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John Wei

Showing results (61-70 of 78) with videos related to

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JU Open Plus|February 19, 2026
Combining Serum Prostate Health Index With Urinary PCA3 and TMPRSS2:ERG RNA Testing Improves Detection of Clinically Significant Prostate CancerNicholas W Eyrich, Yijian Huang, Yingye Zheng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2014
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genesAbdul Noor, Anath C Lionel, Sarah Cohen-Woods, et al.
Plos One|October 3, 2024
Feasibility, reliability and validity of self-measurement of knee range-of-motion using an accelerometer-based smartphone application by patients with total knee arthroplastyEleanor Shuxian Chew, Ee-Lin Woon, Juanita Krysten Miao-Shi Low, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
A high-resolution copy-number variation resource for clinical and population geneticsMohammed Uddin, Bhooma Thiruvahindrapuram, Susan Walker, et al.
Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
JU Open Plus|February 19, 2026
Combining Serum Prostate Health Index With Urinary PCA3 and TMPRSS2:ERG RNA Testing Improves Detection of Clinically Significant Prostate CancerNicholas W Eyrich, Yijian Huang, Yingye Zheng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2014
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genesAbdul Noor, Anath C Lionel, Sarah Cohen-Woods, et al.
Plos One|October 3, 2024
Feasibility, reliability and validity of self-measurement of knee range-of-motion using an accelerometer-based smartphone application by patients with total knee arthroplastyEleanor Shuxian Chew, Ee-Lin Woon, Juanita Krysten Miao-Shi Low, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
A high-resolution copy-number variation resource for clinical and population geneticsMohammed Uddin, Bhooma Thiruvahindrapuram, Susan Walker, et al.
Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Pageof 8