Advanced search
Start date

Marília Moreira Montenegro

CV Lattes

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

graduation at Biomedicina from Faculdades Metropolitanas Unidas (2004), master's at Medicina (Pediatria) from Instituto da criança, HC-FMUSP (2012) and doctorate at Patologia from Faculdade de Medicina da Universidade de São Paulo (2017). Has experience in Genetics, acting on the following subjects: mlpa, cariótipo, citogenômica, duplo y and sd. williams-beuren. (Source: Lattes Curriculum)

News published in Agência FAPESP Newsletter about the researcher
Articles published in other media outlets (0 total):
More itemsLess items
Scholarships in Brazil
FAPESP support in numbers * Updated January 22, 2022
Total / Available in English
1 / 1   Completed scholarships in Brazil

Associated processes
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 (7)
(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)

DUTRA, ROBERTA L.; PIAZZON, FLAVIA B.; ZANARDO, EVELIN A.; MOURA MACHADO COSTA, THAIS VIRGINIA; MONTENEGRO, MARILIA M.; NOVO-FILHO, GIL M.; DIAS, ALEXANDRE T.; NASCIMENTO, AMOM M.; KIM, CHONG AE; KULIKOWSKI, LESLIE D.. Rare Genomic Rearrangement in a Boy with Williams-Beuren Syndrome Associated to XYY Syndrome and Intriguing Behavior. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 167, n. 12, p. 3197-3203, . Web of Science Citations: 1. (09/53105-9)

CERONI, J. R. M.; DUTRA, R. L.; HONJO, R. S.; LLERENA, JR., J. C.; ACOSTA, A. X.; MEDEIROS, P. F. V.; GALERA, M. F.; ZANARDO, E. A.; PIAZZON, F. B.; DIAS, A. T.; et al. A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability. SCIENTIFIC REPORTS, v. 8, . Web of Science Citations: 0. (09/53105-9, 09/53864-7, 14/11572-8, 08/58238-4, 12/25247-6)

GASPARINI, YANCA; MONTENEGRO, MARILIA M.; NOVO-FILHO, GIL M.; CERONI, JOSE R. M.; HONJO, RACHEL S.; ZANARDO, EVELIN A.; DIAS, ALEXANDRE T.; NASCIMENTO, AMOM M.; COSTA, THAIS V. M. M.; MADIA, FABRICIA A.; et al. Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines. Cytogenetic and Genome Research, v. 157, n. 3, p. 153-157, . Web of Science Citations: 1. (16/09452-0, 16/19360-5)

NOVO-FILHO, GIL M.; CARVALHO, GLEYSON F. S.; NASCIMENTO, AMOM M.; MONTENEGRO, MARILIA M.; DAMASCENO, JULLIAN G.; ZANARDO, EVELIN A.; CHEHIMI, SAMAR N.; OLIVEIRA, YANCA G.; DIAS, ALEXANDRE T.; KIM, CHONG A.; et al. Identifying NAHR mechanism between two distinct Alu elements through breakpoint junction mapping by NGS. META GENE, v. 24, . Web of Science Citations: 0. (16/09452-0)

CHEHIMI, SAMAR N.; ZANARDO, EVELIN A.; CERONI, JOSE R. M.; NASCIMENTO, AMOM M.; MADIA, FABRICIA A. R.; DIAS, ALEXANDRE T.; FILHO, GIL M. N.; MONTENEGRO, MARLIA M.; DAMASCENO, JULLIAN; COSTA, THAS V. M. M.; et al. Breakpoint delineation in 5p- patients leads to new insights about microcephaly and the typical high-pitched cry. MOLECULAR GENETICS & GENOMIC MEDICINE, . Web of Science Citations: 0. (16/09452-0)

MONTENEGRO, MARILIA M.; QUAIO, CAIO R.; PALMEIRA, PATRICIA; GASPARINI, YANCA; RANGEL-SANTOS, ANDREIA; DAMASCENO, JULIAN; NOVAK, ESTELA M.; GIMENEZ, THAMIRES M.; YAMAMOTO, GUILHERME L.; RONJO, RACHEL S.; et al. Gene expression profile suggesting immunological dysregulation in two Brazilian Bloom's syndrome cases. MOLECULAR GENETICS & GENOMIC MEDICINE, . Web of Science Citations: 0. (17/08981-1)

Please report errors in researcher information by writing to:

Report errors in this page

Error details: