Most cited papers from Cégep de Chicoutimi

Cégep de Chicoutimi

What are the most cited papers from Cégep de Chicoutimi?

The most cited paper from Cégep de Chicoutimi is "Triglyceride-rich lipoproteins and their remnants: metabolic insights, role in atherosclerotic cardiovascular disease, and emerging therapeutic strategies—a consensus statement from the European Atherosclerosis Society" (Henry N. Ginsberg et al., 2021), with 966 citations. Next come "Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease" (785) and "Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors" (664).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 80 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Triglyceride-rich lipoproteins and their remnants: metabolic insights, role in atherosclerotic cardiovascular disease, and emerging therapeutic strategies—a consensus statement from the European Atherosclerosis Society Henry N. Ginsberg et al. · European Heart Journal Open access	30 Jul 2021	966
2	Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease John David Rioux et al. · Nature Genetics	Oct 2001	785
3	Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors Nicole M. Warrington et al. · Nature Genetics Open access208 authors	May 2019	664
4	ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF James C. Engert, Pierre R. Bérubé, Jocelyne Mercier et al. · Nature Genetics	Feb 2000	439
5	A 10-year study of mortality in a cohort of patients with myotonic dystrophy Jean Mathieu, Per O. Allard, Lynne A. Potvin et al. · Neurology	May 1999	416
6	Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trial Daniel Gaudet, Julie Méthot, Stéphane Déry et al. · Gene Therapy Open access	21 Jun 2012	407
7	Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium Gemma C. Sharp et al. · Human Molecular Genetics Open access	18 Jul 2017	295
8	The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum Heidi Carmen Howard et al. · Nature Genetics	7 Oct 2002	283
9	CARD15 Genetic Variation in a Quebec Population: Prevalence, Genotype-Phenotype Relationship, and Haplotype Structure Severine A.R.A. Vermeire, Gary Wild, Kerry Kocher et al. · The American Journal of Human Genetics Open access	Jul 2002	277
10	Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion Laura Montermini et al. · Annals of Neurology	May 1997	273
11	Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight Leanne K. Küpers et al. · Nature Communications ReviewOpen access127 authors	23 Apr 2019	271
12	Gestational diabetes mellitus epigenetically affects genes predominantly involved in metabolic diseases Stéphanie-May Ruchat, Andrée-Anne Houde, Grégory Voisin et al. · Epigenetics Open access	16 Aug 2013	268
13	Leptin Gene Epigenetic Adaptation to Impaired Glucose Metabolism During Pregnancy Luigi Bouchard, Stéphanie Thibault, Simon‐Pierre Guay et al. · Diabetes Care Open access	19 Aug 2010	236
14	Neurologic Crises in Hereditary Tyrosinemia Grant A. Mitchell, Jean Larochelle, Marie A. Lambert et al. · New England Journal of Medicine	15 Feb 1990	235
15	Altered DNA Methylation of Long Noncoding RNA H19 in Calcific Aortic Valve Disease Promotes Mineralization by Silencing NOTCH1 Fayez Hadji, Marie‐Chloé Boulanger, Simon‐Pierre Guay et al. · Circulation	28 Oct 2016	232
16	A Randomized Trial of Antioxidant Vitamins to Prevent Second Primary Cancers in Head and Neck Cancer Patients Isabelle Bairati, François Meyer, Malorie Gélinas et al. · JNCI Journal of the National Cancer Institute	5 Apr 2005	231
17	Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in Quebec points to a locus of major effect on chromosome 12q23-q24 Jean-Philippe Morissette, André Villeneuve, Lise Bordeleau et al. · American Journal of Medical Genetics	15 Oct 1999	218
18	Placental Adiponectin Gene DNA Methylation Levels Are Associated With Mothers’ Blood Glucose Concentration Luigi Bouchard, Marie‐France Hivert, Simon‐Pierre Guay et al. · Diabetes Open access	7 Mar 2012	213
19	Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics Robin N. Beaumont et al. · Human Molecular Genetics Open access	2 Jan 2018	202
20	Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder Nicholas Barden, Mario Harvey, Bernard Gagné et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics	3 May 2006	202
21	Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia Marie‐Claude Vohl, Patricia Lepage, Daniel Gaudet et al. · Journal of Lipid Research Open access	Jun 2000	177
22	New concepts in the diagnosis and management of choroidal metastases Thibaud Mathis, Pauline Jardel, Olivier J. Loria et al. · Progress in Retinal and Eye Research Open access	19 Sep 2018	176
23	Antioxidant vitamins supplementation and mortality: A randomized trial in head and neck cancer patients Isabelle Bairati, François Meyer, Édith Jobin et al. · International Journal of Cancer	13 Jul 2006	171
24	Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium Janine F. Felix et al. · International Journal of Epidemiology Open access124 authors	24 Aug 2017	169
25	IGF2 DNA methylation is a modulator of newborn’s fetal growth and development Julie St‐Pierre, Marie‐France Hivert, Patrice Perron et al. · Epigenetics Open access	6 Sep 2012	163
