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André Uchimura Bastos

CV Lattes ResearcherID ORCID


Universidade de São Paulo (USP). Instituto de Ciências Biomédicas (ICB)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

graduation at Licenciatura Plena em Ciências Biológicas from Centro Universitário Fundação Santo André (2009), graduation at Ciências Biológicas from Centro Universitário Fundação Santo André (2010) and doctorate at Biologia Estrutural e Funcional from Universidade Federal de São Paulo (2016). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: rearranjos ret/ptc, carcinoma papilífero da tiróide, braf, men2a and medullary thyroid carcinoma. (Source: Lattes Curriculum)

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Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (3)
(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)

VIEIRA CORDIOLI, MARIA ISABEL C.; MORAES, LAIS; BASTOS, ANDRE U.; BESSON, PALOMA; DE SEIXAS ALVES, MARIA TERESA; DELCELO, ROSANA; MONTE, OSMAR; LONGUI, CARLOS; CURY, ADRIANO NAMO; CERUTTI, JANETE M.. Fusion Oncogenes Are the Main Genetic Events Found in Sporadic Papillary Thyroid Carcinomas from Children. THYROID, v. 27, n. 2, p. 182-188, . Web of Science Citations: 14. (13/03867-5)

PEDROSO, JOSE LUIZ; MUNFORD, VERIDIANA; BASTOS, ANDRE UCHIMURA; DE CASTRO, LIGIA PEREIRA; MARUSSI, VICTOR HUGO ROCHA; SILVA, GISELE SAMPAIO; ARITA, JULIANA HARUMI; MENCK, CARLOS F. M.; BARSOTTINI, ORLANDO G.. LMNB1 mutation causes cerebellar involvement and a genome instability defect. JOURNAL OF THE NEUROLOGICAL SCIENCES, v. 379, p. 249-252, . Web of Science Citations: 0. (14/15982-6, 13/21075-9)

OLIVEIRA, MARIANA N. L.; HEMERLY, JEFFERSON P.; BASTOS, ANDRE U.; TAMANAHA, ROSANA; LATINI, FLAVIA R. M.; CAMACHO, CLEBER P.; IMPELLIZZERI, ANELISE; MACIEL, RUI M. B.; CERUTTI, JANETE M.. The RET p.G533C Mutation Confers Predisposition to Multiple Endocrine Neoplasia Type 2A in a Brazilian Kindred and Is Able to Induce a Malignant Phenotype In Vitro and In Vivo. THYROID, v. 21, n. 9, p. 975-985, . Web of Science Citations: 18. (06/60402-1, 09/11257-7, 05/60330-8)

HEMERLY, JEFFERSON PESSOA; BASTOS, ANDRE UCHIMURA; CERUTTI, JANETE M.. Identification of several novel non-p.R132 IDH1 variants in thyroid carcinomas. EUROPEAN JOURNAL OF ENDOCRINOLOGY, v. 163, n. 5, p. 747-755, . Web of Science Citations: 53. (09/11257-7, 05/60330-8)

BASTOS, ANDRE UCHIMURA; DE JESUS, ANA CAROLINA; CERUTTI, JANETE MARIA. ETV6-NTRK3 and STRN-ALK kinase fusions are recurrent events in papillary thyroid cancer of adult population. EUROPEAN JOURNAL OF ENDOCRINOLOGY, v. 178, n. 1, p. 83-91, . Web of Science Citations: 9. (13/03867-5, 12/06221-6)

CARREGOSA PINHEIRO DOS SANTOS, MARIA JOSE; BASTOS, ANDRE UCHIMURA; DA COSTA, VITOR RODRIGUES; DELCELO, ROSANA; LINDSEY, SUSAN CHOW; COLOZZA-GAMA, GABRIEL AVELAR; PENG, HONGZHUANG; RAUSCHER, III, FRANK J.; OLER, GISELE; CERUTTI, JANETE MARIA. LIMD2 Is Overexpressed in BRAF V600E-Positive Papillary Thyroid Carcinomas and Matched Lymph Node Metastases. ENDOCRINE PATHOLOGY, v. 29, n. 3, p. 222-230, . Web of Science Citations: 3. (14/06570-6)

DE JESUS PANIZA, ANA CAROLINA; MENDES, THAIS BIUDE; BORGES VIANNA, MATHEUS DUARTE; DIAS THOMAZ, DEBORA MOTA; CHIAPPINI, PAULA B. O.; COLAZZA-GAMA, GABRIEL A.; LINDSEY, SUSAN CHOW; DE CARVALHO, MARCOS BRASILINO; FERREIRA ALVES, VENANCIO AVANCINI; CURIONI, OTAVIO; et al. Revised criteria for diagnosis of NIFTP reveals a better correlation with tumor biological behavior. ENDOCRINE CONNECTIONS, v. 8, n. 11, p. 1529-1538, . Web of Science Citations: 0. (17/06487-0, 14/06570-6, 16/25784-2, 17/16315-1)

BASTOS, ANDRE UCHIMURA; OLER, GISELE; NAKANO NOZIMA, BRUNO HEIDI; MOYSES, RAQUEL AJUB; CERUTTI, JANETE MARIA. BRAF V600E and decreased NIS and TPO expression are associated with aggressiveness of a subgroup of papillary thyroid microcarcinoma. EUROPEAN JOURNAL OF ENDOCRINOLOGY, v. 173, n. 4, p. 525-540, . Web of Science Citations: 24. (12/02902-9, 11/10787-2, 13/03867-5)

VALENTE, F. O. F.; DA SILVA, M. R. DIAS; CAMACHO, C. P.; KUNII, I. S.; BASTOS, A. U.; DA FONSECA, C. C. N.; SIMIAO, H. P. C.; TAMANAHA, R.; MACIEL, R. M. B.; CERUTTI, J. M.. Comprehensive analysis of RET gene should be performed in patients with multiple endocrine neoplasia type 2 (MEN 2) syndrome and no apparent genotype- phenotype correlation: An appraisal of p.Y791F and p.C634Y RET mutations in five unrelated Brazilian families. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, v. 36, n. 11, p. 975-981, . Web of Science Citations: 10. (09/11257-7)

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