Association study of the trinucleotide repeat polymorphism within <it>SMARCA2 </it>and schizophrenia by Danics Zoltan, Tabbane Karim, Benkelfat Chawki, Fathalli Ferid, Xiong Lan, Sengupta Sarojini, Labelle Alain, Lal Samarthji, Krebs Marie-Odile, Rouleau Guy, Joober Ridha

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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion by Spataro, Rossella, Kousi, Maria, Farhan, Sali M K, Willer, Jason R, Ross, Jay P, Dion, Patrick A, Rouleau, Guy A, Daly, Mark J, Neale, Benjamin M, La Bella, Vincenzo, Katsanis, Nicholas

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Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation by Marra Marco, Lemyre Emmanuelle, Langlois Sylvie, Lam Wan L, Eydoux Patrice, Delaney Allen, Coe Bradley P, Chénier Sébastien, Chan Susanna, Chai David, Montpetit Alexandre, Tucker Tracy, Qian Hong, Rouleau Guy A, Vincent David, Michaud Jacques L, Friedman Jan M

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Genome screen in familial intracranial aneurysm by Langefeld Carl, Bailey-Wilson Joan E, Meissner Irene, Hornung Richard, Deka Ranjan, Flaherty Matthew L, Kleindorfer Dawn, Woo Daniel, Anderson Craig, Brown Robert, Sauerbeck Laura, Foroud Tatiana, Rouleau Guy, Connolly E Sander, Lai Dongbing, Koller Daniel L, Huston John, Broderick Joseph P

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Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization by Li H Irene, Lemyre Emmanuelle, Langlois Sylvie, Gibson William T, Flibotte Stephane, Delaney Allen D, Chai David, Chan Susanna, Boerkoel Cornelius, Birch Patricia, Baross Agnes, Armstrong Linlea, Arbour Laura, Adam Shelin, Friedman JM, MacLeod Patrick, Mathers Joan, Michaud Jacques L, McGillivray Barbara C, Patel Millan S, Qian Hong, Rouleau Guy A, Van Allen Margot I, Yong Siu-Li, Zahir Farah R, Eydoux Patrice, Marra Marco A

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