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Victor Cavalcanti Pardini

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
1997 · G. Velho, H. Blanché, et al. · Diabetologia · 266
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Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
1998 · J.-C. Chèvre, E. H. Hani, et al. · Diabetologia · 143
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Leptin Levels, β-Cell Function, and Insulin Sensitivity in Families with Congenital and Acquired Generalized Lipoatropic Diabetes1
1998 · Victor C. Pardini, Ivana M. N. Victória, et al. · The Journal of Clinical Endocrinology & Metabolism · 86
Clinical and molecular aspects of Berardinelli–Seip Congenital Lipodystrophy (BSCL)
2009 · Karina Braga Gomes, Victor Cavalcanti Pardini, et al. · Clinica Chimica Acta · 43
Mutations in the Seipin and AGPAT2 Genes Clustering in Consanguineous Families with Berardinelli-Seip Congenital Lipodystrophy from Two Separate Geographical Regions of Brazil
2004 · Karina Braga Gomes, Ana Paula Fernandes, et al. · The Journal of Clinical Endocrinology & Metabolism · 39
Leptin Levels, -Cell Function, and Insulin Sensitivity in Families with Congenital and Acquired Generalized Lipoatropic Diabetes
1998 · V. C. Pardini · The Journal of Clinical Endocrinology & Metabolism · 37
Updated Brazilian STR allele frequency data using over 100,000 individuals: An analysis of CSF1PO, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, FGA, Penta D, Penta E, TH01, TPOX and vWA loci
2011 · Vitor Rezende da Costa Aguiar, Eldamária de Vargas Wolfgramm, et al. · Forensic Science International Genetics · 29
Frequency of islet cell autoantibodies (IA-2 and GAD) in young Brazilian type 1 diabetes patients
1999 · V.C. Pardini, D.M. Mourão, et al. · Brazilian Journal of Medical and Biological Research · 28
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Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli–Seip congenital lipodystrophy patients
2005 · K. B. Gomes, V. Cavalcanti Pardini, et al. · Journal of Inherited Metabolic Disease · 25
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Frequency of FMR1 premutation in individuals with ataxia and/or tremorand/or parkinsonism
2008 · A.H.O. Reis, A.C.S. Ferreira, et al. · Genetics and Molecular Research · 23
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An Automated Fluorescent Single-Strand Conformation Polymorphism Technique for Screening Mutations in the Hepatocyte Nuclear Factor-1α Gene (Maturity-Onset Diabetes of the Young)
1997 · Philippe Boutin, Jean Claude Chévre, et al. · Diabetes · 19
Prevalence of C282Y and H63D mutations in the HFE gene of Brazilian individuals with clinical suspicion of hereditary hemochromatosis
2008 · Alessandro C. S. Ferreira, Vanessa C. Oliveira, et al. · Revista Brasileira de Hematologia e Hemoterapia · 17
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Antibodies to Bovine Serum Albumin in Brazilian Children and Young Adults With IDDM
1996 · Victor C Pardini, José G H Vieira, et al. · Diabetes Care · 17
Cryopreservation does not alter karyotype, multipotency, or NANOG/SOX2 gene expression of amniotic fluid mesenchymal stem cells
2012 · P.C. Ângelo, A.C.S. Ferreira, et al. · Genetics and Molecular Research · 16
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Epidemic Spread of SARS-CoV-2 Lineage B.1.1.7 in Brazil
2021 · Filipe R. R. Moreira, Diego M. Bonfim, et al. · Viruses · 15
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Type 1 diabetes susceptibility determined by HLA alleles and CTLA-4 and insulin genes polymorphisms in Brazilians
2009 · Alessandro Clayton Souza Ferreira, Karina Braga Gomes, et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 15
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Assessment of microsatellite instability in colorectal cancer patients from Brazil
2009 · Sinara M. O. Leite, Karina B. Gomes, et al. · Molecular Biology Reports · 12
Mutações predisponentes à trombofilia em indivíduos de Minas Gerais - Brasil com suspeita clínica de trombose
2009 · Sabrina P. Guimarães, Jerusa B. B. Soares, et al. · Revista Brasileira de Hematologia e Hemoterapia · 8
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Frequency of the S65C mutation in the hemochromatosis gene in Brazil
2009 · V.C. Oliveira, F.A. Caxito, et al. · Genetics and Molecular Research · 8
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Fetal hemoglobin levels are related to metabolic control in diabetic subjects
1999 · V.C. Pardini, I.M.N. Victória, et al. · Brazilian Journal of Medical and Biological Research · 8
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Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli‐Seip Congenital Lipodystrophy in a Cluster from Brazil
2007 · K. B. Gomes, V. C. Pardini, et al. · Annals of Human Genetics · 6
Isolamento, diferenciação e aspectos bioquímicos de células-tronco de líquido amniótico
2008 · Antônio Carlos Vieira Cabral, Patrícia Caroline Ângelo, et al. · Revista da Associação Médica Brasileira · 4
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Specific insulin and proinsulin secretion in glucokinase-deficient individuals
1999 · V.C. Pardini, G. Velho, et al. · Brazilian Journal of Medical and Biological Research · 2
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A novel RT-qPCR assay for detection of SARS-CoV-2 variantsbased on RhAmp technology (IDT technologies) v1
2021 · Victor Emmanuel Viana Geddes, Filipe Moreira, et al. · 1
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Corrigendum to “Updated Brazilian STR allele frequency data using over 100,000 individuals: An analysis of CSF1PO, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, FGA, Penta D, Penta E, TH01, TPOX and vWA loci” [Forensic Sci. Int.: Genet. 6 (4) (2012) 504–509]
2012 · Vitor Rezende da Costa Aguiar, Eldamária de Vargas Wolfgramm, et al. · Forensic Science International Genetics · 1
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Works count: 39
Citation count: 870
H-index: 15
I10-index: 17
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