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Simone Sanna

Showing results (121-130 of 149) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic SyndromeTiffany Tu, Alejandro Ochoa, Amika Sood, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Plos Genetics|June 28, 2012
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysisKrzysztof Kiryluk, Yifu Li, Simone Sanna-Cherchi, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
The New England Journal of Medicine|July 19, 2013
Mutations in DSTYK and dominant urinary tract malformationsSimone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, et al.
The New England Journal of Medicine|December 27, 2018
Diagnostic Utility of Exome Sequencing for Kidney DiseaseEmily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, et al.
American Journal of Human Genetics|November 4, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.
American Journal of Human Genetics|December 9, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.
American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.
Pageof 15

Showing results (121-130 of 149) with videos related to

Sort By:
Pageof 15
Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic SyndromeTiffany Tu, Alejandro Ochoa, Amika Sood, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Plos Genetics|June 28, 2012
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysisKrzysztof Kiryluk, Yifu Li, Simone Sanna-Cherchi, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
The New England Journal of Medicine|July 19, 2013
Mutations in DSTYK and dominant urinary tract malformationsSimone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, et al.
The New England Journal of Medicine|December 27, 2018
Diagnostic Utility of Exome Sequencing for Kidney DiseaseEmily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, et al.
American Journal of Human Genetics|November 4, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.
American Journal of Human Genetics|December 9, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.
American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.
Pageof 15