| Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients W Arlt, DS Willis, SH Wild, N Krone, EJ Doherty, S Hahner, TS Han, ... The Journal of Clinical Endocrinology & Metabolism 95 (11), 5110-5121, 2010 | 487 | 2010 |
| Urine steroid metabolomics as a biomarker tool for detecting malignancy in adrenal tumors W Arlt, M Biehl, AE Taylor, S Hahner, R Libe, BA Hughes, P Schneider, ... The Journal of Clinical Endocrinology & Metabolism 96 (12), 3775-3784, 2011 | 460 | 2011 |
| Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany N Krone, A Braun, AA Roscher, D Knorr, HP Schwarz The Journal of Clinical Endocrinology & Metabolism 85 (3), 1059-1065, 2000 | 444 | 2000 |
| Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass … N Krone, BA Hughes, GG Lavery, PM Stewart, W Arlt, CHL Shackleton The Journal of steroid biochemistry and molecular biology 121 (3-5), 496-504, 2010 | 433 | 2010 |
| Genetics of congenital adrenal hyperplasia N Krone, W Arlt Best practice & research clinical endocrinology & metabolism 23 (2), 181-192, 2009 | 309 | 2009 |
| Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015) SF Ahmed, JC Achermann, W Arlt, A Balen, G Conway, Z Edwards, ... Clinical endocrinology 84 (5), 771-788, 2016 | 237 | 2016 |
| 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 | 202 | 2022 |
| UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development SF Ahmed, JC Achermann, W Arlt, AH Balen, G Conway, ZL Edwards, ... Clinical Endocrinology 75 (1), 12-26, 2011 | 184 | 2011 |
| Adrenal insufficiency ES Husebye, SH Pearce, NP Krone, O Kämpe The Lancet 397 (10274), 613-629, 2021 | 182 | 2021 |
| Inactivating PAPSS2 mutations in a patient with premature pubarche C Noordam, V Dhir, JC McNelis, F Schlereth, NA Hanley, N Krone, ... New England Journal of Medicine 360 (22), 2310-2318, 2009 | 170 | 2009 |
| Premature adrenarche: novel lessons from early onset androgen excess J Idkowiak, GG Lavery, V Dhir, TG Barrett, PM Stewart, N Krone, W Arlt European Journal of Endocrinology 165 (2), 189-207, 2011 | 166 | 2011 |
| Congenital adrenal hyperplasia and P450 oxidoreductase deficiency N Krone, V Dhir, HE Ivison, W Arlt Clinical endocrinology 66 (2), 162-172, 2007 | 156 | 2007 |
| Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency LA Metherell, D Naville, G Halaby, M Begeot, A Huebner, G Nurnberg, ... The Journal of Clinical Endocrinology & Metabolism 94 (10), 3865-3871, 2009 | 155 | 2009 |
| Health problems in congenital adrenal hyperplasia due to 21-hydroxylase deficiency N Reisch, W Arlt, N Krone Hormone research in paediatrics 76 (2), 73-85, 2011 | 135 | 2011 |
| Genetics in endocrinology: approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM … L Audí, SF Ahmed, N Krone, M Cools, K McElreavey, PM Holterhus, ... European Journal of Endocrinology 179 (4), R197-R206, 2018 | 133 | 2018 |
| Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency N Krone, N Reisch, J Idkowiak, V Dhir, HE Ivison, BA Hughes, IT Rose, ... The Journal of Clinical Endocrinology & Metabolism 97 (2), E257-E267, 2012 | 128 | 2012 |
| Changes over time in sex assignment for disorders of sex development Z Kolesinska, SF Ahmed, M Niedziela, J Bryce, M Molinska-Glura, ... Pediatrics 134 (3), e710-e715, 2014 | 127 | 2014 |
| Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium‐chain acyl‐CoA dehydrogenase deficiency EM Maier, B Liebl, W Röschinger, U Nennstiel‐Ratzel, R Fingerhut, ... Human Mutation 25 (5), 443-452, 2005 | 125 | 2005 |
| Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal … N Krone, IT Rose, DS Willis, J Hodson, SH Wild, EJ Doherty, S Hahner, ... The Journal of Clinical Endocrinology & Metabolism 98 (2), E346-E354, 2013 | 113 | 2013 |
| Novel associations in disorders of sex development: findings from the I-DSD Registry K Cox, J Bryce, J Jiang, M Rodie, R Sinnott, M Alkhawari, W Arlt, L Audi, ... The Journal of Clinical Endocrinology & Metabolism 99 (2), E348-E355, 2014 | 110 | 2014 |
Faisal AhmedSamson Gemmell Chair of Child Health, University of GlasgowVerified email at glasgow.ac.uk
