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Joseph T Glessner

Showing results (91-100 of 124) with videos related to

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Diabetes|January 17, 2008
A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association studyHakon Hakonarson, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genome Biology|March 7, 2017
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genomeRyan L Collins, Harrison Brand, Claire E Redin, et al.
Diabetes|October 9, 2008
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetesStruan F A Grant, Hui-Qi Qu, Jonathan P Bradfield, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Nature Genetics|September 2, 2008
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel diseaseSubra Kugathasan, Robert N Baldassano, Jonathan P Bradfield, et al.
Human Molecular Genetics|February 24, 2010
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsKai Wang, Robert Baldassano, Haitao Zhang, et al.
BMC Medical Genetics|March 24, 2016
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibilityTerri H Finkel, Jin Li, Zhi Wei, et al.
Journal of Hepatology|August 12, 2023
Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genesJoseph T Glessner, Mylarappa B Ningappa, Kim A Ngo, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.
Pageof 13

Showing results (91-100 of 124) with videos related to

Sort By:
Pageof 13
Diabetes|January 17, 2008
A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association studyHakon Hakonarson, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genome Biology|March 7, 2017
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genomeRyan L Collins, Harrison Brand, Claire E Redin, et al.
Diabetes|October 9, 2008
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetesStruan F A Grant, Hui-Qi Qu, Jonathan P Bradfield, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Nature Genetics|September 2, 2008
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel diseaseSubra Kugathasan, Robert N Baldassano, Jonathan P Bradfield, et al.
Human Molecular Genetics|February 24, 2010
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsKai Wang, Robert Baldassano, Haitao Zhang, et al.
BMC Medical Genetics|March 24, 2016
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibilityTerri H Finkel, Jin Li, Zhi Wei, et al.
Journal of Hepatology|August 12, 2023
Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genesJoseph T Glessner, Mylarappa B Ningappa, Kim A Ngo, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.
Pageof 13