| The polycystic ovary syndrome: a position statement from the European Society of Endocrinology G Conway, D Dewailly, E Diamanti-Kandarakis, HF Escobar-Morreale, ... European journal of endocrinology 171 (4), P1-P29, 2014 | 905 | 2014 |
| Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism N Pitteloud, C Zhang, D Pignatelli, JD Li, T Raivio, LW Cole, L Plummer, ... Proceedings of the National Academy of Sciences 104 (44), 17447-17452, 2007 | 300 | 2007 |
| 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 | 280 | 2000 |
| 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 | 236 | 2006 |
| Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular … L Groussin, LS Kirschner, C Vincent-Dejean, K Perlemoine, E Jullian, ... The American Journal of Human Genetics 71 (6), 1433-1442, 2002 | 209 | 2002 |
| Adrenarche in the rat D Pignatelli, F Xiao, AM Gouveia, JG Ferreira, GP Vinson Journal of Endocrinology 191 (1), 301-308, 2006 | 178 | 2006 |
| The phenotype of hirsute women: a comparison of polycystic ovary syndrome and 21-hydroxylase–deficient nonclassic adrenal hyperplasia M Pall, R Azziz, J Beires, D Pignatelli Fertility and sterility 94 (2), 684-689, 2010 | 127 | 2010 |
| 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 | 112 | 2018 |
| Direct effects of stress on adrenocortical function D Pignatelli, MM Magalhaes, MC Magalhaes Hormone and metabolic research 30 (06/07), 464-474, 1998 | 104 | 1998 |
| European survey of diagnosis and management of the polycystic ovary syndrome: results of the ESE PCOS Special Interest Group's Questionnaire G Conway, D Dewailly, E Diamanti-Kandarakis, HF Escobar-Morreale, ... European journal of endocrinology 171 (4), 489-498, 2014 | 98 | 2014 |
| Von Hippel–Lindau disease: a single gene, several hereditary tumors J Crespigio, LCL Berbel, MA Dias, RF Berbel, SS Pereira, D Pignatelli, ... Journal of endocrinological investigation 41, 21-31, 2018 | 80 | 2018 |
| The complexities in genotyping of congenital adrenal hyperplasia: 21-hydroxylase deficiency D Pignatelli, BL Carvalho, A Palmeiro, A Barros, SG Guerreiro, D Macut Frontiers in Endocrinology 10, 432, 2019 | 63 | 2019 |
| Melanocortin 5 receptor activates ERK1/2 through a PI3K-regulated signaling mechanism AR Rodrigues, D Pignatelli, H Almeida, AM Gouveia Molecular and Cellular Endocrinology 303 (1-2), 74-81, 2009 | 57 | 2009 |
| Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants C Xu, D Cassatella, AM van der Sloot, R Quinton, M Hauschild, ... Genetics in medicine 20 (8), 872-881, 2018 | 46 | 2018 |
| Non-classic adrenal hyperplasia due to the deficiency of 21-hydroxylase and its relation to polycystic ovarian syndrome D Pignatelli Polycystic Ovary Syndrome 40, 158-170, 2013 | 46 | 2013 |
| Increased extracellular signal regulated kinases phosphorylation in the adrenal gland in response to chronic ACTH treatment JG Ferreira, CD Cruz, D Neves, D Pignatelli Journal of endocrinology 192 (3), 647-658, 2007 | 44 | 2007 |
| Immunohistochemical study of heat shock proteins 27, 60 and 70 in the normal human adrenal and in adrenal tumors with suppressed ACTH production D Pignatelli, J Ferreira, P Soares, M José Costa, M Conceição Magalhães Microscopy research and technique 61 (3), 315-323, 2003 | 43 | 2003 |
| Proliferation of capsular stem cells induced by ACTH in the rat adrenal cortex D Pignatelli, J Ferreira, P Vendeira, MC Magalhaes, GP Vinson Endocrine research 28 (4), 683-691, 2002 | 43 | 2002 |
| MAPK/ERK pathway inhibition is a promising treatment target for adrenocortical tumors SS Pereira, MP Monteiro, MM Costa, J Ferreira, MG Alves, PF Oliveira, ... Journal of cellular biochemistry 120 (1), 894-906, 2019 | 39 | 2019 |
