Lan Xiong

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Juliane Winkelmann, Barbara Schormair, Peter Lichtner et al. · Nature Genetics · 2007 · 690 citations

Genome-wide Association Study, Genetic Disorder, Genetics +5

Increased exonic de novo mutation rate in individuals with schizophrenia

Simon Girard, Julie Gauthier, Anne Noreau et al. · Nature Genetics · 2011 · 442 citations

Risk Prediction, Psychiatry, Genetic Disorder +8

De novo mutations in the gene encoding the synaptic scaffolding protein <i>SHANK3</i> in patients ascertained for schizophrenia

Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière et al. · Proceedings of the National Academy of Sciences · 2010 · 379 citations · Full text

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Clyde Francks, Shinji Maegawa, Juha Laurén et al. · Molecular Psychiatry · 2007 · 357 citations · Full text

Chromatin, Psychiatry, Genetic Disorder +8

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Amélie Piton, J Gauthier, Fadi F. Hamdan et al. · Molecular Psychiatry · 2010 · 315 citations

Systematic Resequencing, X-chromosome Synaptic Genes, Genetic Disorder +8