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Discovery of Autoantibodies Targeting Nephrin in Minimal Change Disease Supports a Novel Autoimmune Etiology

Journal of the American Society of Nephrology, 2022-01, Vol.33 (1), p.238-252

2022

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Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome

Journal of the American Society of Nephrology, 2018-07, Vol.29 (7), p.2000-2013

2018

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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis

Nature communications, 2019-04, Vol.10 (1), p.1847-1847, Article 1847

2019

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Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

Nature communications, 2023-04, Vol.14 (1), p.2229-16, Article 2229

2023

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Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets

PloS one, 2015-06, Vol.10 (6), p.e0130729

2015

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Defining nephrotic syndrome from an integrative genomics perspective

Pediatric nephrology (Berlin, West), 2015-01, Vol.30 (1), p.51-63

2015

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Analyzing and reconciling colocalization and transcriptome-wide association studies from the perspective of inferential reproducibility

American journal of human genetics, 2022-05, Vol.109 (5), p.825-837

2022

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APOL1 Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K Variant

Glomerular diseases, 2024-02, Vol.4 (1), p.43-48

2024

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The Democratization of Genomic Inquiry Empowers Our Understanding of Nephrotic Syndrome

Transplantation, 2017-12, Vol.101 (12), p.2814-2815

Sampson, Matthew G.

2017

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Quantify and control reproducibility in high-throughput experiments

Nature methods, 2020-12, Vol.17 (12), p.1207-1213

2020

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Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era

Seminars in nephrology, 2015-05, Vol.35 (3), p.212-221

2015

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Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) Investigators

Glomerular diseases, 2023-08, Vol.3 (1), p.178-188

2023

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Glomerular and tubulointerstitial eQTLs for genomic discovery

Nature reviews. Nephrology, 2019-01, Vol.15 (1), p.3-4

Sampson, Matthew G

2019

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Genetics of Nephrotic Syndrome Presenting in Childhood: Core Curriculum 2019

American journal of kidney diseases, 2019-10, Vol.74 (4), p.549-557

2019

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Using and producing publicly available genomic data to accelerate discovery in nephrology

Nature reviews. Nephrology, 2019-09, Vol.15 (9), p.523-524

2019

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Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome

PloS one, 2013-11, Vol.8 (11), p.e81062-e81062

2013

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APOL1 at 10 years: progress and next steps

Kidney international, 2021-06, Vol.99 (6), p.1296-1302

2021

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A guide to gene–disease relationships in nephrology

Nature reviews. Nephrology, 2024-10

2024

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Author Correction: Using and producing publicly available genomic data to accelerate discovery in nephrology

Nature reviews. Nephrology, 2019-09, Vol.15 (9), p.590-590

2019

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Meeting report of the 2017 KidGen Renal Genetics Symposium

Human genomics, 2018-01, Vol.12 (1), p.5-5, Article 5

2018

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Introduction to Genomics of Kidney Disease: Implications, Discovery, and Translation

Clinical journal of the American Society of Nephrology, 2020-02, Vol.15 (2), p.267-267

2020

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A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

The Journal of clinical investigation, 2016-04, Vol.126 (4), p.1603-1603

2016

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Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive model

Proceedings of the National Academy of Sciences - PNAS, 2022-12, Vol.119 (51), p.e2212810119

2022

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Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects

Journal of the American Society of Nephrology, 2016-03, Vol.27 (3), p.814-823

2016

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UBD modifies APOL1-induced kidney disease risk

Proceedings of the National Academy of Sciences - PNAS, 2018-03, Vol.115 (13), p.3446-3451

2018

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Discovery of Autoantibodies Targeting Nephrin in Minimal Change Disease Supports a Novel Autoimmune Etiology

Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome

Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets

Defining nephrotic syndrome from an integrative genomics perspective

Analyzing and reconciling colocalization and transcriptome-wide association studies from the perspective of inferential reproducibility

APOL1 Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K Variant

The Democratization of Genomic Inquiry Empowers Our Understanding of Nephrotic Syndrome

Quantify and control reproducibility in high-throughput experiments

Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era

Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) Investigators

Glomerular and tubulointerstitial eQTLs for genomic discovery

Genetics of Nephrotic Syndrome Presenting in Childhood: Core Curriculum 2019

Using and producing publicly available genomic data to accelerate discovery in nephrology

Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome

APOL1 at 10 years: progress and next steps

A guide to gene–disease relationships in nephrology

Author Correction: Using and producing publicly available genomic data to accelerate discovery in nephrology

Meeting report of the 2017 KidGen Renal Genetics Symposium

Introduction to Genomics of Kidney Disease: Implications, Discovery, and Translation

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive model

Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects

UBD modifies APOL1-induced kidney disease risk

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