| Genetic diagnosis by whole exome capture and massively parallel DNA sequencing M Choi, UI Scholl, W Ji, T Liu, IR Tikhonova, P Zumbo, A Nayir, ... Proceedings of the National Academy of Sciences 106 (45), 19096-19101, 2009 | 1820 | 2009 |
| K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension M Choi, UI Scholl, P Yue, P Björklund, B Zhao, C Nelson-Williams, W Ji, ... Science 331 (6018), 768-772, 2011 | 1080 | 2011 |
| Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism UI Scholl, G Goh, G Stölting, RC de Oliveira, M Choi, JD Overton, ... Nature genetics 45 (9), 1050-1054, 2013 | 610 | 2013 |
| Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10 UI Scholl, M Choi, T Liu, VT Ramaekers, MG Häusler, J Grimmer, ... Proceedings of the National Academy of Sciences 106 (14), 5842-5847, 2009 | 482 | 2009 |
| Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism UI Scholl, G Stölting, C Nelson-Williams, AA Vichot, M Choi, E Loring, ... eLife 4, e06315, 2015 | 323 | 2015 |
| Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5 UI Scholl, C Nelson-Williams, P Yue, R Grekin, RJ Wyatt, MJ Dillon, ... Proceedings of the National Academy of Sciences 109 (7), 2533-2538, 2012 | 277 | 2012 |
| Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors G Goh, UI Scholl, JM Healy, M Choi, ML Prasad, C Nelson-Williams, ... Nature genetics 46 (6), 613-617, 2014 | 232 | 2014 |
| CLCN2 chloride channel mutations in familial hyperaldosteronism type II UI Scholl, G Stölting, J Schewe, A Thiel, H Tan, C Nelson-Williams, ... Nature genetics 50 (3), 349-354, 2018 | 227 | 2018 |
| Kidney physiology and susceptibility to acute kidney injury: implications for renoprotection H Scholz, FJ Boivin, KM Schmidt-Ott, S Bachmann, KU Eckardt, UI Scholl, ... Nature Reviews Nephrology 17 (5), 335-349, 2021 | 180 | 2021 |
| Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinoma CC Juhlin, G Goh, JM Healy, AL Fonseca, UI Scholl, A Stenman, ... The Journal of Clinical Endocrinology & Metabolism 100 (3), E493-E502, 2015 | 160 | 2015 |
| KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1) C Zhang, L Wang, J Zhang, XT Su, DH Lin, UI Scholl, G Giebisch, ... Proceedings of the National Academy of Sciences 111 (32), 11864-11869, 2014 | 150 | 2014 |
| Diagnosis and treatment of primary aldosteronism M Reincke, I Bancos, P Mulatero, UI Scholl, M Stowasser, TA Williams The Lancet Diabetes & Endocrinology 9 (12), 876-892, 2021 | 141 | 2021 |
| Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype UI Scholl, JM Healy, A Thiel, AL Fonseca, TC Brown, JW Kunstman, ... Clinical Endocrinology 83 (6), 779-789, 2015 | 130 | 2015 |
| Barttin modulates trafficking and function of ClC-K channels U Scholl, S Hebeisen, AGH Janssen, G Müller-Newen, A Alekov, ... Proceedings of the National Academy of Sciences 103 (30), 11411-11416, 2006 | 124 | 2006 |
| Comprehensive DNA methylation analysis of benign and malignant adrenocortical tumors AL Fonseca, J Kugelberg, LF Starker, U Scholl, M Choi, P Hellman, ... Genes, Chromosomes and Cancer 51 (10), 949-960, 2012 | 116 | 2012 |
| Disease-causing dysfunctions of barttin in Bartter syndrome type IV AGH Janssen, U Scholl, C Domeyer, D Nothmann, A Leinenweber, ... Journal of the American Society of Nephrology 20 (1), 145-153, 2009 | 101 | 2009 |
| Predicting functional effects of missense variants in voltage-gated sodium and calcium channels HO Heyne, D Baez-Nieto, S Iqbal, DS Palmer, A Brunklaus, P May, ... Science translational medicine 12 (556), eaay6848, 2020 | 98 | 2020 |
| Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome S Riazuddin, S Anwar, M Fischer, ZM Ahmed, SY Khan, AGH Janssen, ... The American Journal of Human Genetics 85 (2), 273-280, 2009 | 90 | 2009 |
| PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases A Thiel, AC Reis, M Haase, G Goh, M Schott, HS Willenberg, UI Scholl Eur J Endocrinol 172 (6), 677-685, 2015 | 75 | 2015 |
| Macrolides selectively inhibit mutant KCNJ5 potassium channels that cause aldosterone-producing adenoma UI Scholl, L Abriola, C Zhang, EN Reimer, M Plummer, BI Kazmierczak, ... The Journal of Clinical Investigation 127 (7), 2017 | 65 | 2017 |
Murim ChoiSeoul National UniversityVerified email at snu.ac.kr
