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What genetics tells us about the causes and mechanisms of Parkinson's disease
What genetics tells us about the causes and mechanisms of Parkinson's disease
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What genetics tells us about the causes and mechanisms of Parkinson's disease

Corti, Olga ; Lesage, Suzanne ; Brice, Alexis

Physiological reviews, 2011-10, Vol.91 (4), p.1161-1218 [Periódico revisado por pares]

United States: American Physiological Society

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2
Special Issue "Parkinson's Disease: Genetics and Pathogenesis"
Special Issue "Parkinson's Disease: Genetics and Pathogenesis"
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Special Issue "Parkinson's Disease: Genetics and Pathogenesis"

Lesage, Suzanne ; Trinh, Joanne

Genes, 2023-03, Vol.14 (3), p.737 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions (“mimics”)
The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions (“mimics”)
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The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions (“mimics”)

Hening, Wayne A ; Allen, Richard P ; Washburn, Mystinna ; Lesage, Suzanne R ; Earley, Christopher J

Sleep medicine, 2009-10, Vol.10 (9), p.976-981 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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4
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

Trinh, Joanne, BSc ; Gustavsson, Emil K, MSc ; Vilariño-Güell, Carles, PhD ; Bortnick, Stephanie, BSc ; Latourelle, Jeanne, PhD ; McKenzie, Marna B, BSc ; Tu, Chelsea Szu, MSc ; Nosova, Ekaterina, PhD ; Khinda, Jaskaran, BSc ; Milnerwood, Austen, PhD ; Lesage, Suzanne, PhD ; Brice, Alexis, MD ; Tazir, Meriem, MD ; Aasly, Jan O, MD ; Parkkinen, Laura, PhD ; Haytural, Hazal, MSc ; Foroud, Tatiana, PhD ; Myers, Richard H, PhD ; Sassi, Samia Ben, MD ; Hentati, Emna, MD ; Nabli, Fatma, MD ; Farhat, Emna, MD ; Amouri, Rim, PhD ; Hentati, Fayçal, MD ; Farrer, Matthew J, Dr

Lancet neurology, 2016-11, Vol.15 (12), p.1248-1256 [Periódico revisado por pares]

England: Elsevier Ltd

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5
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry
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Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry

Lee, Annie J. ; Wang, Yuanjia ; Alcalay, Roy N. ; Mejia‐Santana, Helen ; Saunders‐Pullman, Rachel ; Bressman, Susan ; Corvol, Jean‐Christophe ; Brice, Alexis ; Lesage, Suzanne ; Mangone, Graziella ; Tolosa, Eduardo ; Pont‐Sunyer, Claustre ; Vilas, Dolores ; Schüle, Birgitt ; Kausar, Farah ; Foroud, Tatiana ; Berg, Daniela ; Brockmann, Kathrin ; Goldwurm, Stefano ; Siri, Chiara ; Asselta, Rosanna ; Ruiz‐Martinez, Javier ; Mondragón, Elisabet ; Marras, Connie ; Ghate, Taneera ; Giladi, Nir ; Mirelman, Anat ; Marder, Karen

Movement disorders, 2017-10, Vol.32 (10), p.1432-1438 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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6
Analysis of blood-based gene expression in idiopathic Parkinson disease
Analysis of blood-based gene expression in idiopathic Parkinson disease
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Analysis of blood-based gene expression in idiopathic Parkinson disease

Shamir, Ron ; Amar, David

Neurology, 2017-10, Vol.89 (16), p.1676-1683 [Periódico revisado por pares]

United States: American Academy of Neurology

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7
Characterization of Recessive Parkinson Disease in a Large Multicenter Study
Characterization of Recessive Parkinson Disease in a Large Multicenter Study
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Characterization of Recessive Parkinson Disease in a Large Multicenter Study

Lesage, Suzanne ; Lunati, Ariane ; Houot, Marion ; Romdhan, Sawssan Ben ; Clot, Fabienne ; Tesson, Christelle ; Mangone, Graziella ; Toullec, Benjamin Le ; Courtin, Thomas ; Larcher, Kathy ; Benmahdjoub, Mustapha ; Arezki, Mohamed ; Bouhouche, Ahmed ; Anheim, Mathieu ; Roze, Emmanuel ; Viallet, François ; Tison, François ; Broussolle, Emmanuel ; Emre, Murat ; Hanagasi, Hasmet ; Bilgic, Basar ; Tazir, Meriem ; Djebara, Mouna Ben ; Gouider, Riadh ; Tranchant, Christine ; Vidailhet, Marie ; Le Guern, Eric ; Corti, Olga ; Mhiri, Chokri ; Lohmann, Ebba ; Singleton, Andrew ; Corvol, Jean‐Christophe ; Brice, Alexis ; Lesage, Suzanne ; Lunati, Ariane ; Houot, Marion ; Ben Romdhan, Sawssan ; Clot, Fabienne ; Tesson, Christelle ; Mangone, Graziella ; Le Toullec, Benjamin ; Courtin, Thomas ; Larcher, Kathy ; Benmahdjoub, Mustapha ; Arezki, Mohammed ; Bouhouche, Ahmed ; Anheim, Mathieu ; Roze, Emmanuel ; Viallet, François ; Tison, François ; Broussolle, Emmanuel ; Emre, Murat ; Hanagasi, Hasmet ; Bilgic, Basar ; Ben Djebara, Mouna ; Gouider, Riadh ; Tazir, Meriem ; Tranchant, Christine ; Vidailhet, Marie ; Le Guern, Eric ; Corti, Olga ; Mhiri, Chokri ; Lohmann, Ebba ; Singleton, Andy ; Corvol, Jean‐Christophe ; Brice, Alexis

Annals of neurology, 2020-10, Vol.88 (4), p.843-850 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
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De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Nava, Caroline ; Dalle, Carine ; Rastetter, Agnès ; Striano, Pasquale ; de Kovel, Carolien G F ; Nabbout, Rima ; Cancès, Claude ; Ville, Dorothée ; Brilstra, Eva H ; Gobbi, Giuseppe ; Raffo, Emmanuel ; Bouteiller, Delphine ; Marie, Yannick ; Trouillard, Oriane ; Robbiano, Angela ; Keren, Boris ; Agher, Dahbia ; Roze, Emmanuel ; Lesage, Suzanne ; Nicolas, Aude ; Brice, Alexis ; Baulac, Michel ; Vogt, Cornelia ; El Hajj, Nady ; Schneider, Eberhard ; Suls, Arvid ; Weckhuysen, Sarah ; Gormley, Padhraig ; Lehesjoki, Anna-Elina ; De Jonghe, Peter ; Helbig, Ingo ; Baulac, Stéphanie ; Zara, Federico ; Koeleman, Bobby P C ; Haaf, Thomas ; LeGuern, Eric ; Depienne, Christel

Nature genetics, 2014-06, Vol.46 (6), p.640-645 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Genetic characteristics of leucine-rich repeat kinase 2 ( LRRK2 ) associated Parkinson’s disease
Genetic characteristics of leucine-rich repeat kinase 2 ( LRRK2 ) associated Parkinson’s disease
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Genetic characteristics of leucine-rich repeat kinase 2 ( LRRK2 ) associated Parkinson’s disease

Bardien, Soraya ; Lesage, Suzanne ; Brice, Alexis ; Carr, Jonathan

Parkinsonism & related disorders, 2011-08, Vol.17 (7), p.501-508 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

Nalls, Mike A, PhD ; McLean, Cory Y, PhD ; Rick, Jacqueline, PhD ; Eberly, Shirley, MS ; Hutten, Samantha J, PhD ; Gwinn, Katrina, MD ; Sutherland, Margaret, PhD ; Martinez, Maria, PhD ; Heutink, Peter, PhD ; Williams, Nigel M, PhD ; Hardy, John, PhD ; Gasser, Thomas, MD ; Brice, Alexis, MD ; Price, T Ryan, MS ; Nicolas, Aude, PhD ; Keller, Margaux F, PhD ; Molony, Cliona, PhD ; Gibbs, J Raphael, MS ; Chen-Plotkin, Alice, MD ; Suh, Eunran, PhD ; Letson, Christopher, BS ; Fiandaca, Massimo S, MD ; Mapstone, Mark, PhD ; Federoff, Howard J, MD ; Noyce, Alastair J, MRCP ; Morris, Huw, MD ; Van Deerlin, Vivianna M, MD ; Weintraub, Daniel, MD ; Zabetian, Cyrus, MD ; Hernandez, Dena G, MS ; Lesage, Suzanne, PhD ; Mullins, Meghan, BA ; Conley, Emily Drabant, PhD ; Northover, Carrie A M, PhD ; Frasier, Mark, PhD ; Marek, Ken, MD ; Day-Williams, Aaron G, PhD ; Stone, David J, PhD ; Ioannidis, John P A, Prof ; Singleton, Andrew B, Dr

Lancet neurology, 2015-10, Vol.14 (10), p.1002-1009 [Periódico revisado por pares]

England: Elsevier Ltd

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