Betsie Boucher - Concepedia

Concepedia

Author

Betsie Boucher

Royal Victoria Hospital

Also Known As

B Boucher, Betsie Boucher

12

Publications

1.1K

Citations

11

H-Index

32

Concepts

All Affiliations

Royal Victoria Hospital McGill University Montreal Heart Institute Royal Victoria Regional Health Centre Montreal Clinical Research Institute

BB

About

Betsie Boucher is an author at Royal Victoria Hospital specializing in medicine, pathology, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	633
2	Public Health	2	2	76
3	Biochemistry	2	2	95
4	Engineering	1	1	32
5	Biomolecular Engineering	1	1	32

Betsie Boucher

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11

Publications

1.1K

Citations

11

H-Index

	Year	Citations
Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux Michel Marcil, Angela Brooks‐Wilson, Susanne M. Clee, The Lancet Abc 1Mendelian DisorderFamilial Hdl DeficiencyGenetic DisorderGenetics	1999	357
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes Susanne M. Clee, John J.P. Kastelein, Marjel van Dam, Journal of Clinical Investigation	2000	318
Cellular Cholesterol Transport and Efflux in Fibroblasts Are Abnormal in Subjects With Familial HDL Deficiency Michel Marcil, Lu Yu, Larbi Krimbou, Arteriosclerosis Thrombosis and Vascular Biology	1999	89
Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations Stephanie Mott, Lu Yu, Michel Marcil, Atherosclerosis Lipid DisorderCellular Cholesterol EffluxFamilial HypoalphalipoproteinemiaGenetic DisorderGenetics	2000	80
Fenofibrate raises plasma homocysteine levels in the fasted and fed states Rachel Bissonnette, Eileen P. Treacy, Rima Rozen, Atherosclerosis BiochemistryFed StatesMedicinePhysiologyMetabolism	2001	63
A novel nonsense apolipoprotein A-I mutation (apoA-IE136X) causes low HDL cholesterol in French Canadians Zari Dastani, Carole Dangoisse, Betsie Boucher, Atherosclerosis Lipid DisorderOxysterolCardiovascular DiseaseFrench CanadiansGenetics	2005	41
Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects Michel Marcil, Betsie Boucher, Éric Gagné, Journal of Lipid Research	1996	40
Severe Familial HDL Deficiency in French-Canadian Kindreds Michel Marcil, Betsie Boucher, Larbi Krimbou, Arteriosclerosis Thrombosis and Vascular Biology Vascular DiseaseGenetic EpidemiologySmall Hdl ParticlesPathologyHyperlipidemia	1995	35
Structural modification of plasma HDL by phospholipids promotes efficient ABCA1-mediated cholesterol release Houssein Hajj Hassan, Sacha Blain, Betsie Boucher, Journal of Lipid Research Proteinlipid InteractionEngineeringNative PlasmaPlasma HdlLipid Movement	2005	32
Cellular cholesterol efflux is modulated by phospholipid-derived signaling molecules in familial HDL deficiency/Tangier disease fibroblasts Bassam Haidar, Stephanie Mott, Betsie Boucher, Journal of Lipid Research	2001	30

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