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Journal of Medical Genetics
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May 4, 2019
Homozygous mutations in <i>SPEF2</i> induce multiple morphological abnormalities of the sperm flagella and male infertility
Chunyu 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 disease
Tianxiao 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 Diseases
Chunyu 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 associations
Cuihua 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 Associations
Cuihua 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 flagella
Yang 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 Diseases
Chunyu 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 ancestry
Chunyu 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 Study
Chathurangi 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 disease
Su-Jeong Kim, Brendan Miller, Nicolas G Hartel, et al.
Page
of 75
Search research articles
Search
Showing results (601-610 of 749) with videos related to
Sort By:
Page
of 75
Journal of Medical Genetics
|
May 4, 2019
Homozygous mutations in <i>SPEF2</i> induce multiple morphological abnormalities of the sperm flagella and male infertility
Chunyu 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 disease
Tianxiao 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 Diseases
Chunyu 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 associations
Cuihua 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 Associations
Cuihua 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 flagella
Yang 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 Diseases
Chunyu 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 ancestry
Chunyu 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 Study
Chathurangi 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 disease
Su-Jeong Kim, Brendan Miller, Nicolas G Hartel, et al.
Page
of 75