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Nature Cell Biology|July 25, 2006
A regulated interaction with the UIM protein Eps15 implicates parkin in EGF receptor trafficking and PI(3)K-Akt signallingLara Fallon, Catherine M L Bélanger, Amadou T Corera, et al.
Brain : a Journal of Neurology|May 24, 2003
Parkin mutations are frequent in patients with isolated early-onset parkinsonismMagali Periquet, Morwena Latouche, Ebba Lohmann, et al.
Cell Reports|November 29, 2018
The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21Iréna Lassot, Stéphan Mora, Suzanne Lesage, et al.
Annals of Neurology|September 30, 2005
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14Stephan Klebe, Alexandra Durr, Alexander Rentschler, et al.
Neurobiology of Aging|October 20, 2018
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriersClémence Fournier, Mathieu Barbier, Agnès Camuzat, et al.
Journal of Alzheimer'S Disease : JAD|April 24, 2010
Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysisJean-Charles Lambert, Benjamin Grenier-Boley, Vincent Chouraki, et al.
JAMA Neurology|September 18, 2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosisIsabelle Le Ber, Agnès Camuzat, Rita Guerreiro, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 31, 2016
Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriersPaola Caroppo, Agnès Camuzat, Anne De Septenville, et al.
Acta Neuropathologica Communications|July 21, 2016
Reduced Tau protein expression is associated with frontotemporal degeneration with progranulin mutationAnthony Papegaey, Sabiha Eddarkaoui, Vincent Deramecourt, et al.
Neurology. Genetics|January 31, 2018
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 functionNatalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, et al.
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