82 Publications (Page 2 of 4)
2014
A statistical framework for testing the causal effects of fetal driveLiu, Nianjun⋅Liu, Nianjun⋅Archer, Edward⋅Archer, Edward⋅Srinivasasainagendra, Vinodh⋅Srinivasasainagendra, Vinodh⋅Allison, David B and Allison, David BFrontiers in genetics, vol. 5, pp. 464, 2014-00-00.
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A unified GMDR method for detecting gene-gene interactions in family and unrelated samples with application to nicotine dependence.Chen, Guo-Bo⋅Chen, Guo-Bo⋅Liu, Nianjun⋅Liu, Nianjun⋅Klimentidis, Yann C⋅Klimentidis, Yann⋅Zhu, Xiaofeng⋅Zhu, Xiaofeng⋅Zhi, Degui⋅Zhi, Degui⋅Wang, Xujing⋅Wang, Xujing⋅Lou, Xiang-Yang and Lou, Xiang-YangHuman genetics, vol. 133, (no. 2), pp. 139-50, 2014/Feb.
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Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.Yan, Qi⋅Yan, Qi⋅Tiwari, Hemant K⋅Tiwari, Hemant K.⋅Yi, Nengjun⋅Yi, Nengjun⋅Lin, Wan Yu⋅Lin, Wan Yu⋅Gao, Guimin⋅Gao, Guimin⋅Lou, Xiang-Yang⋅Lou, Xiang-Yang⋅Cui, Xiangqin⋅Cui, Xiangqin⋅Liu, Nianjun and Liu, NianjunGenetic epidemiology, vol. 38, (no. 5), pp. 447-456, July 2014.
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Multivariate Dimensionality Reduction Approaches to Identify Gene-Gene and Gene-Environment Interactions Underlying Multiple Complex TraitsXu, Hai-Ming⋅Xu, Hai-Ming⋅Xu, Hai-Ming⋅Sun, Xi-Wei⋅Sun, Xi-Wei⋅Sun, Xi-Wei⋅Qi, Ting⋅Qi, Ting⋅Qi, Ting⋅Lin, Wan-Yu⋅Lin, Wan Yu⋅Lin, Wan Yu⋅Liu, Nianjun⋅Liu, Nianjun⋅Liu, Nianjun⋅Lou, Xiang-Yang⋅Lou, Xiang-Yang and Lou, Xiang-YangPloS one, vol. 9, (no. 9), pp. e108103, 2014-00-00.
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Rare variant association testing by adaptive combination of P-values.Lin, Wan Yu⋅Lin, Wan Yu⋅Lou, Xiang-Yang⋅Lou, Xiang-Yang⋅Gao, Guimin⋅Gao, Guimin⋅Liu, Nianjun and Liu, NianjunPloS one, vol. 9, (no. 1), pp. e85728, 2014.
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2013
A Rapid Association Test Procedure Robust under Different Genetic Models Accounting for Population StratificationChen, Wenan⋅Chen, Sam⋅Archer, Kellie J⋅Liu, Nianjun⋅Li, Qizhai⋅Zhao, Zhongming⋅Sun, Shumei and Gao, GuiminHuman Heredity, vol. 75, (no. 1), pp. 23-33, May 2013.
