Tu Nguyen-Dumont
Tu Nguyen-Dumont
Senior Research Fellow, Monash University
Verified email at monash.edu
Cited by
Cited by
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
DJ Park, F Lesueur, T Nguyen-Dumont, M Pertesi, F Odefrey, F Hammet, ...
The American Journal of Human Genetics 90 (4), 734-739, 2012
Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus
S Garritano, F Gemignani, C Voegele, T Nguyen-Dumont, ...
BMC genetics 10 (1), 5, 2009
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation …
F Le Calvez-Kelm, F Lesueur, F Damiola, M Vallée, C Voegele, ...
Breast Cancer Research 13 (1), R6, 2011
Description and validation of high‐throughput simultaneous genotyping and mutation scanning by high‐resolution melting curve analysis
T Nguyen‐Dumont, FL Calvez‐Kelm, N Forey, S McKay‐Chopin, ...
Human mutation 30 (6), 884-890, 2009
A high-plex PCR approach for massively parallel sequencing
T Nguyen-Dumont, BJ Pope, F Hammet, MC Southey, DJ Park
Biotechniques 55 (2), 69-74, 2013
Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families
ZL Teo, DJ Park, E Provenzano, CA Chatfield, FA Odefrey, ...
Breast Cancer Res 15 (1), R17, 2013
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome–spectrum cancers
DJ Park, K Tao, F Le Calvez-Kelm, T Nguyen-Dumont, N Robinot, ...
Cancer discovery 4 (7), 804-815, 2014
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
MC Southey, DJ Park, T Nguyen-Dumont, I Campbell, E Thompson, ...
Breast Cancer Research 15 (3), 1-2, 2013
Multigene testing of moderate-risk genes: be mindful of the missense
EL Young, BJ Feng, AW Stark, F Damiola, G Durand, N Forey, TC Francy, ...
Journal of medical genetics 53 (6), 366-376, 2016
Tumour morphology predicts PALB2 germline mutation status
ZL Teo, E Provenzano, GS Dite, DJ Park, C Apicella, SD Sawyer, ...
British journal of cancer 109 (1), 154-163, 2013
PALB2: research reaching to clinical outcomes for women with breast cancer
MC Southey, I Winship, T Nguyen-Dumont
Hereditary Cancer in Clinical Practice 14 (1), 1, 2016
Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry
T Nguyen-Dumont, F Hammet, M Mahmoodi, H Tsimiklis, ZL Teo, R Li, ...
Breast cancer research and treatment 149 (2), 547-554, 2015
Differential allelic expression in leukoblast from patients with acute myeloid leukemia suggests genetic regulation of CDA, DCK, NT5C2, NT5C3, and TP53
LP Jordheim, T Nguyen-Dumont, X Thomas, C Dumontet, SV Tavtigian
Drug Metabolism and Disposition 36 (12), 2419-2423, 2008
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families
X Yang, G Leslie, A Doroszuk, S Schneider, J Allen, B Decker, ...
Journal of Clinical Oncology, 2019
ROVER variant caller: read-pair overlap considerate variant-calling software applied to PCR-based massively parallel sequencing datasets
BJ Pope, T Nguyen-Dumont, F Hammet, DJ Park
Source code for biology and medicine 9 (1), 1-5, 2014
FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine
T Nguyen-Dumont, A Myszka, P Karpinski, MM Sasiadek, H Akopyan, ...
BMC medical genetics 19 (1), 12, 2018
Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2
T Nguyen-Dumont, ZL Teo, BJ Pope, F Hammet, M Mahmoodi, H Tsimiklis, ...
BMC medical genomics 6 (1), 48, 2013
Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients
HN Hasmad, KN Lai, WX Wen, DJ Park, T Nguyen-Dumont, PCE Kang, ...
Gynecologic oncology 141 (2), 318-322, 2016
Cross-platform compatibility of Hi-Plex, a streamlined approach for targeted massively parallel sequencing
T Nguyen-Dumont, BJ Pope, F Hammet, M Mahmoodi, H Tsimiklis, ...
Analytical biochemistry 442 (2), 127-129, 2013
FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
BJ Pope, T Nguyen-Dumont, F Odefrey, F Hammet, R Bell, K Tao, ...
BMC bioinformatics 14 (1), 1-9, 2013
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