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Lan Xiong
Lan Xiong
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Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
J Winkelmann, B Schormair, P Lichtner, S Ripke, L Xiong, S Jalilzadeh, ...
Nature genetics 39 (8), 1000-1006, 2007
7672007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ...
Molecular psychiatry 12 (12), 1129-1139, 2007
4812007
Increased exonic de novo mutation rate in individuals with schizophrenia
SL Girard, J Gauthier, A Noreau, L Xiong, S Zhou, L Jouan, ...
Nature genetics 43 (9), 860-863, 2011
4732011
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
J Gauthier, N Champagne, RG Lafrenière, L Xiong, D Spiegelman, ...
Proceedings of the National Academy of Sciences 107 (17), 7863-7868, 2010
4272010
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
A Piton, J Gauthier, FF Hamdan, RG Lafreniere, Y Yang, E Henrion, ...
Molecular psychiatry 16 (8), 867-880, 2011
3502011
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
B Schormair, D Kemlink, D Roeske, G Eckstein, L Xiong, P Lichtner, ...
Nature genetics 40 (8), 946-948, 2008
3112008
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts
P Awadalla, J Gauthier, RA Myers, F Casals, FF Hamdan, AR Griffing, ...
The American Journal of Human Genetics 87 (3), 316-324, 2010
2872010
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia
J Tarabeux, O Kebir, J Gauthier, FF Hamdan, L Xiong, A Piton, ...
Translational psychiatry 1 (11), e55-e55, 2011
2552011
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ...
The Lancet Neurology 16 (11), 898-907, 2017
2132017
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12. 1
J Winkelmann, D Czamara, B Schormair, F Knauf, EC Schulte, ...
PLoS genetics 7 (7), e1002171, 2011
2112011
Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity
A Desautels, G Turecki, J Montplaisir, L Xiong, AS Walters, BL Ehrenberg, ...
Archives of neurology 62 (4), 591-596, 2005
1642005
A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13
A Levchenko, S Provost, JY Montplaisir, L Xiong, J St-Onge, P Thibodeau, ...
Neurology 67 (5), 900-901, 2006
1312006
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12
L Xiong, M Labuda, DS Li, TJ Hudson, R Desbiens, G Patry, S Verret, ...
The American Journal of Human Genetics 65 (6), 1698-1710, 1999
1221999
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels
L Xiong, H Catoire, P Dion, C Gaspar, RG Lafrenière, SL Girard, ...
Human molecular genetics 18 (6), 1065-1074, 2009
1112009
Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis
H Catoire, PA Dion, L Xiong, M Amari, R Gaudet, SL Girard, A Noreau, ...
Annals of neurology 70 (1), 170-175, 2011
1022011
De novo variants in sporadic cases of childhood onset schizophrenia
A Ambalavanan, SL Girard, K Ahn, S Zhou, A Dionne-Laporte, ...
European Journal of Human Genetics 24 (6), 944-948, 2016
942016
The 14q restless legs syndrome locus in the French Canadian population
A Levchenko, JY Montplaisir, MP Dubé, JB Riviere, J St‐Onge, G Turecki, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
922004
Familial association of neuropsychological traits in patients with generalized and partial seizure disorders
M Levav, AF Mirsky, J Herault, L Xiong, N Amir, E Andermann
Journal of Clinical and Experimental Neuropsychology 24 (3), 311-326, 2002
922002
Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism
L Mottron, P Duret, S Mueller, RD Moore, B Forgeot d’Arc, S Jacquemont, ...
Molecular autism 6, 1-19, 2015
892015
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12
SF Berkovic, JM Serratosa, HA Phillips, L Xiong, E Andermann, ...
Epilepsia 45 (9), 1054-1060, 2004
872004
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