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Suely Kazue Nagahashi Marie
Suely Kazue Nagahashi Marie
Professor Associado de Medicina
Verified email at usp.br
Title
Cited by
Cited by
Year
An integrated genomic analysis of human glioblastoma multiforme
DW Parsons, S Jones, X Zhang, JCH Lin, RJ Leary, P Angenendt, ...
science 321 (5897), 1807-1812, 2008
67862008
Detection of circulating tumor DNA in early-and late-stage human malignancies
C Bettegowda, M Sausen, RJ Leary, I Kinde, Y Wang, N Agrawal, ...
Science translational medicine 6 (224), 224ra24-224ra24, 2014
45742014
Altered telomeres in tumors with ATRX and DAXX mutations
CM Heaphy, RF De Wilde, Y Jiao, AP Klein, BH Edil, C Shi, C Bettegowda, ...
Science 333 (6041), 425-425, 2011
11632011
SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas
AJ Bass, H Watanabe, CH Mermel, S Yu, S Perner, RG Verhaak, SY Kim, ...
Nature genetics 41 (11), 1238-1242, 2009
10572009
The genetic landscape of the childhood cancer medulloblastoma
DW Parsons, M Li, X Zhang, S Jones, RJ Leary, JCH Lin, SM Boca, ...
science 331 (6016), 435-439, 2011
8002011
Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas
Y Jiao, PJ Killela, ZJ Reitman, BA Rasheed, CM Heaphy, RF De Wilde, ...
Oncotarget 3 (7), 709, 2012
6752012
Transcriptomic analysis of purified human cortical microglia reveals age-associated changes
TF Galatro, IR Holtman, AM Lerario, ID Vainchtein, N Brouwer, PR Sola, ...
Nature neuroscience 20 (8), 1162-1171, 2017
6222017
Mutations in CIC and FUBP1 contribute to human oligodendroglioma
C Bettegowda, N Agrawal, Y Jiao, M Sausen, LD Wood, RH Hruban, ...
Science 333 (6048), 1453-1455, 2011
6002011
Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord
Y Wang, S Springer, M Zhang, KW McMahon, I Kinde, L Dobbyn, J Ptak, ...
Proceedings of the National Academy of Sciences 112 (31), 9704-9709, 2015
4132015
Evaluation of DNA from the Papanicolaou test to detect ovarian and endometrial cancers
I Kinde, C Bettegowda, Y Wang, J Wu, N Agrawal, IM Shih, R Kurman, ...
Science translational medicine 5 (167), 167ra4-167ra4, 2013
4052013
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)
S Rosemberg, SKN Marie, S Kliemann
Pediatric neurology 11 (1), 50-56, 1994
2411994
Selection of suitable housekeeping genes for expression analysis in glioblastoma using quantitative RT-PCR
V Valente, SA Teixeira, L Neder, OK Okamoto, SM Oba-Shinjo, ...
BMC molecular biology 10, 1-11, 2009
231*2009
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
2271996
Gene expression profile analysis of primary glioblastomas and non-neoplastic brain tissue: identification of potential target genes by oligonucleotide microarray and real-time …
CA Scrideli, CG Carlotti, OK Okamoto, VS Andrade, MAA Cortez, ...
Journal of neuro-oncology 88, 281-291, 2008
2202008
PIK3CA Gene Mutations in Pediatric and Adult Glioblastoma Multiforme
GL Gallia, V Rand, IM Siu, CG Eberhart, CD James, SKN Marie, ...
Molecular Cancer Research 4 (10), 709-714, 2006
2082006
Therapeutic impact of cytoreductive surgery and irradiation of posterior fossa ependymoma in the molecular era: a retrospective multicohort analysis
V Ramaswamy, T Hielscher, SC Mack, A Lassaletta, T Lin, KW Pajtler, ...
Journal of Clinical Oncology 34 (21), 2468, 2016
1872016
Effects of somatosensory stimulation on motor function in chronic cortico-subcortical strokes
AB Conforto, LG Cohen, RL Santos, M Scaff, SKN Marie
Journal of neurology 254, 333-339, 2007
1852007
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M Zatz, SK Marie, A Cerqueira, M Vainzof, RCM Pavanello, ...
American journal of medical genetics 77 (2), 155-161, 1998
1851998
Metabolism and brain cancer
SKN Marie, SMO Shinjo
Clinics 66, 33-43, 2011
1842011
New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
TC Pan, RZ Zhang, DG Sudano, SK Marie, CG Bönnemann, ML Chu
The American Journal of Human Genetics 73 (2), 355-369, 2003
1832003
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