| Congenital adrenal hyperplasia due to 21-hydroxylase deficiency PC White, PW Speiser Endocrine reviews 21 (3), 245-291, 2000 | 1860 | 2000 |
| Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline PW Speiser, R Azziz, LS Baskin, L Ghizzoni, TW Hensle, DP Merke, ... The Journal of Clinical Endocrinology & Metabolism 95 (9), 4133-4160, 2010 | 1447 | 2010 |
| Congenital adrenal hyperplasia PW Speiser, PC White New England Journal of Medicine 349 (8), 776-788, 2003 | 1236 | 2003 |
| Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practice guideline PW Speiser, W Arlt, RJ Auchus, LS Baskin, GS Conway, DP Merke, ... The Journal of Clinical Endocrinology & Metabolism 103 (11), 4043-4088, 2018 | 1094 | 2018 |
| Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase T Mune, FM Rogerson, H Nikkilä, AK Agarwal, PC White Nature genetics 10 (4), 394-399, 1995 | 773 | 1995 |
| 11β-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess PC White, T Mune, AK Agarwal Endocrine reviews 18 (1), 135-156, 1997 | 748 | 1997 |
| Structure of human steroid 21-hydroxylase genes. PC White, MI New, BO Dupont Proceedings of the National Academy of Sciences 83 (14), 5111-5115, 1986 | 715 | 1986 |
| A modular analysis framework for blood genomics studies: application to systemic lupus erythematosus D Chaussabel, C Quinn, J Shen, P Patel, C Glaser, N Baldwin, ... Immunity 29 (1), 150-164, 2008 | 702 | 2008 |
| Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. PW Speiser, J Dupont, D Zhu, J Serrat, M Buegeleisen, MT Tusie-Luna, ... The Journal of clinical investigation 90 (2), 584-595, 1992 | 693 | 1992 |
| Congenital adrenal hyperplasia PC White, MI New, BO Dupont New England Journal of Medicine 316 (24), 1519-1524, 1987 | 677* | 1987 |
| Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. PC White, D Grossberger, BJ Onufer, DD Chaplin, MI New, B Dupont, ... Proceedings of the National Academy of Sciences 82 (4), 1089-1093, 1985 | 615 | 1985 |
| Characterization of two genes encoding human steroid 11β-hydroxylase (P-45011β) E Mornet, J Dupont, A Vitek, PC White Journal of Biological Chemistry 264 (35), 20961-20967, 1989 | 587 | 1989 |
| Cloning and expression of rat cDNA encoding corticosteroid 11β-dehydrogenase AK Agarwal, C Monder, B Eckstein, PC White Journal of Biological Chemistry 264 (32), 18939-18943, 1989 | 587 | 1989 |
| The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. GM Tannin, AK Agarwal, C Monder, MI New, PC White Journal of Biological Chemistry 266 (25), 16653-16658, 1991 | 568 | 1991 |
| Chemical characterization of a neural cell adhesion molecule purified from embryonic brain membranes. S Hoffman, BC Sorkin, PC White, R Brackenbury, R Mailhammer, ... Journal of Biological Chemistry 257 (13), 7720-7729, 1982 | 553 | 1982 |
| The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex KM Curnow, MT Tusie-Luna, L Pascoe, R Natarajan, JL Gu, JL Nadler, ... Molecular Endocrinology 5 (10), 1513-1522, 1991 | 457 | 1991 |
| Disorders of steroid 11β-hydroxylase isozymes PC White, KM Curnow, L Pascoe Endocrine reviews 15 (4), 421-438, 1994 | 446 | 1994 |
| Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function M Kupari, A Hautanen, L Lankinen, P Koskinen, J Virolainen, H Nikkila, ... Circulation 97 (6), 569-575, 1998 | 383 | 1998 |
| Mutations in the genes encoding 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency N Draper, EA Walker, IJ Bujalska, JW Tomlinson, SM Chalder, W Arlt, ... Nature genetics 34 (4), 434-439, 2003 | 373 | 2003 |
| Congenital adrenal hyperplasia—current insights in pathophysiology, diagnostics, and management HL Claahsen-van der Grinten, PW Speiser, SF Ahmed, W Arlt, RJ Auchus, ... Endocrine reviews 43 (1), 91-159, 2022 | 362 | 2022 |