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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 [Peer Reviewed Journal]

England: Oxford University Press

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2
Polygenic risk of Parkinson disease is correlated with disease age at onset
Polygenic risk of Parkinson disease is correlated with disease age at onset
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Polygenic risk of Parkinson disease is correlated with disease age at onset

Escott-Price, Valentina ; Nalls, Mike A. ; Morris, Huw R. ; Lubbe, Steven ; Brice, Alexis ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W. ; Hardy, John ; Singleton, Andrew B. ; Williams, Nigel M.

Annals of neurology, 2015-04, Vol.77 (4), p.582-591 [Peer Reviewed Journal]

United States: Blackwell Publishing Ltd

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3
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers

MENCACCI, Niccolò E ; ISAIAS, Ioannis U ; NOYCE, Alastair J ; MOK, Kin Y ; OPLADEN, Thomas ; KUNSTMANN, Erdmute ; HODECKER, Sybille ; MÜNCHAU, Alexander ; VOLKMANN, Jens ; SAMNICK, Samuel ; SIDLE, Katie ; NANJI, Tina ; REICH, Martin M ; SWEENEY, Mary G ; HOULDEN, Henry ; BATLA, Amit ; ZECCHINELLI, Anna L ; PEZZOLI, Gianni ; MAROTTA, Giorgio ; LEES, Andrew ; ALEGRIA, Paulo ; KRACK, Paul ; CORMIER-DEQUAIRE, Florence ; GANOS, Christos ; LESAGE, Suzanne ; BRICE, Alexis ; HEUTINK, Peter ; GASSER, Thomas ; LUBBE, Steven J ; MORRIS, Huw R ; TABA, Pille ; KOKS, Sulev ; MAJOUNIE, Elisa ; GIBBS, J. Raphael ; PLAGNOL, Vincent ; SINGLETON, Andrew ; HARDY, John ; KLEBE, Stephan ; BHATIA, Kailash P ; WOOD, Nicholas W ; POLKE, James M ; BRAS, Jose ; HERSHESON, Joshua ; STAMELOU, Maria ; PITTMAN, Alan M

Brain (London, England : 1878), 2014-09, Vol.137 (Pt 9), p.2480-2492 [Peer Reviewed Journal]

Oxford: Oxford University Press

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4
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
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Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

Blauwendraat, Cornelis ; Heilbron, Karl ; Vallerga, Costanza L. ; Bandres‐Ciga, Sara ; von Coelln, Rainer ; Pihlstrøm, Lasse ; Simón‐Sánchez, Javier ; Schulte, Claudia ; Sharma, Manu ; Krohn, Lynne ; Siitonen, Ari ; Iwaki, Hirotaka ; Leonard, Hampton ; Noyce, Alastair J. ; Tan, Manuela ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Scholz, Sonja W. ; Jankovic, Joseph ; Shulman, Lisa M. ; Lesage, Suzanne ; Corvol, Jean‐Christophe ; Brice, Alexis ; van Hilten, Jacobus J. ; Marinus, Johan ; Eerola‐Rautio, Johanna ; Tienari, Pentti ; Majamaa, Kari ; Toft, Mathias ; Grosset, Donald G. ; Gasser, Thomas ; Heutink, Peter ; Shulman, Joshua M. ; Wood, Nicolas ; Hardy, John ; Morris, Huw R. ; Hinds, David A. ; Gratten, Jacob ; Visscher, Peter M. ; Gan‐Or, Ziv ; Nalls, Mike A. ; Singleton, Andrew B.

Movement disorders, 2019-06, Vol.34 (6), p.866-875 [Peer Reviewed Journal]

Chichester, UK: John Wiley & Sons, Ltd

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5
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

Blauwendraat, Cornelis ; Reed, Xylena ; Krohn, Lynne ; Heilbron, Karl ; Bandres-Ciga, Sara ; Tan, Manuela ; Gibbs, J Raphael ; Hernandez, Dena G ; Kumaran, Ravindran ; Langston, Rebekah ; Bonet-Ponce, Luis ; Alcalay, Roy N ; Hassin-Baer, Sharon ; Greenbaum, Lior ; Iwaki, Hirotaka ; Leonard, Hampton L ; Grenn, Francis P ; Ruskey, Jennifer A ; Sabir, Marya ; Ahmed, Sarah ; Makarious, Mary B ; Pihlstrøm, Lasse ; Toft, Mathias ; van Hilten, Jacobus J ; Marinus, Johan ; Schulte, Claudia ; Brockmann, Kathrin ; Sharma, Manu ; Siitonen, Ari ; Majamaa, Kari ; Eerola-Rautio, Johanna ; Tienari, Pentti J ; Pantelyat, Alexander ; Hillis, Argye E ; Dawson, Ted M ; Rosenthal, Liana S ; Albert, Marilyn S ; Resnick, Susan M ; Ferrucci, Luigi ; Morris, Christopher M ; Pletnikova, Olga ; Troncoso, Juan ; Grosset, Donald ; Lesage, Suzanne ; Corvol, Jean-Christophe ; Brice, Alexis ; Noyce, Alastair J ; Masliah, Eliezer ; Wood, Nick ; Hardy, John ; Shulman, Lisa M ; Jankovic, Joseph ; Shulman, Joshua M ; Heutink, Peter ; Gasser, Thomas ; Cannon, Paul ; Scholz, Sonja W ; Morris, Huw ; Cookson, Mark R ; Nalls, Mike A ; Gan-Or, Ziv ; Singleton, Andrew B

Brain (London, England : 1878), 2020-01, Vol.143 (1), p.234-248 [Peer Reviewed Journal]

England: Oxford University Press

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6
Genetic comorbidities in Parkinson's disease
Genetic comorbidities in Parkinson's disease
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Genetic comorbidities in Parkinson's disease

Nalls, Mike A ; Saad, Mohamad ; Noyce, Alastair J ; Keller, Margaux F ; Schrag, Anette ; Bestwick, Jonathan P ; Traynor, Bryan J ; Gibbs, J Raphael ; Hernandez, Dena G ; Cookson, Mark R ; Morris, Huw R ; Williams, Nigel ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Hardy, John ; Martinez, Maria ; Singleton, Andrew B

Human molecular genetics, 2014-02, Vol.23 (3), p.831-841 [Peer Reviewed Journal]

England: Oxford University Press

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7
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

Robak, Laurie A ; Jansen, Iris E ; van Rooij, Jeroen ; Uitterlinden, André G ; Kraaij, Robert ; Jankovic, Joseph ; Heutink, Peter ; Shulman, Joshua M

Brain (London, England : 1878), 2017-12, Vol.140 (12), p.3191-3203 [Peer Reviewed Journal]

England: Oxford University Press

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8
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

Nalls, Mike A ; Bras, Jose ; Hernandez, Dena G ; Keller, Margaux F ; Majounie, Elisa ; Renton, Alan E ; Saad, Mohamad ; Jansen, Iris ; Guerreiro, Rita ; Lubbe, Steven ; Plagnol, Vincent ; Gibbs, J. Raphael ; Schulte, Claudia ; Pankratz, Nathan ; Sutherland, Margaret ; Bertram, Lars ; Lill, Christina M ; DeStefano, Anita L ; Faroud, Tatiana ; Eriksson, Nicholas ; Tung, Joyce Y ; Edsall, Connor ; Nichols, Noah ; Brooks, Janet ; Arepalli, Sampath ; Pliner, Hannah ; Letson, Chris ; Heutink, Peter ; Martinez, Maria ; Gasser, Thomas ; Traynor, Bryan J ; Wood, Nick ; Hardy, John ; Singleton, Andrew B

Neurobiology of aging, 2015-03, Vol.36 (3), p.1605.e7-1605.e12 [Peer Reviewed Journal]

United States: Elsevier Inc

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9
SNCA variants are associated with increased risk for multiple system atrophy
SNCA variants are associated with increased risk for multiple system atrophy
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SNCA variants are associated with increased risk for multiple system atrophy

Scholz, Sonja W. ; Houlden, Henry ; Schulte, Claudia ; Sharma, Manu ; Li, Abi ; Berg, Daniela ; Melchers, Anna ; Paudel, Reema ; Gibbs, J. Raphael ; Simon-Sanchez, Javier ; Paisan-Ruiz, Coro ; Bras, Jose ; Ding, Jinhui ; Chen, Honglei ; Traynor, Bryan J. ; Arepalli, Sampath ; Zonozi, Ryan R. ; Revesz, Tamas ; Holton, Janice ; Wood, Nick ; Lees, Andrew ; Oertel, Wolfgang ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Illig, Thomas ; Riess, Olaf ; Fernandez, Hubert H. ; Rodriguez, Ramon L. ; Okun, Michael S. ; Poewe, Werner ; Wenning, Gregor K. ; Hardy, John A. ; Singleton, Andrew B. ; Gasser, Thomas

Annals of neurology, 2009-05, Vol.65 (5), p.610-614 [Peer Reviewed Journal]

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

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10
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 [Peer Reviewed Journal]

United States: Public Library of Science

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