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Chunyu Liu

Showing results (641-650 of 749) with videos related to

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Nature Communications|September 20, 2018
Author Correction: Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular diseaseChen Yao, George Chen, Ci Song, et al.
American Journal of Human Genetics|July 4, 2020
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male InfertilityChunyu Liu, Haruhiko Miyata, Yang Gao, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWASYu Chen, Sihan Liu, Zongyao Ren, et al.
Human Genetics|July 13, 2021
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouseQunshan Shen, Guillaume Martinez, Hongbin Liu, et al.
Journal of Medical Genetics|November 12, 2018
Novel homozygous <i>CFAP69</i> mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagellaXiaojin He, Weiyu Li, Huan Wu, et al.
Aging Cell|October 24, 2025
Association of Epigenetic Age Acceleration and Mitochondrial DNA-Based Aging Metrics Provides Insights Into Mechanisms of Aging-Related DiseasesMengyao Wang, Yinan Zheng, Meng Lai, et al.
Journal of Medical Genetics|September 11, 2019
Biallelic mutations in <i>CFAP65</i> cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and miceWeiyu Li, Huan Wu, Fuping Li, et al.
Epigenomics|November 28, 2017
Maternal alcohol consumption and offspring DNA methylation: findings from six general population-based birth cohortsGemma C Sharp, Ryan Arathimos, Sarah E Reese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Intronic (TTTGA)<sub>n</sub> insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsyZhidong Cen, You Chen, Dehao Yang, et al.
American Journal of Human Genetics|June 30, 2015
Improving Phenotypic Prediction by Combining Genetic and Epigenetic AssociationsSonia Shah, Marc J Bonder, Riccardo E Marioni, et al.
Pageof 75

Showing results (641-650 of 749) with videos related to

Sort By:
Pageof 75
Nature Communications|September 20, 2018
Author Correction: Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular diseaseChen Yao, George Chen, Ci Song, et al.
American Journal of Human Genetics|July 4, 2020
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male InfertilityChunyu Liu, Haruhiko Miyata, Yang Gao, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWASYu Chen, Sihan Liu, Zongyao Ren, et al.
Human Genetics|July 13, 2021
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouseQunshan Shen, Guillaume Martinez, Hongbin Liu, et al.
Journal of Medical Genetics|November 12, 2018
Novel homozygous <i>CFAP69</i> mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagellaXiaojin He, Weiyu Li, Huan Wu, et al.
Aging Cell|October 24, 2025
Association of Epigenetic Age Acceleration and Mitochondrial DNA-Based Aging Metrics Provides Insights Into Mechanisms of Aging-Related DiseasesMengyao Wang, Yinan Zheng, Meng Lai, et al.
Journal of Medical Genetics|September 11, 2019
Biallelic mutations in <i>CFAP65</i> cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and miceWeiyu Li, Huan Wu, Fuping Li, et al.
Epigenomics|November 28, 2017
Maternal alcohol consumption and offspring DNA methylation: findings from six general population-based birth cohortsGemma C Sharp, Ryan Arathimos, Sarah E Reese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Intronic (TTTGA)<sub>n</sub> insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsyZhidong Cen, You Chen, Dehao Yang, et al.
American Journal of Human Genetics|June 30, 2015
Improving Phenotypic Prediction by Combining Genetic and Epigenetic AssociationsSonia Shah, Marc J Bonder, Riccardo E Marioni, et al.
Pageof 75