Advanced search
Start date
Betweenand

Ana Beatriz Alvarez Perez

CV Lattes GoogleMyCitations ResearcherID


Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Escola Paulista de Medicina (EPM)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

graduate at MEDICINA from Centro Universitário Lusíada (1982), master's at Morphology from Universidade Federal de São Paulo (1991) and ph.d. at Paediatrics from Universidade Federal de São Paulo (1997). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: genética médica, genética molecular, mutation, síndrome malformativa and homocisteína. (Source: Lattes Curriculum)

Research grants
FAPESP support in numbers * Updated August 01, 2020
Total / Available in English
6 / 2 Completed research grants

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 (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)

Publications3
Citations10
Cit./Article3.3
Data from Web of Science

COLOVATI, MILENY E. S.; BRAGAGNOLO, SILVIA; GUILHERME, ROBERTA S.; DANTAS, ANELISA G.; SOARES, MARIA F.; KIM, CHONG A.; PEREZ, ANA B. A.; MELARAGNO, MARIA I.. Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum Phenotype. Cytogenetic and Genome Research, v. 147, n. 2-3, p. 130-134, . Web of Science Citations: 4. (13/04623-2)

BRAGAGNOLO, SILVIA; COLOVATI, MILENY E. S.; SOUZA, MALU Z.; DANTAS, ANELISE G.; DE SOARES, MARIA F. F.; MELARAGNO, MARIA I.; PEREZ, ANA B.. Clinical and cytogenomic findings in OAV spectrum. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 176, n. 3, p. 638-648, . Web of Science Citations: 4. (13/04623-2, 13/19897-0)

BRAGAGNOLO, SILVIA; COLOVATI, MILENY E. S.; GUILHERME, ROBERTA S.; DANTAS, ANELISA G.; DE SOUZA, MALU ZAMARIOLLI; DE SOARES, MARIA F.; MELARAGNO, MARIA I.; PEREZ, ANA B.. Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy. Cytogenetic and Genome Research, v. 150, n. 1, p. 17-22, . Web of Science Citations: 2. (13/04623-2)

Please report errors in researcher information by writing to: cdi@fapesp.br.
X

Report errors in this page


Error details: