Alexandre Dionne-Laporte
Overview
Explore the profile of Alexandre Dionne-Laporte including associated specialties, affiliations and a list of published articles.
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51
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1920
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Recent Articles
1.
Khlaifia A, Jadhav V, Danik M, Badra T, Berryer M, Dionne-Laporte A, et al.
eNeuro
. 2023 Apr;
10(5).
PMID: 37072176
haploinsufficiency in humans causes intellectual disability (ID). SYNGAP1 is highly expressed in cortical excitatory neurons and, reducing its expression in mice accelerates the maturation of excitatory synapses during sensitive developmental...
2.
Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung N, Tardif J, Dieterich K, Dabir T, et al.
Genet Med
. 2020 Sep;
23(1):237.
PMID: 32934366
No abstract available.
3.
Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung N, Tardif J, Dieterich K, Dabir T, et al.
Genet Med
. 2020 Sep;
23(1):149-154.
PMID: 32873933
Purpose: Biallelic variants in TBC1D24, which encodes a protein that regulates vesicular transport, are frequently identified in patients with DOORS (deafness, onychodystrophy, osteodystrophy, intellectual disability [previously referred to as mental...
4.
Ross J, Leblond C, Laurent S, Spiegelman D, Dionne-Laporte A, Camu W, et al.
Neurogenetics
. 2020 May;
21(3):227-242.
PMID: 32385536
"Oligogenic inheritance" is used to describe cases where more than one rare pathogenic variant is observed in the same individual. While multiple variants can alter disease presentation, the necessity of...
5.
Sardaar S, Qi B, Dionne-Laporte A, Rouleau G, Rabbany R, Trakadis Y
BMC Psychiatry
. 2020 Mar;
20(1):92.
PMID: 32111185
Background: Machine learning (ML) algorithms and methods offer great tools to analyze large complex genomic datasets. Our goal was to compare the genomic architecture of schizophrenia (SCZ) and autism spectrum...
6.
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross J, et al.
PLoS One
. 2019 Nov;
14(11):e0225186.
PMID: 31725784
Restless legs syndrome is a common complex disorder with different genetic and environmental risk factors. Here we used human cell lines to conduct an RNA-Seq study and observed how the...
7.
Accogli A, Calabretta S, St-Onge J, Boudrahem-Addour N, Dionne-Laporte A, Joset P, et al.
Am J Hum Genet
. 2019 Oct;
105(4):854-868.
PMID: 31585109
Cadherins constitute a family of transmembrane proteins that mediate calcium-dependent cell-cell adhesion. The extracellular domain of cadherins consists of extracellular cadherin (EC) domains, separated by calcium binding sites. The EC...
8.
Leveille E, Estiar M, Krohn L, Spiegelman D, Dionne-Laporte A, Dupre N, et al.
J Hum Genet
. 2019 Sep;
64(11):1145-1151.
PMID: 31515523
More than 80 known or suspected genes/loci have been reported to be involved in hereditary spastic paraplegia (HSP). Genetic and clinical overlap have been reported between HSP and other neurological...
9.
Zhou S, Xie P, Quoibion A, Ambalavanan A, Dionne-Laporte A, Spiegelman D, et al.
Proc Natl Acad Sci U S A
. 2019 Jul;
116(32):16012-16017.
PMID: 31332017
The Canadian Inuit have a distinct population background that may entail particular implications for the health of its individuals. However, the number of genetic studies examining this Inuit population is...
10.
Callaghan D, Rogic S, Tan P, Calli K, Qiao Y, Baldwin R, et al.
Clin Genet
. 2019 May;
96(3):199-206.
PMID: 31038196
Autism spectrum disorder (ASD) is a highly heterogeneous genetic disorder with strong evidence of ASD-association currently available only for a small number of genes. This makes it challenging to identify...