Victor Ferraz

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Milena Jorge Simões FlóriaProfessor Doutor, Universidade de São PauloVerified email at usp.br
Ida SchwartzProfessor, Federal University of Rio Grande do SulVerified email at hcpa.edu.br
Antonia Paula Marques de FariaProfessor Associado, Departamento de Genética Médica, FCM-UNICAMPVerified email at fcm.unicamp.br
Temis Maria FelixHospital de Clínicas de Porto AlegreVerified email at hcpa.edu.br
Dirce Maria CarraroHead, Genomics and Molecular Biology Laboratory, AC Camargo HospitalVerified email at cipe.accamargo.org.br
Roberto GiuglianiHead of Rare Diseases DASA, Founder CASA DOS RAROS, Med Genet Serv HCPA, Dep Genetics & PPGBM UFRGSVerified email at hcpa.edu.br
Débora Gusmão MeloProfessora de Genética Médica, Universidade Federal de São Paulo, Escola Paulista de MedicinaVerified email at unifesp.br
Fernando ChahudProfessor of Pathology, University of São PauloVerified email at fmrp.usp.br
Domingos AlvesDepartamento de Medicina Social, FMRP -USPVerified email at fmrp.usp.br
decio brunoniProfessor of Medical Genetics, Universidade Presbiteriana Mackenzie Verified email at mackenzie.br
Carlos Alberto Nogueira-de-AlmeidaProfessor Adjunto da Universidade Federal de São CarlosVerified email at ufscar.br
Juliana Maria Ferraz SallumProfa Livre Docente da Pós graduação Oftalmologia da UNIFESPVerified email at pobox.com
Ivan Maynart TavaresProfessor and Chair, Ophthalmology Dept., Universidade Federal de Sao Paulo - Escola Paulista deVerified email at unifesp.br
RUBENS BELFORT JRUniversidade Federal de São Paulo - Escola Paulista de Medicina -Vision InstituteVerified email at clinicabelfort.com.br
Tereza Cristina Scatena VillaEscola de Enfermagem de Ribeirão Preto, USPVerified email at eerp.usp.br
Israel GomyUniversidade de São PauloVerified email at usp.br
Benedito Mauro RossiProfessor de Oncologia, Pós-Graduação, Hospital Sírio Libanês, São PauloVerified email at oncocentro.com
Oliveira LP; Ligia Petrolini de Oliveira;...Docente, Medicina, USCSVerified email at prof.uscs.edu.br
Ester Silveira RamosFaculdade de Medicina de Ribeirão Preto-Universidade de São PauloVerified email at fmrp.usp.br
Camila Maria CenziDoutoranda em Enfermagem Fundamental Universidade de São PauloVerified email at usp.br

Victor Ferraz

Professor - Departamento de Genética da Faculdade de Medicina de Ribeirão Preto, Universidade de São

Verified email at usp.br

medical genetics hereditary cancer genetic deafness ophthalmic genetics


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Genetic services and testing in Brazil DDG Horovitz, VE de Faria Ferraz, S Dain, AP Marques-de-Faria Journal of community genetics 4, 355-375, 2013	130	2013
Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis? T Vieira, I Schwartz, V Munoz, L Pinto, C Steiner, M Ribeiro, R Boy, ... American Journal of Medical Genetics Part A 146 (13), 1741-1747, 2008	127	2008
Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and Barber-Say syndromes S Marchegiani, T Davis, F Tessadori, G Van Haaften, F Brancati, ... The American Journal of Human Genetics 97 (1), 99-110, 2015	77	2015
Genetics and genomics in Brazil: a promising future MR Passos-Bueno, D Bertola, DDG Horovitz, VE de Faria Ferraz, LA Brito Molecular genetics & genomic medicine 2 (4), 280, 2014	77	2014
Clinical genetics in developing countries: the case of Brazil AP Marques-de-Faria, VEF Ferraz, AX Acosta, D Brunoni Public Health Genomics 7 (2-3), 95-105, 2004	63	2004
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population S da Costa e Silva Carvalho, NM Cury, DB Brotto, LF De Araujo, ... BMC medical genomics 13, 1-24, 2020	55	2020
Genetic education, knowledge and experiences between nurses and physicians in primary care in Brazil: A cross‐sectional study LC Lopes‐Júnior, PM Carvalho Junior, VE de Faria Ferraz, ... Nursing & health sciences 19 (1), 66-74, 2017	51	2017
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families NM Cury, VEF Ferraz, WA Silva Hereditary cancer in clinical practice 12, 1-8, 2014	40	2014
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil MB de Melo, AK Mandal, IM Tavares, MH Ali, M Kabra, ... PLoS One 10 (5), e0127147, 2015	29	2015
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN) TM Félix, BM de Oliveira, M Artifon, I Carvalho, FA Bernardi, IVD Schwartz, ... Orphanet Journal of Rare Diseases 17 (1), 84, 2022	27	2022
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 … M Flória-Santos, LC Lopes-Júnior, LM Alvarenga, MS Ribeiro, VEF Ferraz, ... Genetics and molecular biology 39, 178-183, 2016	27	2016
Ablepharon‐macrostomia syndrome: First report of familial occurrence VEF Ferraz, DG Melo, SE Hansing, AAV Cruz, JM Pina‐Neto American journal of medical genetics 94 (4), 281-283, 2000	27	2000
Obesidade infanto-juvenil: uma proposta de classificação clínica CAN de Almeida, MEC Baptista, GAN de Almeida, VE de Faria Ferraz Pediatria (São Paulo) 26 (4), 257-67, 2004	26	2004
Percepção de causas e risco oncológico, história familiar e comportamentos preventivos de usuários em aconselhamento oncogenético TBC Silva, DJ MacDonald, VEF Ferraz, LC Nascimento, CB Santos, ... Revista da Escola de Enfermagem da USP 47, 377-384, 2013	23	2013
Congenital shortening of the anterior lamella of all eyelids: the so-called ablepharon macrostomia syndrome AAV Cruz, FC Guimarães, HN Obeid, VEF Ferraz, TR Noce, FE Martinez Ophthalmic Plastic & Reconstructive Surgery 11 (4), 284-287, 1995	23	1995
Aggravation of eyelid and conjunctival malignancies following photodynamic therapy in DeSanctis-Cacchione syndrome F Procianoy, AAV Cruz, A Baccega, V Ferraz, F Chahud Ophthalmic Plastic & Reconstructive Surgery 22 (6), 498-499, 2006	21	2006
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect GA De Molfetta, TM Felix, M Riegel, VEF Ferraz, JM Pina Neto Arquivos de Neuro-Psiquiatria 60, 1011-1014, 2002	20	2002
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries EM Monteiro Santos, MD Valentin, F Carneiro, LP de Oliveira, ... BMC cancer 12, 1-9, 2012	17	2012
Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1 LG Darrigo Junior, VEF Ferraz, MCV Cormedi, LHH Araujo, ... Brain and Behavior 12 (6), e2599, 2022	16	2022
Familial occurrence of ablepharon macrostomia syndrome: eyelid structure and surgical considerations AAV Cruz, CA Souza, VEF Ferraz, CAC Monteiro, FA Martins Archives of ophthalmology 118 (3), 429-430, 2000	16	2000

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