Amirthagowri Ambalavanan

Amirthagowri Ambalavanan

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Amirthagowri Ambalavanan

Amirthagowri Ambalavanan

Publications by authors named "Amirthagowri Ambalavanan"

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25Publications

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Genetic architecture and adaptations of Nunavik Inuit.

Proc Natl Acad Sci U S A 2019 Aug 22;116(32):16012-16017. Epub 2019 Jul 22.

Montreal Neurological Institute and Hospital, McGill University, Montréal, Québec, Canada H3A 2B4;

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http://dx.doi.org/10.1073/pnas.1810388116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689950PMC
August 2019

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population.

Neurobiol Aging 2018 08 10;68:160.e1-160.e7. Epub 2018 Mar 10.

School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China; Centre for Genome Sciences, The University of Hong Kong, Hong Kong, China; State Key Laboratory for Cognitive and Brain Sciences, The University of Hong Kong, Hong Kong, China; HKU-SIRI/ZIRI, The University of Hong Kong, Hong Kong, China; HKU-SUSTech Joint Laboratories of Matrix Biology and Diseases, The University of Hong Kong, Hong Kong, China. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.03.006DOI Listing
August 2018

No rare deleterious variants from , , and are associated with essential tremor.

Neurol Genet 2017 Oct 19;3(5):e195. Epub 2017 Oct 19.

Montreal Neurological Institute and Hospital (G.H., A.A., J.-F.S., C.S.L., D.S., S.B.L., C.V.B., P.A.D., G.A.R.), Quebec, Canada; Department of Human Genetics (G.H., A.A., C.S.L., P.A.D., G.A.R.) and Department of Neurology and Neurosurgery (J.-F.S., P.A.D., G.A.R.), McGill University, Montreal, Quebec, Canada; Xenon Pharmaceuticals Inc (C.G.), Burnaby, British Columbia, Canada; André Barbeau Movement Disorders Unit (M.P., S.C.), Centre Hospitalier Universitaire de Montréal (CHUM)-Notre-Dame, Quebec, Canada; Department of Medicine (N.D.), Faculty of Medicine, Laval University, Quebec, Canada; Département des Sciences Neurologiques (N.D.), CHU de Québec (Enfant-Jésus), Quebec, Canada; Department of Medical Genetics (C.V.-G.), University of British Columbia, Vancouver, British Columbia, Canada; Division of Neurology (A.R.), Saskatchewan Movement Disorders Program, University of Saskatchewan, Saskatoon Health Region, Saskatoon, Canada; and Département des Sciences Fondamentales (S.L.G.), Université du Québec à Chicoutimi, Saguenay, Canada.

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http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
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http://dx.doi.org/10.1212/NXG.0000000000000195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281551PMC
October 2017

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population.

Am J Hum Genet 2016 Nov 13;99(5):1072-1085. Epub 2016 Oct 13.

Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.09.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097946PMC
November 2016

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

Neurol Genet 2016 Oct 8;2(5):e104. Epub 2016 Sep 8.

Montreal Neurological Institute (V.M., J.P.R., A.A., P.A.D., G.A.R., Z.G.-O.), Department of Human Genetics (J.P.R., A.A., G.A.R., Z.G.-O.), Department of Neurology and Neurosurgery (P.A.D., G.A.R., Z.G.-O.), McGill University, Quebec, Canada; Department of Neurology and Taub Institute for Research on Alzheimer's Disease and the Aging Brain (R.N.A.), College of Physicians and Surgeons, Columbia University, New York, NY; and Section on Molecular Neurogenetics (E.S.), Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD.

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http://dx.doi.org/10.1212/NXG.0000000000000104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017539PMC
October 2016

Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.

Neurobiol Aging 2016 09 3;45:212.e13-212.e17. Epub 2016 May 3.

Department of Human Genetics, McGill University, Montréal, Quebec, Canada; Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2016.04.023DOI Listing
September 2016

The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder.

Neurobiol Aging 2016 07 6;43:180.e7-180.e13. Epub 2016 Apr 6.

Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada; Department of Human Genetics, McGill University, Montréal, Quebec, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2016.03.029DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892956PMC
July 2016

Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Mol Genet Genomic Med 2016 Jul 11;4(4):447-56. Epub 2016 Mar 11.

Department of Neurology and NeurosurgeryMontreal Neurological InstituteMcGill University3801 UniversityMontrealQuebecH3A 2B4Canada; Department of BiologyUniversity of British ColumbiaKelownaBC. V1V 1V7Canada.

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http://dx.doi.org/10.1002/mgg3.215DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947863PMC
July 2016

Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.

PLoS One 2015 26;10(5):e0128255. Epub 2015 May 26.

Montreal Neurological Institute and Hospital, McGill University, Montréal (Que), Canada; Department of Neurology and Neurosurgery, McGill University, Montréal (Que), Canada.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0128255PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444093PMC
April 2016

Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome.

Sleep Med 2015 Sep 17;16(9):1151-5. Epub 2015 Jun 17.

Montreal Neurological Institute and McGill University, Montréal, QC, Canada; Department of Human Genetics, McGill University, Montréal, QC, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.sleep.2015.06.002DOI Listing
September 2015

Family-based association study of common variants, rare mutation study and epistatic interaction detection in HDAC genes in schizophrenia.

Schizophr Res 2014 Dec 18;160(1-3):97-103. Epub 2014 Oct 18.

Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine Paris Descartes, Service Hospitalo-Universitaire, Centre Hospitalier Sainte-Anne, Paris, France; INSERM, U894, Laboratory "Pathophysiology of Psychiatric Disorders", Centre of Psychiatry and Neurosciences, Paris, France; Institut de Psychiatrie-GDR 3557 de Psychiatrie, France. Electronic address:

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http://dx.doi.org/10.1016/j.schres.2014.09.029DOI Listing
December 2014

Methylation of BDNF in women with bulimic eating syndromes: associations with childhood abuse and borderline personality disorder.

Prog Neuropsychopharmacol Biol Psychiatry 2014 Oct 5;54:43-9. Epub 2014 May 5.

Eating Disorders Program, Douglas University Institute, Montreal, Quebec, Canada; Psychiatry Department, McGill University, Montreal, Quebec, Canada; Research Centre, Douglas University Institute, Montreal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.pnpbp.2014.04.010DOI Listing
October 2014