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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association studyPerera, Minoli A⋅Perera, M.A.⋅Perera, Minoli A⋅Perera, Minoli A.⋅Perera, Minoli A⋅Perera, Minoli⋅Cavallari, Larisa H.⋅Cavallari, Larisa H⋅Cavallari, Larisa H⋅Cavallari, Larisa H⋅Cavallari, L.H.⋅Cavallari, Larisa H⋅Limdi, Nita⋅Limdi, Nita A⋅Limdi, Nita A⋅Limdi, Nita A⋅Limdi, Nita A.⋅Limdi, N.A.⋅Gamazon, Eric R⋅Gamazon, Eric R⋅Gamazon, Eric R⋅Gamazon, Eric R⋅Gamazon, E.R.⋅Gamazon, Eric R.⋅Konkashbaev, Anuar⋅Konkashbaev, A.⋅Konkashbaev, Anuar⋅Konkashbaev, Anuar⋅Konkashbaev, Anuar⋅Konkashbaev, Anuar⋅Daneshjou, Roxana⋅Daneshjou, Roxana⋅Daneshjou, Roxana R⋅Daneshjou, Roxana⋅Daneshjou, Roxana⋅Daneshjou, R.⋅Pluzhnikov, Anna⋅Pluzhnikov, Anna⋅Pluzhnikov, Anna⋅Pluzhnikov, Anna⋅Pluzhnikov, A.⋅Pluzhnikov, Anna⋅Crawford, Dana C.⋅Crawford, Dana C⋅Crawford, D.C.⋅Crawford, Dana C⋅Crawford, Dana⋅Crawford, Dana C⋅Wang, Jelai⋅Wang, Jelai⋅Wang, Jelai⋅Wang, Jelai⋅Wang, Jelai⋅Wang, J.⋅Liu, Nianjun⋅Liu, Nianjun⋅Liu, Nianjun⋅Liu, N.⋅Liu, Nianjun⋅Liu, Nianjun⋅Tatonetti, Nicholas⋅Tatonetti, Nicholas⋅al.⋅Tatonetti, Nicholas⋅Tatonetti, N.⋅Tatonetti, Nicholas⋅Bourgeois, S.⋅Bourgeois, Stephane⋅Bourgeois, Stephane⋅Bourgeois, Stephane⋅Bourgeois, Stephane⋅Takahashi, Harumi⋅Takahashi, H.⋅Takahashi, Harumi⋅Takahashi, Harumi⋅Takahashi, Harumi⋅Bradford, Yukiko⋅Bradford, Yukiko⋅Bradford, Yukiko⋅Bradford, Yukiko⋅Bradford, Y.⋅Burkley, Benjamin M⋅Burkley, Benjamin M⋅Burkley, Benjamin M⋅Burkley, B.M.⋅Burkley, Benjamin M⋅Desnick, Robert J⋅Desnick, Robert J⋅Desnick, R.J.⋅Desnick, Robert J⋅Desnick, Robert J⋅Halperin, Jonathan L⋅Halperin, J.L.⋅Halperin, Jonathan L⋅Halperin, Jonathan L⋅Halperin, Jonathan L⋅Khalifa, Sherief I⋅Khalifa, S.I.⋅Khalifa, Sherief I⋅Khalifa, Sherief I⋅Khalifa, Sherief I⋅Langaee, Taimour Y⋅Langaee, Taimour Y⋅Langaee, Taimour Y⋅Langaee, T.Y.⋅Langaee, Taimour Y⋅Lubitz, Steven A⋅Lubitz, Steven A⋅Lubitz, Steven A⋅Lubitz, S.A.⋅Lubitz, Steven A⋅Nutescu, Edith A⋅Nutescu, E.A.⋅Nutescu, Edith A⋅Nutescu, Edith A⋅Nutescu, Edith A⋅Oetjens, Matthew⋅Oetjens, Matthew⋅Oetjens, Matthew⋅Oetjens, Matthew⋅Oetjens, M.⋅Shahin, Mohamed H⋅Shahin, Mohamed H⋅Shahin, Mohamed H⋅Shahin, Mohamed H⋅Shahin, M.H.⋅Patel, Shitalben R⋅Patel, Shitalben R⋅Patel, Shitalben R⋅Patel, S.R.⋅Patel, Shitalben R⋅Sagreiya, Hersh⋅Sagreiya, Hersh⋅Sagreiya, Hersh⋅Sagreiya, H.