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Matthew G Sampson

Showing results (11-20 of 94) with videos related to

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BMJ Case Reports|September 1, 2019
Unique association of multiple endocrine neoplasia 2A and congenital anomalies of the kidney and urinary tract in a child with a <i>RET</i> mutationOlivia R Wood, Tobias Else, Matthew G Sampson
Pediatric Nephrology (Berlin, Germany)|June 4, 2014
Defining nephrotic syndrome from an integrative genomics perspectiveMatthew G Sampson, Jeffrey B Hodgin, Matthias Kretzler
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 21, 2025
Gaining a Genomic Foothold on Unexplained Kidney FailureJanewit Wongboonsin, Michelle T McNulty, Matthew G Sampson
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 9, 2019
Genetics of Nephrotic Syndrome Presenting in Childhood: Core Curriculum 2019Andreia Watanabe, Luciana S Feltran, Matthew G Sampson
Kidney International|April 1, 2021
APOL1 at 10 years: progress and next stepsBarry I Freedman, Jeffrey B Kopp, Matthew G Sampson, et al.
Bioinformatics (Oxford, England)|July 26, 2015
GeneVetter: a web tool for quantitative monogenic assessment of rare diseasesChristopher E Gillies, Catherine C Robertson, Matthew G Sampson, et al.
American Journal of Human Genetics|May 6, 2022
Analyzing and reconciling colocalization and transcriptome-wide association studies from the perspective of inferential reproducibilityAbhay Hukku, Matthew G Sampson, Francesca Luca, et al.
Plos One|November 22, 2013
Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndromeMatthew G Sampson, Christopher E Gillies, Wenjun Ju, et al.
Nature Reviews. Nephrology|October 24, 2024
A guide to gene-disease relationships in nephrologyZornitza Stark, Alicia B Byrne, Matthew G Sampson, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2025
Next-generation nephrology: part 1-an aid for genetic and genomic testing in pediatric nephrologyAsheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Pageof 10

Showing results (11-20 of 94) with videos related to

Sort By:
Pageof 10
BMJ Case Reports|September 1, 2019
Unique association of multiple endocrine neoplasia 2A and congenital anomalies of the kidney and urinary tract in a child with a <i>RET</i> mutationOlivia R Wood, Tobias Else, Matthew G Sampson
Pediatric Nephrology (Berlin, Germany)|June 4, 2014
Defining nephrotic syndrome from an integrative genomics perspectiveMatthew G Sampson, Jeffrey B Hodgin, Matthias Kretzler
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 21, 2025
Gaining a Genomic Foothold on Unexplained Kidney FailureJanewit Wongboonsin, Michelle T McNulty, Matthew G Sampson
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 9, 2019
Genetics of Nephrotic Syndrome Presenting in Childhood: Core Curriculum 2019Andreia Watanabe, Luciana S Feltran, Matthew G Sampson
Kidney International|April 1, 2021
APOL1 at 10 years: progress and next stepsBarry I Freedman, Jeffrey B Kopp, Matthew G Sampson, et al.
Bioinformatics (Oxford, England)|July 26, 2015
GeneVetter: a web tool for quantitative monogenic assessment of rare diseasesChristopher E Gillies, Catherine C Robertson, Matthew G Sampson, et al.
American Journal of Human Genetics|May 6, 2022
Analyzing and reconciling colocalization and transcriptome-wide association studies from the perspective of inferential reproducibilityAbhay Hukku, Matthew G Sampson, Francesca Luca, et al.
Plos One|November 22, 2013
Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndromeMatthew G Sampson, Christopher E Gillies, Wenjun Ju, et al.
Nature Reviews. Nephrology|October 24, 2024
A guide to gene-disease relationships in nephrologyZornitza Stark, Alicia B Byrne, Matthew G Sampson, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2025
Next-generation nephrology: part 1-an aid for genetic and genomic testing in pediatric nephrologyAsheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Pageof 10