Maria Tereza Matias Baptista

Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome

Ana Paula Abreu, Ericka Barbosa Trarbach, Margaret de Castro et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 120 citations · Full text

Medicine, Endocrinology, Genetics +17

Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia

Ericka Barbosa Trarbach, Elaine Maria Frade Costa, Beatriz R. Versiani et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 108 citations · Full text

Life Sciences, Endocrinology, Genetics +14

Nonsense Mutations in<i>FGF8</i>Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Ericka Barbosa Trarbach, Ana Paula Abreu, Letícia Ferreira Gontijo Silveira et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 79 citations

Life Sciences, Endocrinology, Genetics +17

Gonadotropin-Independent Precocious Puberty Due to Luteinizing Hormone Receptor Mutations in Brazilian Boys: A Novel Constitutively Activating Mutation in the First Transmembrane Helix¹

Ana Cláudia Latronico, H. Shinozaki, Gil Guerra‐Júnior et al. · The Journal of Clinical Endocrinology & Metabolism · 2000 · 55 citations · Full text

Medicine, Endocrinology, Genetics +17

XX Maleness and XX True Hermaphroditism in<i>SRY</i>-Negative Monozygotic Twins: Additional Evidence for a Common Origin

Andréa Trevas Maciel‐Guerra, Maricilda Palandi de Mello, Fernanda Boechers Coeli et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 48 citations

Life Sciences, Genetics, Molecular Genetics +17