⋅Sagreiya, Hersh⋅Tector, M.⋅Tector, Matthew⋅Tector, Matthew⋅Tector, Matthew⋅Tector, Matthew⋅Weck, Karen E⋅Weck, K.E.⋅Weck, Karen E⋅Weck, Karen E⋅Weck, Karen E⋅Rieder, Mark J⋅Rieder, M.J.⋅Rieder, Mark J⋅Rieder, Mark J⋅Rieder, Mark J⋅Scott, Stuart A⋅Scott, Stuart⋅Scott, Stuart A⋅Scott, Stuart A⋅Scott, S.A.⋅Wu, Alan H⋅Wu, Alan H⋅Wu, Alan H⋅Wu, Alan H⋅Wu, A.H.B.⋅Burmester, James K⋅Burmester, James K⋅Burmester, J.K.⋅Burmester, James K⋅Burmester, James K⋅Wadelius, Mia⋅Wadelius, M.⋅Wadelius, Mia⋅Wadelius, Mia⋅Wadelius, Mia⋅Deloukas, Panos⋅Deloukas, P.⋅Deloukas, Panos⋅Deloukas, Panos⋅Deloukas, Panos⋅Wagner, Michael J⋅Wagner, M.J.⋅Wagner, Michael J⋅Wagner, Michael J⋅Wagner, Michael J⋅Mushiroda, Taisei⋅Mushiroda, T.⋅Mushiroda, Taisei⋅Mushiroda, Taisei⋅Mushiroda, Taisei⋅Kubo, Michiaki⋅Kubo, Michiaki⋅Kubo, Michiaki⋅Kubo, M.⋅Kubo, Michiaki⋅Roden, Dan M⋅Roden, Dan M⋅Roden, D.M.⋅Roden, Dan M⋅Roden, Dan M⋅Cox, Nancy J⋅Cox, Nancy J⋅Cox, Nancy J⋅Cox, Nancy J⋅Cox, N.J.⋅Altman, R.B.⋅Altman, Russ B⋅Altman, Russ B⋅Altman, Russ B⋅Altman, Russ B⋅Klein, Teri E⋅Klein, T.E.⋅Klein, Teri E⋅Klein, Teri E⋅Klein, Teri E⋅Nakamura, Yusuke⋅Nakamura, Yusuke⋅Nakamura, Y.⋅Nakamura, Yusuke⋅Nakamura, Yusuke⋅Johnson, Julie A⋅Johnson, J.A.⋅Johnson, Julie A⋅Johnson, Julie A and Johnson, Julie AThe Lancet, vol. 382, (no. 9894), pp. 790-6, Aug 31, 2013.
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Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Lin, Wan-Yu⋅Lin, Wan Yu⋅Lin, Wan Yu⋅Yi, Nengjun⋅Yi, Nengjun⋅Yi, Nengjun⋅Lou, Xiang-Yang⋅Lou, Xiang-Yang⋅Lou, Xiang-Yang⋅Zhi, Degui⋅Zhi, Degui⋅Zhi, Degui⋅Zhang, Kui⋅Zhang, Kui⋅Zhang, Kui⋅Gao, Guimin⋅Gao, Guimin⋅Gao, Guimin⋅Tiwari, Hemant K⋅Tiwari, Hemant K⋅Tiwari, Hemant K.⋅Liu, Nianjun⋅Liu, Nianjun and Liu, NianjunGenetic epidemiology, vol. 37, (no. 6), pp. 560-70, 2013/Sep.
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Long-Term Changes in Adiposity and Glycemic Control Are Associated With Past Adenovirus InfectionLin, Wan Yu⋅WY, Lin⋅Dubuisson, Olga⋅O, Dubuisson⋅Rubicz, Rohina⋅R, Rubicz⋅Liu, Nianjun⋅N, Liu⋅Allison, David B⋅DB, Allison⋅JE, Curran⋅Curran, Joanne E⋅AG, Comuzzie⋅Comuzzie, Anthony G⋅Blangero, John⋅J, Blangero⋅Leach, Charles T⋅CT, Leach⋅Göring, Harald⋅H, Göring⋅Dhurandhar, Nikhil V and NV, DhurandharDiabetes Care, vol. 36, (no. 3), pp. 701-707, Mar 2013.
