| A GPR54-activating mutation in a patient with central precocious puberty MG Teles, SDC Bianco, VN Brito, EB Trarbach, W Kuohung, S Xu, ... New England Journal of Medicine 358 (7), 709-715, 2008 | 719 | 2008 |
| 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 | 159 | 2014 |
| Classificação do diabetes M Rodacki, M Teles, M Gabbay, R Montenegro, M Bertoluci Diretriz Oficial da Sociedade Brasileira de Diabetes, 557753.2022-1, 2022 | 136 | 2022 |
| Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency EB Trarbach, AP Abreu, LFG Silveira, HM Garmes, MTM Baptista, ... The Journal of Clinical Endocrinology & Metabolism 95 (7), 3491-3496, 2010 | 101 | 2010 |
| Factors determining normal adult height in girls with gonadotropin-dependent precocious puberty treated with depot gonadotropin-releasing hormone analogs VN Brito, AC Latronico, P Cukier, MG Teles, LFG Silveira, IJP Arnhold, ... The Journal of Clinical Endocrinology & Metabolism 93 (7), 2662-2669, 2008 | 91 | 2008 |
| KISS1R intracellular trafficking and degradation: effect of the Arg386Pro disease-associated mutation SDC Bianco, L Vandepas, M Correa-Medina, B Gereben, A Mukherjee, ... Endocrinology 152 (4), 1616-1626, 2011 | 90 | 2011 |
| A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism MG Teles, EB Trarbach, SD Noel, G Guerra-Junior, A Jorge, D Beneduzzi, ... European journal of endocrinology 163 (1), 29-34, 2010 | 71 | 2010 |
| New genetic factors implicated in human GnRH-dependent precocious puberty: the role of kisspeptin system MG Teles, LFG Silveira, C Tusset, AC Latronico Molecular and cellular endocrinology 346 (1-2), 84-90, 2011 | 62 | 2011 |
| DLK1, notch signaling and the timing of puberty DB Macedo, UB Kaiser Seminars in reproductive medicine 37 (04), 174-181, 2019 | 57 | 2019 |
| A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation I Hussain, N Patni, M Ueda, E Sorkina, CM Valerio, E Cochran, RJ Brown, ... The Journal of Clinical Endocrinology & Metabolism 103 (3), 1005-1014, 2018 | 56 | 2018 |
| PDX1 ‐MODY and dorsal pancreatic agenesis: New phenotype of a rare disease LA Caetano, LS Santana, AD Costa‐Riquetto, AM Lerario, M Nery, ... Clinical genetics 93 (2), 382-386, 2018 | 46 | 2018 |
| Acquired lipodystrophy associated with nivolumab in a patient with advanced renal cell carcinoma CK Falcao, MCS Cabral, JM Mota, ST Arbache, AD Costa-Riquetto, ... The Journal of Clinical Endocrinology & Metabolism 104 (8), 3245-3248, 2019 | 41 | 2019 |
| Targeted sequencing identifies novel variants in common and rare MODY genes LS de Santana, LA Caetano, AD Costa‐Riquetto, PC Franco, RP Dotto, ... Molecular Genetics & Genomic Medicine 7 (12), e962, 2019 | 36 | 2019 |
| Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation‐dependent probe amplification: detection of a hemizygosis for the … EB Trarbach, MG Teles, EMF Costa, AP Abreu, HM Garmes, G Guerra, ... Clinical endocrinology 72 (3), 371-376, 2010 | 31 | 2010 |
| Clinical application of ACMG‐AMP guidelines in HNF1A and GCK variants in a cohort of MODY families LS Santana, LA Caetano, AD Costa‐Riquetto, EPS Quedas, M Nery, ... Clinical genetics 92 (4), 388-396, 2017 | 30 | 2017 |
| Maturity-onset diabetes of the young (MODY) in Brazil: establishment of a national registry and appraisal of available genetic and clinical data FMA Giuffrida, RS Moises, LS Weinert, LE Calliari, T Della Manna, ... Diabetes research and clinical practice 123, 134-142, 2017 | 30 | 2017 |
| Role of kisspeptin/GPR54 system in human reproductive axis LFG Silveira, MG Teles, EB Trarbach, AC Latronico Kallmann Syndrome and Hypogonadotropic Hypogonadism 39, 13-24, 2010 | 30 | 2010 |
| Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disorders P Cukier, H Wright, T Rulfs, LFG Silveira, MG Teles, BB Mendonca, ... Hormone research in paediatrics 80 (4), 257-266, 2013 | 25 | 2013 |
| COVID-19 pandemic triggers telemedicine regulation and intensifies diabetes management technology adoption in Brazil M Teles, T Sacchetta, Y Matsumoto Journal of Diabetes Science and Technology 14 (4), 797-798, 2020 | 22 | 2020 |
| Homozygous and heterozygous nuclear lamin A p. R582C mutation: different lipodystrophic phenotypes in the same kindred RM Montenegro Jr, AD Costa-Riquetto, VO Fernandes, ... Frontiers in endocrinology 9, 458, 2018 | 19 | 2018 |
Ana Claudia LatronicoProfessora Titular da Endocrinologia, Departamento de Clínica Médica da Faculdade da USPAdresse e-mail validée de usp.br
