| Year |
Citation |
Score |
| 2010 |
Dastani Z, Pajukanta P, Marcil M, Rudzicz N, Ruel I, Bailey SD, Lee JC, Lemire M, Faith J, Platko J, Rioux J, Hudson TJ, Gaudet D, Engert JC, Genest J. Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects. European Journal of Human Genetics : Ejhg. 18: 342-7. PMID 19844255 DOI: 10.1038/Ejhg.2009.157 |
0.378 |
|
| 2009 |
Meyer P, Nigam A, Marcil M, Tardif JC. The therapeutic potential of high-density lipoprotein mimetic agents in coronary artery disease. Current Atherosclerosis Reports. 11: 329-33. PMID 19664374 DOI: 10.1007/S11883-009-0049-Z |
0.49 |
|
| 2009 |
Rashid S, Marcil M, Ruel I, Genest J. Identification of a novel human cellular HDL biosynthesis defect. European Heart Journal. 30: 2204-12. PMID 19553242 DOI: 10.1093/Eurheartj/Ehp250 |
0.498 |
|
| 2009 |
Solymoss BC, Bourassa MG, Marcil M, Levesque S, Varga S, Campeau L. Long-term rates of cardiovascular events in patients with the metabolic syndrome according to severity of coronary-angiographic alterations Coronary Artery Disease. 20: 1-8. PMID 19050599 DOI: 10.1097/Mca.0B013E32831624A5 |
0.617 |
|
| 2008 |
Lee JC, Weissglas-Volkov D, Kyttälä M, Dastani Z, Cantor RM, Sobel EM, Plaisier CL, Engert JC, van Greevenbroek MM, Kane JP, Malloy MJ, Pullinger CR, Huertas-Vazquez A, Aguilar-Salinas CA, Tusie-Luna T, ... ... Marcil M, et al. WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. American Journal of Human Genetics. 83: 180-92. PMID 18674750 DOI: 10.1016/J.Ajhg.2008.07.002 |
0.391 |
|
| 2008 |
Awan Z, Alrasadi K, Francis GA, Hegele RA, McPherson R, Frohlich J, Valenti D, de Varennes B, Marcil M, Gagne C, Genest J, Couture P. Vascular calcifications in homozygote familial hypercholesterolemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 28: 777-85. PMID 18239150 DOI: 10.1161/Atvbaha.107.160408 |
0.384 |
|
| 2008 |
Krimbou L, Ruel I, Dastani Z, Alrasadi K, Hajj Hassan H, Iatan I, Marcil M, Genest J. Disorders of high‐density lipoprotein biogenesis Annals of Medicine. 40: 39-47. DOI: 10.1080/07853890701689637 |
0.445 |
|
| 2007 |
Dastani Z, Ruel IL, Engert JC, Genest J, Marcil M. Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants do not contribute to low levels of high-density lipoprotein cholesterol. Bmc Medical Genetics. 8: 79. PMID 18088425 DOI: 10.1186/1471-2350-8-79 |
0.466 |
|
| 2007 |
Grenon SM, Lachapelle K, Marcil M, Omeroglu A, Genest J, de Varennes B. Surgical strategies for severe calcification of the aorta (porcelain aorta) in two patients with homozygous familial hypercholesterolemia. The Canadian Journal of Cardiology. 23: 1159-61. PMID 18060104 DOI: 10.1016/S0828-282X(07)70889-9 |
0.376 |
|
| 2006 |
Dastani Z, Engert JC, Genest J, Marcil M. Genetics of high-density lipoproteins. Current Opinion in Cardiology. 21: 329-35. PMID 16755202 DOI: 10.1097/01.Hco.0000231403.94856.Cd |
0.401 |
|
| 2006 |
Krimbou L, Marcil M, Genest J. New insights into the biogenesis of human high-density lipoproteins. Current Opinion in Lipidology. 17: 258-67. PMID 16680030 DOI: 10.1097/01.Mol.0000226117.43178.7C |
0.401 |
|
| 2006 |
Hassan HH, Denis M, Krimbou L, Marcil M, Genest J. Cellular cholesterol homeostasis in vascular endothelial cells. The Canadian Journal of Cardiology. 22: 35B-40B. PMID 16498511 DOI: 10.1016/S0828-282X(06)70985-0 |
0.385 |
|
| 2006 |
Alrasadi K, Ruel IL, Marcil M, Genest J. Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency. Atherosclerosis. 188: 281-91. PMID 16343503 DOI: 10.1016/J.Atherosclerosis.2005.10.048 |
0.351 |
