Marcia MacDonald

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Michael HaydenKillam Professor, University of British ColumbiaVerified email at cmmt.ubc.ca
Marie-Pierre DubéProfessor of Medicine, Université de MontréalVerified email at umontreal.ca
Tomas GanzDistinguished Professor of Medicine and Pathology, UCLAVerified email at mednet.ucla.edu
Elizabeta NemethProfessor of Medicine, UCLAVerified email at mednet.ucla.edu
marianna politouNational and Kapodistrian University of AthensVerified email at med.uoa.gr
Ajamete KaykasNovartis Institutes for Biomedical ResearchVerified email at novartis.com
Bart StaelsProfesseur Université LilleVerified email at pasteur-lille.fr
Gibson WTProfessor, University of British ColumbiaVerified email at cfri.ubc.ca
Brian WongDepartment of Surgery, Washington University School of MedicineVerified email at wustl.edu
John CHAPMANSorbonne University and Pitie-Salpetriere University HospitalVerified email at upmc.fr
Mahmoud A. PouladiAssociate Professor, Department of Medical Genetics, University of British ColumbiaVerified email at ubc.ca
Joanna KarasinskaPancreas Centre BCVerified email at cmmt.ubc.ca
Angela Brooks-WilsonHead of Cancer Genetics, Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency ProfessorVerified email at bcgsc.ca
Bruce A VallanceUniversity of British ColumbiaVerified email at cw.bc.ca
Simon WarbyUniversity of MontrealVerified email at umontreal.ca
Stefanie Butlandhttps://www.openscapes.org/Verified email at cmmt.ubc.ca
Roger C. GreenFaculty of Medicine, Memorial University of NewfoundlandVerified email at mun.ca
Francis OuelletteOrigin BioinformaticsVerified email at bioinformatics.ca
Guy RouleauMontreal Neurological Institute-Hospital, McGill UniversityVerified email at mcgill.ca
Melissa Beth GlierResearch Scientist | BC Centre for Disease Control

Marcia MacDonald

Research for the Front Lines

Verified email at researchforthefrontlines.ca - Homepage

community-led research biomarkers anti-doping genomics/proteomics metabolic syndrome


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Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis G Papanikolaou, ME Samuels, EH Ludwig, MLE MacDonald, ... Nature genetics 36 (1), 77-82, 2004	1253	2004
Loss‐of‐function mutations in the Nav1. 7 gene underlie congenital indifference to pain in multiple human populations YP Goldberg, J MacFarlane, ML MacDonald, J Thompson, M Dube, ... Clinical genetics 71 (4), 311-319, 2007	565	2007
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy J Robitaille, MLE MacDonald, A Kaykas, LC Sheldahl, J Zeisler, MP Dubé, ... Nature genetics 32 (2), 326-330, 2002	544	2002
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates RG Lafrenière, MLE MacDonald, MP Dubé, J MacFarlane, M O’Driscoll, ... The American Journal of Human Genetics 74 (5), 1064-1073, 2004	172	2004
Allele replacement: an application that permits rapid manipulation of herpes simplex virus type 1 genomes BC Horsburgh, MM Hubinette, D Qiang, MLE MacDonald, F Tufaro Gene therapy 6 (5), 922-930, 1999	143	1999
Compositions and methods for silencing apolipoprotein C-III expression M MacDonald, ACH Lee, I Maclachlan US Patent 9,023,820, 2015	117	2015
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis MLE MacDonald, M van Eck, RB Hildebrand, BWC Wong, N Bissada, ... Arteriosclerosis, thrombosis, and vascular biology 29 (3), 341-347, 2009	116	2009
Compositions and methods for silencing apolipoprotein C-III expression M MacDonald, ACH Lee, I Maclachlan US Patent 9,428,751, 2016	81	2016
Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice MLE MacDonald, RR Singaraja, N Bissada, P Ruddle, R Watts, ... Journal of lipid research 49 (1), 217-229, 2008	79	2008
Identification and functional analysis of a naturally occurring E89K mutation in the ABCA1 gene of the WHAM chicken AD Attie, Y Hamon, AR Brooks-Wilson, MP Gray-Keller, MLE MacDonald, ... Journal of lipid research 43 (10), 1610-1617, 2002	74	2002
Genetic variants of frizzled‐4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity MLE MacDonald, YP Goldberg, J Macfarlane, ME Samuels, MT Trese, ... Clinical genetics 67 (4), 363-366, 2005	68	2005
Methods for identifying analgesic agents ML MacDonald, ME Samuels, R Sherrington, YP Goldberg US Patent 7,659,082, 2010	17	2010
Absence of stearoyl-CoA desaturase-1 does not promote DSS-induced acute colitis MLE MacDonald, N Bissada, BA Vallance, MR Hayden Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2009	13	2009
Juvenile hemochromatosis gene (hfe2a), expression products and uses thereof M Samuels, E Ludwig, M MacDonald, P Franchini, Y Goldberg, R Kamboj, ... US Patent App. 10/552,158, 2007	12	2007
Methods for identifying analgesic agents ML MacDonald, ME Samuels, R Sherrington, YP Goldberg US Patent 9,086,420, 2015	9*	2015
Ironing out neurodegeneration: Mutations in a phospholipase A2 cause neurodegenerative diseases with iron accumulation MLE MacDonald Clinical genetics 70 (4), 306-307, 2006	4	2006
The metabolic phenotype of SCD1-deficient mice is independent of melanin-concentrating hormone MB Glier, P Pissios, SL Babich, MLE Macdonald, MR Hayden, ... Peptides 31 (1), 123-129, 2010	3	2010
Mutations in a G protein‐coupled receptor cause hypogonadotropic hypogonadism in humans and mice MLE MacDonald Clinical genetics 65 (3), 177-178, 2004	2	2004
Pharmacogenetics of antidepressants: serotonin 2A receptor genotype strongly associated with treatment outcome M Macdonald Clinical genetics 70 (1), 14-15, 2006	1	2006
Mutations in TGF‐β receptor type‐2 cause Marfan's syndrome JR Helm, MLE MacDonald Clinical genetics 67 (1), 26-27, 2005	1	2005

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