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Hôpital de Chicoutimi

Alternate names: Chicoutimi Hospital, Hôpital de Marine, Hôtel-Dieu Saint-Vallier
ROR: 01thfx675
OpenAlex ID: I4405283524
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
2000 · David Altshuler, Joel N. Hirschhorn, et al. · Nature Genetics · 1,772
Hypertriglyceridemic Waist
2000 · Isabelle Lemieux, Agnès Pascot, et al. · Circulation · 953
Evinacumab for Homozygous Familial Hypercholesterolemia
2020 · Frederick J. Raal, Robert S. Rosenson, et al. · New England Journal of Medicine · 833
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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
1998 · Bernard Brais, Jean-Pierre Bouchard, et al. · Nature Genetics · 814
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
2019 · Nicole M. Warrington, Robin N. Beaumont, et al. · Nature Genetics · 600
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Targeting APOC3 in the Familial Chylomicronemia Syndrome
2014 · Daniel Gaudet, Diane Brisson, et al. · New England Journal of Medicine · 500
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Efficacy and Safety of Ezetimibe Coadministered With Atorvastatin or Simvastatin in Patients With Homozygous Familial Hypercholesterolemia
2002 · Claude Gagné, Daniel Gaudet, et al. · Circulation · 485
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF
2000 · James C. Engert, Pierre Bérubé, et al. · Nature Genetics · 440
Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trial
2012 · D Gaudet, J Méthot, et al. · Gene Therapy · 409
2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance
2023 · Marina Cuchel, Frederick J Raal, et al. · European Heart Journal · 403
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Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region
2004 · Jose C. Florez, Noël Burtt, et al. · Diabetes · 307
Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium
2017 · Gemma C Sharp, Lucas A Salas, et al. · Human Molecular Genetics · 294
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Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight
2016 · Jessica Tyrrell, Rebecca C. Richmond, et al. · JAMA · 282
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Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion
1997 · Laura Montermini, Andrea Richeter, et al. · Annals of Neurology · 278
Gestational diabetes mellitus epigenetically affects genes predominantly involved in metabolic diseases
2013 · Stephanie-May Ruchat, Andrée-Anne Houde, et al. · Epigenetics · 269
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Convalescent plasma for hospitalized patients with COVID-19: an open-label, randomized controlled trial
2021 · Philippe Bégin, Jeannie Callum, et al. · Nature Medicine · 265
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Leptin Gene Epigenetic Adaptation to Impaired Glucose Metabolism During Pregnancy
2010 · Luigi Bouchard, Stéphanie Thibault, et al. · Diabetes Care · 245
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Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
2019 · Leanne K. Küpers, Claire Monnereau, et al. · Nature Communications · 239
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Circulating miRNAs as sensitive and specific biomarkers for the diagnosis and monitoring of human diseases: Promises and challenges
2013 · V. De Guire, R. Robitaille, et al. · Clinical Biochemistry · 232
Altered DNA Methylation of Long Noncoding RNA H19 in Calcific Aortic Valve Disease Promotes Mineralization by Silencing NOTCH1
2016 · Fayez Hadji, Marie-Chloé Boulanger, et al. · Circulation · 231
Neurologic Crises in Hereditary Tyrosinemia
1990 · Grant Mitchell, Jean Larochelle, et al. · New England Journal of Medicine · 230
Increased frequency of DRB1*11:01 in anti–hydroxymethylglutaryl‐coenzyme A reductase–associated autoimmune myopathy
2012 · Andrew L. Mammen, Daniel Gaudet, et al. · Arthritis Care & Research · 228
Rare dyslipidaemias, from phenotype to genotype to management: a European Atherosclerosis Society task force consensus statement
2019 · Robert A Hegele, Jan Borén, et al. · The Lancet Diabetes & Endocrinology · 227
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Placental Adiponectin Gene DNA Methylation Levels Are Associated With Mothers’ Blood Glucose Concentration
2012 · Luigi Bouchard, Marie-France Hivert, et al. · Diabetes · 213
Rarity of anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase antibodies in statin users, including those with self‐limited musculoskeletal side effects
2011 · Andrew L. Mammen, Katherine Pak, et al. · Arthritis Care & Research · 204
Works count: 421
Citation count: 69,300
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