|
| 2006 |
Dastani Z, Quiogue L, Plaisier C, Engert JC, Marcil M, Genest J, Pajukanta P. Evidence for a gene influencing high-density lipoprotein cholesterol on chromosome 4q31.21. Arteriosclerosis, Thrombosis, and Vascular Biology. 26: 392-7. PMID 16322534 DOI: 10.1161/01.Atv.0000198243.83781.A3 |
0.473 |
|
| 2006 |
Ching YL, Lesimple A, Denis M, Vincent J, Larsen A, Mamer O, Krimbou L, Genest J, Marcil M. Increased sphingomyelin content impairs HDL biogenesis and maturation in human Niemann-Pick disease type B Journal of Lipid Research. 47: 622-632. PMID 16319418 DOI: 10.1194/Jlr.M500487-Jlr200 |
0.45 |
|
| 2006 |
Dastani Z, Dangoisse C, Boucher B, Desbiens K, Krimbou L, Dufour R, Hegele RA, Pajukanta P, Engert JC, Genest J, Marcil M. A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians. Atherosclerosis. 185: 127-36. PMID 16023124 DOI: 10.1016/J.Atherosclerosis.2005.05.028 |
0.489 |
|
| 2005 |
Ruel IL, Lamarche B, Mauger JF, Badellino KO, Cohn JS, Marcil M, Couture P. Effect of fenofibrate on plasma lipoprotein composition and kinetics in patients with complete hepatic lipase deficiency. Arteriosclerosis, Thrombosis, and Vascular Biology. 25: 2600-7. PMID 16224048 DOI: 10.1161/01.Atv.0000190700.76493.Bb |
0.34 |
|
| 2005 |
Alawadhi M, Thanassoulis G, Marcil M, Genest J. Genetic lipoprotein disorders and coronary atherosclerosis. Current Atherosclerosis Reports. 7: 196-203. PMID 15811253 DOI: 10.1007/S11883-005-0006-4 |
0.409 |
|
| 2004 |
Denis M, Haidar B, Marcil M, Bouvier M, Krimbou L, Genest J. Characterization of oligomeric human ATP binding cassette transporter A1. Potential implications for determining the structure of nascent high density lipoprotein particles. The Journal of Biological Chemistry. 279: 41529-36. PMID 15280376 DOI: 10.1074/Jbc.M406881200 |
0.352 |
|
| 2004 |
Ruel IL, Couture P, Cohn JS, Bensadoun A, Marcil M, Lamarche B. Evidence that hepatic lipase deficiency in humans is not associated with proatherogenic changes in HDL composition and metabolism. Journal of Lipid Research. 45: 1528-37. PMID 15175359 DOI: 10.1194/Jlr.M400090-Jlr200 |
0.451 |
|
| 2004 |
Marcil M, O'Connell B, Krimbou L, Genest J. High-density lipoproteins: multifunctional vanguards of the cardiovascular system. Expert Review of Cardiovascular Therapy. 2: 417-30. PMID 15151487 DOI: 10.1586/14779072.2.3.417 |
0.513 |
|
| 2004 |
Alenezi MY, Marcil M, Blank D, Sherman M, Genest J. Is the decreased high-density lipoprotein cholesterol in the metabolic syndrome due to cellular lipid efflux defect? The Journal of Clinical Endocrinology and Metabolism. 89: 761-4. PMID 14764793 DOI: 10.1210/Jc.2003-031213 |
0.482 |
|
| 2004 |
Krimbou L, Denis M, Haidar B, Carrier M, Marcil M, Genest J. Molecular interactions between apoE and ABCA1: impact on apoE lipidation. Journal of Lipid Research. 45: 839-48. PMID 14754908 DOI: 10.1194/Jlr.M300418-Jlr200 |
0.412 |
|
| 2004 |
Solymoss BC, Bourassa MG, Campeau L, Sniderman A, Marcil M, Lespérance J, Lévesque S, Varga S. Effect of increasing metabolic syndrome score on atherosclerotic risk profile and coronary artery disease angiographic severity. The American Journal of Cardiology. 93: 159-64. PMID 14715340 DOI: 10.1016/J.Amjcard.2003.09.032 |
0.673 |
|
| 2004 |
Denis M, Haidar B, Marcil M, Bouvier M, Krimbou L, Genest J. Molecular and cellular physiology of apolipoprotein A-I lipidation by the ATP-binding cassette transporter A1 (ABCA1). The Journal of Biological Chemistry. 279: 7384-94. PMID 14660648 DOI: 10.1074/Jbc.M306963200 |
