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Chunyu Liu

Showing results (601-610 of 749) with videos related to

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Journal of Medical Genetics|May 4, 2019
Homozygous mutations in <i>SPEF2</i> induce multiple morphological abnormalities of the sperm flagella and male infertilityChunyu Liu, Mingrong Lv, Xiaojin He, et al.
Nature Communications|September 21, 2019
Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular diseaseTianxiao Huan, Roby Joehanes, Ci Song, et al.
Medrxiv : the Preprint Server for Health Sciences|May 13, 2022
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of DiseasesChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Molecular Psychiatry|December 21, 2024
Genetic analysis of psychosis Biotypes: shared Ancestry-adjusted polygenic risk and unique genomic associationsCuihua Xia, Ney Alliey-Rodriguez, Carol A Tamminga, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Genetic Analysis of Psychosis Biotypes: Shared Ancestry-Adjusted Polygenic Risk and Unique Genomic AssociationsCuihua Xia, Ney Alliey-Rodriguez, Carol A Tamminga, et al.
Reproductive Biomedicine Online|March 27, 2021
Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagellaYang Gao, Shixiong Tian, Yanwei Sha, et al.
Research Square|June 6, 2022
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of DiseasesChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Mitochondrion|July 24, 2021
Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestryChunyu Liu, Jessica L Fetterman, Yong Qian, et al.
Journal of Medical Internet Research|January 20, 2021
Adherence of Mobile App-Based Surveys and Comparison With Traditional Surveys: eCohort StudyChathurangi H Pathiravasan, Yuankai Zhang, Ludovic Trinquart, et al.
Molecular Psychiatry|January 3, 2024
A naturally occurring variant of SHLP2 is a protective factor in Parkinson's diseaseSu-Jeong Kim, Brendan Miller, Nicolas G Hartel, et al.
Pageof 75

Showing results (601-610 of 749) with videos related to

Sort By:
Pageof 75
Journal of Medical Genetics|May 4, 2019
Homozygous mutations in <i>SPEF2</i> induce multiple morphological abnormalities of the sperm flagella and male infertilityChunyu Liu, Mingrong Lv, Xiaojin He, et al.
Nature Communications|September 21, 2019
Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular diseaseTianxiao Huan, Roby Joehanes, Ci Song, et al.
Medrxiv : the Preprint Server for Health Sciences|May 13, 2022
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of DiseasesChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Molecular Psychiatry|December 21, 2024
Genetic analysis of psychosis Biotypes: shared Ancestry-adjusted polygenic risk and unique genomic associationsCuihua Xia, Ney Alliey-Rodriguez, Carol A Tamminga, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Genetic Analysis of Psychosis Biotypes: Shared Ancestry-Adjusted Polygenic Risk and Unique Genomic AssociationsCuihua Xia, Ney Alliey-Rodriguez, Carol A Tamminga, et al.
Reproductive Biomedicine Online|March 27, 2021
Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagellaYang Gao, Shixiong Tian, Yanwei Sha, et al.
Research Square|June 6, 2022
Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of DiseasesChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Mitochondrion|July 24, 2021
Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestryChunyu Liu, Jessica L Fetterman, Yong Qian, et al.
Journal of Medical Internet Research|January 20, 2021
Adherence of Mobile App-Based Surveys and Comparison With Traditional Surveys: eCohort StudyChathurangi H Pathiravasan, Yuankai Zhang, Ludovic Trinquart, et al.
Molecular Psychiatry|January 3, 2024
A naturally occurring variant of SHLP2 is a protective factor in Parkinson's diseaseSu-Jeong Kim, Brendan Miller, Nicolas G Hartel, et al.
Pageof 75