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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
Multiple system atrophy: the application of genetics in understanding etiology
Multiple system atrophy: the application of genetics in understanding etiology
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Multiple system atrophy: the application of genetics in understanding etiology

Federoff, Monica ; Schottlaender, Lucia V. ; Houlden, Henry ; Singleton, Andrew

Clinical autonomic research, 2015-02, Vol.25 (1), p.19-36 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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3
SORL1 mutation in a Greek family with Parkinson's disease and dementia
SORL1 mutation in a Greek family with Parkinson's disease and dementia
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SORL1 mutation in a Greek family with Parkinson's disease and dementia

Xiromerisiou, Georgia ; Bourinaris, Thomas ; Houlden, Henry ; Lewis, Patrick A. ; Senkevich, Konstantin ; Hammer, Monia ; Federoff, Monica ; Khan, Alaa ; Spanaki, Cleanthe ; Hadjigeorgiou, Georgios M. ; Bonstanjopoulou, Sevasti ; Fidani, Liana ; Ermolaev, Aleksey ; Gan‐Or, Ziv ; Singleton, Andrew ; Vandrovcova, Jana ; Hardy, John

Annals of clinical and translational neurology, 2021-10, Vol.8 (10), p.1961-1969 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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4
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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5
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies
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ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies

Blauwendraat, Cornelis ; Nalls, Mike A. ; Federoff, Monica ; Pletnikova, Olga ; Ding, Jinhui ; Letson, Christopher ; Geiger, Joshua T. ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Troncoso, Juan C. ; Simón‐Sánchez, Javier ; Scholz, Sonja W.

Movement disorders, 2017-02, Vol.32 (2), p.298-299 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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6
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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