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Victor Evangelista de Faria Ferraz

Observed names: Evangelista de Faria Ferraz, Victor, Ferraz, Victor, Ferraz, Victor Evangelista De Faria, V. E. F. Ferraz, V.E.F. Ferraz, Victor E. F. Ferraz, Victor E. Faria Ferraz, Victor E.F. Ferraz, Victor EF Ferraz, Victor EF. Ferraz, Victor Evangelista De Faria Ferraz, Victor Evangelista F. Ferraz, Victor Evangelista Faria Ferraz, Victor Evangelista Ferraz, Victor Ferraz
Observed institutions: Universidade de Ribeirão Preto, Universidade de São Paulo, Hospital de Clínicas de Porto Alegre, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Clinics Hospital of Ribeirão Preto, Universidade Estadual Paulista (Unesp)
ORCID: 0000-0003-0337-4588
Observed ORCID: 0000-0003-0337-4588
OpenAlex ID: A5014365256
Mucopolysaccharidoses in Brazil: What happens from birth to biochemical diagnosis?
2008 · Taiane Vieira, Ida Schwartz, et al. · American Journal of Medical Genetics Part A · 87
Genetics and genomics in Brazil: a promising future
2014 · Maria Rita Passos‐Bueno, Debora Bertola, et al. · Molecular Genetics & Genomic Medicine · 83
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Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes
2015 · Shannon Marchegiani, Taylor Davis, et al. · The American Journal of Human Genetics · 73
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Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population
2020 · Simone da Costa e Silva Carvalho, Nathalia Moreno Cury, et al. · BMC Medical Genomics · 52
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Genetic education, knowledge and experiences between nurses and physicians in primary care in Brazil: A cross‐sectional study
2016 · Luís Carlos Lopes‐Júnior, Paulo Marcondes Carvalho Júnior, et al. · Nursing and Health Sciences · 50
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Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN)
2022 · Têmis Maria Félix, Bibiana Mello de Oliveira, et al. · Orphanet Journal of Rare Diseases · 49
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Clinical Genetics in Developing Countries: The Case of Brazil
2004 · Antonia Paula Marques-de-Faria, Victor E. Faria Ferraz, et al. · Public Health Genomics · 47
Health Policies for Rare Disease Patients: A Scoping Review
2022 · Luís Carlos Lopes-Júnior, Victor Evangelista Faria Ferraz, et al. · International Journal of Environmental Research and Public Health · 36
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TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families
2014 · Nathalia M Cury, Victor EF Ferraz, et al. · Hereditary Cancer in Clinical Practice · 31
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Aggravation of Eyelid and Conjunctival Malignancies Following Photodynamic Therapy in DeSanctis-Cacchione Syndrome
2006 · Fernando Procianoy, Antonio A.V. Cruz, et al. · Ophthalmic Plastic and Reconstructive Surgery · 24
Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1
2022 · Luiz Guilherme Darrigo Junior, Victor Evangelista de Faria Ferraz, et al. · Brain and Behavior · 23
Ablepharon-Macrostomia syndrome: First report of familial occurrence
2000 · Victor E.F. Ferraz, D�bora G. Melo, et al. · American Journal of Medical Genetics · 23
Congenital Shortening of the Anterior Lamella of All Eyelids
1995 · Antonio Augusto V. Cruz, Fernando C. Guimarães, et al. · Ophthalmic Plastic and Reconstructive Surgery · 22
Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network
2024 · Bibiana Mello de Oliveira, Filipe Andrade Bernardi, et al. · Orphanet Journal of Rare Diseases · 21
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Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study
2016 · Milena Flória-Santos, Luís Carlos Lopes-Júnior, et al. · Genetics and Molecular Biology · 21
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Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil
2015 · Mônica Barbosa de Melo, Anil K. Mandal, et al. · PLoS ONE · 21
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Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies
2024 · Dafne Dain Gandelman Horovitz, Têmis Maria Félix, et al. · Genes · 17
Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach
2020 · Reginaldo Cruz Alves Rosa, Jessica Oliveira Santis, et al. · Gynecologic Oncology · 14
Perfil de Competência em Genética para Médicos do Brasil: uma Proposta da Sociedade Brasileira de Genética Médica e Genômica
2019 · Débora Gusmão Melo, André Anjos da Silva, et al. · Revista Brasileira de Educação Médica · 14
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Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries
2012 · Erika Maria Monteiro Santos, Mev Dominguez Valentin, et al. · BMC Cancer · 14
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Familial Occurrence of Ablepharon Macrostomia Syndrome: Eyelid Structure and Surgical Considerations
2000 · Antonio A. V. Cruz, Carmo A. Souza, et al. · Archives of Ophthalmology · 14
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers
2015 · Mariana Fitarelli-Kiehl, Juliana Giacomazzi, et al. · Familial Cancer · 11
Percepção de causas e risco oncológico, história familiar e comportamentos preventivos de usuários em aconselhamento oncogenético
2013 · Barreto de Castro e Silva, Tiago, MacDonald, Deborah J., et al. · Redalyc (Universidad Autónoma del Estado de México) · 10
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS–FREM complex disorders
2013 · Denny Schanze, Magdalena Harakalova, et al. · American Journal of Medical Genetics Part A · 9
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect
2002 · Greice Andreotti De Molfetta, Temis Maria Felix, et al. · Arquivos de Neuro-Psiquiatria · 8
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Works count: 66
Citation count: 845
H-index: 17
I10-index: 23
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