| A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B R Bashir, S Britton, T Strachan, S Keers, E Vafiadaki, M Lako, I Richard, ... Nature genetics 20 (1), 37-42, 1998 | 795 | 1998 |
| Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, ... Nature genetics 14 (2), 195-198, 1996 | 547 | 1996 |
| Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin ES Moreira, TJ Wiltshire, G Faulkner, A Nilforoushan, M Vainzof, ... Nature genetics 24 (2), 163-166, 2000 | 427 | 2000 |
| Caveolin-3 in muscular dystrophy EM McNally, E de Sá Moreira, DJ Duggan, CG Bönnemann, MP Lisanti, ... Human molecular genetics 7 (5), 871-877, 1998 | 287 | 1998 |
| The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ... Human molecular genetics 5 (12), 1963-1969, 1996 | 227 | 1996 |
| Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. EM McNally, MR Passos-Bueno, CG Bönnemann, M Vainzof, ... American journal of human genetics 59 (5), 1040, 1996 | 212 | 1996 |
| The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12 ES Moreira, M Vainzof, SK Marie, AL Sertie, M Zatz, MR Passos-Bueno The American Journal of Human Genetics 61 (1), 151-159, 1997 | 163 | 1997 |
| The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome AA Camargo, HPB Samaia, E Dias-Neto, DF Simão, IA Migotto, ... Proceedings of the National Academy of Sciences 98 (21), 12103-12108, 2001 | 160 | 2001 |
| Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E) CG Bönnemann, MR Passos-Bueno, EM McNally, M Vainzof, ES Moreira, ... Human molecular genetics 5 (12), 1953-1961, 1996 | 153 | 1996 |
| Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33–34 (LGMD2F) and indicates that there is at least one more subtype of … MR Passos-Bueno, ES Moreira, M Vainzof, SK Marie, M Zatz Human molecular genetics 5 (6), 815-820, 1996 | 136 | 1996 |
| Seven autosomal recessive limb‐girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G MR Passos‐Bueno, M Vainzof, ES Moreira, M Zatz American journal of medical genetics 82 (5), 392-398, 1999 | 134 | 1999 |
| Lithium reduces Gsk3b mRNA levels: implications for Alzheimer disease CT Mendes, FB Mury, E de Sá Moreira, FL Alberto, OV Forlenza, ... European archives of psychiatry and clinical neuroscience 259 (1), 16-22, 2009 | 128 | 2009 |
| A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22. 3 AL Sertie, M Quimby, ES Moreira, J Murray, M Zatz, SE Antonarakis, ... Human molecular genetics 5 (6), 843-847, 1996 | 110 | 1996 |
| Dysferlin protein analysis in limb-girdle muscular dystrophies M Vainzof, LVB Anderson, EM McNally, DB Davis, G Faulkner, G Valle, ... Journal of Molecular Neuroscience 17 (1), 71-80, 2001 | 102 | 2001 |
| A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma P Iughetti, O Suzuki, PHC Godoi, VAF Alves, AL Sertié, T Zorick, F Soares, ... Cancer research 61 (20), 7375-7378, 2001 | 98 | 2001 |
| 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 |
| Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. MR Passos-Bueno, ES Moreira, SK Marie, R Bashir, L Vasquez, DR Love, ... Journal of medical genetics 33 (2), 97-102, 1996 | 68 | 1996 |
| Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations ES Moreira, M Vainzof, OT Suzuki, RCM Pavanello, M Zatz, ... Journal of medical genetics 40 (2), e12-e12, 2003 | 67 | 2003 |
| A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian … ES Moreira, M Vainzof, SK Marie, V Nigro, M Zatz, MR Passos-Bueno Journal of medical genetics 35 (11), 951-953, 1998 | 65 | 1998 |
| Molecular screening for microdeletions at 9p22‐p24 and 11q23‐q24 in a large cohort of patients with trigonocephaly FS Jehee, D Johnson, LG Alonso, DP Cavalcanti, E de Sa Moreira, ... Clinical genetics 67 (6), 503-510, 2005 | 64 | 2005 |
Maria Rita Passos-BuenoDepartamento de Genetica e Biologia Evolutiva, Instituto de Biociências, Universidade de São PauloVerified email at ib.usp.br
