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Milena Gurgel Teles Bezerra

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

Milena Gurgel Teles Bezerra in research grants and scholarships supported by FAPESP.

Research grants
Scholarships in Brazil
FAPESP support in numbers * Updated July 04, 2020
Total / Available in English
2 / 2 Completed research grants
1 / 1 Ongoing scholarships in Brazil
1 / 0 Completed scholarships in Brazil
4 / 3 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 (5)

(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)

Publications4
Citations11
Cit./Article2.8
Data from Web of Science

SANTANA, L. S.; CAETANO, L. A.; COSTA-RIQUETTO, A. D.; QUEDAS, E. P. S.; NERY, M.; COLLETT-SOLBERG, P.; BOGUSZEWSKI, M. C. S.; VENDRAMINI, M. F.; CRISOSTOMO, L. G.; FLOH, F. O.; et al. Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families. Clinical Genetics, v. 92, n. 4, p. 388-396, . Web of Science Citations: 6. (13/19920-2)

DE SANTANA, LUCAS S.; CAETANO, LILIAN A.; COSTA-RIQUETTO, ALINE D.; FRANCO, PEDRO C.; DOTTO, RENATA P.; REIS, ANDRE F.; WEINERT, LETICIA S.; SILVEIRO, SANDRA P.; VENDRAMINI, MARCIO F.; DO PRADO, FLAVIENE A.; et al. Targeted sequencing identifies novel variants in common and rare MODY genes. MOLECULAR GENETICS & GENOMIC MEDICINE, v. 7, n. 12, . Web of Science Citations: 0. (17/14703-4, 13/19920-2, 17/15365-5, 15/05123-9, 13/02162-8)

TELES, MILENA GURGEL; BIANCO, SUZY D. C.; BRITO, VINICIUS NAHIME; TRARBACH, ERICKA B.; KUOHUNG, WENDY; XU, SHUYUN; SEMINARA, STEPHANIE B.; MENDONCA, BERENICE B.; KAISER, URSULA B.; LATRONICO, ANA CLAUDIA. A GPR54-activating mutation in a patient with central precocious puberty. New England Journal of Medicine, v. 358, n. 7, p. 709-715, . (05/04726-0)

CAETANO, L. A.; SANTANA, L. S.; COSTA-RIQUETTO, A. D.; LERARIO, A. M.; NERY, M.; NOGUEIRA, G. F.; ORTEGA, C. D.; ROCHA, M. S.; JORGE, A. A. L.; TELES, M. G.. PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease. Clinical Genetics, v. 93, n. 2, p. 382-386, . Web of Science Citations: 3. (13/02162-8, 13/19920-2)

MONTENEGRO, JR., RENAN MAGALHAES; COSTA-RIQUETTO, ALINE DANTAS; FERNANDES, VIRGINIA OLIVEIRA; DIAS RANGEL MONTENEGRO, ANA PAULA; DE SANTANA, LUCAS SANTOS; DE LIMA JORGE, ALEXANDER AUGUSTO; DE AZEVEDO SOUZA KARBAGE, LIA BEATRIZ; AGUIAR, LINDENBERG BARBOSA; COSTA CARVALHO, FRANCISCO HERLANIO; TELES, MILENA GURGEL; et al. Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred. FRONTIERS IN ENDOCRINOLOGY, v. 9, . Web of Science Citations: 2. (13/19920-2, 13/02162-8)

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