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Molecular Genetics & Genomic Medicine|July 29, 2016
Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signalingRhalena A Thomas, Amirthagowri Ambalavanan, Guy A Rouleau, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|May 8, 2014
Methylation of BDNF in women with bulimic eating syndromes: associations with childhood abuse and borderline personality disorderLea Thaler, Lise Gauvin, Ridha Joober, et al.
Neurology. Genetics|September 21, 2016
GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysisVictoria Mallett, Jay P Ross, Roy N Alcalay, et al.
Genome|November 19, 2013
Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorderCristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, et al.
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2019
Genetic architecture and adaptations of Nunavik InuitSirui Zhou, Pingxing Xie, Amélie Quoibion, et al.
Molecular Psychiatry|June 14, 2018
Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophreniaBoris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, et al.
Plos One|May 27, 2015
Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit populationSirui Zhou, Lan Xiong, Pingxing Xie, et al.
Neurobiology of Aging|May 30, 2016
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's diseaseJay P Ross, Nicolas Dupre, Yves Dauvilliers, et al.
Schizophrenia Research|December 3, 2014
Family-based association study of common variants, rare mutation study and epistatic interaction detection in HDAC genes in schizophreniaOussama Kebir, Boris Chaumette, Mar Fatjó-Vilas, et al.
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