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Matthew G Sampson

Showing results (21-30 of 94) with videos related to

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Pediatric Nephrology (Berlin, Germany)|February 28, 2025
Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspectiveAsheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Human Genomics|February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics SymposiumKushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Kidney International Reports|December 23, 2017
A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 PathwayJoseph Wang, Beth Vogt, Sidharth Kumar Sethi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 12, 2022
Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive modelSeong Kyu Han, Yoshiharu Muto, Parker C Wilson, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
Glomerular Diseases|March 18, 2024
<i>APOL1</i> Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K VariantRasheed Gbadegesin, Elena Martinelli, Yask Gupta, et al.
Plos One|June 25, 2015
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic RicketsSara L Ma, Virginia Vega-Warner, Christopher Gillies, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 18, 2016
An investigation of APOL1 risk genotypes and preterm birth in African American population cohortsCatherine C Robertson, Christopher E Gillies, Rosemary K B Putler, et al.
Pediatric Nephrology (Berlin, Germany)|March 29, 2017
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
Pediatric Nephrology (Berlin, Germany)|February 28, 2025
Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspectiveAsheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Human Genomics|February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics SymposiumKushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Kidney International Reports|December 23, 2017
A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 PathwayJoseph Wang, Beth Vogt, Sidharth Kumar Sethi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 12, 2022
Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive modelSeong Kyu Han, Yoshiharu Muto, Parker C Wilson, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
Glomerular Diseases|March 18, 2024
<i>APOL1</i> Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K VariantRasheed Gbadegesin, Elena Martinelli, Yask Gupta, et al.
Plos One|June 25, 2015
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic RicketsSara L Ma, Virginia Vega-Warner, Christopher Gillies, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 18, 2016
An investigation of APOL1 risk genotypes and preterm birth in African American population cohortsCatherine C Robertson, Christopher E Gillies, Rosemary K B Putler, et al.
Pediatric Nephrology (Berlin, Germany)|March 29, 2017
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
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