Coro Paisán Ruiz
Title
Cited by
Cited by
Year
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ...
Neuron 44 (4), 595-600, 2004
21842004
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308, 2009
16322009
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
WC Nichols, N Pankratz, D Hernandez, C Paisán-Ruíz, S Jain, CA Halter, ...
The Lancet 365 (9457), 410-412, 2005
4762005
Characterization of PLA2G6 as a locus for dystonia‐parkinsonism
C Paisan‐Ruiz, KP Bhatia, A Li, D Hernandez, M Davis, NW Wood, ...
Annals of neurology 65 (1), 19-23, 2009
4212009
SNCA variants are associated with increased risk for multiple system atrophy
SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
2562009
The genetics of Parkinson's syndromes: a critical review
J Hardy, P Lewis, T Revesz, A Lees, C Paisan-Ruiz
Current opinion in genetics & development 19 (3), 254-265, 2009
2352009
The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early‐Onset Progressive Parkinsonism with Generalized Seizures
CE Krebs, S Karkheiran, JC Powell, M Cao, V Makarov, H Darvish, ...
Human mutation 34 (9), 1200-1207, 2013
2342013
Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
C Paisán‐Ruiz, R Guevara, M Federoff, H Hanagasi, F Sina, E Elahi, ...
Movement Disorders 25 (12), 1791-1800, 2010
2232010
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA)
MC Kruer, C Paisán‐Ruiz, N Boddaert, MY Yoon, H Hama, A Gregory, ...
Annals of neurology 68 (5), 611-618, 2010
1922010
LRRK2 gene in Parkinson disease: mutation analysis and case control association study
C Paisan-Ruiz, AE Lang, T Kawarai, C Sato, S Salehi-Rad, GK Fisman, ...
Neurology 65 (5), 696-700, 2005
1902005
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA
S Camargos, S Scholz, J Simón-Sánchez, C Paisán-Ruiz, P Lewis, ...
The Lancet Neurology 7 (3), 207-215, 2008
1872008
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Human molecular genetics 20 (2), 345-353, 2011
1802011
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)
KJ Dick, M Eckhardt, C Paisán‐Ruiz, AA Alshehhi, C Proukakis, ...
Human mutation 31 (4), E1251-E1260, 2010
1652010
Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations
C Paisán-Ruiz, A Li, SA Schneider, JL Holton, R Johnson, D Kidd, ...
Neurobiology of aging 33 (4), 814-823, 2012
1632012
ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation
SA Schneider, C Paisan‐Ruiz, NP Quinn, AJ Lees, H Houlden, J Hardy, ...
Movement Disorders 25 (8), 979-984, 2010
1602010
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2
DG Hernandez, C Paisán‐Ruíz, A McInerney‐Leo, S Jain, ...
Annals of neurology 57 (3), 453-456, 2005
1232005
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
M Narooie-Nejad, SH Paylakhi, S Shojaee, Z Fazlali, M Rezaei Kanavi, ...
Human molecular genetics 18 (20), 3969-3977, 2009
1212009
Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course
N Setó‐Salvia, J Pagonabarraga, H Houlden, B Pascual‐Sedano, ...
Movement Disorders 27 (3), 393-399, 2012
1192012
GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias
SA Schneider, C Paisan‐Ruiz, I Garcia‐Gorostiaga, NP Quinn, YG Weber, ...
Movement disorders: official journal of the Movement Disorder Society 24 (11 …, 2009
1172009
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal
J Bras, C Paisan-Ruiz, R Guerreiro, MH Ribeiro, A Morgadinho, ...
Neurobiology of aging 30 (9), 1515-1517, 2009
1122009
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