0.365 |
|
| 2004 |
Alenezi MY, Marcil M, Genest J. High-density lipoproteins: target for cardiovascular disease prevention Drug Discovery Today: Disease Mechanisms. 1: 159-164. DOI: 10.1016/J.Ddmec.2004.09.008 |
0.423 |
|
| 2003 |
Solymoss BC, Bourassa MG, Campeau L, Lespérance J, Marcil M, Varga S. Incidence, coronary risk profile and angiographic characteristics of prediabetic and diabetic patients in a population with ischemic heart disease. The Canadian Journal of Cardiology. 19: 1155-60. PMID 14532941 |
0.556 |
|
| 2003 |
Solymoss BC, Bourassa MG, Lespérance J, Levesque S, Marcil M, Varga S, Campeau L. Incidence and clinical characteristics of the metabolic syndrome in patients with coronary artery disease Coronary Artery Disease. 14: 207-212. PMID 12702923 DOI: 10.1097/01.Mca.0000065744.52558.9F |
0.68 |
|
| 2003 |
Marcil M, Bissonnette R, Vincent J, Krimbou L, Genest J. Cellular phospholipid and cholesterol efflux in high-density lipoprotein deficiency. Circulation. 107: 1366-71. PMID 12642355 DOI: 10.1161/01.Cir.0000056764.53152.F9 |
0.523 |
|
| 2003 |
Krimbou L, Marcil M, Chiba H, Genest J. Structural and functional properties of human plasma high density-sized lipoprotein containing only apoE particles. Journal of Lipid Research. 44: 884-92. PMID 12611904 DOI: 10.1194/Jlr.M200273-Jlr200 |
0.442 |
|
| 2003 |
Lee CY, Krimbou L, Vincent J, Bernard C, Larramée P, Genest J, Marcil M. Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol. Human Genetics. 112: 552-62. PMID 12607113 DOI: 10.1007/S00439-002-0893-1 |
0.53 |
|
| 2002 |
Haidar B, Denis M, Krimbou L, Marcil M, Genest J. cAMP induces ABCA1 phosphorylation activity and promotes cholesterol efflux from fibroblasts. Journal of Lipid Research. 43: 2087-94. PMID 12454270 DOI: 10.1194/Jlr.M200235-Jlr200 |
0.384 |
|
| 2002 |
Wellington CL, Yang YZ, Zhou S, Clee SM, Tan B, Hirano K, Zwarts K, Kwok A, Gelfer A, Marcil M, Newman S, Roomp K, Singaraja R, Collins J, Zhang LH, et al. Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol. Journal of Lipid Research. 43: 1939-49. PMID 12401893 DOI: 10.1194/Jlr.M200277-Jlr200 |
0.327 |
|
| 2001 |
Krimbou L, Marcil M, Davignon J, Genest J. Interaction of Lecithin:Cholesterol Acyltransferase (LCAT)·α 2-macroglobulin complex with low density Lipoprotein Receptor-related Protein (LRP): Evidence for an α 2-macroglobulin/LRP receptor-mediated system participating in LCAT clearance Journal of Biological Chemistry. 276: 33241-33248. PMID 11435418 DOI: 10.1074/Jbc.M100326200 |
0.391 |
|
| 2000 |
Clee SM, Kastelein JJ, van Dam M, Marcil M, Roomp K, Zwarts KY, Collins JA, Roelants R, Tamasawa N, Stulc T, Suda T, Ceska R, Boucher B, Rondeau C, DeSouich C, et al. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. The Journal of Clinical Investigation. 106: 1263-70. PMID 11086027 DOI: 10.1172/Jci10727 |
0.531 |
|
| 2000 |
Mott S, Yu L, Marcil M, Boucher B, Rondeau C, Genest J. Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations. Atherosclerosis. 152: 457-68. PMID 10998475 DOI: 10.1016/S0021-9150(99)00498-0 |
0.516 |
|
| 1999 |
Marcil M, Brooks-Wilson A, Clee SM, Roomp K, Zhang LH, Yu L, Collins JA, van Dam M, Molhuizen HO, Loubster O, Ouellette BF, Sensen CW, Fichter K, Mott S, Denis M, et al. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. Lancet. 354: 1341-6. PMID 10533863 DOI: 10.1016/S0140-6736(99)07026-9 |
0.392 |
|
| 1999 |
