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| 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 | 652 | 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 | 596 | 1999 |
| Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage Nature biotechnology 29 (12), 1132-1144, 2011 | 588 | 2011 |
| Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome L Pereira, M D'Alessio, F Ramirez, J R. Lynch, B Sykes, T Pangilinan, ... Human molecular genetics 2 (7), 961-968, 1993 | 495 | 1993 |
| 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 | 471 | 1997 |
| Aberrant patterns of X chromosome inactivation in bovine clones F Xue, XC Tian, F Du, C Kubota, M Taneja, A Dinnyes, Y Dai, H Levine, ... Nature genetics 31 (2), 216-220, 2002 | 399 | 2002 |
| Fibrillins 1 and 2 perform partially overlapping functions during aortic development L Carta, L Pereira, E Arteaga-Solis, SY Lee-Arteaga, B Lenart, B Starcher, ... Journal of Biological Chemistry 281 (12), 8016-8023, 2006 | 287 | 2006 |
| Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic amplicons. G Nijbroek, S Sood, I McIntosh, CA Francomano, E Bull, L Pereira, ... American journal of human genetics 57 (1), 8, 1995 | 287 | 1995 |
| Quality control guidelines for clinical-grade human induced pluripotent stem cell lines S Sullivan, GN Stacey, C Akazawa, N Aoyama, R Baptista, P Bedford, ... Regenerative medicine 13 (7), 859-866, 2018 | 195 | 2018 |
| Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1) EH Schuchman, O Levran, LV Pereira, RJ Desnick Genomics 12 (2), 197-205, 1992 | 178 | 1992 |
| A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome L Pereira, O Levran, F Ramirez, JR Lynch, B Sykes, RE Pyeritz, HC Dietz New England Journal of Medicine 331 (3), 148-153, 1994 | 171 | 1994 |
| The fibrillins F Ramirez, L Pereira The international journal of biochemistry & cell biology 31 (2), 255-259, 1999 | 155 | 1999 |
| Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome JC Moreira de Mello, ÉSS Araújo, R Stabellini, AM Fraga, JES Souza, ... PloS one 5 (6), e10947, 2010 | 154 | 2010 |
| 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 | 139 | 2004 |
| Human dental pulp cells: a new source of cell therapy in a mouse model of compressive spinal cord injury FM de Almeida, SA Marques, BS Ramalho, RF Rodrigues, DV Cadilhe, ... Journal of neurotrauma 28 (9), 1939-1949, 2011 | 113 | 2011 |
| A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression BL Lima, EJC Santos, GR Fernandes, C Merkel, MRB Mello, JPA Gomes, ... PloS one 5 (11), e14136, 2010 | 99 | 2010 |
| Early X chromosome inactivation during human preimplantation development revealed by single-cell RNA-sequencing JC Moreira de Mello, GR Fernandes, MD Vibranovski, LV Pereira Scientific reports 7 (1), 10794, 2017 | 94 | 2017 |
| A importância do uso das células tronco para a saúde pública LV Pereira Ciência & saúde coletiva 13, 07-14, 2008 | 87 | 2008 |
| A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy MRP Bueno, ES Moreira, M Vainzof, J Chamberlain, SK Marle, L Pereira, ... Human molecular genetics 4 (7), 1163-1167, 1995 | 82 | 1995 |
