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Nadia Prigoda-Lee
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Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies
DE Rushlow, BM Mol, JY Kennett, S Yee, S Pajovic, BL Thériault, ...
The lancet oncology 14 (4), 327-334, 2013
4012013
Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma
H Dimaras, V Khetan, W Halliday, M Orlic, NL Prigoda, B Piovesan, ...
Human molecular genetics 17 (10), 1363-1372, 2008
3292008
SMAD4 mutations found in unselected HHT patients
CJ Gallione, JA Richards, TGW Letteboer, D Rushlow, NL Prigoda, ...
Journal of medical genetics 43 (10), 793-797, 2006
2732006
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP–HHT syndrome
C Gallione, AS Aylsworth, J Beis, T Berk, B Bernhardt, RD Clark, ...
American journal of medical genetics Part A 152 (2), 333-339, 2010
1812010
Detection of mosaic RB1 mutations in families with retinoblastoma
D Rushlow, B Piovesan, K Zhang, NL Prigoda‐Lee, MN Marchong, ...
Human mutation 30 (5), 842-851, 2009
1762009
Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations
NL Prigoda, S Savas, SA Abdalla, B Piovesan, D Rushlow, ...
Journal of medical genetics 43 (9), 722-728, 2006
1442006
Phenotypic and Genotypic Expression of Self-incompatibility Haplotypes in Arabidopsis lyrata Suggests Unique Origin of Alleles in Different Dominance Classes
NL Prigoda, A Nassuth, BK Mable
Molecular Biology and Evolution 22 (7), 1609-1620, 2005
822005
FGFR3 mutations, but not FGFR3 expression and FGFR3 copy-number variations, are associated with favourable non-muscle invasive bladder cancer
Y Neuzillet, BWG van Rhijn, NL Prigoda, B Bapat, L Liu, PJ Bostrom, ...
Virchows Archiv 465, 207-213, 2014
292014
Identification of clinically relevant mosaicism in type I hereditary haemorrhagic telangiectasia
NP Lee, D Matevski, D Dumitru, B Piovesan, D Rushlow, BL Gallie
Journal of medical genetics 48 (5), 353-357, 2011
162011
Retinoblastoma: The evidence does matter
NL Prigoda-Leea, D Rushlowa, B Piovesan, K Zhang, H Dimaras, ...
Analytical Cellular Pathology 31, 249-250, 2009
12009
A family with a novel chromosomal rearrangement: A resource to identify a further gene for pulmonary arteriovenous malformations and hereditary haemorrhagic telangiectasia
CL Shovlin, N Prigoda, FS Govani
Thorax 62, A115-A115, 2007
12007
Phenotypic and molecular expression of self-incompatibility alleles in Arabidopsis lyrata
N Prigoda
University of Guelph, 2004
12004
NOT KNUDSON'S RETINOBLASTOMA: ONE HIT CANCER INITIATED BY THE MYCN ONCOGENE?
BL Gallie, D Rushlow, KY Jennifer, B Mol, S Yee, S Pajovic, R Pang, ...
PEDIATRIC BLOOD & CANCER 59 (6), 986-986, 2012
2012
Loss of RB1 is insufficient to cause human retinoblastoma
H Dimaras, V Khetan, W Halliday, M Orlic, N Prigoda, B Piovesan, ...
Cancer Research 68 (9_Supplement), 4548-4548, 2008
2008
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