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1
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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2
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

Lubbe, Steven J ; Escott-Price, Valentina ; Gibbs, J Raphael ; Nalls, Mike A ; Bras, Jose ; Price, T Ryan ; Nicolas, Aude ; Jansen, Iris E ; Mok, Kin Y ; Pittman, Alan M ; Tomkins, James E ; Lewis, Patrick A ; Noyce, Alastair J ; Lesage, Suzanne ; Sharma, Manu ; Schiff, Elena R ; Levine, Adam P ; Brice, Alexis ; Gasser, Thomas ; Hardy, John ; Heutink, Peter ; Wood, Nicholas W ; Singleton, Andrew B ; Williams, Nigel M ; Morris, Huw R

Human molecular genetics, 2016-12, Vol.25 (24), p.5483-5489 [Revista revisada por pares]

England: Oxford University Press

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3
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations:Evidence for oligogenic inheritance
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations:Evidence for oligogenic inheritance
Material Type:
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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations:Evidence for oligogenic inheritance

Lubbe, Steven J ; Escott-Price, Valentina ; Gibbs, J. Raphael ; Nalls, Mike A ; Bras, Jose ; Price, T. Ryan ; Nicolas, Aude ; Jansen, Iris E ; Mok, Kin Y ; Pittman, Alan M ; Tomkins, James E ; Lewis, Patrick A ; Noyce, Alastair J ; Lesage, Suzanne ; Sharma, Manu ; Schiff, Elena R ; Levine, Adam P ; Brice, Alexis ; Gasser, Thomas ; Hardy, John ; Heutink, Peter ; Wood, Nicholas W ; Singleton, Andrew B ; Williams, Nigel M ; Morris, Huw R

2016-12

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4
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
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Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease

Brown, Emmeline E. ; Blauwendraat, Cornelis ; Trinh, Joanne ; Rizig, Mie ; Nalls, Mike A. ; Leveille, Etienne ; Ruskey, Jennifer A. ; Jonvik, Hallgeir ; Tan, Manuela M.X. ; Bandres-Ciga, Sara ; Hassin-Baer, Sharon ; Brockmann, Kathrin ; Infante, Jon ; Tolosa, Eduardo ; Ezquerra, Mario ; Ben Romdhan, Sawssan ; Benmahdjoub, Mustapha ; Arezki, Mohamed ; Mhiri, Chokri ; Hardy, John ; Singleton, Andrew B. ; Alcalay, Roy N. ; Gasser, Thomas ; Grosset, Donald G. ; Williams, Nigel M. ; Pittman, Alan ; Gan-Or, Ziv ; Fernandez-Santiago, Ruben ; Brice, Alexis ; Lesage, Suzanne ; Farrer, Matthew ; Wood, Nicholas ; Morris, Huw R.

Neurobiology of aging, 2021-01, Vol.97, p.148.e17-148.e24 [Revista revisada por pares]

United States: Elsevier Inc

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5
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
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Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Holmans, Mohamad Saad Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O'Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

Archives of neurology (Chicago), 2013-10, Vol.70 (10), p.1268-1268

Chicago: American Medical Association

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6
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Material Type:
Artículo 		Añadir a Mi Portal

Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamad ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J. Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O’Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

JAMA neurology, 2013-10, Vol.70 (10), p.1268-1276 [Revista revisada por pares]

United States: American Medical Association

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7
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
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Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

Martinez, Maria ; Brice, Alexis ; Vaughan, Jenny R. ; Zimprich, Alexander ; Breteler, Monique M.B. ; Meco, Giuseppe ; Filla, Alessandro ; Farrer, Matthew J. ; Bétard, Christine ; Singleton, Andrew ; Hardy, John ; De Michele, Giuseppe ; Bonifati, Vincenzo ; Oostra, Ben A. ; Gasser, Thomas ; Wood, Nick W. ; Dürr, Alexandra

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-07, Vol.136B (1), p.72-74 [Revista revisada por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
Material Type:
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Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

MARTINEZ, Maria ; BRICE, Alexis ; HARDY, John ; DE MICHELE, Giuseppe ; BONIFATI, Vincenzo ; OOSTRA, Ben A ; GASSER, Thomas ; WOOD, Nick W ; DÜRR, Alexandra ; VAUGHAN, Jenny R ; ZIMPRICH, Alexander ; BRETELER, Monique M. B ; MECO, Giuseppe ; FILLA, Alessandro ; FATTER, Matthew J ; BETARD, Christine ; SINGLETON, Andrew

American journal of medical genetics, 2005, Vol.136B (1), p.72-74 [Revista revisada por pares]

New York, NY: Wiley-Liss

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9
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

Simón-Sánchez, Javier ; Kilarski, Laura L ; Nalls, Michael A ; Martinez, Maria ; Schulte, Claudia ; Holmans, Peter ; Gasser, Thomas ; Hardy, John ; Singleton, Andrew B ; Wood, Nicholas W ; Brice, Alexis ; Heutink, Peter ; Williams, Nigel ; Morris, Huw R Lewin, Alfred

PloS one, 2012-03, Vol.7 (3), p.e28787-e28787 [Revista revisada por pares]

United States: Public Library of Science

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10
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Mok, Kin Y ; Sheerin, Una ; Simon-Sanchez, Javier ; Salaka, Afnan ; Chester, Lucy ; Escott-Price, Valentina ; Mantripragada, Kiran ; Doherty, Karen M ; Noyce, Alastair J ; Mencacci, Niccolo E ; Lubbe, Steven J ; Williams-Gray, Caroline H ; Barker, Roger A ; van Dijk, Karin ; Berendse, Henk W ; Heutink, Peter ; Corvol, Jean-Christophe ; Cormier, Florence ; Lesage, Suzanne ; Brice, Alexis ; Brockmann, Kathrin ; Schulte, Claudia ; Gasser, Thomas ; Foltynie, Thomas ; Limousin, Patricia ; Morrison, Karen E ; Clarke, Carl E ; Sawcer, Stephen ; Warner, Tom T ; Lees, Andrew J ; Morris, Huw R ; Nalls, Mike A ; Singleton, Andrew B ; Hardy, John ; Abramov, Andrey Y ; Plagnol, Vincent ; Williams, Nigel M ; Wood, Nicholas W

2016-05

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