Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Huei San Leong"'
Autor:
Michael Parsons, Michael Anderson, Windy Berkofsky-Fessler, Sandrine Caputo, Raymond Chan, Melissa Cline, Fergus Couch, Miguel de la Hoya, Bing-Jian Feng, David Goldgar, Encarna Gomez-Garcia, Susan Hiraki, Megan Holdren, Claude Houdayer, Paul James, Rachid Karam, Huei San Leong, Alexandra Martins, Arjen Mensenkamp, Alvaro Monteiro, Vaishnavi Nathan, Robert O'Connor, Tina Pesaran, Paolo Radice, Marcy Richardson, Gunnar Schmidt, Inge Sokilde Pedersen, Melissa Southey, Sean Tavtigian, Bryony Thompson, Amanda Toland, Emma Tudini, Clare Turnbull, Maaike Vreeswijk, Logan Walker, Lauren Zec, Amanda Spurdle
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100095- (2023)
Externí odkaz:
https://doaj.org/article/4293f81e35c44437b2760aac2b4577ae
Autor:
Huei San Leong, Marnie Blewitt
Publikováno v:
Bio-Protocol, Vol 3, Iss 15 (2013)
Cellular transformation is a widely used method to artificially induce cells to form tumours in vivo. Here, we describe the methodology for malignant transformation of mouse embryonic fibroblasts (MEFs) for transplantation into immunodeficient nude m
Externí odkaz:
https://doaj.org/article/95f9f1cf7a6c487398b221044a604cd4
Autor:
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Liying Zhang, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam
Publikováno v:
Journal of Medical Genetics, 60, 568-575
Journal of Medical Genetics, 60, 6, pp. 568-575
Journal of Medical Genetics, 60, 6, pp. 568-575
BackgroundGermline pathogenic variants inCDH1are associated with increased risk of diffuse gastric cancer and lobular breast cancer. Risk reduction strategies include consideration of prophylactic surgery, thereby making accurate interpretation of ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b92564af059677ad97db8e84364c32ac
https://hdl.handle.net/2066/293518
https://hdl.handle.net/2066/293518
Autor:
Marnie E. Blewitt, Douglas J. Hilton, Warren S. Alexander, Gordon K. Smyth, Ian J. Majewski, James M. Murphy, Miha Pakusch, Jason Corbin, Stanley Lee, Yifang Hu, Kelan Chen, Huei San Leong
Supplementary Material PDF file - 709K, Supplementary Tables 1 and 2, supplementary methods, supplementary figure legends and supplementary figures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55111f649031bfd4f5f7e664a7ea78d5
https://doi.org/10.1158/0008-5472.22398279.v1
https://doi.org/10.1158/0008-5472.22398279.v1
Autor:
Marnie E. Blewitt, Douglas J. Hilton, Warren S. Alexander, Gordon K. Smyth, Ian J. Majewski, James M. Murphy, Miha Pakusch, Jason Corbin, Stanley Lee, Yifang Hu, Kelan Chen, Huei San Leong
Supplementary Tables S3-S4 XLSX file - 576K, Gene set analysis (Camera) and differentially expressed genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1826c40b4776a691d89e58e2f08c66cb
https://doi.org/10.1158/0008-5472.22398276
https://doi.org/10.1158/0008-5472.22398276
Autor:
Xi, Luo, Jamie L, Maciaszek, Bryony A, Thompson, Huei San, Leong, Katherine, Dixon, Sónia, Sousa, Michael, Anderson, Maegan E, Roberts, Kristy, Lee, Amanda B, Spurdle, Arjen R, Mensenkamp, Terra, Brannan, Carolina, Pardo, Liying, Zhang, Tina, Pesaran, Sainan, Wei, Grace-Ann, Fasaye, Chimene, Kesserwan, Brian H, Shirts, Jeremy L, Davis, Carla, Oliveira, Sharon E, Plon, Kasmintan A, Schrader, Rachid, Karam
