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Allison A. Dilliott, PhD
Allison A. Dilliott, PhD
Department of Neurology and Neurosurgery, Montreal Neurological Institute McGill University
Verified email at mcgill.ca
Title
Cited by
Cited by
Year
Polygenic versus monogenic causes of hypercholesterolemia ascertained clinically
J Wang, JS Dron, MR Ban, JF Robinson, AD McIntyre, M Alazzam, ...
Arteriosclerosis, thrombosis, and vascular biology 36 (12), 2439-2445, 2016
2162016
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
S Zhang, J Cooper-Knock, AK Weimer, M Shi, T Moll, JNG Marshall, ...
Neuron 110 (6), 992-1008. e11, 2022
742022
Targeted next-generation sequencing and bioinformatics pipeline to evaluate genetic determinants of constitutional disease
AA Dilliott, SMK Farhan, M Ghani, C Sato, E Liang, M Zhang, AD McIntyre, ...
JoVE (Journal of Visualized Experiments), e57266, 2018
472018
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration
SMK Farhan, AA Dilliott, M Ghani, C Sato, E Liang, M Zhang, AD McIntyre, ...
NPJ Genomic Medicine 1 (1), 1-11, 2016
312016
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection
L Badalato, SMK Farhan, AA Dilliott, Care4Rare Canada Consortium, ...
American Journal of Medical Genetics Part A 173 (1), 183-189, 2017
262017
Loss-of-Function CREB3L3 Variants in Patients With Severe Hypertriglyceridemia
JS Dron, AA Dilliott, A Lawson, AD McIntyre, BD Davis, J Wang, H Cao, ...
Arteriosclerosis, Thrombosis, and Vascular Biology 40 (8), 1935-1941, 2020
202020
Characteristics of the Ontario neurodegenerative disease research initiative cohort
KM Sunderland, D Beaton, SR Arnott, P Kleinstiver, D Kwan, ...
Alzheimer's & Dementia 19 (1), 226-243, 2023
192023
Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter Hyperintensities
J Ramirez, AA Dilliott, MA Binns, DP Breen, EC Evans, D Beaton, ...
Movement Disorders 35 (11), 2090-2095, 2020
192020
Contribution of rare variant associations to neurodegenerative disease presentation
AA Dilliott, A Abdelhady, KM Sunderland, SMK Farhan, A Abrahao, ...
NPJ Genomic Medicine 6 (1), 80, 2021
152021
DnaJC7 in amyotrophic lateral sclerosis
AA Dilliott, CM Andary, M Stoltz, AA Petropavlovskiy, SMK Farhan, ...
International Journal of Molecular Sciences 23 (8), 4076, 2022
142022
MRI-visible perivascular space volumes, sleep duration and daytime dysfunction in adults with cerebrovascular disease
J Ramirez, MF Holmes, C Berezuk, D Kwan, B Tan, D Beaton, CJM Scott, ...
Sleep Medicine 83, 83-88, 2021
142021
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia
PK Gill, JS Dron, AA Dilliott, AD McIntyre, H Cao, J Wang, IG Movsesyan, ...
Journal of Clinical Lipidology 15 (1), 88-96, 2021
132021
A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner …
LR Wang, A Radonjic, AA Dilliott, AD McIntyre, RA Hegele
Journal of Investigative Medicine High Impact Case Reports 6, 2324709618786770, 2018
132018
Matrin3: Disorder and ALS pathogenesis
A Salem, CJ Wilson, BS Rutledge, A Dilliott, S Farhan, WY Choy, ...
Frontiers in Molecular Biosciences 8, 794646, 2022
122022
Genetic and epigenetic study of an Alzheimer’s disease family with monozygotic triplets
M Zhang, AA Dilliott, R Khallaf, JF Robinson, RA Hegele, M Comishen, ...
Brain 142 (11), 3375-3381, 2019
122019
Association of apolipoprotein E variation with cognitive impairment across multiple neurodegenerative diagnoses
AA Dilliott, KM Sunderland, PM McLaughlin, AC Roberts, EC Evans, ...
Neurobiology of Aging 105, 378. e1-378. e9, 2021
112021
The Ontario neurodegenerative disease research initiative
KM Sunderland, D Beaton, SR Arnott, P Kleinstiver, D Kwan, ...
medRxiv, 2020.07. 30.20165456, 2020
102020
Genetic variation in the ontario neurodegenerative disease research initiative
AA Dilliott, EC Evans, SMK Farhan, M Ghani, C Sato, M Zhang, ...
Canadian Journal of Neurological Sciences 46 (5), 491-498, 2019
82019
Soluble epoxide hydrolase derived linoleic acid oxylipins, small vessel disease markers, and neurodegeneration in stroke
D Yu, N Liang, J Zebarth, Q Shen, M Ozzoude, M Goubran, JS Rabin, ...
Journal of the American Heart Association 12 (1), e026901, 2023
72023
Clinical testing panels for ALS: global distribution, consistency, and challenges
AA Dilliott, A Al Nasser, M Elnagheeb, J Fifita, L Henden, IM Keseler, ...
Amyotrophic lateral sclerosis and frontotemporal degeneration 24 (5-6), 420-435, 2023
42023
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