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A large study reveals no association between APOE and Parkinson's disease
A large study reveals no association between APOE and Parkinson's disease
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A large study reveals no association between APOE and Parkinson's disease

Federoff, Monica ; Jimenez-Rolando, Belen ; Nalls, Michael A ; Singleton, Andrew B

Neurobiology of disease, 2012-05, Vol.46 (2), p.389-392 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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Genome-wide association study reveals genetic risk underlying Parkinson's disease

Singleton, Andrew B ; Gasser, Thomas ; Simón-Sánchez, Javier ; Schulte, Claudia ; Bras, Jose M ; Sharma, Manu ; Gibbs, J Raphael ; Berg, Daniela ; Paisan-Ruiz, Coro ; Lichtner, Peter ; Scholz, Sonja W ; Hernandez, Dena G ; Krüger, Rejko ; Federoff, Monica ; Klein, Christine ; Goate, Alison ; Perlmutter, Joel ; Bonin, Michael ; Nalls, Michael A ; Illig, Thomas ; Gieger, Christian ; Houlden, Henry ; Steffens, Michael ; Okun, Michael S ; Racette, Brad A ; Cookson, Mark R ; Foote, Kelly D ; Fernandez, Hubert H ; Traynor, Bryan J ; Schreiber, Stefan ; Arepalli, Sampath ; Zonozi, Ryan ; Gwinn, Katrina ; van der Brug, Marcel ; Lopez, Grisel ; Chanock, Stephen J ; Schatzkin, Arthur ; Park, Yikyung ; Hollenbeck, Albert ; Gao, Jianjun ; Huang, Xuemei ; Wood, Nick W ; Lorenz, Delia ; Deuschl, Günther ; Chen, Honglei ; Riess, Olaf ; Hardy, John A

Nature genetics, 2009-12, Vol.41 (12), p.1308-1312 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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3
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease

Lesage, Suzanne ; Bras, Jose ; Cormier-Dequaire, Florence ; Condroyer, Christel ; Nicolas, Aude ; Darwent, Lee ; Guerreiro, Rita ; Majounie, Elisa ; Federoff, Monica ; Heutink, Peter ; Wood, Nicholas W ; Gasser, Thomas ; Hardy, John ; Tison, François ; Singleton, Andrew ; Brice, Alexis

Neurology, 2015-06, Vol.1 (1), p.e9-e9 [Periódico revisado por pares]

United States: American Academy of Neurology

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4
Lack of replication of association between GIGYF2 variants and Parkinson disease
Lack of replication of association between GIGYF2 variants and Parkinson disease
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Lack of replication of association between GIGYF2 variants and Parkinson disease

Bras, Jose ; Simón-Sánchez, Javier ; Federoff, Monica ; Morgadinho, Ana ; Januario, Cristina ; Ribeiro, Maria ; Cunha, Luis ; Oliveira, Catarina ; Singleton, Andrew B.

Human molecular genetics, 2009-01, Vol.18 (2), p.341-346 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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Genome-wide association study reveals genetic risk underlying Parkinson's disease

Simón-Sánchez, Javier ; Schulte, Claudia ; Bras, Jose M ; Sharma, Manu ; Gibbs, J Raphael ; Berg, Daniela ; Paisan-Ruiz, Coro ; Lichtner, Peter ; Scholz, Sonja W ; Hernandez, Dena G ; Krüger, Rejko ; Federoff, Monica ; Klein, Christine ; Goate, Alison ; Perlmutter, Joel ; Bonin, Michael ; Nalls, Michael A ; Illig, Thomas ; Gieger, Christian ; Houlden, Henry ; Steffens, Michael ; Okun, Michael S ; Racette, Brad A ; Cookson, Mark R ; Foote, Kelly D ; Fernandez, Hubert H ; Traynor, Bryan J ; Schreiber, Stefan ; Arepalli, Sampath ; Zonozi, Ryan ; Gwinn, Katrina ; van der Brug, Marcel ; Lopez, Grisel ; Chanock, Stephen J ; Schatzkin, Arthur ; Park, Yikyung ; Hollenbeck, Albert ; Gao, Jianjun ; Huang, Xuemei ; Wood, Nick W ; Lorenz, Delia ; Deuschl, Günther ; Chen, Honglei ; Riess, Olaf ; Hardy, John A ; Singleton, Andrew B ; Gasser, Thomas

Nature (London), 2010-08, p.S24 [Periódico revisado por pares]

London: Nature Publishing Group

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6
A genome-wide association study in multiple system atrophy
A genome-wide association study in multiple system atrophy
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A genome-wide association study in multiple system atrophy

Sailer, Anna ; Scholz, Sonja W ; Nalls, Michael A ; Schulte, Claudia ; Federoff, Monica ; Price, T Ryan ; Lees, Andrew ; Ross, Owen A ; Dickson, Dennis W ; Mok, Kin ; Mencacci, Niccolo E ; Schottlaender, Lucia ; Chelban, Viorica ; Ling, Helen ; O'Sullivan, Sean S ; Wood, Nicholas W ; Traynor, Bryan J ; Ferrucci, Luigi ; Federoff, Howard J ; Mhyre, Timothy R ; Morris, Huw R ; Deuschl, Günther ; Quinn, Niall ; Widner, Hakan ; Albanese, Alberto ; Infante, Jon ; Bhatia, Kailash P ; Poewe, Werner ; Oertel, Wolfgang ; Höglinger, Günter U ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Ferreira, Joaquim ; Tolosa, Eduardo ; Bloem, Bastiaan R ; Rascol, Olivier ; Meissner, Wassilios G ; Hardy, John A ; Revesz, Tamas ; Holton, Janice L ; Gasser, Thomas ; Wenning, Gregor K ; Singleton, Andrew B ; Houlden, Henry ; Calandra-Buonaura, Giovanna ; Capellari, Sabina ; Cortelli, Pietro

Neurology, 2016-10, Vol.87 (15), p.1591-1598

eScholarship, University of California

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7
Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia
Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia
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Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

Bettencourt, Conceição ; Salpietro, Vincenzo ; Efthymiou, Stephanie ; Chelban, Viorica ; Hughes, Deborah ; Pittman, Alan ; Federoff, Monica ; Bourinaris, Thomas ; Spilioti, Martha ; Deretzi, Georgia ; Kalantzakou, Triantafyllia ; Houlden, Henry ; Singleton, Andrew ; Xiromerisiou, Georgia

Figshare 2017

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