Detalhe da pesquisa
1.
Identification of gene fusions associated with amyotrophic lateral sclerosis.
Muscle Nerve;
69(4): 477-489, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38305586
2.
Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes.
Brain;
146(11): 4608-4621, 2023 11 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37394881
3.
Association of plasma biomarkers with cognition, cognitive decline, and daily function across and within neurodegenerative diseases: Results from the Ontario Neurodegenerative Disease Research Initiative.
Alzheimers Dement;
20(3): 1753-1770, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38105605
4.
Characteristics of the Ontario Neurodegenerative Disease Research Initiative cohort.
Alzheimers Dement;
19(1): 226-243, 2023 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36318754
5.
Rare neurovascular genetic and imaging markers across neurodegenerative diseases.
Alzheimers Dement;
19(12): 5583-5595, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37272523
6.
DnaJC7 in Amyotrophic Lateral Sclerosis.
Int J Mol Sci;
23(8)2022 Apr 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35456894
7.
Loss-of-Function CREB3L3 Variants in Patients With Severe Hypertriglyceridemia.
Arterioscler Thromb Vasc Biol;
40(8): 1935-1941, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32580631
8.
Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter Hyperintensities.
Mov Disord;
35(11): 2090-2095, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32573853
9.
A novel homozygous variant in REN in a family presenting with classic features of disorders involving the renin-angiotensin pathway, without renal tubular dysgenesis.
Am J Med Genet A;
182(10): 2284-2290, 2020 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33043632
10.
Genetic and epigenetic study of an Alzheimer's disease family with monozygotic triplets.
Brain;
142(11): 3375-3381, 2019 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31580390
11.
Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative.
Can J Neurol Sci;
46(5): 491-498, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31217043
12.
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection.
Am J Med Genet A;
173(1): 183-189, 2017 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27991736
13.
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically.
Arterioscler Thromb Vasc Biol;
36(12): 2439-2445, 2016 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27765764
14.
Transcriptomics of Human Brain Tissue in Parkinson's Disease: a Comparison of Bulk and Single-cell RNA Sequencing.
Mol Neurobiol;
2024 Apr 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38578357
15.
Cost-effectiveness of a gene sequencing test for Alzheimer's disease in Ontario.
J Community Genet;
14(2): 135-147, 2023 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36434378
16.
Soluble Epoxide Hydrolase Derived Linoleic Acid Oxylipins, Small Vessel Disease Markers, and Neurodegeneration in Stroke.
J Am Heart Assoc;
12(1): e026901, 2023 01 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36583428
17.
Clinical testing panels for ALS: global distribution, consistency, and challenges.
Amyotroph Lateral Scler Frontotemporal Degener;
24(5-6): 420-435, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36896705
18.
Association of Dual-Task Gait Cost and White Matter Hyperintensity Burden Poststroke: Results From the ONDRI.
Neurorehabil Neural Repair;
37(7): 434-443, 2023 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37269105
19.
Lack of association of TP73 with amyotrophic lateral sclerosis in a large cohort of cases.
Neurobiol Aging;
115: 109-111, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35512496
20.
Sex-stratified RNA-seq analysis reveals traumatic brain injury-induced transcriptional changes in the female hippocampus conducive to dementia.
Front Neurol;
13: 1026448, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36619915