Brooks-Wilson A, Marcil M, Clee SM, Zhang LH, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HO, Loubser O, Ouelette BF, Fichter K, Ashbourne-Excoffon KJ, Sensen CW, et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nature Genetics. 22: 336-45. PMID 10431236 DOI: 10.1038/11905 |
0.454 |
|
| 1999 |
Marcil M, Yu L, Krimbou L, Boucher B, Oram JF, Cohn JS, Genest J. Cellular Cholesterol Transport and Efflux in Fibroblasts Are Abnormal in Subjects With Familial HDL Deficiency Arteriosclerosis, Thrombosis, and Vascular Biology. 19: 159-169. PMID 9888879 DOI: 10.1161/01.Atv.19.1.159 |
0.481 |
|
| 1997 |
Genest J, Marcil M, Yu L, Batal R, Krimbou L, Boucher B, Davignon J, Oram JF, Cohn JS. 4.P.338 Familial HDL deficiency: A cellular cholesterol transport defect Atherosclerosis. 134: 367. DOI: 10.1016/S0021-9150(97)89864-4 |
0.378 |
|
| 1997 |
Genest J, Marcil M. 4.W22.2 Genetic lipoprotein disorders in premature coronary artery disease Atherosclerosis. 134: 291. DOI: 10.1016/S0021-9150(97)89506-8 |
0.414 |
|
| 1996 |
Marcil M, Krimbou L, Boucher B, Solymoss BC, Cohn JS, Genest J. Abnormal HDL3and apo Al-mediated cellular cholesterol efflux in subjects with familial HDL deficiency Journal of the American College of Cardiology. 27: 385. DOI: 10.1016/S0735-1097(96)82468-5 |
0.391 |
|
| 1995 |
Marcil M, Boucher B, Krimbou L, Solymoss BC, Davignon J, Frohlich J, Genest J. Severe familial HDL deficiency in French-Canadian kindreds. Clinical, biochemical, and molecular characterization. Arteriosclerosis, Thrombosis, and Vascular Biology. 15: 1015-24. PMID 7627690 DOI: 10.1161/01.Atv.15.8.1015 |
0.68 |
|
| 1995 |
Solymoss BC, Marcil M, Chaour M, Gilfix BM, Poitras AM, Campeau L. Fasting hyperinsulinism, insulin resistance syndrome, and coronary artery disease in men and women. The American Journal of Cardiology. 76: 1152-6. PMID 7484901 DOI: 10.1016/S0002-9149(99)80326-9 |
0.634 |
|
| 1994 |
Solymoss BC, Marcil M, Gilfix BM, Gelinas F, Poitras AM, Campeau L. The place of ferritin among risk factors associated with coronary artery disease. Coronary Artery Disease. 5: 231-5. PMID 8199737 |
0.637 |
|
| 1994 |
Marcil M, Boucher B, Solymos BC, Davignon J, Frolich J, Genest J. Severe familial primary hypoalphalipoproteinemia in French Canadian kindred: no association with the apo A-I/C-III/A-IV and A-II gene loci, normal LCAT activity, normal triglyceride levels and lack of clinical manifestations of Tangier Disease Atherosclerosis. 109: 229-230. DOI: 10.1016/0021-9150(94)93921-7 |
0.329 |
|
| 1993 |
Qiu S, Théroux P, Marcil M, Solymoss BC. Plasma endothelin-1 levels in stable and unstable angina. Cardiology. 82: 12-9. PMID 8519005 |
0.611 |
|
| 1993 |
Solymoss BC, Marcil M, Wesolowska E, Lesperance J, Pelletier LC, Campeau L. Risk factors of venous aortocoronary bypass graft disease noted at late symptom-directed angiographic study. The Canadian Journal of Cardiology. 9: 80-4. PMID 8439832 |
0.564 |
|
| 1993 |
Solymoss BC, Marcil M, Wesolowska E, Gilfix BM, Lespérance J, Campeau L. Relation of coronary artery disease in women < 60 years of age to the combined elevation of serum lipoprotein (a) and total cholesterol to high-density cholesterol ratio. The American Journal of Cardiology. 72: 1215-9. PMID 8256694 DOI: 10.1016/0002-9149(93)90286-L |
0.675 |
|
| 1991 |
Qiu SQ, Théroux P, Genest J, Solymoss BC, Robitaille D, Marcil M. Lipoprotein (a) blood levels in unstable angina pectoris, acute myocardial infarction, and after thrombolytic therapy. The American Journal of Cardiology. 67: 1175-9. PMID 1827942 DOI: 10.1016/0002-9149(91)90922-8 |
0.604 |
|
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