Matthew Gordon Sampson

24PUBLICATIONS
166CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthNeurogeneticsMedical genetics (excl. cancer genetics)Epigenetics (incl. genome methylation and epigenomics)
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Publications (24)

|May 21, 2026
Gene-disease relationships for glomerular phenotypes: expert recommendations from ClinGen.

|Jan 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract.

Lisanne M Vendrig, Juntao Ke, Michael W T Tanck

|Dec 22, 2025
The landscape of allele-specific expression in human kidneys.

Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas

|Nov 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.

Florian Buerger, Daanya Salmanullah, Lorrin Liang

|Oct 24, 2024
A guide to gene-disease relationships in nephrology.

Zornitza Stark, Alicia B Byrne, Matthew G Sampson

|Apr 02, 2024
Recessive variants in the intergenic <i>NOS1AP-C1orf226</i> locus cause monogenic kidney disease responsive to anti-proteinuric treatment.

Florian Buerger, Daanya Salmanullah, Lorrin Liang

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Frequent Collaborators

5 joint publications

Friedhelm Hildebrandt

5 joint publications

Simone Sanna-Cherchi

4 joint publications

Ali Gharavi

4 joint publications

Miguel Verbitsky