MEIS1 and Restless Legs Syndrome: A Comprehensive Review

por Sarayloo, Faezeh, Dion, Patrick A., Rouleau, Guy A.
Publicado 2019

Progress in the genetics of restless legs syndrome: the path ahead in the era of whole-genome sequencing

por Akçimen, Fulya, Dion, Patrick A, Rouleau, Guy A
Publicado 2022

Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms

por Vande Velde, Christine, Dion, Patrick A., Rouleau, Guy A.
Publicado 2011

Exome sequencing in genetic disease: recent advances and considerations

por Ross, Jay P., Dion, Patrick A., Rouleau, Guy A.
Publicado 2020

Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans

por Therrien, Martine, Rouleau, Guy A., Dion, Patrick A., Parker, J. Alex
Publicado 2013

FET proteins regulate lifespan and neuronal integrity

por Therrien, Martine, Rouleau, Guy A., Dion, Patrick A., Parker, J. Alex
Publicado 2016

Reliability and correlation of mixture cell correction in methylomic and transcriptomic blood data

por Chaumette, Boris, Kebir, Oussama, Dion, Patrick A., Rouleau, Guy A., Krebs, Marie-Odile
Publicado 2020

Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum

por Noreau, Anne, Beauchemin, Philippe, Dionne-Laporte, Alexandre, Dion, Patrick A, Rouleau, Guy A, Dupré, Nicolas
Publicado 2014

Screening of novel restless legs syndrome–associated genes in French-Canadian families

por Akçimen, Fulya, Spiegelman, Dan, Dionne-Laporte, Alexandre, Gan-Or, Ziv, Dion, Patrick A., Rouleau, Guy A.
Publicado 2018

De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

por Leblond, Claire S., Webber, Alina, Gan-Or, Ziv, Moore, Fraser, Dagher, Alain, Dion, Patrick A., Rouleau, Guy A.
Publicado 2016

WNK1/HSN2 Mutation in Human Peripheral Neuropathy Deregulates KCC2 Expression and Posterior Lateral Line Development in Zebrafish (Danio rerio)

por Bercier, Valérie, Brustein, Edna, Liao, Meijiang, Dion, Patrick A., Lafrenière, Ronald G., Rouleau, Guy A., Drapeau, Pierre
Publicado 2013

Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes

por Liao, Calwing, Laporte, Alexandre D., Spiegelman, Dan, Akçimen, Fulya, Joober, Ridha, Dion, Patrick A., Rouleau, Guy A.
Publicado 2019

Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study

por Alipour, Paria, Senkevich, Konstantin, Ross, Jay P., Spiegelman, Dan, Manousaki, Despoina, Dion, Patrick A., Rouleau, Guy A.
Publicado 2022

Comparative Analysis of the Expression Profile of Wnk1 and Wnk1/Hsn2 Splice Variants in Developing and Adult Mouse Tissues

por Shekarabi, Masoud, Lafrenière, Ron G., Gaudet, Rébecca, Laganière, Janet, Marcinkiewicz, Martin M., Dion, Patrick A., Rouleau, Guy A.
Publicado 2013

Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes

por Akçimen, Fulya, Sarayloo, Faezeh, Liao, Calwing, Ross, Jay P., Oliveira, Rachel De Barros, Dion, Patrick A., Rouleau, Guy A.
Publicado 2020

GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis

por Mallett, Victoria, Ross, Jay P., Alcalay, Roy N., Ambalavanan, Amirthagowri, Sidransky, Ellen, Dion, Patrick A., Rouleau, Guy A., Gan-Or, Ziv
Publicado 2016

Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissues

por Ross, Jay P., Leblond, Claire S., Catoire, Hélène, Volkening, Kathryn, Strong, Michael, Zinman, Lorne, Robertson, Janice, Dion, Patrick A., Rouleau, Guy A.
Publicado 2019

The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosis

por Salmon, Kristiana, Ross, Jay P., Bertone, Vanessa, Gobbo, Maria, Anoja, Nancy, Karamchandani, Jason, Dion, Patrick A., Rouleau, Guy A., Genge, Angela
Publicado 2022

Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the disease

por Jouan, Loubna, Girard, Simon L, Dobrzeniecka, Sylvia, Ambalavanan, Amirthagowri, Krebs, Marie-Odile, Joober, Ridha, Gauthier, Julie, Dion, Patrick A, Rouleau, Guy A
Publicado 2013

Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor

por Castonguay, Charles-Etienne, Liao, Calwing, Khayachi, Anouar, Liu, Yumin, Medeiros, Miranda, Houle, Gabrielle, Ross, Jay P., Dion, Patrick A., Rouleau, Guy A.
Publicado 2022