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Chunyu Liu

Showing results (611-620 of 749) with videos related to

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Biorxiv : the Preprint Server for Biology|October 24, 2023
The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia riskQiuman Liang, Yi Jiang, Annie W Shieh, et al.
Journal of Medical Genetics|August 5, 2021
Homozygous mutations in <i>CCDC34</i> cause male infertility with oligoasthenoteratozoospermia in humans and miceJiangshan Cong, Xiong Wang, Amir Amiri-Yekta, et al.
Nature Communications|November 28, 2025
Impact of common variants on brain gene expression from RNA to protein to schizophrenia riskQiuman Liang, Yi Jiang, Annie W Shieh, et al.
Nature Communications|November 4, 2017
Epigenome-wide association studies identify DNA methylation associated with kidney functionAudrey Y Chu, Adrienne Tin, Pascal Schlosser, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Integrating Whole Genome and Transcriptome Sequencing to Characterize the Genetic Architecture of Isoform Variation and its Implications for Health and DiseaseChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
<i>CFAP47</i> is a novel causative gene implicated in X-linked polycystic kidney diseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
Ebiomedicine|May 1, 2022
Complex trait methylation scores in the prediction of major depressive disorderMiruna C Barbu, Carmen Amador, Alex S F Kwong, et al.
Scientific Reports|November 24, 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.
American Journal of Human Genetics|November 19, 2019
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and MiceChunyu Liu, Xiaojin He, Wangjie Liu, et al.
Pageof 75

Showing results (611-620 of 749) with videos related to

Sort By:
Pageof 75
Biorxiv : the Preprint Server for Biology|October 24, 2023
The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia riskQiuman Liang, Yi Jiang, Annie W Shieh, et al.
Journal of Medical Genetics|August 5, 2021
Homozygous mutations in <i>CCDC34</i> cause male infertility with oligoasthenoteratozoospermia in humans and miceJiangshan Cong, Xiong Wang, Amir Amiri-Yekta, et al.
Nature Communications|November 28, 2025
Impact of common variants on brain gene expression from RNA to protein to schizophrenia riskQiuman Liang, Yi Jiang, Annie W Shieh, et al.
Nature Communications|November 4, 2017
Epigenome-wide association studies identify DNA methylation associated with kidney functionAudrey Y Chu, Adrienne Tin, Pascal Schlosser, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Integrating Whole Genome and Transcriptome Sequencing to Characterize the Genetic Architecture of Isoform Variation and its Implications for Health and DiseaseChunyu Liu, Roby Joehanes, Jiantao Ma, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
<i>CFAP47</i> is a novel causative gene implicated in X-linked polycystic kidney diseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
Ebiomedicine|May 1, 2022
Complex trait methylation scores in the prediction of major depressive disorderMiruna C Barbu, Carmen Amador, Alex S F Kwong, et al.
Scientific Reports|November 24, 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.
American Journal of Human Genetics|November 19, 2019
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and MiceChunyu Liu, Xiaojin He, Wangjie Liu, et al.
Pageof 75