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Tania Aparecida Sartori Sanchez Bachega

CV Lattes GoogleMyCitations


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

graduate at Medicina from Universidade de Santo Amaro (1987) and ph.d. at Endocrinology from Universidade de São Paulo (1997). Has experience in Medicine, focusing on Clinical Medicine, acting on the following subjects: deficiência da 21-hidroxilase, 21-hidroxilase, hiperplasia adrenal congênita, adrenal and 17ohp. (Source: Lattes Curriculum)

Research grants
Scholarships in Brazil
FAPESP support in numbers * Updated November 30, 2019
Total / Available in English
9 / 6 Completed research grants
9 / 2 Completed scholarships in Brazil
1 / 0 Completed scholarships abroad
19 / 8 All research grants and scholarships

Associated processes
Most frequent collaborators in research granted by FAPESP
Contact researcher

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 (19)

(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)

Publications16
Citations115
Cit./Article7.2
Data from Web of Science

HAYASHI, GISELLE; FAURE, CLAUDIA; BRONDI, MARIA FERNANDA; VALLEJOS, CARLA; SOARES, DAIANA; OLIVEIRA, ERICA; BRITO, VINICIUS N.; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 55, n. 8, p. 632-637, . Web of Science Citations: 11.

MOREIRA, RICARDO P. P.; BACHEGA, TANIA A. S. S.; MACHADO, MARCIO C.; MENDONCA, BERENICE B.; BRONSTEIN, MARCELLO D.; VILLARES FRAGOSO, MARIA CANDIDA B.. Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease. Clinics, v. 68, n. 5, p. 579-585, . Web of Science Citations: 3.

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.

MOREIRA, RICARDO P. P.; JORGE, ALEXANDER A. L.; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Frequency of genetic polymorphisms of PXR gene in the Brazilian population. Clinics, v. 66, n. 6, p. 1041-1044, . Web of Science Citations: 6. (05/04726-0)

KAUPERT, L. C.; LEMOS-MARINI, S. H. V.; DE MELLO, M. P.; MOREIRA, R. P.; BRITO, V. N.; JORGE, A. A. L.; LONGUI, C. A.; GUERRA, JR., G.; MENDONCA, B. B.; BACHEGA, T. A.. The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia. Clinical Genetics, v. 84, n. 5, p. 482-488, . Web of Science Citations: 6.

MOREIRA, RICARDO P. P.; VILLARES, SANDRA M.; MADUREIRA, GUIOMAR; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics, v. 80, n. 2, p. 111-118, . Web of Science Citations: 10.

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.; 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)

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)

SILVEIRA, E. L.; ELNECAVE, R. H.; DOS SANTOS, E. P.; MOURA, V.; PINTO, E. M.; NADER, I. VAN DER LINDEN; MENDONCA, B. B.; BACHEGA, T. A. S. S.. Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia. Clinical Genetics, v. 76, n. 6, p. 503-510, . Web of Science Citations: 15.

BACHEGA‚ T.A.S.S.; BILLERBECK‚ A.E.C.; MARCONDES‚ J.A.M.; MADUREIRA‚ G.; ARNHOLD‚ I.J.P.; MENDONCA‚ B.B.. Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinical Endocrinology, v. 52, n. 5, p. 601-607, .

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.

T.A.S.S. BACHEGA; A.E.C. BILLERBECK; G. MADUREIRA; J.A.M. MARCONDES; C.A. LONGUI; M.V. LEITE; I.J.P. ARNHOLD; B.B. MENDONÇA. 21-Hydroxylase deficiency in Brazil. Brazilian Journal of Medical and Biological Research, v. 33, n. 10, p. 1211-1216, .

ARAUJO‚ R.S.; BILLERBECK‚ A.E.C.; MADUREIRA‚ G.; MENDONCA‚ B.B.; BACHEGA‚ T.A.S.S.. Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation. Clinical Endocrinology, v. 62, n. 2, p. 132-136, .

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)

HAYASHI, GISELLE Y.; CARVALHO, DANIEL F.; DE MIRANDA, MIRELA C.; FAURE, CLAUDIA; VALLEJOS, CARLA; BRITO, VINICIUS N.; RODRIGUES, ANDRESA DE SANTI; MADUREIRA, GUIOMAR; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Neonatal 17-hydroxyprogesterone levels adjusted according to age at sample collection and birthweight improve the efficacy of congenital adrenal hyperplasia newborn screening. Clinical Endocrinology, v. 86, n. 4, p. 480-487, . Web of Science Citations: 9. (14/07878-4)

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)

KAUPERT, LAURA C.; BILLERBECK, ANA ELISA C.; BRITO, VINICIUS N.; MENDONCA, BERENICE B.; BACHEGA, TANIA A. S. S.. Could the Leukocyte X Chromosome Inactivation Pattern Be Extrapolated to Hair Bulbs?. Hormone Research in Paediatrics, v. 73, n. 4, p. 238-243, . Web of Science Citations: 3.

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: 10.

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)

MOURA, Vivian de Oliveira. Análise de genes moduladores do fenótipo da forma não clássica da deficiência da 21-hidroxilase. 2011. Dissertação (Mestrado) - Faculdade de Medicina. Universidade de São Paulo (USP). São Paulo. (08/51624-6)

KAUPERT, Laura Cesar. Análise de genes moduladores do fenótipo de virilização genital em mulheres com a forma clássica da deficiência da 21-hidroxilase. 2012. Tese (Doutorado) – Faculdade de Medicina. Universidade de São Paulo (USP). São Paulo. (08/55546-0)

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