Publikováno v:
J Med Genet
BACKGROUND: Germline pathogenic variants in CDH1 are associated with increased risk for diffuse gastric cancer and lobular breast cancer. Risk-reduction strategies include consideration of prophylactic surgery, thereby making accurate interpretation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed92a5ffe0a6e46f2cb612ad82e06503
https://pubmed.ncbi.nlm.nih.gov/36600593
https://pubmed.ncbi.nlm.nih.gov/36600593
Autor:
Emma Tudini, James Andrews, David M. Lawrence, Sarah L. King-Smith, Naomi Baker, Leanne Baxter, John Beilby, Bruce Bennetts, Victoria Beshay, Michael Black, Tiffany F. Boughtwood, Kristian Brion, Pak Leng Cheong, Michael Christie, John Christodoulou, Belinda Chong, Kathy Cox, Mark R. Davis, Lucas Dejong, Marcel E. Dinger, Kenneth D. Doig, Evelyn Douglas, Andrew Dubowsky, Melissa Ellul, Andrew Fellowes, Katrina Fisk, Cristina Fortuno, Kathryn Friend, Renee L. Gallagher, Song Gao, Emma Hackett, Johanna Hadler, Michael Hipwell, Gladys Ho, Georgina Hollway, Amanda J. Hooper, Karin S. Kassahn, Rahul Krishnaraj, Chiyan Lau, Huong Le, Huei San Leong, Ben Lundie, Sebastian Lunke, Anthony Marty, Mary McPhillips, Lan T. Nguyen, Katia Nones, Kristen Palmer, John V. Pearson, Michael C.J. Quinn, Lesley H. Rawlings, Simon Sadedin, Louisa Sanchez, Andreas W. Schreiber, Emanouil Sigalas, Aygul Simsek, Julien Soubrier, Zornitza Stark, Bryony A. Thompson, James U, Cassandra G. Vakulin, Amanda V. Wells, Cheryl A. Wise, Rick Woods, Andrew Ziolkowski, Marie-Jo Brion, Hamish S. Scott, Natalie P. Thorne, Amanda B. Spurdle, Lauren Akesson, Richard Allcock, Katie Ashton, Damon A. Bell, Anna Brown, Michael Buckley, John R. Burnett, Linda Burrows, Alicia Byrne, Eva Chan, Corrina Cliffe, Roderick Clifton-Bligh, Susan Dooley, Miriam Fanjul Fernandez, Elizabeth Farnsworth, Thuong Ha, Denae Henry, Duncan Holds, Katherine Holman, Matilda Jackson, Sinlay Kang, Catherine Luxford, Sam McManus, Rachael Mehrtens, Cliff Meldrum, David Mossman, Sarah-Jane Pantaleo, Dean Phelan, Electra Pontikinas, Anja Ravine, Tony Roscioli, Rodney Scott, Keryn Simons, Oliver Vanwageningen
Publikováno v:
Am J Hum Genet
Sharing genomic variant interpretations across laboratories promotes consistency in variant assertions. A landscape analysis of Australian clinical genetic-testing laboratories in 2017 identified that, despite the national-accreditation-body recommen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3847493e457643efaf7244e001b19ac0
https://pubmed.ncbi.nlm.nih.gov/36332611
https://pubmed.ncbi.nlm.nih.gov/36332611
Autor:
Sven Mahner, Robertson Mackenzie, Aline Talhouk, Linda E. Kelemen, Gottfried E. Konecny, Jennifer Alsop, Rosalind Glasspool, Chiu-Chen Tseng, Joy Hendley, Dennis J. Slamon, Jennifer A. Doherty, Andrew Berchuck, Anna H. Wu, Anna M. Piskorz, Chen Wang, Cristina Rodríguez-Antona, D.G.H. de Silva, Valerie Rhenius, Peter A. Fasching, Stacey J. Winham, Gary L. Keeney, Teodora Goranova, Joshy George, Jan Lubinski, Michelle J. Henderson, Rex C. Bentley, Jenny Lester, Sabine Behrens, Joellen M. Schildkraut, Michael E. Carney, Timothy