Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities LM Boyden, M Choi, KA Choate, CJ Nelson-Williams, A Farhi, HR Toka, ... Nature 482 (7383), 98-102, 2012 | 654 | 2012 |
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA FH Wilson, A Hariri, A Farhi, H Zhao, KF Petersen, HR Toka, ... Science 306 (5699), 1190-1194, 2004 | 429 | 2004 |
Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule MD Lalioti, J Zhang, HM Volkman, KT Kahle, KE Hoffmann, HR Toka, ... Nature genetics 38 (10), 1124-1132, 2006 | 377 | 2006 |
PDE3A mutations cause autosomal dominant hypertension with brachydactyly PG Maass, A Aydin, FC Luft, C Schächterle, A Weise, S Stricker, ... Nature genetics 47 (6), 647-653, 2015 | 185 | 2015 |
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12 H Schuster, TF Wienker, S Bähring, N Bilginturan, HR Toka, H Neitzel, ... Nature genetics 13 (1), 98-100, 1996 | 172 | 1996 |
Congenital anomalies of kidney and urinary tract HR Toka, O Toka, A Hariri, HT Nguyen Seminars in nephrology 30 (4), 374-386, 2010 | 169 | 2010 |
Deficiency of the calcium-sensing receptor in the kidney causes parathyroid hormone–independent hypocalciuria HR Toka, K Al-Romaih, JM Koshy, S DiBartolo III, CH Kos, SJ Quinn, ... Journal of the American Society of Nephrology 23 (11), 1879-1890, 2012 | 150 | 2012 |
Mutations in PAX2 associate with adult-onset FSGS M Barua, E Stellacci, L Stella, A Weins, G Genovese, V Muto, V Caputo, ... Journal of the American Society of Nephrology 25 (9), 1942-1953, 2014 | 142 | 2014 |
Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly R Naraghi, H Schuster, HR Toka, S Bähring, O Toka, O Öztekin, ... Stroke 28 (9), 1749-1754, 1997 | 95 | 1997 |
Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension H Schuster, TF Wienker, HR Toka, S Bähring, E Jeschke, O Toka, ... Hypertension 28 (6), 1085-1092, 1996 | 90 | 1996 |
WNK kinases: molecular regulators of integrated epithelial ion transport KT Kahle, FH Wilson, M Lalioti, H Toka, H Qin, RP Lifton Current opinion in nephrology and hypertension 13 (5), 557-562, 2004 | 82 | 2004 |
Severely impaired baroreflex-buffering in patients with monogenic hypertension and neurovascular contact J Jordan, HR Toka, K Heusser, O Toka, JR Shannon, J Tank, A Diedrich, ... Circulation 102 (21), 2611-2618, 2000 | 75 | 2000 |
Parathyroid hormone controls paracellular Ca2+ transport in the thick ascending limb by regulating the tight-junction protein Claudin14 T Sato, M Courbebaisse, N Ide, Y Fan, J Hanai, J Kaludjerovic, ... Proceedings of the National Academy of Sciences 114 (16), E3344-E3353, 2017 | 69 | 2017 |
Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasia Y Fan, W Liu, R Bi, MJ Densmore, T Sato, M Mannstadt, Q Yuan, X Zhou, ... Proceedings of the National Academy of Sciences 115 (16), E3749-E3758, 2018 | 67 | 2018 |
Comparative expression of the extracellular calcium-sensing receptor in the mouse, rat, and human kidney JAZ Graca, M Schepelmann, SC Brennan, J Reens, W Chang, P Yan, ... American Journal of Physiology-Renal Physiology 310 (6), F518-F533, 2016 | 67 | 2016 |
Mitochondrial DNA mutations in renal disease: an overview LP Govers, HR Toka, A Hariri, SB Walsh, D Bockenhauer Pediatric Nephrology 36 (1), 9-17, 2021 | 58 | 2021 |
Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12 S Bähring, A Rauch, O Toka, C Schroeder, C Hesse, H Siedler, ... Hypertension 43 (2), 471-476, 2004 | 53 | 2004 |
Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension HR Toka, S Bahring, D Chitayat, JC Melby, R Whitehead, E Jeschke, ... Annals of internal medicine 129 (3), 204-208, 1998 | 47 | 1998 |
Calcium sensing in the renal tubule HR Toka, MR Pollak, P Houillier Physiology 30 (4), 317-326, 2015 | 43 | 2015 |
Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family. S Bähring, T Nagai, HR Toka, I Nitz, O Toka, A Aydin, A Mühl, TF Wienker, ... American journal of human genetics 60 (3), 732, 1997 | 43 | 1997 |