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S. Marie

Human Molecular Genetics, Molecular Cancer Research, American journal of medical genetics, Journal of Neuro-Oncology, American Journal of Human Genetics, Journal of Neurological Sciences, Cancer Immunity Show more
10
Role
Title
Level Year L/R
🐜 The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
12 auth. M. Vainzof, M. Passos-Bueno, M. Cánovas, E. Moreira, R. Pavanello, S. Marie, ... L. Anderson, C. Bönnemann, E. McNally, V. Nigro, L. Kunkel, M. Zatz 		7 1996
7
🐜
🐜 PIK3CA Gene Mutations in Pediatric and Adult Glioblastoma Multiforme
14 auth. G. Gallia, V. Rand, I. Siu, C. Eberhart, C. James, S. Marie, S. Oba-Shinjo, C. Carlotti, O. Caballero, A. Simpson, ... M. Brock, P. Massion, B. Carson, G. Riggins 		7 2006
7
🐜
🐬 The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.
M. Zatz, S. Marie, A. Cerqueira, M. Vainzof, R. Pavanello, M. Passos-Bueno 		7 1998
7
🐬
🐜 Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
12 auth. Carsten G. Bönnemann, Carsten G. Bönnemann, M. Passos-Bueno, Elizabeth M. McNally, M. Vainzof, E. S. Moreira, ... S. Marie, R. Pavanello, Satoru Noguchi, Eijiro Ozawa, Mayana Zatz, Louis M. Kunkel 		6 1996
6
🐜
🐜 Gene expression profile analysis of primary glioblastomas and non-neoplastic brain tissue: identification of potential target genes by oligonucleotide microarray and real-time quantitative PCR
12 auth. C. Scrideli, C. Carlotti, O. Okamoto, Vanessa da Silva S. Andrade, M. Cortez, F. Motta, ... A. K. Lucio-Eterovic, L. Neder, S. Rosemberg, S. Oba-Shinjo, S. Marie, L. Tone 		6 2008
6
🐜
🐜 High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.
9 auth. M. Zatz, S. Marie, M. Passos-Bueno, M. Vainzof, S. Campiotto, A. Cerqueira, ... C. Wijmenga, G. Padberg, R. Frants 		6 1995
6
🐜
🐬 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 AR LGMD.
M. Passos-Bueno, E. Moreira, M. Vainzof, S. Marie, M. Zatz 		6 1996
6
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🐬 Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
M. Vainzof, M. Passos-Bueno, R. Pavanello, S. Marie, A. Oliveira, M. Zatz 		6 1999
6
🐬
🐬 Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
M. Zatz, M. Passos-Bueno, A. Cerqueira, S. Marie, M. Vainzof, R. Pavanello 		6 1995
6
🐬
🐢 Cancer-testis (CT) antigen expression in medulloblastoma.
7 auth. S. Oba-Shinjo, O. Caballero, A. Jungbluth, S. Rosemberg, L. Old, A. Simpson, ... S. Marie 		5 2008
5
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