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Ericka Barbosa Trarbach

CV Lattes

Universidade de São Paulo (USP). Faculdade de Medicina (FM)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

Graduate at Licenciatura em Ciências Biológicas from Universidade Federal do Espírito Santo (1996), master's at Genetics from Universidade Estadual de Campinas (2000) and ph.d. at Genetics from Universidade Estadual de Campinas (2004). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: pituitary tumors, genetics and epigenetics, and Kallmann syndrome. (Source: Lattes Curriculum)

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Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (10)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

Data from Web of Science

MONTENEGRO, LUCIANA RIBEIRO; SILVEIRA, LETICIA F. G.; TUSSET, CINTIA; DE CASTRO, MARGARET; VERSIANI, BEATRIZ R.; LATRONICO, ANA CLAUDIA; MENDONCA, BERENICE BILHARINHO; TRARBACH, ERICKA B.. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome. Fertility and Sterility, v. 100, n. 3, p. 854-859, . Web of Science Citations: 7. (05/04726-0)

ABREU, ANA PAULA; TRARBACH, ERICKA BARBOSA; DE CASTRO, MARGARET; FRADE COSTA, ELAINE MARIA; VERSIANI, BEATRIZ; MATIAS BAPTISTA, MARIA TEREZA; GARMES, HERALDO MENDES; MENDONCA, BERENICE BILHARINHO; LATRONICO, ANA CLAUDIA. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, v. 93, n. 10, p. 4113-4118, . Web of Science Citations: 69. (05/04726-0)

BATISTA, RAFAEL LOCH; TRARBACH, ERICKA BARBOSA; MARQUES, MATEUS DINIZ; CESCATO, VALTER ANGELO; DA SILVA, GILBERTO OCHMAN; BORBA HERKENHOFF, CLARISSA G.; CUNHA-NETO, MALEBRANCHE BERARDO; MUSOLINO, NINA ROSA. Nonfunctioning Pituitary Adenoma Recurrence and Its Relationship with Sex, Size, and Hormonal Immunohistochemical Profile. WORLD NEUROSURGERY, v. 120, p. E241-E246, . Web of Science Citations: 1. (14/16327-1)

BATISTA, RAFAEL L.; MUSOLINO, NINA R. C.; CESCATO, VALTER A. S.; DA SILVA, GILBERTO O.; MEDEIROS, RAPHAEL S. S.; HERKENHOFF, CLARISSA G. B.; TRARBACH, ERICKA B.; CUNHA-NETO, MALEBRANCHE B.. Cabergoline in the Management of Residual Nonfunctioning Pituitary Adenoma A Single-Center, Open-Label, 2-Year Randomized Clinical Trial. AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, v. 42, n. 2, p. 221-227, . Web of Science Citations: 1. (14/16327-1)

TRARBACH, ERICKA B.; ABREU, ANA PAULA; GONTIJO SILVEIRA, LETICIA FERREIRA; GARMES, HERALDO MENDES; BAPTISTA, MARIA TEREZA M.; TELES, MILENA GURGEL; COSTA, ELAINE M. F.; MOHAMMADI, MOOSA; PITTELOUD, NELLY; MENDONCA, BERENICE B.; et al. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, v. 95, n. 7, p. 3491-3496, . Web of Science Citations: 44. (05/04726-0)

TRARBACH, ERICKA BARBOSA; TELES, MILENA GURGEL; FRADE COSTA, ELAINE MARIA; ABREU, ANA PAULA; GARMES, HERALDO MENDES; GUERRA-JUNIOR, GIL; MATIAS BAPTISTA, MARIA TEREZA; DE CASTRO, MARGARET; MENDONCA, BERENICE BILHARINHO; LATRONICO, ANA CLAUDIA. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. CLINICAL ENDOCRINOLOGY, v. 72, n. 3, p. 371-376, . Web of Science Citations: 13. (05/04726-0)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

TRARBACH, Ericka Barbosa. Estudo citogenetico e molecular em pacientes com hipogonadismo hipogonadotrofico com e sem anosmia : sindorme de Kallmann e hipogonadismo hipogonadotropico. Tese (Doutorado) -  Instituto de Biologia.  Universidade Estadual de Campinas.  (00/08834-8

SHINZATO, Amanda. Investigação molecular dos genes PTEN e DREAM em pacientes portadores de bócio multinodular. Dissertação (Mestrado) -  Faculdade de Medicina.  Universidade de São Paulo (USP).  São Paulo.  (12/11479-2

TRARBACH, Ericka Barbosa. Estudos citogeneticos em pacientes com sindrome de Kallmann. Dissertação (Mestrado) -  Instituto de Biologia.  Universidade Estadual de Campinas.  (97/14568-4

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