Budden, David G. Huntsman, Oleg Oszurek, Michael S. Anglesio, Jacek Gronwald, Ruby Yun-Ju Huang, Martin Köbel, Javier Benitez, Martin Widschwendter, Melissa C. Larson, Raghwa Sharma, Clara Bodelon, Usha Menon, Janusz Menkiszak, Blake Gilks, María Josefa Mosteiro García, Jesús García-Donas, Wafaa Elatre, Scott H. Kaufmann, Paul Haluska, Pamela J. Thompson, Boris Winterhoff, Susan J. Ramus, Louise A. Brinton, Simon A. Gayther, Mary Anne Rossing, Georgia Chenevix-Trench, Hugh Luk, Jolanta Lissowska, Marc T. Goodman, Billy Chen, Beth Y. Karlan, Naveena Singh, Sian Fereday, Mark E. Sherman, Ana Osorio, Lynne R. Wilkens, Maria P. Intermaggio, Brenda Y. Hernandez, Britton Trabert, Esther Herpel, Mercedes Jimenez-Linan, Janine Senz, Geyi Liu, Celeste Leigh Pearce, Samuel C Y Leong, Iain A. McNeish, Isabelle Ray-Coquard, Susana Banerjee, Malcolm C. Pike, Liz-Anne Lewsley, Helen Steed, Honglin Song, Samantha Hinsley, David D.L. Bowtell, James D. Brenton, Holly R. Harris, Tuan Zea Tan, Cezary Cybulski, Alicia Beeghly-Fadiel, A. Toloczko, Nikilyn Nevins, Robert S. Brown, Darren Ennis, Stephanie Chen, Euan A. Stronach, José Palacios, Sandra Orsulic, Anna deFazio, Geoff Macintyre, Kara L. Cushing-Haugen, Mila Volchek, Aleksandra Gentry-Maharaj, Jenny Chang-Claude, Ellen L. Goode, Paul D.P. Pharoah, Hanwei Sudderuddin, Stefan Kommoss, Derek S. Chiu, Huei San Leong, Peter Sinn, Catherine J. Kennedy, Chloe Karpinskyj, Alison Brand, Amy Lum, Veronica Chow, Nicolas Wentzensen, Tayyebeh M. Nazeran, Nadia Traficante, Dustin Johnson, Yoke-Eng Chiew, Casey S. Greene, Jennifer M Koziak, Renée T. Fortner
Publikováno v:
Clinical Cancer Research. 26:5411-5423
Purpose: Gene expression–based molecular subtypes of high-grade serous tubo-ovarian cancer (HGSOC), demonstrated across multiple studies, may provide improved stratification for molecularly targeted trials. However, evaluation of clinical utility h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bde75a52c672f987ad27c063d5669c57
https://doi.org/10.1158/1078-0432.ccr-20-0103
https://doi.org/10.1158/1078-0432.ccr-20-0103
Autor:
Paul A. James, Amanda B. Spurdle, Victoria Beshay, Jill S. Dolinsky, Jeffrey N. Weitzel, Kelly McGoldrick, Tina Pesaran, Huei San Leong, Lily Hoang, Cristina Fortuno
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(3)
Some variants identified by multigene panel testing of DNA from blood present with low variant allele fraction (VAF), often a manifestation of clonal hematopoiesis. Research has shown that the proportion of variants with low VAF is especially high in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a782c99759c7d648e5004c6c987bab98
https://pubmed.ncbi.nlm.nih.gov/34906512
https://pubmed.ncbi.nlm.nih.gov/34906512
Autor:
Richard Lupat, Jason Li, Jason Ellul, Satwica Yerneni, Anthony T. Papenfuss, Georgina L Ryland, Andrew Fellowes, Piers Blombery, Stephen B. Fox, Ella R. Thompson, Huei San Leong, Michael Dickinson, Amit Kumar, John F. Markham, Wasanthi De Silva
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-2 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2df8ba8c815c11673a9440c90a92ba
https://doi.org/10.1038/s41598-020-67205-0
https://doi.org/10.1038/s41598-020-67205-0