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Showing results (491-500 of 573) with videos related to

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JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Kidney International|June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndromeSimone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Journal of the American Society of Nephrology : JASN|October 15, 2011
APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathyNatalia Papeta, Krzysztof Kiryluk, Ami Patel, et al.
Plos Genetics|February 11, 2017
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathwayKrzysztof Kiryluk, Yifu Li, Zina Moldoveanu, et al.
Journal of Neurology|October 27, 2023
Genetic testing in adults with neurologic disorders: indications, approach, and clinical impactsLaynie Dratch, Meron Azage, Aaron Baldwin, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Kidney International Reports|June 11, 2020
Persistent Disease Activity in Patients With Long-Standing Glomerular DiseaseElisa Delbarba, Maddalena Marasa, Pietro A Canetta, et al.
Contemporary Clinical Trials Communications|April 14, 2021
Improving data quality in observational research studies: Report of the Cure Glomerulonephropathy (CureGN) networkBrenda W Gillespie, Louis-Philippe Laurin, Dawn Zinsser, et al.
JAMA Network Open|August 4, 2021
Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx AncestryCong Liu, Nur Zeinomar, Wendy K Chung, et al.
Kidney International Reports|August 7, 2023
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney DiseaseMaddalena Marasa, Dina F Ahram, Atteeq U Rehman, et al.
Pageof 58

Showing results (491-500 of 573) with videos related to

Sort By:
Pageof 58
JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Kidney International|June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndromeSimone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Journal of the American Society of Nephrology : JASN|October 15, 2011
APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathyNatalia Papeta, Krzysztof Kiryluk, Ami Patel, et al.
Plos Genetics|February 11, 2017
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathwayKrzysztof Kiryluk, Yifu Li, Zina Moldoveanu, et al.
Journal of Neurology|October 27, 2023
Genetic testing in adults with neurologic disorders: indications, approach, and clinical impactsLaynie Dratch, Meron Azage, Aaron Baldwin, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Kidney International Reports|June 11, 2020
Persistent Disease Activity in Patients With Long-Standing Glomerular DiseaseElisa Delbarba, Maddalena Marasa, Pietro A Canetta, et al.
Contemporary Clinical Trials Communications|April 14, 2021
Improving data quality in observational research studies: Report of the Cure Glomerulonephropathy (CureGN) networkBrenda W Gillespie, Louis-Philippe Laurin, Dawn Zinsser, et al.
JAMA Network Open|August 4, 2021
Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx AncestryCong Liu, Nur Zeinomar, Wendy K Chung, et al.
Kidney International Reports|August 7, 2023
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney DiseaseMaddalena Marasa, Dina F Ahram, Atteeq U Rehman, et al.
Pageof 58