Suely Kazue Nagahashi Marie

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Zatz MUniversidade de S. PauloEmail verificata su usp.br
Maria Rita Passos-BuenoDepartamento de Genetica e Biologia Evolutiva, Instituto de Biociências, Universidade de São PauloEmail verificata su ib.usp.br
Mariz VainzofCentro de Estudos do Genoma Humano e Células Tronco, IBUSPEmail verificata su usp.br
Manoel Jacobsen TeixeiraProfessor Titular da Disciplina de Neurocirurgia da FMUSPEmail verificata su usp.br
Mari Cleide Sogayar Professor de Bioquímica, Universidade de São PauloEmail verificata su iq.usp.br
Carlos G Carlotti JrProfessor de Neurocirurgia FMRP-USPEmail verificata su fmrp.usp.br
Antonio GuimaraesProfessor de Sociologia, Universidade de São PauloEmail verificata su usp.br
scrideli OR scridelli OR scrilelliFaculdade de Medicina de Ribeirão Preto - Universidade de São PauloEmail verificata su fmrp.usp.br
Luiz Gonzaga ToneProfessor Titular Faculdade de Medicina de Ribeirão Preto-USPEmail verificata su fmrp.usp.br
Alzira CarvalhoProfessora de Neurologia da FMABCEmail verificata su fmabc.br
Ricardo NitriniProfessor de Neurologia, Faculdade de Medicina da Universidade de Sao PauloEmail verificata su usp.br
Oswaldo Keith OkamotoUniversidade de São PauloEmail verificata su usp.br
CLAUDIA DA COSTA LEITEProfessora Associada do Departamento de Radiologia da Faculdade de Medicina da Universidade de SaoEmail verificata su hc.fm.usp.br
Bert VogelsteinJohns HopkinsEmail verificata su jhmi.edu
Kenneth KinzlerJohns Hopkins UniversityEmail verificata su jhmi.edu
Yuchen JiaoCancer Hospital and Institute, CAMSEmail verificata su cicams.ac.cn
Leonardo G CohenHuman Cortical Physiology and Neurorehabilitation Section, National Institutes of Health, NIHEmail verificata su ninds.nih.gov
Marcela GimenezFaculdade de Ciências Médicas da Santa Casa de São PauloEmail verificata su fcmsantacasasp.edu.br
Christian Bowman-ColinModerna Inc.Email verificata su modernatx.com
Anamaria Aranha CamargoCentro de Oncologia Molecular Hospital Sírio LibanêsEmail verificata su mochsl.org.br

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Suely Kazue Nagahashi Marie

Professor Associado de Medicina

Email verificata su usp.br

Medicina


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
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	6834	2008
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	4675	2014
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	1176	2011
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	1053	2009
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	808	2011
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	682	2012
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	643	2017
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	606	2011
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	425	2015
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	412	2013
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	239	1994
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	227	1996
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	224	2008
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	214	2006
Metabolism and brain cancer SKN Marie, SMO Shinjo Clinics 66, 33-43, 2011	191	2011
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	191	2003
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	187	2016
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	185	2007
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	185	1998

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