Resultats de la cerca - Simone M. Rowley

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  1. 1
    Pre-Invasive Ovarian Mucinous Tumors Are Characterized by <i>CDKN2A</i> and <i>RAS</i> Pathway Aberrations

    Pre-Invasive Ovarian Mucinous Tumors Are Characterized by <i>CDKN2A</i> and <i>RAS</i> Pathway Aberrations per Sally M. Hunter, Kylie L. Gorringe, Michael Christie, Simone M. Rowley, David D.L. Bowtell, Ian Campbell

    Publicat 2012
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  2. 2
    Mutational Landscape of Ovarian Adult Granulosa Cell Tumors from Whole Exome and Targeted <i>TERT</i> Promoter Sequencing

    Mutational Landscape of Ovarian Adult Granulosa Cell Tumors from Whole Exome and Targeted <i>TERT</i> Promoter Sequencing per Maria Alexiadis, Simone M. Rowley, Simon Chu, Dilys T.H. Leung, Colin J.R. Stewart, Kaushalya Amarasinghe, Ian Campbell, Peter J. Fuller

    Publicat 2018
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  3. 3
    <i><scp>RNF43</scp></i> is a tumour suppressor gene mutated in mucinous tumours of the ovary

    <i><scp>RNF43</scp></i> is a tumour suppressor gene mutated in mucinous tumours of the ovary per Georgina L. Ryland, Sally M. Hunter, Maria Doyle, Simone M. Rowley, Michael Christie, Prue E. Allan, David D.L. Bowtell, Kylie L. Gorringe, Ian Campbell

    Publicat 2012
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  4. 4
    Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

    Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors per Georgina L. Ryland, Sally M. Hunter, Maria Doyle, Franco Caramia, Jason Li, Simone M. Rowley, Michael Christie, Prue E. Allan, Andrew N. Stephens, David D.L. Bowtell, Ian Campbell, Kylie L. Gorringe

    Publicat 2015
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  5. 5
    Loss of heterozygosity: what is it good for?

    Loss of heterozygosity: what is it good for? per Georgina L. Ryland, Maria Doyle, David L. Goode, Samantha E. Boyle, David Y.H. Choong, Simone M. Rowley, Jason Li, David D.L. Bowtell, Richard W. Tothill, Ian Campbell, Kylie L. Gorringe

    Publicat 2015
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  6. 6
    Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue

    Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue per Tanjina Kader, David L. Goode, Stephen Q. Wong, Jacquie Connaughton, Simone M. Rowley, Lisa Devereux, David J. Byrne, Stephen B. Fox, Gisela Mir Arnau, Richard W. Tothill, Ian Campbell, Kylie L. Gorringe

    Publicat 2016
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  7. 7
    Erratum to: Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

    Erratum to: Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors per Georgina L. Ryland, Sally M. Hunter, Maria Doyle, Franco Caramia, Jason Li, Simone M. Rowley, Michael Christie, Prue E. Allan, Andrew N. Stephens, David D.L. Bowtell, Ian Campbell, Kylie L. Gorringe

    Publicat 2017
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  8. 8
    Copy number analysis of ductal carcinoma in situ with and without recurrence

    Copy number analysis of ductal carcinoma in situ with and without recurrence per Kylie L. Gorringe, Sally M. Hunter, Jia‐Min Pang, Ken Opeskin, Prue Hill, Simone M. Rowley, David Y.H. Choong, Ella R. Thompson, Alexander Dobrovic, Stephen B. Fox, G. Bruce Mann, Ian Campbell

    Publicat 2015
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  9. 9
    Population-based genetic testing of asymptomatic women for breast and ovarian cancer susceptibility

    Population-based genetic testing of asymptomatic women for breast and ovarian cancer susceptibility per Simone M. Rowley, Lyon Mascarenhas, Lisa Devereux, Na Li, Kaushalya Amarasinghe, Magnus Zethoven, Jue Er Amanda Lee, Alexandra Lewis, James Morgan, Sharne Limb, Mary‐Anne Young, Paul A. James, Alison H. Trainer, Ian Campbell

    Publicat 2018
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  10. 10
    Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles

    Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles per Ella R. Thompson, Maria Doyle, Georgina L. Ryland, Simone M. Rowley, David Y.H. Choong, Richard W. Tothill, Heather Thorne, Daniel R. Barnes, Jason Li, Jason Ellul, Gayle K. Philip, Yoland C. Antill, Paul A. James, Alison H. Trainer, Gillian Mitchell, Ian Campbell

    Publicat 2012
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  11. 11
    Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes

    Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes per Sally M. Hunter, Michael S. Anglesio, Georgina L. Ryland, Raghwa Sharma, Yoke-Eng Chiew, Simone M. Rowley, Maria Doyle, Jason Li, C. Blake Gilks, Phillip Moss, Prue E. Allan, Andrew N. Stephens, David G. Huntsman, Anna deFazio, David D.L. Bowtell, Kylie L. Gorringe, Ian Campbell

    Publicat 2015
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  12. 12
    <i>FXN</i> methylation predicts expression and clinical outcome in Friedreich ataxia

    <i>FXN</i> methylation predicts expression and clinical outcome in Friedreich ataxia per Marguerite V. Evans‐Galea, Nissa Carrodus, Simone M. Rowley, Louise A. Corben, Geneieve Tai, Richard Saffery, John C. Galati, Nicholas C. Wong, Jeffrey M. Craig, David R. Lynch, Sean R. Regner, Alicia Brocht, Susan Perlman, Khalaf Bushara, Christopher M. Gómez, George Wilmot, Lingli Li, Elizabeth Varley, Martin B. Delatycki, Joseph P. Sarsero

    Publicat 2011
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  13. 13
    Therapeutic options for mucinous ovarian carcinoma

    Therapeutic options for mucinous ovarian carcinoma per Kylie L. Gorringe, Dane Cheasley, Matthew J. Wakefield, Georgina L. Ryland, Prue E. Allan, Kathryn Alsop, Kaushalya Amarasinghe, Sumitra Ananda, David D.L. Bowtell, Michael Christie, Yoke-Eng Chiew, Michael Churchman, Anna deFazio, Sián Fereday, C. Blake Gilks, Charlie Gourley, Alison Hadley, Joy Hendley, Sally M. Hunter, Scott H. Kaufmann, Catherine J. Kennedy, Martin Köbel, Cécile Le Page, Jason Li, Richard Lupat, Orla McNally, Jessica N. McAlpine, Jan Pyman, Simone M. Rowley, Carolina Salazar, Hugo Saunders, Timothy Semple, Andrew N. Stephens, Niko Thio, Michelle C. Torres, Nadia Traficante, Magnus Zethoven, Yoland Antill, Ian Campbell, Clare L. Scott

    Publicat 2020
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  14. 14
    Integrated multi-omics for rapid rare disease diagnosis on a national scale

    Integrated multi-omics for rapid rare disease diagnosis on a national scale per Sebastian Lunke, Sophie E. Bouffler, Chirag Patel, Sarah A. Sandaradura, Meredith Wilson, Jason Pinner, Matthew F. Hunter, Christopher Barnett, Mathew Wallis, Benjamin Kamien, Tiong Yang Tan, Mary‐Louise Freckmann, Belinda Chong, Dean Phelan, David Francis, Karin S. Kassahn, Thuong Ha, Song Gao, Peer Arts, Matilda R. Jackson, Hamish S. Scott, Stefanie Eggers, Simone M. Rowley, Kirsten Boggs, Ana Rakonjac, Gemma R. Brett, M. De Silva, Amanda Springer, Michelle C. Ward, Kirsty Stallard, Cas Simons, Thomas Conway, Andreas Halman, Nicole J. Van Bergen, Tim Sikora, Liana N. Semcesen, David A. Stroud, Alison G. Compton, David R. Thorburn, Katrina M. Bell, Simon Sadedin, Kathryn N. North, John Christodoulou, Zornitza Stark

    Publicat 2023
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  15. 15
    The molecular origin and taxonomy of mucinous ovarian carcinoma

