| Testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone–receptor gene AC Latronico, J Anasti, IJP Arnhold, R Rapaport, BB Mendonca, W Bloise, ... New England journal of medicine 334 (8), 507-512, 1996 | 433 | 1996 |
| Mutations of the KISS1 Gene in Disorders of Puberty LG Silveira, SD Noel, AP Silveira-Neto, AP Abreu, VN Brito, MG Santos, ... The Journal of Clinical Endocrinology & Metabolism 95 (5), 2276-2280, 2010 | 402 | 2010 |
| 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 |
| The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency JD Cogan, W Wu, JA Phillips III, IJP Arnhold, A Agapito, OV Fofanova, ... The Journal of Clinical Endocrinology & Metabolism 83 (9), 3346-3349, 1998 | 262 | 1998 |
| Diagnostic value of fluorometric assays in the evaluation of precocious puberty VN Brito, MC Batista, MF Borges, AC Latronico, MBF Kohek, ACP Thirone, ... The journal of Clinical endocrinology & metabolism 84 (10), 3539-3544, 1999 | 244 | 1999 |
| 46, XY disorders of sex development (DSD) BB Mendonca, S Domenice, IJP Arnhold, EMF Costa Clinical endocrinology 70 (2), 173-187, 2009 | 234 | 2009 |
| Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene KFS Melo, BB Mendonca, AEC Billerbeck, EMF Costa, M Inácio, ... The Journal of Clinical Endocrinology & Metabolism 88 (7), 3241-3250, 2003 | 217 | 2003 |
| Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301, G302 in the PROP1 gene BB Mendonca, MGF Osorio, AC Latronico, V Estefan, LSS Lo, IJP Arnhold The Journal of Clinical Endocrinology & Metabolism 84 (3), 942-945, 1999 | 198 | 1999 |
| Molecular mechanisms of pituitary organogenesis: in search of novel regulatory genes SW Davis, F Castinetti, LR Carvalho, BS Ellsworth, MA Potok, RH Lyons, ... Molecular and cellular endocrinology 323 (1), 4-19, 2010 | 191 | 2010 |
| Growth hormone (GH) pharmacogenetics: influence of GH receptor exon 3 retention or deletion on first-year growth response and final height in patients with severe GH deficiency AAL Jorge, FG Marchisotti, LR Montenegro, LR Carvalho, BB Mendonca, ... The Journal of Clinical Endocrinology & Metabolism 91 (3), 1076-1080, 2006 | 191 | 2006 |
| Update on the etiology, diagnosis and therapeutic management of sexual precocity VN Brito, AC Latronico, IJP Arnhold, BB Mendonça Arquivos Brasileiros de Endocrinologia & Metabologia 52, 18-31, 2008 | 170 | 2008 |
| Male Pseudohermaphroditism Due to Steroid 5α-Reductase 2 Deficiency Diagnosis, Psychological Evaluation, and Management BB Mendonca, M Inacio, EMF Costa, IJP Arnhold, FAQ Silva, W Nicolau, ... Medicine 75 (2), 64-76, 1996 | 169 | 1996 |
| 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 | 159 | 2018 |
| A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction LR Carvalho, KS Woods, BB Mendonca, N Marcal, AL Zamparini, S Stifani, ... The Journal of clinical investigation 112 (8), 1192-1201, 2003 | 158 | 2003 |
| Pituitary Magnetic Resonance Imaging and Function in Patients with Growth Hormone Deficiency with and without Mutations in GHRH-R, GH-1, or PROP-1 Genes MGF Osorio, S Marui, AAL Jorge, AC Latronico, LSS Lo, CC Leite, ... The Journal of Clinical Endocrinology & Metabolism 87 (11), 5076-5084, 2002 | 153 | 2002 |
| 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 |
| Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3 DB Macedo, AP Abreu, ACS Reis, LR Montenegro, A Dauber, ... The Journal of Clinical Endocrinology & Metabolism 99 (6), E1097-E1103, 2014 | 150 | 2014 |
| A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface … AC Latronico, Y Chai, IJP Arnhold, X Liu, BB Mendonca, DL Segaloff Molecular Endocrinology 12 (3), 442-450, 1998 | 147 | 1998 |
| Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency TASS Bachega, AEC Billerbeck, G Madureira, JAM Marcondes, ... The Journal of Clinical Endocrinology & Metabolism 83 (12), 4416-4419, 1998 | 146 | 1998 |
| Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene BB Mendonca, MV Leite, M de Castro, T Kino, LLK Elias, TAS Bachega, ... The Journal of Clinical Endocrinology & Metabolism 87 (4), 1805-1809, 2002 | 142 | 2002 |
