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Lucilene Arilho Ribeiro Bicudo

CV Lattes

Universidade de São Paulo (USP). Hospital de Reabilitação de Anomalias Craniofaciais (HRAC)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

Graduation at Biological Sciences from UNESP, Botucatu Campus (1993), a Master's Degree in Biological Sciences (Genetics) from UNESP, Campus de Botucatu (1996) and PhD in Biological Sciences (Molecular Genetics) from UNESP and New York University, USA (2000). Professor at the Federal University of Goias (UFG), teaching the subjects of Genetics and Molecular Genetics for Nutrition, Biomedicine and Nursing courses. Professor of the Postgraduate Program in Biological Sciences of the UFG and a collaborating professor of the IBB Graduate Program at Unesp, Botucatu. Experience in the field of Human and Medical Genetics, with emphasis on Molecular Genetics, working mainly on the following topics: genetics of midline defects, intellectual deficiency and congenital heart diseases; genomics and syndromology and mutation and developmental genes. (Source: Lattes Curriculum)

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Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (6)

(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)

Data from Web of Science

BERTOLACINI, C. D. P.; RIBEIRO-BICUDO, L. A.; PETRIN, A.; RICHIERI-COSTA, A.; MURRAY, J. C.. Clinical findings in patients with GLI2 mutations - phenotypic variability. Clinical Genetics, v. 81, n. 1, p. 70-75, . Web of Science Citations: 28.

PEREIRA BERTOLACINI, CLAUDIA DANIELLI; RICHIERI-COSTA, ANTONIO; RIBEIRO-BICUDO, LUCILENE ARILHO. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly. BRAIN & DEVELOPMENT, v. 32, n. 3, p. 217-222, . Web of Science Citations: 6.

GAMBA, BRUNO FAULIN; RICHIERI-COSTA, ANTONIO; COSTA, SILVIA; ROSENBERG, CARLA; RIBEIRO-BICUDO, LUCILENE ARILHO. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, v. 290, n. 6, p. 2213-2216, . Web of Science Citations: 8. (11/07012-9, 10/18740-2)

GAMBA, BRUNO F.; ROSENBERG, CARLA; COSTA, SILVIA; RICHIERI-COSTA, ANTONIO; RIBEIRO-BICUDO, LUCILENE A.. Cleft Lip/Palate, Short Stature, and Developmental Delay in a Boy with a 5.6-Mb Interstitial Deletion Involving 10p15.3p14. MOLECULAR SYNDROMOLOGY, v. 6, n. 1, p. 39-43, . Web of Science Citations: 1. (11/07012-9, 10/18740-2)

RIBEIRO, LUCILENE ARILHO; PEREIRA BERTOLACINI, CLAUDIA DANIELLI; QUIEZI, RODRIGO GONCALVES; RICHIERI-COSTA, ANTONIO. A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis. CLINICAL DYSMORPHOLOGY, v. 20, n. 3, p. 160-162, . Web of Science Citations: 1.

RICHIERI-COSTA, ANTONIO; RIBEIRO, LUCILENE ARILHO. Holoprosencephaly and Holoprosencephaly-Like Phenotypes: Review of Facial and Molecular Findings in Patients From a Craniofacial Hospital in Brazil. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, v. 154C, n. 1, p. 149-157, . Web of Science Citations: 7.

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