| Sleep characteristics of adolescents: a longitudinal study MMM Andrade, AA Benedito-Silva, S Domenice, IJP Arnhold, ... Journal of Adolescent Health 14 (5), 401-406, 1993 | 290 | 1993 |
| An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors AC Latronico, EM Pinto, S Domenice, MCBV Fragoso, RM Martin, ... The Journal of Clinical Endocrinology & Metabolism 86 (10), 4970-4973, 2001 | 251 | 2001 |
| 46, XY disorders of sex development (DSD) BB Mendonca, S Domenice, IJP Arnhold, EMF Costa Clinical endocrinology 70 (2), 173-187, 2009 | 234 | 2009 |
| Cushing’s Syndrome Secondary to Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia due to Activating Mutations of GNAS1 Gene MCBV Fragoso, S Domenice, AC Latronico, RM Martin, MAA Pereira, ... The Journal of Clinical Endocrinology & Metabolism 88 (5), 2147-2151, 2003 | 197 | 2003 |
| Ectopic ACTH syndrome: our experience with 25 cases LR Salgado, MCBV Fragoso, M Knoepfelmacher, MC Machado, ... European Journal of Endocrinology 155 (5), 725-733, 2006 | 179 | 2006 |
| A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency RV Correa, S Domenice, NC Bingham, AEC Billerbeck, WE Rainey, ... The Journal of Clinical Endocrinology & Metabolism 89 (4), 1767-1772, 2004 | 171 | 2004 |
| Androgen insensitivity syndrome: a review RL Batista, EMF Costa, AS Rodrigues, NL Gomes, JA Faria Jr, MY Nishi, ... Archives of endocrinology and metabolism 62, 227-235, 2018 | 160 | 2018 |
| A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty AC Latronico, J Anasti, IJ Arnhold, BB Mendonca, S Domenice, ... The Journal of Clinical Endocrinology & Metabolism 80 (8), 2490-2494, 1995 | 151 | 1995 |
| Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors EM Pinto, AEC Billerbeck, MCBF Villares, S Domenice, BB Mendonça, ... Arquivos Brasileiros de Endocrinologia & Metabologia 48, 647-650, 2004 | 144 | 2004 |
| Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthood BB Mendonca, AM Lucon, CAV Menezes, LB Saldanha, AC Latronico, ... The Journal of urology 154 (6), 2004-2009, 1995 | 133 | 1995 |
| Wide spectrum of NR5A1‐related phenotypes in 46, XY and 46, XX individuals S Domenice, AZ Machado, FM Ferreira, B Ferraz‐de‐Souza, AM Lerario, ... Birth Defects Research Part C: Embryo Today: Reviews 108 (4), 309-320, 2016 | 113 | 2016 |
| The role of desmopressin in bilateral and simultaneous inferior petrosal sinus sampling for differential diagnosis of ACTH‐dependent Cushing's syndrome MC Machado, SV De Sa, S Domenice, MCBV Fragoso, P Puglia Jr, ... Clinical endocrinology 66 (1), 136-142, 2007 | 107 | 2007 |
| Management of 46, XY differences/disorders of sex development (DSD) throughout life AB Wisniewski, RL Batista, EMF Costa, C Finlayson, MHP Sircili, ... Endocrine Reviews 40 (6), 1547-1572, 2019 | 105 | 2019 |
| Disorders of sex development: effect of molecular diagnostics JC Achermann, S Domenice, TASS Bachega, MY Nishi, BB Mendonca Nature Reviews Endocrinology 11 (8), 478-488, 2015 | 100 | 2015 |
| 46, XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency BB Mendonca, NL Gomes, EMF Costa, M Inacio, RM Martin, MY Nishi, ... The Journal of steroid biochemistry and molecular biology 165, 79-85, 2017 | 97 | 2017 |
| Steroid 5α-reductase 2 deficiency BB Mendonca, RL Batista, S Domenice, EMF Costa, IJP Arnhold, ... The Journal of steroid biochemistry and molecular biology 163, 206-211, 2016 | 97 | 2016 |
| Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene S Domenice, AC Latronico, VN Brito, IJP Arnhold, F Kok, BB Mendonca The Journal of Clinical Endocrinology & Metabolism 86 (9), 4068-4071, 2001 | 92 | 2001 |
| Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients S Domenice, RV Correa, EMF Costa, MY Nishi, E Vilain, IJP Arnhold, ... Brazilian journal of medical and biological research 37, 145-150, 2004 | 87 | 2004 |
| A novel missense mutation (S18N) in the 5′ non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives S Domenice, M Yumie Nishi, AE Correia Billerbeck, AC Latronico, ... Human genetics 102, 213-215, 1998 | 81 | 1998 |
| Quality of life of patients with 46, XX and 46, XY disorders of sex development RC Amaral, M Inacio, VN Brito, TASS Bachega, S Domenice, IJP Arnhold, ... Clinical endocrinology 82 (2), 159-164, 2015 | 78* | 2015 |
