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Dingge Ying

Showing results (11-20 of 25) with videos related to

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Briefings in Bioinformatics|September 22, 2025
Clinical and data-driven optimization of Genomiser for rare disease patients: experience from the Hong Kong Genome ProjectAnson Man Chun Xi, Denis Long Him Yeung, Wei Ma, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Monoallelic Mutations in <i>CC2D1A</i> Suggest a Novel Role in Human Heterotaxy and Ciliary DysfunctionAlvin Chun Hang Ma, Christopher Chun Yu Mak, Kit San Yeung, et al.
Genome Biology|March 18, 2017
cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genesMulin Jun Li, Miaoxin Li, Zipeng Liu, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 20, 2016
Prenatal Tobacco Exposure Shortens Telomere Length in ChildrenPatrick Ip, Brian Hon Yin Chung, Frederick Ka Wing Ho, et al.
Molecular Autism|January 4, 2018
Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autismKit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2026
Whole genome sequencing for CKD of unexplained cause in Hong KongBecky Mingyao Ma, Shirley Pik Ying Hue, Wei Ma, et al.
Cell Reports|October 14, 2025
Integrated genomic and transcriptomic profiling of glioblastoma reveals ecDNA-driven heterogeneity and microenvironmental reprogrammingWenshu Tang, Wing Lun Lee, Cario W S Lo, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
<i>CFTR</i> founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Annals of Human Genetics|April 26, 2013
Epistatic interaction between genetic variants in susceptibility gene ETS1 correlates with IL-17 levels in SLE patientsJing Zhang, Yan Zhang, Lu Zhang, et al.
Plos Genetics|February 20, 2010
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosusWanling Yang, Nan Shen, Dong-Qing Ye, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Briefings in Bioinformatics|September 22, 2025
Clinical and data-driven optimization of Genomiser for rare disease patients: experience from the Hong Kong Genome ProjectAnson Man Chun Xi, Denis Long Him Yeung, Wei Ma, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Monoallelic Mutations in <i>CC2D1A</i> Suggest a Novel Role in Human Heterotaxy and Ciliary DysfunctionAlvin Chun Hang Ma, Christopher Chun Yu Mak, Kit San Yeung, et al.
Genome Biology|March 18, 2017
cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genesMulin Jun Li, Miaoxin Li, Zipeng Liu, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 20, 2016
Prenatal Tobacco Exposure Shortens Telomere Length in ChildrenPatrick Ip, Brian Hon Yin Chung, Frederick Ka Wing Ho, et al.
Molecular Autism|January 4, 2018
Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autismKit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2026
Whole genome sequencing for CKD of unexplained cause in Hong KongBecky Mingyao Ma, Shirley Pik Ying Hue, Wei Ma, et al.
Cell Reports|October 14, 2025
Integrated genomic and transcriptomic profiling of glioblastoma reveals ecDNA-driven heterogeneity and microenvironmental reprogrammingWenshu Tang, Wing Lun Lee, Cario W S Lo, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
<i>CFTR</i> founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Annals of Human Genetics|April 26, 2013
Epistatic interaction between genetic variants in susceptibility gene ETS1 correlates with IL-17 levels in SLE patientsJing Zhang, Yan Zhang, Lu Zhang, et al.
Plos Genetics|February 20, 2010
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosusWanling Yang, Nan Shen, Dong-Qing Ye, et al.
Pageof 3