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Jun Z Li

Showing results (91-100 of 107) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|September 17, 2020
A Novel Recurrent <i>COL5A1</i> Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular DysplasiaJulie Richer, Hannah L Hill, Yu Wang, et al.
Human Genetics|September 5, 2013
Genome-wide association study and meta-analysis of intraocular pressureA Bilge Ozel, Sayoko E Moroi, David M Reed, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 7, 2009
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryLaura J Scott, Pierandrea Muglia, Xiangyang Q Kong, et al.
Plos Genetics|May 4, 2019
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in miceSarah J Garnai, Michelle L Brinkmeier, Ben Emery, et al.
American Journal of Human Genetics|July 16, 2021
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiencyPeter Gergics, Cathy Smith, Hironori Bando, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Cell Genomics|March 27, 2024
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Nature Communications|April 21, 2022
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Arteriosclerosis, Thrombosis, and Vascular Biology|September 17, 2020
A Novel Recurrent <i>COL5A1</i> Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular DysplasiaJulie Richer, Hannah L Hill, Yu Wang, et al.
Human Genetics|September 5, 2013
Genome-wide association study and meta-analysis of intraocular pressureA Bilge Ozel, Sayoko E Moroi, David M Reed, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 7, 2009
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryLaura J Scott, Pierandrea Muglia, Xiangyang Q Kong, et al.
Plos Genetics|May 4, 2019
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in miceSarah J Garnai, Michelle L Brinkmeier, Ben Emery, et al.
American Journal of Human Genetics|July 16, 2021
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiencyPeter Gergics, Cathy Smith, Hironori Bando, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Cell Genomics|March 27, 2024
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Nature Communications|April 21, 2022
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
Pageof 11