| Isolation and characterization of a population of immature dental pulp stem cells expressing OCT-4 and other embryonic stem cell markers I Kerkis, A Kerkis, D Dozortsev, GC Stukart-Parsons, SM Gomes Massironi, ... Cells Tissues Organs 184 (3-4), 105-116, 2007 | 662 | 2007 |
| Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1 L Pereira, SY Lee, B Gayraud, K Andrikopoulos, SD Shapiro, T Bunton, ... Proceedings of the National Academy of Sciences 96 (7), 3819-3823, 1999 | 606 | 1999 |
| Targetting of the gene encoding fibrillin–1 recapitulates the vascular aspect of Marfan syndrome L Pereira, K Andrikopoulos, J Tian, SY Lee, DR Keene, R Ono, ... Nature genetics 17 (2), 218-222, 1997 | 476 | 1997 |
| Crotamine is a novel cell‐penetrating protein from the venom of rattlesnake Crotalus durissus terrificus A Kerkis, I Kerkis, G Rádis‐Baptista, EB Oliveira, AM Vianna‐Morgante, ... The FASEB journal 18 (12), 1407-1409, 2004 | 146 | 2004 |
| Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15. 1→ p15. 4 L da Veiga Pereira, RJ Desnick, DA Adler, CM Disteche, EH Schuchman Genomics 9 (2), 229-234, 1991 | 114 | 1991 |
| A importância do uso das células tronco para a saúde pública LV Pereira Ciência & Saúde Coletiva 13, 07-14, 2008 | 89 | 2008 |
| Association between Parkinson's disease and glucocerebrosidase mutations in Brazil M Spitz, R Rozenberg, L da Veiga Pereira, ER Barbosa Parkinsonism & related disorders 14 (1), 58-62, 2008 | 74 | 2008 |
| The fibrillin‐Marfan syndrome connection F Ramirez, L Pereira, H Zhang, B Lee Bioessays 15 (9), 589-594, 1993 | 70 | 1993 |
| Establishment of new murine embryonic stem cell lines for the generation of mouse models of human genetic diseases MA Sukoyan, AY Kerkis, MRB Mello, IE Kerkis, JA Visintin, LV Pereira Brazilian Journal of Medical and Biological Research 35, 535-542, 2002 | 62 | 2002 |
| Ribozymes and the anti-gene therapy: how a catalytic RNA can be used to inhibit gene function AR Muotri, L da Veiga Pereira, L dos Reis Vasques, CFM Menck Gene 237 (2), 303-310, 1999 | 61 | 1999 |
| Marfan Syndrome: New Clues to Genotype—Phenotype Correlations F Ramirez, B Gayraud, L Pereira Annals of medicine 31 (3), 202-207, 1999 | 60 | 1999 |
| Clonagem: fatos e mitos LV Pereira Conferências, 2002 | 44 | 2002 |
| The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program R Rozenberg, LV Pereira São Paulo Medical Journal 119, 146-149, 2001 | 42 | 2001 |
| Detection of 12 new mutations in Gaucher disease Brazilian patients R Rozenberg, DC Fox, E Sobreira, LV Pereira Blood Cells, Molecules, and Diseases 37 (3), 204-209, 2006 | 35 | 2006 |
| High frequency of mutation G377S in Brazilian type 3 Gaucher disease patients R Rozenberg, FT Araujo, DC Fox, P Aranda, A Nonino, C Micheletti, ... Brazilian journal of medical and biological research 39, 1171-1179, 2006 | 31 | 2006 |
| Mutations of extracellular matrix components in vascular disease F Ramirez, L Pereira The Annals of thoracic surgery 67 (6), 1857-1858, 1999 | 24 | 1999 |
| A report from a workshop of the international stem cell banking initiative, held in collaboration of global alliance for iPSC therapies and the harvard stem cell institute … JH Kim, A Alderton, JM Crook, N Benvenisty, C Brandsten, M Firpo, ... Stem Cells 37 (9), 1130-1135, 2019 | 23 | 2019 |
| Diagnosis and molecular characterization of nonclassic forms of tay-sachs disease in Brazil R Rozenberg, F Kok, MG Burin, MC Sá Miranda, C Vasques, ... Journal of child neurology 21 (6), 540-544, 2006 | 23 | 2006 |
| X chromosome inactivation: how human are mice? LR Vasques, MN Klöckner, LV Pereira Cytogenetic and genome research 99 (1-4), 30-35, 2002 | 22 | 2002 |
| Identification of 8 new mutations in Brazilian families with Marfan syndrome ABA Perez, LV Pereira, D Brunoni, M Zatz, MR Passos‐Bueno Human Mutation 13 (1), 84-84, 1999 | 20 | 1999 |
