Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mingrui Yu

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Ebiomedicine|June 13, 2024
Contribution of copy number variants on antipsychotic treatment response in Han Chinese patients with schizophreniaYaoyao Sun, Yuyanan Zhang, Zhe Lu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
The accuracy of polygenic score models for anthropometric traits and Type II Diabetes in the Native Hawaiian PopulationYing-Chu Lo, Tsz Fung Chan, Soyoung Jeon, et al.
Cell Genomics|August 15, 2024
Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traitsChia-Yen Chen, Tzu-Ting Chen, Yen-Chen Anne Feng, et al.
Cell Genomics|December 20, 2023
Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traitsChia-Yen Chen, Tzu-Ting Chen, Yen-Chen Anne Feng, et al.
Communications Biology|April 24, 2025
The accuracy of polygenic score models for BMI and Type II diabetes in the Native Hawaiian populationYing-Chu Lo, He Tian, Tsz Fung Chan, et al.
Journal of Medicinal Chemistry|July 16, 2024
Development of Zalfermin, a Long-Acting Proteolytically Stabilized FGF21 AnalogKristian Sass-Ørum, Tina Møller Tagmose, Jørgen Olsen, et al.
Nature Genetics|August 26, 2024
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Exome sequencing directly implicates 68 genes in inflammatory bowel diseaseRuifei Zhu, Qian Zhang, Kai Yuan, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerToni A Boltz, Benjamin B Chu, Calwing Liao, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Ebiomedicine|June 13, 2024
Contribution of copy number variants on antipsychotic treatment response in Han Chinese patients with schizophreniaYaoyao Sun, Yuyanan Zhang, Zhe Lu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
The accuracy of polygenic score models for anthropometric traits and Type II Diabetes in the Native Hawaiian PopulationYing-Chu Lo, Tsz Fung Chan, Soyoung Jeon, et al.
Cell Genomics|August 15, 2024
Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traitsChia-Yen Chen, Tzu-Ting Chen, Yen-Chen Anne Feng, et al.
Cell Genomics|December 20, 2023
Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traitsChia-Yen Chen, Tzu-Ting Chen, Yen-Chen Anne Feng, et al.
Communications Biology|April 24, 2025
The accuracy of polygenic score models for BMI and Type II diabetes in the Native Hawaiian populationYing-Chu Lo, He Tian, Tsz Fung Chan, et al.
Journal of Medicinal Chemistry|July 16, 2024
Development of Zalfermin, a Long-Acting Proteolytically Stabilized FGF21 AnalogKristian Sass-Ørum, Tina Møller Tagmose, Jørgen Olsen, et al.
Nature Genetics|August 26, 2024
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Exome sequencing directly implicates 68 genes in inflammatory bowel diseaseRuifei Zhu, Qian Zhang, Kai Yuan, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerToni A Boltz, Benjamin B Chu, Calwing Liao, et al.
Pageof 4