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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 Yu⋅WY, Lin⋅Dubuisson, Olga⋅O, Dubuisson⋅Rubicz, Rohina⋅R, Rubicz⋅Liu, Nianjun⋅N, Liu⋅Allison, David B⋅DB, Allison⋅JE, Curran⋅Curran, Joanne E⋅AG, Comuzzie⋅Comuzzie, Anthony G⋅Blangero, John⋅J, Blangero⋅Leach, Charles T⋅CT, Leach⋅Göring, Harald⋅H, Göring⋅Dhurandhar, Nikhil V and NV, DhurandharDiabetes care, vol. 36, (no. 9), pp. e162, 2013/Sep.
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2012
A Generalized Sequential Bonferroni Procedure Using Smoothed Weights for Genome-Wide Association Studies Incorporating Information on Hardy-Weinberg Disequilibrium among CasesGao, Guimin⋅Kang, Guolian⋅Wang, Jiexun⋅Chen, Wenan⋅Qin, Huaizen⋅Jiang, Bo⋅Li, Qizhai⋅Sun, Chuanyu⋅Liu, Nianjun⋅Archer, Kellie J and Allison, David BHuman Heredity, vol. 73, (no. 1), pp. 1-13, Mar 2012.
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Genotype calling from next-generation sequencing data using haplotype information of reads.Zhi, Degui⋅Zhi, Degui⋅Wu, Jihua⋅Wu, Jihua⋅Liu, Nianjun⋅Liu, Nianjun⋅Zhang, Kui and Zhang, KuiBioinformatics (Oxford, England), vol. 28, (no. 7), pp. 938-46, 2012/Apr/1.
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Haplotype-based methods for detecting uncommon causal variants with common SNPs.Lin, Wan Yu⋅Lin, Wan-Yu⋅Lin, Wan Yu⋅Yi, Nengjun⋅Yi, Nengjun⋅Yi, Nengjun⋅Zhi, Degui⋅Zhi, Degui⋅Zhi, Degui⋅Zhang, Kui⋅Zhang, Kui⋅Zhang, Kui⋅Gao, Guimin⋅Gao, Guimin⋅Gao, Guimin⋅Tiwari, Hemant K⋅Tiwari, Hemant K⋅Tiwari, Hemant K.⋅Liu, Nianjun⋅Liu, Nianjun and Liu, NianjunGenetic epidemiology, vol. 36, (no. 6), pp. 572-82, 2012/Sep.
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Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness.Lin, Wan Yu and Liu, NianjunFrontiers in genetics, vol. 3, pp. 107, 2012.
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Similarity-Based Multimarker Association Tests for Continuous TraitsLin, Wan Yu⋅Lin, Wan-Yu⋅Lin, Wan Yu⋅Tiwari, Hemant K⋅Tiwari, Hemant K⋅Tiwari, Hemant K.⋅Gao, Guimin⋅Gao, Guimin⋅Gao, Guimin⋅Zhang, Kui⋅Zhang, Kui⋅Zhang, Kui⋅Arcaroli, John J⋅Arcaroli, John J⋅Arcaroli, John J.⋅Abraham, Edward⋅Abraham, Edward⋅Abraham, Edward⋅Liu, Nianjun⋅Liu, Nianjun and Liu, NianjunAnnals of Human Genetics, vol. 76, (no. 3), pp. 260, 2012-05-00.
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2011
Association between IL-32 genotypes and outcome in infection-associated acute lung injury.Arcaroli, John J⋅Liu, Nianjun⋅Yi, Nengjun and Abraham, EdwardCritical care (London, England), vol. 15, (no. 3), pp. R138, 2011.
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Controlling Population Structure in Human Genetic Association Studies with Samples of Unrelated Individuals.Liu, Nianjun⋅Zhao, Hongyu⋅Patki, Amit⋅Limdi, Nita A and Allison, David BStatistics and its interface, vol. 4, (no. 3), pp. 317-326, 2011.
