Co-Authors
This is a "connection" page, showing publications co-authored by DARYL SCOTT and ZEYNEP COBAN-AKDEMIR.
Connection Strength
0.085
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Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension. JCI Insight. 2024 05 08; 9(9).
Score: 0.054
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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: 0.032