Co-Authors
This is a "connection" page, showing publications co-authored by SARAH SWARTZ and MIR REZA BEKHEIRNIA.
Connection Strength
0.197
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Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. Genet Med. 2017 04; 19(4):412-420.
Score: 0.142
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Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes. Front Med (Lausanne). 2023; 10:1089159.
Score: 0.056