    The molecular origin and taxonomy of mucinous ovarian carcinoma per Dane Cheasley, Matthew J. Wakefield, Georgina L. Ryland, Prue E. Allan, Kathryn Alsop, Kaushalya Amarasinghe, Sumitra Ananda, Michael S. Anglesio, George Au‐Yeung, Maret Böhm, David D.L. Bowtell, Alison H. Brand, Georgia Chenevix‐Trench, Michael Christie, Yoke-Eng Chiew, Michael Churchman, Anna deFazio, Renee Demeo, Rhiannon Dudley, Nicole Fairweather, Clare G. Fedele, Sián Fereday, Stephen B. Fox, C. Blake Gilks, Charlie Gourley, Neville F. Hacker, Alison Hadley, Joy Hendley, Gwo‐Yaw Ho, Siobhan Hughes, David G. Hunstman, Sally M. Hunter, Tom Jobling, Kimberly R. Kalli, Scott H. Kaufmann, Catherine J. Kennedy, Martin Köbel, Cécile Le Page, Jason Li, Richard Lupat, Orla McNally, Jessica N. McAlpine, Anne‐Marie Mes‐Masson, Linda Mileshkin, Diane Provencher, Jan Pyman, Kurosh Rahimi, Simone M. Rowley, Carolina Salazar, Goli Samimi, Hugo Saunders, Timothy Semple, R. Sharma, Alice J. Sharpe, Andrew N. Stephens, Niko Thio, Michelle C. Torres, Nadia Traficante, Zhongyue Xing, Magnus Zethoven, Yoland Antill, Clare L. Scott, Ian Campbell, Kylie L. Gorringe

    Publicat 2019
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  16. 16
    No evidence that protein truncating variants in<i>BRIP1</i>are associated with breast cancer risk: implications for gene panel testing

    No evidence that protein truncating variants in<i>BRIP1</i>are associated with breast cancer risk: implications for gene panel testing per Douglas F. Easton, Fabienne Lesueur, Brennan Decker, Kyriaki Michailidou, Jun Li, Jamie Allen, Craig Luccarini, Karen A. Pooley, Mitul Shah, Manjeet K. Bolla, Sophia Wang, Joe Dennis, Jamil Ahmad, Ella R. Thompson, Francesca Damiola, Maroulio Pertesi, Catherine Voegele, Noura Mebirouk, Nivonirina Robinot, Geoffroy Durand, Nathalie Forey, Robert Luben, Shahana Ahmed, Kristiina Aittomäki, Hoda Anton‐Culver, Volker Arndt, Caroline Baynes, Matthias W. Beckman, Javier Benı́tez, David Van Den Berg, William J. Blot, Natalia Bogdanova, Stig E. Bojesen, Hermann Brenner, Jenny Chang‐Claude, Kee Seng Chia, Ji‐Yeob Choi, Don Conroy, Angela Cox, Simon S. Cross, Kamila Czene, Hatef Darabi, Peter Devilee, Mikael Eriksson, Peter A. Fasching, Jonine D. Figueroa, Henrik Flyger, Florentia Fostira, Montserrat García‐Closas, Graham G. Giles, Gord Glendon, Anna González‐Neira, Pascal Guénel, Christopher A. Haiman, Per Hall, Steven N. Hart, Mikael Hartman, Maartje J. Hooning, Chia‐Ni Hsiung, Hidemi Ito, Anna Jakubowska, Paul A. James, Esther M. John, Nichola Johnson, Michael E. Jones, Maria Kabisch, Daehee Kang, Veli‐Matti Kosma, Vessela Kristensen, Diether Lambrechts, Na Li, Annika Lindblom, Jirong Long, Artitaya Lophatananon, Jan Lubiński, Graham J. Mann, Siranoush Manoukian, Sara Margolin, Keitaro Matsuo, Alfons Meindl, Gillian Mitchell, Kenneth Muir, Ines Nevelsteen, Ans van den Ouweland, Paolo Peterlongo, Sze Yee Phuah, Katri Pylkäs, Simone M. Rowley, Suleeporn Sangrajrang, Rita K. Schmutzler, Chen‐Yang Shen, Xiao‐Ou Shu, Melissa C. Southey, Harald Surowy, Anthony J. Swerdlow, Soo‐Hwang Teo, Rob A.�E.�M. Tollenaar, Ian Tomlinson, Diana Torres, Thérèse Truong

    Publicat 2016
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