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Jonathan L Haines

Showing results (51-60 of 537) with videos related to

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AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 19, 2026
Leadership, Informatics Expertise, and Resources: Determinants of Institutional Data Sharing in the National Clinical Cohort Collaborative (N3C)Carly M Rose, William S Bush, Mark F Beno, et al.
Human Molecular Genetics|September 26, 2024
Identifying X-chromosome variants associated with age-related macular degenerationMichelle Grunin, Robert P Igo, Yeunjoo E Song, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Identifying X-Chromosome Variants Associated with Age-Related Macular DegenerationMichelle Grunin, Robert P Igo, Yeunjoo E Song, et al.
Investigative Ophthalmology & Visual Science|September 28, 2019
Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular DegenerationAndrea R Waksmunski, Michelle Grunin, Tyler G Kinzy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2008
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3Todd L Edwards, Margaret Pericak-Vance, Johnny R Gilbert, et al.
Medrxiv : the Preprint Server for Health Sciences|July 14, 2025
Institutional Characteristics Associated with Accessing and Sharing EHR Data with the National COVID Cohort Collaborative (N3C)Carly M Rose, William S Bush, Mark F Beno, et al.
Science (New York, N.Y.)|July 3, 2007
Problems with genome-wide association studiesScott M Williams, Jeffrey A Canter, Dana C Crawford, et al.
Experimental Eye Research|August 15, 2015
Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysisBao J Fan, Louis R Pasquale, Jae H Kang, et al.
BMC Medical Genomics|July 8, 2020
Statistical driver genes as a means to uncover missing heritability for age-related macular degenerationAndrea R Waksmunski, Michelle Grunin, Tyler G Kinzy, et al.
Neurogenetics|November 20, 2017
Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorderAnthony J Griswold, Derek Van Booven, Michael L Cuccaro, et al.
Pageof 54

Showing results (51-60 of 537) with videos related to

Sort By:
Pageof 54
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 19, 2026
Leadership, Informatics Expertise, and Resources: Determinants of Institutional Data Sharing in the National Clinical Cohort Collaborative (N3C)Carly M Rose, William S Bush, Mark F Beno, et al.
Human Molecular Genetics|September 26, 2024
Identifying X-chromosome variants associated with age-related macular degenerationMichelle Grunin, Robert P Igo, Yeunjoo E Song, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Identifying X-Chromosome Variants Associated with Age-Related Macular DegenerationMichelle Grunin, Robert P Igo, Yeunjoo E Song, et al.
Investigative Ophthalmology & Visual Science|September 28, 2019
Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular DegenerationAndrea R Waksmunski, Michelle Grunin, Tyler G Kinzy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2008
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3Todd L Edwards, Margaret Pericak-Vance, Johnny R Gilbert, et al.
Medrxiv : the Preprint Server for Health Sciences|July 14, 2025
Institutional Characteristics Associated with Accessing and Sharing EHR Data with the National COVID Cohort Collaborative (N3C)Carly M Rose, William S Bush, Mark F Beno, et al.
Science (New York, N.Y.)|July 3, 2007
Problems with genome-wide association studiesScott M Williams, Jeffrey A Canter, Dana C Crawford, et al.
Experimental Eye Research|August 15, 2015
Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysisBao J Fan, Louis R Pasquale, Jae H Kang, et al.
BMC Medical Genomics|July 8, 2020
Statistical driver genes as a means to uncover missing heritability for age-related macular degenerationAndrea R Waksmunski, Michelle Grunin, Tyler G Kinzy, et al.
Neurogenetics|November 20, 2017
Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorderAnthony J Griswold, Derek Van Booven, Michael L Cuccaro, et al.
Pageof 54