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Pei-Kuan Cong

Showing results (1-10 of 9) with videos related to

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International Journal of Ophthalmology|October 19, 2023
A novel pathogenic splicing mutation of <i>RPGR</i> in a Chinese family with X-linked retinitis pigmentosa verified by minigene splicing assayHui-Qin Wang, Pei-Kuan Cong, Tian He, et al.
Human Molecular Genetics|July 7, 2021
Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral densityWei-Yang Bai, Jiang-Wei Xia, Xiao-Li Rong, et al.
Briefings in Bioinformatics|February 1, 2020
Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversityWei-Yang Bai, Xiao-Wei Zhu, Pei-Kuan Cong, et al.
Communications Biology|November 27, 2021
Observational and genetic evidence highlight the association of human sleep behaviors with the incidence of fractureYu Qian, Jiangwei Xia, Ke-Qi Liu, et al.
Bone|January 23, 2020
Identification of PIEZO1 polymorphisms for human bone mineral densityWei-Yang Bai, Lijun Wang, Zhi-Min Ying, et al.
BMJ Open|June 29, 2021
Cohort profile: the Westlake BioBank for Chinese (WBBC) pilot projectXiao-Wei Zhu, Ke-Qi Liu, Ping-Yu Wang, et al.
Nature Communications|May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot projectPei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Annals of the Rheumatic Diseases|August 2, 2020
Systemic evaluation of the relationship between psoriasis, psoriatic arthritis and osteoporosis: observational and Mendelian randomisation studyJiangwei Xia, Shu-Yang Xie, Ke-Qi Liu, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
International Journal of Ophthalmology|October 19, 2023
A novel pathogenic splicing mutation of <i>RPGR</i> in a Chinese family with X-linked retinitis pigmentosa verified by minigene splicing assayHui-Qin Wang, Pei-Kuan Cong, Tian He, et al.
Human Molecular Genetics|July 7, 2021
Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral densityWei-Yang Bai, Jiang-Wei Xia, Xiao-Li Rong, et al.
Briefings in Bioinformatics|February 1, 2020
Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversityWei-Yang Bai, Xiao-Wei Zhu, Pei-Kuan Cong, et al.
Communications Biology|November 27, 2021
Observational and genetic evidence highlight the association of human sleep behaviors with the incidence of fractureYu Qian, Jiangwei Xia, Ke-Qi Liu, et al.
Bone|January 23, 2020
Identification of PIEZO1 polymorphisms for human bone mineral densityWei-Yang Bai, Lijun Wang, Zhi-Min Ying, et al.
BMJ Open|June 29, 2021
Cohort profile: the Westlake BioBank for Chinese (WBBC) pilot projectXiao-Wei Zhu, Ke-Qi Liu, Ping-Yu Wang, et al.
Nature Communications|May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot projectPei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Annals of the Rheumatic Diseases|August 2, 2020
Systemic evaluation of the relationship between psoriasis, psoriatic arthritis and osteoporosis: observational and Mendelian randomisation studyJiangwei Xia, Shu-Yang Xie, Ke-Qi Liu, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Pageof 1