Post-doctoral Fellow: Genetic basis of immunosuppressant sensitive nephrotic syndrome:
The Sampson Lab studies the genomics of nephrotic syndrome, a rare and often debilitating form of kidney disease. We use a variety of technologies (e.g. SNP arrays, whole genome sequencing, RNA-seq and ATAC-seq of kidney tissues) and methods (e.g. GWAS, eQTL, rare variant association, epidemiologic modeling) to (1) discover genetic drivers of nephrotic syndrome, (2) provide insight on their biological mechanisms, and (3) describe their clinical impact. Current areas of focus include (1) immunosuppressive sensitive nephrotic syndrome, (2) APOL1-associate kidney disease, and (3) gene regulatory circuit mapping in kidney cells to illuminate mechanisms underlying nephrotic syndrome risk loci. Our group is extremely collaborative both through formal participation in consortia and through informal collaborations with medical professionals and experimental groups worldwide.
We are now interested in recruiting a post-doctoral fellow for a project related to immunosuppressant sensitive nephrotic syndrome (ISNS). Through GWAS, our group and others have begun to illuminate the genetic basis of ISNS. Bioinformatic and multiomic integrative analyses of the small but growing number of ISNS GWAS loci point to genes expressed in resident kidney cells and circulating immune cells. This fits our biological and clinical understanding of this disease. We now need to experimentally pursue these GWAS loci to implicate the causal SNPs, the gene(s) they impact, and the cell type(s) in which they exert their effect.
To drive this project, we seek an individual with a strong background in cell or molecular biology, or related fields. We prefer experience with molecular genetics and glomerular biology OR immunology.
Matt Sampson, MD MSCE
Associate Professor of Pediatrics, Harvard Medical School
Warren E. Grupe Chair in Nephrology, Boston Children’s Hospital
Associate Member, Broad Institute
Tagged as: Life Sciences
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