| Year |
Citation |
Score |
| 2008 |
Giguere A, Chagnon P, Hebert J. Deregulated Expression of Ubiquitin-Specific Peptidase Genes in Myeloid Leukemia Blood. 112: 4481-4481. DOI: 10.1182/Blood.V112.11.4481.4481 |
0.324 |
|
| 2006 |
Chagnon P, Schneider R, Hébert J, Fortin PR, Provost S, Belisle C, Gingras M, Bolduc V, Perreault C, Silverman E, Busque L. Identification and characterization of an Xp22.33;Yp11.2 translocation causing a triplication of several genes of the pseudoautosomal region 1 in an XX male patient with severe systemic lupus erythematosus. Arthritis and Rheumatism. 54: 1270-8. PMID 16575839 DOI: 10.1002/Art.21733 |
0.323 |
|
| 2006 |
Giguere A, Hazourli S, Meftah D, Fetni R, Chagnon P, Hebert J. The Ubiquitin Specific Peptidase 42 Gene (USP42) Is Recurrently Involved as a Fusion Gene with RUNX1 in Acute Myeloid Leukemia with the t(7;21)(p22;q22) Cryptic Translocation. Blood. 108: 4273-4273. DOI: 10.1182/Blood.V108.11.4273.4273 |
0.314 |
|
| 2005 |
Hazourli S, Chagnon P, Fetni R, Busque L, Hebert J. Overexpression of MEL1 as a Novel Fusion Partner of AML1 in the Blastic Phase of Chronic Myeloid Leukemia with the Recurrent Cryptic Translocation t(1;21)(p36.3;q22). Blood. 106: 4332-4332. DOI: 10.1182/Blood.V106.11.4332.4332 |
0.315 |
|
| 2005 |
Devaux C, Chagnon P, Belisle C, Soulieres D, Busque L. Hemoglobin Ville-Marie: A New β-Globin Variant (del480C) Causing Oxydative Hemolysis. Blood. 106: 3783-3783. DOI: 10.1182/Blood.V106.11.3783.3783 |
0.33 |
|
| 2002 |
Chagnon P, Michaud J, Mitchell G, Mercier J, Marion JF, Drouin E, Rasquin-Weber A, Hudson TJ, Richter A. A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. American Journal of Human Genetics. 71: 1443-9. PMID 12417987 DOI: 10.1086/344580 |
0.309 |
|
| 1999 |
Chagnon P, Gee M, Filion M, Robitaille Y, Belouchi M, Gauvreau D. Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population. American Journal of Medical Genetics. 85: 20-30. PMID 10377009 DOI: 10.1002/(Sici)1096-8628(19990702)85:1<20::Aid-Ajmg6>3.0.Co;2-K |
0.587 |
|
| 1996 |
Delacourte A, Robitaille Y, Sergeant N, Buée L, Hof PR, Wattez A, Laroche-Cholette A, Mathieu J, Chagnon P, Gauvreau D. Specific pathological Tau protein variants characterize Pick's disease. Journal of Neuropathology and Experimental Neurology. 55: 159-68. PMID 8786374 DOI: 10.1097/00005072-199602000-00004 |
0.58 |
|
| 1995 |
Chagnon P, Bétard C, Robitaille Y, Cholette A, Gauvreau D. Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases. Neuroreport. 6: 711-5. PMID 7605932 DOI: 10.1097/00001756-199503270-00002 |
0.579 |
|
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