Search research articles
Contact Us
Filters
Showing results (61-70 of 71) with videos related to
Page
of 8
Sort By:
Nucleic Acids Research
|
December 21, 2021
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases
Lin Jiang, Hui Jiang, Sheng Dai, et al.
Cell Genomics
|
August 29, 2025
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic loci
Ke Zhao, Yao Zhou, Xueqi Wang, et al.
Hepatology (Baltimore, Md.)
|
November 25, 2014
The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis B
Liang Peng, Qiang Zhao, Qibin Li, et al.
Genome Biology
|
October 31, 2023
Landscape of enhancer disruption and functional screen in melanoma cells
Zhao Wang, Menghan Luo, Qian Liang, et al.
Nature Communications
|
November 6, 2023
LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortality
Ruiyang Li, Wenben Chen, Mingyuan Li, et al.
Human Molecular Genetics
|
November 28, 2017
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca
Jacob S J Hsu, Manting So, Clara S M Tang, et al.
Schizophrenia Bulletin
|
September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese
Emily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
Neurobiology of Aging
|
April 17, 2018
A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population
Binbin Wang, Suying Bao, Zhigang Zhang, et al.
Hepatology (Baltimore, Md.)
|
May 22, 2012
Rare inborn errors associated with chronic hepatitis B virus infection
Qiang Zhao, Liang Peng, Weijun Huang, et al.
Schizophrenia Bulletin
|
May 27, 2014
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations
, Jim van Os, Bart P Rutten, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
Nucleic Acids Research
|
December 21, 2021
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases
Lin Jiang, Hui Jiang, Sheng Dai, et al.
Cell Genomics
|
August 29, 2025
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic loci
Ke Zhao, Yao Zhou, Xueqi Wang, et al.
Hepatology (Baltimore, Md.)
|
November 25, 2014
The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis B
Liang Peng, Qiang Zhao, Qibin Li, et al.
Genome Biology
|
October 31, 2023
Landscape of enhancer disruption and functional screen in melanoma cells
Zhao Wang, Menghan Luo, Qian Liang, et al.
Nature Communications
|
November 6, 2023
LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortality
Ruiyang Li, Wenben Chen, Mingyuan Li, et al.
Human Molecular Genetics
|
November 28, 2017
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca
Jacob S J Hsu, Manting So, Clara S M Tang, et al.
Schizophrenia Bulletin
|
September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese
Emily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
Neurobiology of Aging
|
April 17, 2018
A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population
Binbin Wang, Suying Bao, Zhigang Zhang, et al.
Hepatology (Baltimore, Md.)
|
May 22, 2012
Rare inborn errors associated with chronic hepatitis B virus infection
Qiang Zhao, Liang Peng, Weijun Huang, et al.
Schizophrenia Bulletin
|
May 27, 2014
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations
, Jim van Os, Bart P Rutten, et al.
Page
of 8