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Joseph Glessner

Showing results (61-70 of 95) with videos related to

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Schizophrenia Research|February 7, 2016
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activityAry Gadelha, Jonathan Coleman, Gerome Breen, et al.
BMC Genomics|January 11, 2024
Genome-wide association study between copy number variation and feeding behavior, feed efficiency, and growth traits in Nellore cattleLorena F Benfica, Luiz F Brito, Ricardo D do Bem, et al.
Human Genomics|November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.
Journal of Pediatric Urology|May 8, 2025
Genetic analysis of two bladder exstrophy populations of South Asian and North American originJohn K Weaver, Dana A Weiss, Austin Thompson, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, et al.
Gastroenterology|July 22, 2008
Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejectionRakesh Sindhi, Brandon W Higgs, Daniel E Weeks, et al.
Circulation. Cardiovascular Genetics|February 4, 2010
Common variants in HSPB7 and FRMD4B associated with advanced heart failureThomas P Cappola, Mingyao Li, Jing He, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
Human Mutation|December 6, 2008
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variationBinita M Kamath, Brian D Thiel, Xiaowu Gai, et al.
Nature Communications|March 16, 2026
Multitrait GWAS and functional validation reveal genetic loci for gastric cancerHuanxin Ding, Chuxuan Liu, Qing Sun, et al.
Pageof 10

Showing results (61-70 of 95) with videos related to

Sort By:
Pageof 10
Schizophrenia Research|February 7, 2016
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activityAry Gadelha, Jonathan Coleman, Gerome Breen, et al.
BMC Genomics|January 11, 2024
Genome-wide association study between copy number variation and feeding behavior, feed efficiency, and growth traits in Nellore cattleLorena F Benfica, Luiz F Brito, Ricardo D do Bem, et al.
Human Genomics|November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.
Journal of Pediatric Urology|May 8, 2025
Genetic analysis of two bladder exstrophy populations of South Asian and North American originJohn K Weaver, Dana A Weiss, Austin Thompson, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, et al.
Gastroenterology|July 22, 2008
Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejectionRakesh Sindhi, Brandon W Higgs, Daniel E Weeks, et al.
Circulation. Cardiovascular Genetics|February 4, 2010
Common variants in HSPB7 and FRMD4B associated with advanced heart failureThomas P Cappola, Mingyao Li, Jing He, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
Human Mutation|December 6, 2008
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variationBinita M Kamath, Brian D Thiel, Xiaowu Gai, et al.
Nature Communications|March 16, 2026
Multitrait GWAS and functional validation reveal genetic loci for gastric cancerHuanxin Ding, Chuxuan Liu, Qing Sun, et al.
Pageof 10