Guylaine DAmours
Overview
Explore the profile of Guylaine DAmours including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
128
Followers
0
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Recent Articles
1.
DAmours G, Clausen M, Luca S, Reble E, Kodida R, Assamad D, et al.
BMJ Open
. 2024 Sep;
14(9):e090084.
PMID: 39231549
Introduction: Genetic testing is used across medical disciplines leading to unprecedented demand for genetic services. This has resulted in excessive waitlists and unsustainable pressure on the standard model of genetic...
2.
Assamad D, Majeed S, Aguda V, Grewal S, Butkowsky C, Clausen M, et al.
Public Health Genomics
. 2023 Oct;
26(1):194-200.
PMID: 37883926
No abstract available.
3.
Prenatal pleural effusions and chylothorax: An unusual presentation for CM-AVM syndrome due to RASA1
DAmours G, Brunel-Guitton C, Delrue M, Dubois J, Laberge S, Soucy J
Am J Med Genet A
. 2020 Aug;
182(10):2454-2460.
PMID: 32776686
No abstract available.
4.
Beauregard-Lacroix E, Salian S, Kim H, Ehresmann S, DAmours G, Gauthier J, et al.
Eur J Hum Genet
. 2019 Nov;
28(4):461-468.
PMID: 31695177
Neonatal progeroid syndrome, also known as Wiedemann-Rautenstrauch syndrome, is a rare condition characterized by severe growth retardation, apparent macrocephaly with prominent scalp veins, and lipodystrophy. It is caused by biallelic...
5.
Verheije R, Kupchik G, Isidor B, Kroes H, Lynch S, Hawkes L, et al.
Eur J Hum Genet
. 2018 Oct;
27(2):278-290.
PMID: 30291340
Deletions on chromosome 15q14 are a known chromosomal cause of cleft palate, typically co-occurring with intellectual disability, facial dysmorphism, and congenital heart defects. The identification of patients with loss-of-function variants...
6.
DAmours G, Langlois M, Mathonnet G, Fetni R, Nizard S, Srour M, et al.
BMC Med Genomics
. 2014 Dec;
7:70.
PMID: 25539807
Background: Molecular karyotyping is now the first-tier genetic test for patients affected with unexplained intellectual disability (ID) and/or multiple congenital anomalies (MCA), since it identifies a pathogenic copy number variation...
7.
Hitz M, Lemieux-Perreault L, Marshall C, Feroz-Zada Y, Davies R, Yang S, et al.
PLoS Genet
. 2012 Sep;
8(9):e1002903.
PMID: 22969434
Left-sided congenital heart disease (CHD) encompasses a spectrum of malformations that range from bicuspid aortic valve to hypoplastic left heart syndrome. It contributes significantly to infant mortality and has serious...
8.
DAmours G, Bureau G, Boily M, Cyr M
Behav Brain Res
. 2011 Mar;
221(1):108-17.
PMID: 21376085
Much research has implicated the striatum in motor learning, but the underlying mechanism is still under extensive investigation. In this study, genome-wide analysis of gene expression was conducted in mice...