarin pharmacogenetics
Limdi, Nita AWadelius, MiaCavallari, LarissaEriksson, NiclasCrawford, Dana CLee, Ming-Ta MChen, Chien-HsiunMotsinger-Reif, AlisonSagreiya, HershLiu, NianjunWu, Alan H. BGage, Brian FJorgensen, AndreaPirmohamed, MunirShin, Jae-GookSuarez-Kurtz, GuilhermeKimmel, Stephen EJohnson, Julie AKlein, Teri E and Wagner, Michael J
Blood, vol. 115, (no. 18), pp. 3827, 2010. | Journal Article
 
Warfarin pharmacogenetics
Limdi, Nita AWadelius, MiaCavallari, LarissaEriksson, NiclasCrawford, Dana CLee, Ming-Ta MChen, Chien-HsiunMotsinger-Reif, AlisonSagreiya, HershLiu, NianjunWu, Alan H. BGage, Brian FJorgensen, AndreaPirmohamed, MunirShin, Jae-GookSuarez-Kurtz, GuilhermeKimmel, Stephen EJohnson, Julie AKlein, Teri E and Wagner, Michael J
Blood, vol. 115, (no. 18), pp. 3827, 2010. | Journal Article
 
Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups.
Limdi, Nita AWadelius, MiaCavallari, LarisaEriksson, NiclasCrawford, DanaLee, Ming-Ta MChen, Chien-HsiunMotsinger Reif, AlisonSagreiya, HershLiu, NianjunWu, Alan HGage, Brian FJorgensen, AndreaPirmohamed, MunirShin, Jae-GookSuarez-Kurtz, GuilhermeKimmel, StephenJohnson, Julie AKlein, Teri E and Wagner, Michael J
Blood, vol. 115, (no. 18), pp. 3827-34, 2010/May/6. | Journal Article
2009
Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations.
Chung, Wendy KPatki, AmitMatsuoka, NaokiBoyer, Bert BLiu, NianjunMusani, Solomon KGoropashnaya, Anna VTan, Perciliz LKatsanis, NicholasJohnson, Stephen BGregersen, Peter KAllison, David BLeibel, Rudolph L and Tiwari, Hemant K
Human heredity, vol. 67, (no. 3), pp. 193-205, 2009. | Journal Article