26	Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies M. Geoffrey Hayes et al. · Diabetes Open access	Aug 2013	154
27	Leptin and adiponectin DNA methylation levels in adipose tissues and blood cells are associated with BMI, waist girth and LDL-cholesterol levels in severely obese men and women Andrée-Anne Houde, Cécilia Légaré, Simon Biron et al. · BMC Medical Genetics Open access	30 Apr 2015	148
28	Normal skin wound and hypertrophic scar myofibroblasts have differential responses to apoptotic inductors Véronique J. Moulin, Sébastien Larochelle, Céline Langlois et al. · Journal of Cellular Physiology	16 Sep 2003	146
29	Autosomal recessive spastic ataxia of Charlevoix–Saguenay Jean‐Pierre Bouchard, Andréa Richter, Jean Mathieu et al. · Neuromuscular Disorders	Oct 1998	142
30	Relationship Between Chronic Hypercapnia and Inspiratory-Muscle Weakness in Myotonic Dystrophy Paul Bégin, Jean Mathieu, José Almirall et al. · American Journal of Respiratory and Critical Care Medicine	Jul 1997	141
31	ABCA1 gene promoter DNA methylation is associated with HDL particle profile and coronary artery disease in familial hypercholesterolemia Simon‐Pierre Guay, Diane Brisson, Johannie Munger et al. · Epigenetics Open access	May 2012	136
32	Epidermis promotes dermal fibrosis: role in the pathogenesis of hypertrophic scars Judith Bellemare, Charles J. Roberge, Danielle Bergeron et al. · The Journal of Pathology	17 Mar 2005	135
33	Genealogical reconstruction of myotonic dystrophy in the Saguenay‐Lac‐Saint‐ Jean area (Quebec, Canada) Jean Mathieu, Marc De Braekeleer, Claude Prévost · Neurology	May 1990	132
34	Epigenetic programming of obesity and diabetes by in utero exposure to gestational diabetes mellitus Stéphanie-May Ruchat, Marie‐France Hivert, Luigi Bouchard · Nutrition Reviews	Oct 2013	130
35	Effects of noninvasive ventilation on lung hyperinflation in stable hypercapnic COPD Orlando Díaz, Paul Bégin, Bernardita Torrealba et al. · European Respiratory Journal Open access	Dec 2002	128
36	Sleep complaints in patients with myotonic dystrophy Luc Laberge, Paul Bégin, Jacques Yves Montplaisir et al. · Journal of Sleep Research	23 Feb 2004	127
37	Genes, maternal smoking, and the offspring brain and body during adolescence: Design of the Saguenay Youth Study Zdenka Pausová et al. · Human Brain Mapping Open access	27 Apr 2007	126
38	Genetics of Glucose regulation in Gestation and Growth (Gen3G): a prospective prebirth cohort of mother–child pairs in Sherbrooke, Canada Laetitia Guillemette, Catherine Allard, Marilyn Lacroix et al. · BMJ Open Open access	Feb 2016	117
39	Crushing Virtual Cigarettes Reduces Tobacco Addiction and Treatment Discontinuation Benoît Girard, Benoît Girard, Vincent Turcotte et al. · CyberPsychology & Behavior	Oct 2009	116
40	Myotonic dystrophy Jean Mathieu, Marc De Braekeleer, Claude Prévost et al. · Neurology	1992	115
41	Canadian Cardiovascular Society Position Statement on Familial Hypercholesterolemia Jacques J. Genest, Robert Alexander Hegele, Jean Bergeron et al. · Canadian Journal of Cardiology Open access	3 Oct 2014	114
42	PPARGC1α gene DNA methylation variations in human placenta mediate the link between maternal hyperglycemia and leptin levels in newborns Sandra C. Côté, Valérie Gagné‐Ouellet, Simon‐Pierre Guay et al. · Clinical Epigenetics Open access	22 Jun 2016	105
43	The role of telementoring and telerobotic assistance in the provision of laparoscopic colorectal surgery in rural areas Herawaty Sebajang, Patrick Trudeau, Al Dougall et al. · Surgical Endoscopy	3 Jul 2006	104
44	Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean. C Morin, Grant A. Mitchell, Jonathan R. LaRochelle et al. · PubMed	Aug 1993	101
45	Functional Analysis of LDLR (Low-Density Lipoprotein Receptor) Variants in Patient Lymphocytes to Assess the Effect of Evinacumab in Homozygous Familial Hypercholesterolemia Patients With a Spectrum of LDLR Activity Poulabi Banerjee, Kuo‐Chen Chan, Michel Tarabocchia et al. · Arteriosclerosis Thrombosis and Vascular Biology Open access	3 Oct 2019	96
46	Hereditary motor and sensory neuropathy with agenesis of the corpus callosum Nicolas Dupré, Heidi Carmen Howard, Jean Mathieu et al. · Annals of Neurology	25 Jun 2003	96
47	Effect of liver fatty acid binding protein (FABP) T94A missense mutation on plasma lipoprotein responsiveness to treatment with fenofibrate. Charles Brouillette, Yohan Bossé, Louis Pérusse et al. · PubMed	2004	96
48	Role of Tumor Necrosis Factor-α Gene Locus in Obesity and Obesity-Associated Hypertension in French Canadians Zdenka Pausová, Benoît Deslauriers, Daniel Gaudet et al. · Hypertension	Jul 2000	95
49	Correlates of Body Dissatisfaction in Children Jacinthe Dion, Jennifer Hains, Patrick Vachon et al. · The Journal of Pediatrics	Feb 2016	94
50	Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11 Andréa Richter, John David Rioux, Jean‐Pierre Bouchard et al. · The American Journal of Human Genetics Open access	Mar 1999	94

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.