| Congenital adrenal hyperplasia due to 21-hydroxylase deficiency PC White, PW Speiser Endocrine reviews 21 (3), 245-291, 2000 | 1813 | 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 | 1415 | 2010 |
| Congenital adrenal hyperplasia PW Speiser, PC White New England Journal of Medicine 349 (8), 776-788, 2003 | 1261 | 2003 |
| Childhood obesity PW Speiser, MCJ Rudolf, H Anhalt, C Camacho-Hubner, F Chiarelli, ... The journal of clinical endocrinology & metabolism 90 (3), 1871-1887, 2005 | 1129 | 2005 |
| 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 | 990 | 2018 |
| High frequency of nonclassical steroid 21-hydroxylase deficiency PW Speiser, BO Dupont, P Rubinstein, A Piazza, A Kastelan, MI NEW Obstetrical & Gynecological Survey 41 (4), 244-245, 1986 | 752 | 1986 |
| Prevention and treatment of pediatric obesity: an endocrine society clinical practice guideline based on expert opinion GP August, S Caprio, I Fennoy, M Freemark, FR Kaufman, RH Lustig, ... The Journal of Clinical Endocrinology & Metabolism 93 (12), 4576-4599, 2008 | 714 | 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 | 682 | 1992 |
| Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2. L Pascoe, KM Curnow, L Slutsker, JM Connell, PW Speiser, MI New, ... Proceedings of the National Academy of Sciences 89 (17), 8327-8331, 1992 | 307 | 1992 |
| Update of guidelines for the use of growth hormone in children: the Lawson Wilkins Pediatric Endocrinology Society Drug and Therapeutics Committee TA Wilson, SR Rose, P Cohen, AD Rogol, P Backeljauw, R Brown, ... The Journal of pediatrics 143 (4), 415-421, 2003 | 299 | 2003 |
| Mutations in Prokineticin 2 and Prokineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum LW Cole, Y Sidis, CK Zhang, R Quinton, L Plummer, D Pignatelli, ... The Journal of Clinical Endocrinology & Metabolism 93 (9), 3551-3559, 2008 | 282 | 2008 |
| 21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study C Moran, R Azziz, E Carmina, D Dewailly, F Fruzzetti, L Ibañez, ... American journal of obstetrics and gynecology 183 (6), 1468-1474, 2000 | 281 | 2000 |
| 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 | 260 | 2022 |
| Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8. KM Curnow, L Slutsker, J Vitek, T Cole, PW Speiser, MI New, PC White, ... Proceedings of the National Academy of Sciences 90 (10), 4552-4556, 1993 | 250 | 1993 |
| Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia C Moran, R Azziz, N Weintrob, SF Witchel, V Rohmer, D Dewailly, ... The Journal of Clinical Endocrinology & Metabolism 91 (9), 3451-3456, 2006 | 238 | 2006 |
| Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14, DR1 PW Speiser, MI New, PC White New England Journal of Medicine 319 (1), 19-23, 1988 | 238 | 1988 |
| A Mutation (Pro-30 to Leu) in CYP21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele MT Tusie-Luna, PW Speiser, M Dumic, MI New, PC White Molecular endocrinology 5 (5), 685-692, 1991 | 216 | 1991 |
| Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype GA Bellus, EB Spector, PW Speiser, CA Weaver, AT Garber, CR Bryke, ... The American Journal of Human Genetics 67 (6), 1411-1421, 2000 | 208 | 2000 |
| The adrenal hyperplasia. MI New The Metabolic Basis of Inherited Disease., 1881-1918, 1989 | 193 | 1989 |
| Hormones and handedness: Left‐hand bias in female congenital adrenal hyperplasia patients R Nass, S Baker, P Speiser, R Virdis, A Balsamo, E Cacciari, A Loche, ... Neurology 37 (4), 711-711, 1987 | 182 | 1987 |
