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Larissa Garcia Gomes

CV Lattes GoogleMyCitations ORCID


Secretaria da Saúde (São Paulo - Estado). Hospital das Clínicas da Faculdade de Medicina da USP (HCFMUSP)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

graduate at Medicina from Universidade Federal do Espírito Santo (2000) and ph.d. at Endocrinology from Universidade de São Paulo (2009). Has experience in Medicine, focusing on Endocrinology, acting on the following subjects: endocrinologia, metabologia, deficiência da 21-hidroxilase, p450 oxidoreductase and diabetes. (Source: Lattes Curriculum)

Research grants
FAPESP support in numbers * Updated October 19, 2019
Total / Available in English
1 / 1 Completed research grants
1 / 0 Completed scholarships in Brazil
2 / 1 All research grants and scholarships

Associated processes
Most frequent collaborators in research granted by FAPESP
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Use this Research Supported by FAPESP (BV/FAPESP) channel only to send messages referring to FAPESP-funded scientific projects.


 

 

 

 

Keywords used by the researcher
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)

Publications10
Citations52
Cit./Article5.2
Data from Web of Science

GOMES, LARISSA G.; MADUREIRA, GUIOMAR; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 68, n. 2, p. 147-151, . Web of Science Citations: 2.

MOURA-MASSARI, V. O.; BUGANO, D. D. G.; MARCONDES, J. A. M.; GOMES, L. G.; MENDONCA, B. B.; BACHEGA, T. A. S. S.. CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia. Hormone and Metabolic Research, v. 45, n. 4, p. 301-307, . Web of Science Citations: 10. (08/51624-6, 05/04726-0)

MOREIRA, RICARDO P. P.; GOMES, LARISSA G.; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency. PLoS One, v. 7, n. 9, . Web of Science Citations: 9.

MOREIRA, RICARDO P. P.; JORGE, ALEXANDER A. L.; GOMES, LARISSA G.; KAUPERT, LAURA C.; MASSUD FILHO, JOAO; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 66, n. 8, p. 1361-1365, . Web of Science Citations: 5. (05/04726-0)

ROCHA, THAIS; CRESPO, RAIANE P.; YANCE, VIVIANE V. R.; HAYASHIDA, SYLVIA A.; BARACAT, EDMUND C.; CARVALHO, FILOMENA; DOMENICE, SORAHIA; MENDONCA, BERENICE B.; GOMES, LARISSA G.. Persistent Poor Metabolic Profile in Postmenopausal Women With Ovarian Hyperandrogenism After Testosterone Level Normalization. JOURNAL OF THE ENDOCRINE SOCIETY, v. 3, n. 5, p. 1087-1096, . Web of Science Citations: 0. (15/17350-0)

KAUPERT, LAURA C.; GOMES, LARISSA G.; BRITO, VINICIUS N.; LEMOS-MARINI, SOFIA H. V.; DE MELLO, MARICILDA P.; LONGUI, CARLOS A.; KOCHI, CRISTIANE; DE CASTRO, MARGARET; GUERRA, JR., GIL; MENDONCA, BERENICE B.; et al. A Single Nucleotide Variant in the Promoter Region of 17 beta-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency. Hormone Research in Paediatrics, v. 85, n. 5, p. 333-338, . Web of Science Citations: 3. (14/07878-4)

MOURA-MASSARI, VIVIAN OLIVEIRA; CUNHA, FLAVIA SIQUEIRA; GOMES, LARISSA GARCIA; DINIZ GOMES, DIOGO BUGANO; MIGUEL MARCONDES, JOSE ANTONIO; MADUREIRA, GUIOMAR; DE MENDONCA, BERENICE BILHARINHO; SARTORI SANCHEZ BACHEGA, TANIA A.. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. PLoS One, v. 11, n. 2, . Web of Science Citations: 2. (08/51624-6, 05/04726-0, 14/07878-4)

MOREIRA, RICARDO P. P.; GOMES, LARISSA G.; MADUREIRA, GUIOMAR; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia. INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, . Web of Science Citations: 5.

DE CARVALHO, DANIEL F.; MIRANDA, MIRELA C.; GOMES, LARISSA G.; MADUREIRA, GUIOMAR; MARCONDES, JOSE A. M.; BILLERBECK, ANA ELISA C.; RODRIGUES, ANDRESA S.; PRESTI, PAULA F.; KUPERMAN, HILTON; DAMIANI, DURVAL; et al. Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction. EUROPEAN JOURNAL OF ENDOCRINOLOGY, v. 175, n. 2, p. 107-116, . Web of Science Citations: 15. (14/07878-4)

GAMES, LARISSA G.; CUNHA-SILVA, MARINA; CRESPO, RAIANE P.; RAMOS, CAROLINA O.; MONTENEGRO, LUCIANA R.; CANTON, ANA; LEES, MELISSA; SPOUDEAS, HELEN; DAUBER, ANDREW; MACEDO, DELANIE B.; et al. DLK1 Is a Novel Link Between Reproduction and Metabolism. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, v. 104, n. 6, p. 2112-2120, . Web of Science Citations: 1. (15/17350-0)

Academic Publications

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

GOMES, Larissa Garcia. Estudo da proteína P450 óxido-redutase e dos citocromos hepáticos 2C19 e 3A4 como possíveis moduladores do fenótipo da deficiência da 21-hidroxilase. 2009. 90f. Tese (Doutorado) – Faculdade de Medicina. Universidade de São Paulo (USP). São Paulo. (05/55364-0)

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