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Suely Kazue Nagahashi Marie
Suely Kazue Nagahashi Marie
Professor Associado de Medicina
E-mail confirmado em usp.br
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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
68352008
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
46772014
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
11762011
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
10542009
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
8082011
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
6822012
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
6432017
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
6062011
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
4262015
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
4132013
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
2391994
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
236*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
2242008
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
2142006
Metabolism and brain cancer
SKN Marie, SMO Shinjo
Clinics 66, 33-43, 2011
1912011
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
1912003
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 (3), 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
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