Sevcan A. Bakkaloğlu

Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

Martin Konrad, André Schaller, Dominik Seelow et al. · The American Journal of Human Genetics · 2006 · 522 citations · Full text

Medicine, Genetics, Molecular Genetics +15

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Saskia F. Heeringa, Gil Chernin, Moumita Chaki et al. · Journal of Clinical Investigation · 2011 · 400 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Jillian K. Warejko, Weizhen Tan, Ankana Daga et al. · Clinical Journal of the American Society of Nephrology · 2017 · 235 citations · Full text

Life Sciences, Genetics, Nephrology +15

The bone and mineral disorder of children undergoing chronic peritoneal dialysis

Dagmara Borzych, Lesley Rees, Il Soo Ha et al. · Kidney International · 2010 · 130 citations · Full text

Medicine, Nephrology, Pediatrics +14

Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

Heon Yung Gee, Shazia Ashraf, Xiaoyang Wan et al. · The American Journal of Human Genetics · 2014 · 128 citations · Full text

Medicine, Genetics, Nephrology +12