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List of works by Matthew G Sampson

A Familial Infantile Renal Failure

scientific article published in September 2016

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

scientific article published on 20 February 2017

A reference panel of 64,976 haplotypes for genotype imputation

scientific article

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

scientific article published on 22 February 2016

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

scientific article published on March 2016

APOL1 genotype-associated morphologic changes among patients with focal segmental glomerulosclerosis

scientific article published on 01 March 2021

APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts

scientific article published on 27 April 2016

Actualizing the Benefits of Genomic Discovery in Pediatric Nephrology

scientific article published on 13 August 2015

An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts

scientific article published in December 2017

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 01 April 2019

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

scientific article published on 01 September 2019

Childhood Onset Nephrotic Syndrome

Complete Remission in the Nephrotic Syndrome Study Network

scientific article

Copy-number disorders are a common cause of congenital kidney malformations

scientific article

Defining nephrotic syndrome from an integrative genomics perspective

scientific article

Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach

scientific article published on 16 January 2013

Diagnoses of uncertain significance: kidney genetics in the 21st century

scientific article published on 07 April 2020

Disruption of the exocyst induces podocyte loss and dysfunction

scientific article published on 09 May 2019

Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

scientific article published on 20 October 2016

Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease.

scientific article published in October 2010

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

scientific article published in November 2017

Felic (CIP4b), a novel binding partner with the Src kinase Lyn and Cdc42, localizes to the phagocytic cup

scientific article (publication date: April 2003)

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

scientific article

GeneVetter: a web tool for quantitative monogenic assessment of rare diseases

scientific article published on 23 July 2015

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

scientific article

Glomerular and tubulointerstitial eQTLs for genomic discovery

scientific article published on 01 January 2019

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

scientific article published on 6 July 2015

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

scientific article published on 28 January 2020

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

scientific article (publication date: May 2015)

Quantify and control reproducibility in high-throughput experiments

scientific article published on 12 October 2020

Renal and Cardiovascular Morbidities Associated with APOL1 Status among African-American and Non-African-American Children with Focal Segmental Glomerulosclerosis.

scientific article

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

scientific article published on 23 April 2019

Src kinases in G-CSF receptor signaling

scientific article published on January 2007

The Democratization of Genomic Inquiry Empowers Our Understanding of Nephrotic Syndrome

The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.

scientific article published on 19 May 2017

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 21 December 2018

The human nephrin Y1139RSL motif is essential for podocyte foot process organization and slit diaphragm formation during glomerular development

scientific article published on 31 May 2019

Tissue transcriptome-driven identification of epidermal growth factor as a chronic kidney disease biomarker

scientific article published on December 2015

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

scientific article published on 14 June 2018

Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort

scientific article

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

scientific article published on 01 September 2019

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

scientific article published on 24 June 2015

tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

scientific article

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