Dr. Matthew G Sampson M.D.
Nephrologist (Pediatric) | Pediatric Nephrology
1500 E Medical Center Dr 1st Floor Taubman Ce Ann Arbor MI, 48109About
Dr. Matthew Sampson is a pediatric nephrologist practicing in Ann Arbor, MI. Dr. Sampson specializes in caring for children with chronic conditions such as hypertension, kidney disease, and chronic dialysis. Pediatric nephrologists have extensive knowledge on the dialysis and transplant processes, while simultaneously developing lasting relationships with the families of their young patients.
Education and Training
University of Virginia School of Medicine 2005
Board Certification
PediatricsAmerican Board of PediatricsABP- Pediatric Nephrology
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome.
- Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with
- GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.
- Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.
- 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.
- tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.
- Actualizing the Benefits of Genomic Discovery in Pediatric Nephrology.
- An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts.
- Genes, Exomes, Genomes, Copy Number: What is Their Future in Pediatric Renal Disease.
- Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
- Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
- The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase .
- The Democratization of Genomic Inquiry Empowers Our Understanding of Nephrotic Syndrome.
- A Familial Infantile Renal Failure.
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