| Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome CE Flück, T Tajima, AV Pandey, W Arlt, K Okuhara, CF Verge, EW Jabs, ... Nature genetics 36 (3), 228-230, 2004 | 541 | 2004 |
| Caring for individuals with a difference of sex development (DSD): a consensus statement M Cools, A Nordenström, R Robeva, J Hall, P Westerveld, C Flück, ... Nature Reviews Endocrinology 14 (7), 415-429, 2018 | 441 | 2018 |
| 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 | 414 | 2022 |
| Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials K Clément, E van den Akker, J Argente, A Bahm, WK Chung, H Connors, ... The lancet Diabetes & endocrinology 8 (12), 960-970, 2020 | 392 | 2020 |
| Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis N Huang, AV Pandey, V Agrawal, W Reardon, PD Lapunzina, D Mowat, ... The American Journal of Human Genetics 76 (5), 729-749, 2005 | 364 | 2005 |
| NADPH P450 oxidoreductase: structure, function, and pathology of diseases AV Pandey, CE Flück Pharmacology & therapeutics 138 (2), 229-254, 2013 | 293 | 2013 |
| Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation CE Flück, M Meyer-Böni, AV Pandey, P Kempná, WL Miller, EJ Schoenle, ... The American Journal of Human Genetics 89 (2), 201-218, 2011 | 269 | 2011 |
| “Hot spot” in the PROP1 gene responsible for combined pituitary hormone deficiency J Deladoëy, C Flück, A Büyükgebiz, BV Kuhlmann, A Eblé, ... The Journal of Clinical Endocrinology & Metabolism 84 (5), 1645-1650, 1999 | 265 | 1999 |
| Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg→ Cys at codon 120 (R120C) C Flück, J Deladoey, K Rutishauser, A Eblé, U Marti, W Wu, PE Mullis The Journal of Clinical Endocrinology & Metabolism 83 (10), 3727-3734, 1998 | 254 | 1998 |
| Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study B Köhler, E Kleinemeier, A Lux, O Hiort, A Grüters, U Thyen, ... The Journal of Clinical Endocrinology & Metabolism 97 (2), 577-588, 2012 | 194 | 2012 |
| High prevalence of vitamin D deficiency in children and adolescents with type 1 diabetes M Janner, P Ballinari, PE Mullis, CE Flück Pandey Swiss medical weekly 140, w13091, 2010 | 192 | 2010 |
| The 17, 20-Lyase Activity of Cytochrome P450c17 from Human Fetal Testis Favors the Δ5 Steroidogenic Pathway CE Flück, WL Miller, RJ Auchus The Journal of Clinical Endocrinology & Metabolism 88 (8), 3762-3766, 2003 | 189 | 2003 |
| The adrenal cortex and its disorders WL Miller, CE Flück, DT Breault, BJ Feldman Sperling Pediatric Endocrinology, 425-490, 2021 | 188 | 2021 |
| NADPH–cytochrome P450 oxidoreductase: roles in physiology, pharmacology, and toxicology DS Riddick, X Ding, CR Wolf, TD Porter, AV Pandey, QY Zhang, J Gu, ... Drug Metabolism and Disposition 41 (1), 12-23, 2013 | 164 | 2013 |
| GATA-4 and GATA-6 modulate tissue-specific transcription of the human gene for P450c17 by direct interaction with Sp1 CE Flück, WL Miller Molecular Endocrinology 18 (5), 1144-1157, 2004 | 155 | 2004 |
| Aromatase Deficiency Caused by a Novel P450arom Gene Mutation: Impact of Absent Estrogen Production on Serum Gonadotropin Concentration in a Boy J Deladoëy, C Flück, M Bex, N Yoshimura, N Harada, PE Mullis The Journal of Clinical Endocrinology & Metabolism 84 (11), 4050-4054, 1999 | 154 | 1999 |
| Ten Novel Mutations in the NR5A1 Gene Cause Disordered Sex Development in 46,XY and Ovarian Insufficiency in 46,XX Individuals N Camats, AV Pandey, M Fernandez-Cancio, P Andaluz, M Janner, ... The Journal of Clinical Endocrinology & Metabolism 97 (7), E1294-E1306, 2012 | 145 | 2012 |
| Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase AV Pandey, P Kempna, G Hofer, PE Mullis, CE Fluck Molecular Endocrinology 21 (10), 2579-2595, 2007 | 134 | 2007 |
| Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures D Cassatella, SR Howard, JS Acierno, C Xu, GE Papadakis, FA Santoni, ... European journal of endocrinology 178 (4), 377-388, 2018 | 121 | 2018 |
| Adrenal gland development and defects P Kempná, CE Flück Best practice & research Clinical endocrinology & metabolism 22 (1), 77-93, 2008 | 120 | 2008 |
Amit V PandeyUniversity Children's Hospital Bern, University of BernAdresse e-mail validée de unibe.ch