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Pak Chung Sham

Showing results (181-190 of 224) with videos related to

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Diabetes|April 8, 2017
An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of <i>GCKR</i> That Regulates FGF21 LevelsChloe Y Y Cheung, Clara S Tang, Aimin Xu, et al.
Schizophrenia Bulletin|September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han ChineseEmily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
International Psychogeriatrics|October 22, 2016
Prevalence of anxiety disorders in community dwelling older adults in Hong KongAda Wai Tung Fung, Wai-Chi Chan, Corine Sau-Man Wong, et al.
Molecular Psychiatry|October 4, 2022
A causal association of ANKRD37 with human hippocampal volumeJiayuan Xu, Xianyou Xia, Qiaojun Li, et al.
Scientific Reports|February 18, 2015
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)Yu Chen, Jie Zhou, Zhongshan Cheng, et al.
Ebiomedicine|August 29, 2021
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanismWai-Yee Lam, Clara Sze-Man Tang, Man-Ting So, et al.
American Journal of Hypertension|January 14, 2014
A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han ChineseKuang-Mao Chiang, Hsin-Chou Yang, Yu-Jen Liang, et al.
Human Genetics|June 28, 2011
Mutations in the NRG1 gene are associated with Hirschsprung diseaseClara Sze-Man Tang, Elly Sau-Wai Ngan, Wai-Kiu Tang, et al.
Human Mutation|July 18, 2017
Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosisWenjie Gao, Chong Chen, Taifeng Zhou, et al.
Human Molecular Genetics|December 16, 2011
Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral densitySu-Mei Xiao, Annie Wai Chee Kung, Yi Gao, et al.
Pageof 23

Showing results (181-190 of 224) with videos related to

Sort By:
Pageof 23
Diabetes|April 8, 2017
An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of <i>GCKR</i> That Regulates FGF21 LevelsChloe Y Y Cheung, Clara S Tang, Aimin Xu, et al.
Schizophrenia Bulletin|September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han ChineseEmily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
International Psychogeriatrics|October 22, 2016
Prevalence of anxiety disorders in community dwelling older adults in Hong KongAda Wai Tung Fung, Wai-Chi Chan, Corine Sau-Man Wong, et al.
Molecular Psychiatry|October 4, 2022
A causal association of ANKRD37 with human hippocampal volumeJiayuan Xu, Xianyou Xia, Qiaojun Li, et al.
Scientific Reports|February 18, 2015
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)Yu Chen, Jie Zhou, Zhongshan Cheng, et al.
Ebiomedicine|August 29, 2021
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanismWai-Yee Lam, Clara Sze-Man Tang, Man-Ting So, et al.
American Journal of Hypertension|January 14, 2014
A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han ChineseKuang-Mao Chiang, Hsin-Chou Yang, Yu-Jen Liang, et al.
Human Genetics|June 28, 2011
Mutations in the NRG1 gene are associated with Hirschsprung diseaseClara Sze-Man Tang, Elly Sau-Wai Ngan, Wai-Kiu Tang, et al.
Human Mutation|July 18, 2017
Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosisWenjie Gao, Chong Chen, Taifeng Zhou, et al.
Human Molecular Genetics|December 16, 2011
Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral densitySu-Mei Xiao, Annie Wai Chee Kung, Yi Gao, et al.
Pageof 23