Luigi Bouchard
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Explore the profile of Luigi Bouchard including associated specialties, affiliations and a list of published articles.
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152
Citations
3792
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Recent Articles
1.
Chen Y, Tilves C, Bohn B, Doyon M, Bouchard L, Perron P, et al.
Pediatr Obes
. 2025 Mar;
:e70007.
PMID: 40059505
Objective: To examine gut microbiota diversity, composition and metabolites in relation to overall mass (OM), fat mass (FM) and lean soft tissue mass (LSTM) measured by dual x-ray absorptiometry (DXA)...
2.
Clement A, Legare C, Desgagne V, Thibeault K, White F, Scott M, et al.
BMC Pregnancy Childbirth
. 2025 Mar;
25(1):255.
PMID: 40057749
Background: Gestational hypertension (GH) is linked to an increased risk of cardiometabolic diseases for both mother and child, but we lack reliable biomarkers to identify high-risk women early in pregnancy....
3.
St-Amour S, Tessier L, Harnois J, Allard C, Lavoie A, Caron P, et al.
PLoS One
. 2025 Feb;
20(2):e0305511.
PMID: 39928707
Type 2 diabetes (T2D) is a chronic disorder affecting 462 million worldwide, often managed with metformin as first-line treatment. However, metformin's response varies among individuals, including up to 30% experiencing...
4.
Satkunanathan P, Allard C, Doyon M, Perron P, Bouchard L, Hivert M, et al.
BMC Pregnancy Childbirth
. 2025 Jan;
25(1):41.
PMID: 39833733
Background: Lower maternal insulin sensitivity during pregnancy is associated with greater fetal adiposity. Physical activity can improve insulin sensitivity, but it is not known if physical behaviours influence the known...
5.
Legeay S, Poitras M, Tremblay-Vaillancourt V, Fournier A, Bouchard L, Leblanc J, et al.
BMJ Open
. 2025 Jan;
15(1):e089642.
PMID: 39788778
Introduction: MODY2 (maturity-onset diabetes of the young type 2, MIM125851) is a monogenic diabetes with an autosomal dominant transmission caused by a variant of the gene. MODY2 is often confused...
6.
Guay S, Paquette M, Taschereau A, Desgagne V, Bouchard L, Bernard S, et al.
Clin Biochem
. 2025 Jan;
135():110873.
PMID: 39756670
Background And Aims: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS) are the two main causes of severe hypertriglyceridemia (sHTG). FCS is a rare autosomal recessive form of sHTG,...
7.
Clement A, Legare C, Desgagne V, Thibeault K, White F, Scott M, et al.
Pregnancy Hypertens
. 2024 Nov;
34:95-103.
PMID: 39491415
Objectives: To identify first trimester circulating microRNAs associated with preeclampsia (PE) and assess their predictive value in two independent cohorts METHODS: Circulating microRNAs were quantified from plasma samples collected at...
8.
Diemer E, Tuhkanen J, Sammallahti S, Heinonen K, Neumann A, Robinson S, et al.
Epigenetics
. 2024 Oct;
19(1):2413815.
PMID: 39418282
Low maternal vitamin D concentrations during pregnancy have been associated with a range of offspring health outcomes. DNA methylation is one mechanism by which the maternal vitamin D status during...
9.
Bohn B, Tilves C, Chen Y, Doyon M, Bouchard L, Perron P, et al.
BMJ Open Gastroenterol
. 2024 Aug;
11(1).
PMID: 39209769
Objective: Gut microbes and microbe-dependent metabolites (eg, tryptophan-kynurenine-serotonin pathway metabolites) have been linked to systemic inflammation, but the microbiota-metabolite-inflammation axis remains uncharacterised in children. Here we investigated whether gut microbiota...
10.
Josefson J, Kuang A, Allard C, Bianco M, Lowe Jr W, Scholtens D, et al.
Obesity (Silver Spring)
. 2024 Aug;
32(10):1923-1933.
PMID: 39165088
Objective: This study aimed to identify whether cord blood DNA methylation at specific loci is associated with neonatal adiposity, a key risk factor for childhood obesity. Methods: An epigenome-wide association...