Marcia MacDonald
Marcia MacDonald
World Anti-Doping Agency
Verified email at wada-ama.org - Homepage
Title
Cited by
Cited by
Year
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
11262004
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
4582002
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
4462007
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
1502004
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
1361999
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
972009
Compositions and methods for silencing apolipoprotein C-III expression
M MacDonald, ACH Lee, I Maclachlan
US Patent 9,023,820, 2015
692015
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
682008
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
612005
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
602002
Compositions and methods for silencing apolipoprotein C-III expression
M MacDonald, ACH Lee, I Maclachlan
US Patent 9,428,751, 2016
432016
Methods for identifying analgesic agents
ML MacDonald, ME Samuels, R Sherrington, YP Goldberg
US Patent 9,086,420, 2015
14*2015
Methods for identifying analgesic agents
ML MacDonald, ME Samuels, R Sherrington, YP Goldberg
US Patent 7,659,082, 2010
142010
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
132009
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
122007
Ironing out neurodegeneration: Mutations in a phospholipase A2 cause neurodegenerative diseases with iron accumulation
MLE MacDonald
Clinical genetics 70 (4), 306-307, 2006
42006
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
32010
Mutations in a G protein‐coupled receptor cause hypogonadotropic hypogonadism in humans and mice
MLE MacDonald
Clinical genetics 65 (3), 177-178, 2004
22004
Pharmacogenetics of antidepressants: serotonin 2A receptor genotype strongly associated with treatment outcome
M Macdonald
Clinical genetics 70 (1), 14-15, 2006
12006
Genetic validation of β‐secretase as a drug target for Alzheimer's Disease
MLE MacDonald
Clinical genetics 65 (6), 459-460, 2004
12004
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Articles 1–20