Articles with public access mandates - John S. WayeLearn more
Available somewhere: 12
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ...
Nature genetics 43 (4), 295-301, 2011
Mandates: US National Institutes of Health
Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene
AD Paterson, JM Rommens, B Bharaj, J Blavignac, I Wong, M Diamandis, ...
Blood, The Journal of the American Society of Hematology 115 (6), 1264-1266, 2010
Mandates: Canadian Institutes of Health Research
Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes
M Diamandis, AD Paterson, JM Rommens, DK Veljkovic, J Blavignac, ...
Blood, The Journal of the American Society of Hematology 113 (7), 1543-1546, 2009
Mandates: Canadian Institutes of Health Research, Genome Canada
αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia
L Buitrago, A Rendon, Y Liang, I Simeoni, A Negri, ...
Proceedings of the National Academy of Sciences 112 (15), E1898-E1907, 2015
Mandates: US National Institutes of Health, British Heart Foundation, UK Medical …
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)
MS Lebo, KR Zakoor, K Chun, MD Speevak, JS Waye, E McCready, ...
Genetics in Medicine 20 (3), 294-302, 2018
Mandates: Canadian Institutes of Health Research, Genome Canada
Targeted gene sequencing identifies variants in the protein C and endothelial protein C receptor genes in patients with unprovoked venous thromboembolism
C Wu, DJ Dwivedi, L Pepler, Z Lysov, J Waye, J Julian, K Desch, ...
Arteriosclerosis, thrombosis, and vascular biology 33 (11), 2674-2681, 2013
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by …
CPM Hayward, M Liang, S Tasneem, A Soomro, JS Waye, AD Paterson, ...
PLoS One 12 (3), e0173991, 2017
Mandates: Canadian Institutes of Health Research, Heart and Stroke Foundation of …
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation
MS Badin, JK Iyer, M Chong, L Graf, GE Rivard, JS Waye, AD Paterson, ...
Haemophilia 23 (3), e204-e213, 2017
Mandates: Natural Sciences and Engineering Research Council of Canada
An evaluation of genetic causes and environmental risks for bilateral optic atrophy
AT Chen, L Brady, DE Bulman, ANE Sundaram, AR Rodriguez, ...
PLoS One 14 (11), e0225656, 2019
Mandates: Canadian Institutes of Health Research
Targeted gene sequencing to identify polymorphisms in the protein C and EPCR genes in patients with unprovoked venous thromboembolism
C Wu, D Dwivedi, L Pepler, Z Lysov, J Waye, J Julian, K Desch, ...
Arteriosclerosis, thrombosis, and vascular biology 33 (11), 2674, 2013
Mandates: Canadian Institutes of Health Research, Heart and Stroke Foundation of Canada
Expression of embryonic zeta-globin and epsilon-globin chains in
W Tang, SP Cai, B Eng, MC Poon, JS Waye, N Illum, DH Chui
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
Two novel beta-thalassemia mutations in the 5'and 3'noncoding
SP Cai, B Eng, WH Francombe, NF Olivieri, AG Kendall, JS Waye, ...
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
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