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Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data.Chen, Wenan⋅Chen, Wenan⋅Gao, Xi⋅Gao, Xi⋅Wang, Jiexun⋅Wang, Jiexun⋅Sun, Chuanyu⋅Sun, Chuanyu⋅Wan, Wen⋅Wan, Wen⋅Zhi, Degui⋅Zhi, Degui⋅Liu, Nianjun⋅Liu, Nianjun⋅Chen, Xiangning⋅Chen, Xiangning⋅Gao, Guimin and Gao, GuiminBMC proceedings, vol. 5 Suppl 9, pp. S86, 2011.
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Evaluation of pooled association tests for rare variant identification.Lin, Wan Yu⋅Zhang, Boshao⋅Yi, Nengjun⋅Gao, Guimin and Liu, NianjunBMC proceedings, vol. 5 Suppl 9, pp. S118, 2011.
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Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects.Yi, Nengjun⋅Liu, Nianjun⋅Zhi, Degui and Li, JunPLoS genetics, vol. 7, (no. 12), pp. e1002382, 2011/Dec.
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Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate.Zhang, Boshao⋅Zhang, Boshao⋅Zhi, Degui⋅Zhi, Degui⋅Zhang, Kui⋅Zhang, Kui⋅Gao, Guimin⋅Gao, Guimin⋅Limdi, Nita N⋅Limdi, Nita N⋅Liu, Nianjun and Liu, NianjunStatistics and its interface, vol. 4, (no. 3), pp. 339-352, 2011.
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2010
Warfarin pharmacogenetics
Limdi, Nita A⋅Wadelius, Mia⋅Cavallari, Larissa⋅Eriksson, Niclas⋅Crawford, Dana C⋅Lee, Ming-Ta M⋅Chen, Chien-Hsiun⋅Motsinger-Reif, Alison⋅Sagreiya, Hersh⋅Liu, Nianjun⋅Wu, Alan H. B⋅Gage, Brian F⋅Jorgensen, Andrea⋅Pirmohamed, Munir⋅Shin, Jae-Gook⋅Suarez-Kurtz, Guilherme⋅Kimmel, Stephen E⋅Johnson, Julie A⋅Klein, Teri E and Wagner, Michael J
Blood, vol. 115, (no. 18), pp. 3827, 2010. | Journal Article
Warfarin pharmacogenetics
Limdi, Nita A⋅Wadelius, Mia⋅Cavallari, Larissa⋅Eriksson, Niclas⋅Crawford, Dana C⋅Lee, Ming-Ta M⋅Chen, Chien-Hsiun⋅Motsinger-Reif, Alison⋅Sagreiya, Hersh⋅Liu, Nianjun⋅Wu, Alan H. B⋅Gage, Brian F⋅Jorgensen, Andrea⋅Pirmohamed, Munir⋅Shin, Jae-Gook⋅Suarez-Kurtz, Guilherme⋅Kimmel, Stephen E⋅Johnson, Julie A⋅Klein, 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 A⋅Wadelius, Mia⋅Cavallari, Larisa⋅Eriksson, Niclas⋅Crawford, Dana⋅Lee, Ming-Ta M⋅Chen, Chien-Hsiun⋅Motsinger Reif, Alison⋅Sagreiya, Hersh⋅Liu, Nianjun⋅Wu, Alan H⋅Gage, Brian F⋅Jorgensen, Andrea⋅Pirmohamed, Munir⋅Shin, Jae-Gook⋅Suarez-Kurtz, Guilherme⋅Kimmel, Stephen⋅Johnson, Julie A⋅Klein, Teri E and Wagner, Michael JBlood, vol. 115, (no. 18), pp. 3827-34, 2010/May/6.
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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 K⋅Patki, Amit⋅Matsuoka, Naoki⋅Boyer, Bert B⋅Liu, Nianjun⋅Musani, Solomon K⋅Goropashnaya, Anna V⋅Tan, Perciliz L⋅Katsanis, Nicholas⋅Johnson, Stephen B⋅Gregersen, Peter K⋅Allison, David B⋅Leibel, Rudolph L and Tiwari, Hemant KHuman heredity, vol. 67, (no. 3), pp. 193-205, 2009.
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