Below is a list of highlighted publications from the Sampson Lab.

For a list of all publications involving Matt Sampson, click here. 

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome: https://pubmed.ncbi.nlm.nih.gov/37120605/

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs: https://pubmed.ncbi.nlm.nih.gov/37076491/

A Glomerular Transcriptomic Landscape of Apolipoprotein L1 in Black Patients with Focal Segmental Glomerulosclerosis: https://pubmed.ncbi.nlm.nih.gov/34929253/

APOL1 Genotype-associated Morphologic Changes Among Patients with Focal Segmental Glomerulosclerosis: https://pubmed.ncbi.nlm.nih.gov/33646395/

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome: https://pubmed.ncbi.nlm.nih.gov/32554042/

Using and producing publicly available genomic data to accelerate discovery in nephrology: https://pubmed.ncbi.nlm.nih.gov/31182850/

An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome: https://pubmed.ncbi.nlm.nih.gov/30057032/

Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome: https://pubmed.ncbi.nlm.nih.gov/29903748/

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: https://pubmed.ncbi.nlm.nih.gov/27190333/

Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort: https://pubmed.ncbi.nlm.nih.gov/26534921/

Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects: https://pubmed.ncbi.nlm.nih.gov/26150607/