Hasil Pencarian - Simone M. Rowley

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  1. 1
    Detection of interruptions in the GAA trinucleotide repeat expansion in the FXN gene of Friedreich ataxia

    Detection of interruptions in the GAA trinucleotide repeat expansion in the FXN gene of Friedreich ataxia oleh Timothy P. Holloway, Simone M. Rowley, Martin B. Delatycki, Joseph P. Sarsero

    Diterbitkan 2011-03-01
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  2. 2
    Long range regulation of human FXN gene expression.

    Long range regulation of human FXN gene expression. oleh Novita Puspasari, Simone M Rowley, Lavinia Gordon, Paul J Lockhart, Panos A Ioannou, Martin B Delatycki, Joseph P Sarsero

    Diterbitkan 2011-01-01
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  3. 3
    Analysis of RAD51D in ovarian cancer patients and families with a history of ovarian or breast cancer.

    Analysis of RAD51D in ovarian cancer patients and families with a history of ovarian or breast cancer. oleh Ella R Thompson, Simone M Rowley, Sarah Sawyer, kConfab, Diana M Eccles, Alison H Trainer, Gillian Mitchell, Paul A James, Ian G Campbell

    Diterbitkan 2013-01-01
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  4. 4
    Molecular comparison of pure ovarian fibroma with serous benign ovarian tumours

    Molecular comparison of pure ovarian fibroma with serous benign ovarian tumours oleh Sally M. Hunter, Genevieve V. Dall, Maria A. Doyle, Richard Lupat, Jason Li, Prue Allan, Simone M. Rowley, David Bowtell, On behalf of AOCS, Ian G. Campbell, Kylie L. Gorringe

    Diterbitkan 2020-07-01
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  5. 5
    Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes

    Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes oleh Deepak N. Subramanian, Magnus Zethoven, Simone McInerny, James A. Morgan, Simone M. Rowley, Jue Er Amanda Lee, Na Li, Kylie L. Gorringe, Paul A. James, Ian G. Campbell

    Diterbitkan 2020-04-01
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  6. 6
    Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer

    Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer oleh Belle W. X. Lim, Na Li, Simone M. Rowley, Ella R. Thompson, Simone McInerny, Magnus Zethoven, Rodney J. Scott, Lisa Devereux, Erica K. Sloan, Paul A. James, Ian G. Campbell

    Diterbitkan 2022-01-01
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  7. 7
    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 oleh Tanjina Kader, David L. Goode, Stephen Q. Wong, Jacquie Connaughton, Simone M. Rowley, Lisa Devereux, David Byrne, Stephen B. Fox, Gisela Mir Arnau, Richard W. Tothill, Ian G. Campbell, Kylie L. Gorringe

    Diterbitkan 2016-11-01
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  8. 8
    MicroRNA genes and their target 3'-untranslated regions are infrequently somatically mutated in ovarian cancers.

    MicroRNA genes and their target 3'-untranslated regions are infrequently somatically mutated in ovarian cancers. oleh Georgina L Ryland, Jennifer L Bearfoot, Maria A Doyle, Samantha E Boyle, David Y H Choong, Simone M Rowley, Australian Ovarian Cancer Study Group, Richard W Tothill, Kylie L Gorringe, Ian G Campbell

    Diterbitkan 2012-01-01
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  9. 9
    Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs

    Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs oleh Na Li, Simone M. Rowley, Ella R. Thompson, Simone McInerny, Lisa Devereux, Kaushalya C. Amarasinghe, Magnus Zethoven, Richard Lupat, David Goode, Jason Li, Alison H. Trainer, Kylie L. Gorringe, Paul A. James, Ian G. Campbell

    Diterbitkan 2018-01-01
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  10. 10
    Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study

    Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study oleh Na Li, Belle W. X. Lim, Ella R. Thompson, Simone McInerny, Magnus Zethoven, Dane Cheasley, Simone M. Rowley, Michelle W. Wong-Brown, Lisa Devereux, Kylie L. Gorringe, Erica K. Sloan, Alison Trainer, Rodney J. Scott, Paul A. James, Ian G. Campbell

    Diterbitkan 2021-06-01
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  11. 11
    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. oleh Ella R Thompson, Maria A Doyle, Georgina L Ryland, Simone M Rowley, David Y H Choong, Richard W Tothill, Heather Thorne, kConFab, Daniel R Barnes, Jason Li, Jason Ellul, Gayle K Philip, Yoland C Antill, Paul A James, Alison H Trainer, Gillian Mitchell, Ian G Campbell

    Diterbitkan 2012-09-01
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  12. 12
    The molecular origin and taxonomy of mucinous ovarian carcinoma

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

    Diterbitkan 2019-09-01
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  13. 13
    Meeting abstracts from the Annual Conference on Hereditary Cancers 2015

    Meeting abstracts from the Annual Conference on Hereditary Cancers 2015 oleh Ella R. Thompson, Michelle Wong-Brown, Simone M. Rowley, Susan Dooley, Na Lil, Michael Hipwell, Simone McInerny, Cliff Meldrum, Lisa Devereux, David Mossman, Alison H. Trainer, Briar-Rose Millar, Gillian Mitchell, Cate Smith, Paul A. James, Ian G. Campbell, Rodney J. Scott, Katarzyna Klonowska, Anna Jakubowska, Jelena Maksimenko, Arvids Irmejs, Miki Nakazawa-Miklasevica, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, Edvins Miklasevics, Karolina Tęcza, Jolanta Pamuła-Piłat, Joanna Łanuszewska, Ewa Grzybowska, Edvins Miklasevics, M. Szwiec, J. Tomiczek-Szwiec, M. Gełej, C. Cybulski, T. Huzarski, E. Kilar, Małgorzata Oczko-Wojciechowska, Michał Świerniak, Jolanta Krajewska, Małgorzata Kowalska, Tomasz Tyszkiewicz, Agnieszka Pawlaczek, Michał Jarząb, Monika Kowal, Dagmara Rusinek, Jadwiga Zebracka-Gala, Agnieszka Czarniecka, Barbara Jarzab, Andrzej Plawski, Paweł Borun, Joanna Szczepinska, Monika Siolek, Beata Kozak-Klonowska, Katarzyna Kaczmarek, Magdalena Muszyńska, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska, Jan Lubiński, Grzegorz Sukiennicki, Magdalena Muszyńska, Wojciech Marciniak, Katarzyna Kaczmarek, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska, Jan Lubiński, Michał Post

    Diterbitkan 2017-10-01
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