Torthaí cuardaigh - Kasmintan A. Schrader

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  1. 1
    Cancer Genomics and Inherited Risk

    Cancer Genomics and Inherited Risk de réir Zsofia K. Stadler, Kasmintan A. Schrader, Joseph Vijai, Mark E. Robson, Kenneth Offit

    Foilsithe / Cruthaithe 2014
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  2. 2
    Genetics of gastric cancer: what do we know about the genetic risks?

    Genetics of gastric cancer: what do we know about the genetic risks? de réir Thomas P. Slavin, Jeffrey N. Weitzel, Susan L. Neuhausen, Kasmintan A. Schrader, Carla Oliveíra, Rachid Karam

    Foilsithe / Cruthaithe 2019
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  3. 3
    Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq

    Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq de réir Vahid Akbari, Vincent C. T. Hanlon, Kieran O’Neill, Louis Lefebvre, Kasmintan A. Schrader, Peter M. Lansdorp, Steven J.M. Jones

    Foilsithe / Cruthaithe 2022
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  4. 4
    Germline BRCA1 and BRCA2 Mutations in Ovarian Cancer

    Germline BRCA1 and BRCA2 Mutations in Ovarian Cancer de réir Kasmintan A. Schrader, Jane Hurlburt, Steve E. Kalloger, Samantha Hansford, Sean Young, David G. Huntsman, C. Blake Gilks, Jessica N. McAlpine

    Foilsithe / Cruthaithe 2012
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  5. 5
    Hereditary diffuse gastric cancer: association with lobular breast cancer

    Hereditary diffuse gastric cancer: association with lobular breast cancer de réir Kasmintan A. Schrader, Serena Masciari, Niki Boyd, Sara J. Wiyrick, Pardeep Kaurah, Janine Senz, Wylie Burke, Henry T. Lynch, Judy E. Garber, David G. Huntsman

    Foilsithe / Cruthaithe 2007
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  6. 6
    The cost and cost trajectory of whole‐genome analysis guiding treatment of patients with advanced cancers

    The cost and cost trajectory of whole‐genome analysis guiding treatment of patients with advanced cancers de réir Deirdre Weymann, Janessa Laskin, Robyn Roscoe, Kasmintan A. Schrader, Stephen Chia, Stephen Yip, Winson Y. Cheung, Karen A. Gelmon, Aly Karsan, Daniel J. Renouf, Marco A. Marra, Dean A. Regier

    Foilsithe / Cruthaithe 2017
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  7. 7
    Consensus Statement: Recommendations on Actionable Biomarker Testing for Thyroid Cancer Management

    Consensus Statement: Recommendations on Actionable Biomarker Testing for Thyroid Cancer Management de réir Özgür Mete, Andrée Boucher, Kasmintan A. Schrader, Omar Abdel‐Rahman, Houda Bahig, Cheryl Ho, Olfat Kamel Hasan, Bernard Lemieux, Eric Winquist, Ralph Wong, Jonn Wu, Nicole G. Chau, Shereen Ezzat

    Foilsithe / Cruthaithe 2024
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  8. 8
    The Specificity of the FOXL2 c.402C>G Somatic Mutation: A Survey of Solid Tumors

    The Specificity of the FOXL2 c.402C>G Somatic Mutation: A Survey of Solid Tumors de réir Kasmintan A. Schrader, Bella Gorbatcheva, Janine Senz, Alireza Heravi‐Moussavi, Nataliya Melnyk, Clara Salamanca, Sarah Maines‐Bandiera, Susanna L. Cooke, Peter C. K. Leung, James D. Brenton, C. Blake Gilks, John E. Monahan, David G. Huntsman

    Foilsithe / Cruthaithe 2009
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  9. 9
    The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

    The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results de réir Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan A. Schrader, Michael F. Evans, Adena Scheer, Nancy N. Baxter, Jada G. Hamilton, Jordan Lerner‐Ellis, Kenneth Offit, Mark E. Robson, Andreas Laupacis

    Foilsithe / Cruthaithe 2018
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  10. 10
    Response to angiotensin blockade with irbesartan in a patient with metastatic colorectal cancer

    Response to angiotensin blockade with irbesartan in a patient with metastatic colorectal cancer de réir Martin Jones, Kasmintan A. Schrader, Yaoqing Shen, Erin Pleasance, Carolyn Ch’ng, Nazir Ahmad Dar, Steven Yip, Daniel J. Renouf, Jacquie Schein, Andrew J. Mungall, Yu-Xue Zhao, Richard A. Moore, Y. Ma, Brandon S. Sheffield, Tony Ng, Steven J.M. Jones, Marco A. Marra, Janessa Laskin, Howard J. Lim

    Foilsithe / Cruthaithe 2016
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  11. 11
    Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA

    Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA de réir Kasmintan A. Schrader, Donavan T. Cheng, Joseph Vijai, Meera Prasad, Michael F. Walsh, Ahmet Zehir, Ai Ni, Tinu Thomas, Ryma Benayed, Asad Ashraf, Anne Lincoln, Maria E. Arcila, Zsofia K. Stadler, David B. Solit, David M. Hyman, Liying Zhang, David S. Klimstra, Marc Ladanyi, Kenneth Offit, Michael F. Berger, Mark E. Robson

    Foilsithe / Cruthaithe 2015
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  12. 12
    Homologous recombination deficiency signatures in gastrointestinal and thoracic cancers correlate with platinum therapy duration

    Homologous recombination deficiency signatures in gastrointestinal and thoracic cancers correlate with platinum therapy duration de réir Erica S. Tsang, Veronika Csizmók, Laura M. Williamson, Erin Pleasance, James T. Topham, Joanna M. Karasinska, Emma Titmuss, Kasmintan A. Schrader, Stephen Yip, Basile Tessier‐Cloutier, Karen Mungall, Tony Ng, Sophie Sun, Howard J. Lim, Jonathan M. Loree, Janessa Laskin, Marco A. Marra, Steven J.M. Jones, David F. Schaeffer, Daniel J. Renouf

    Foilsithe / Cruthaithe 2023
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  13. 13
    Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer

    Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer de réir Kara N. Maxwell, Steven N. Hart, Joseph Vijai, Kasmintan A. Schrader, Thomas P. Slavin, Tinu Thomas, Bradley Wubbenhorst, Vignesh Ravichandran, Raymond M. Moore, Chunling Hu, Lucia Guidugli, Brandon M. Wenz, Susan M. Domchek, Mark E. Robson, Csilla I. Szabo, Susan L. Neuhausen, Jeffrey N. Weitzel, Kenneth Offit, Fergus J. Couch, Katherine L. Nathanson

    Foilsithe / Cruthaithe 2016
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  14. 14
    Molecular characterization of metastatic pancreatic neuroendocrine tumors (PNETs) using whole-genome and transcriptome sequencing

    Molecular characterization of metastatic pancreatic neuroendocrine tumors (PNETs) using whole-genome and transcriptome sequencing de réir Hui‐Li Wong, Kevin Yang, Yaoqing Shen, Eric Y. Stutheit-Zhao, Jonathan M. Loree, Hagen F. Kennecke, Steve E. Kalloger, Joanna M. Karasinska, Howard J. Lim, Andrew J. Mungall, Xiaolan Feng, Janine M. Davies, Kasmintan A. Schrader, Chen Zhou, Aly Karsan, Steven J.M. Jones, Janessa Laskin, Marco A. Marra, David F. Schaeffer, Sharon M. Gorski, Daniel J. Renouf

    Foilsithe / Cruthaithe 2017
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  15. 15
    Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies

    Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies de réir Joseph Vijai, Tomas Kirchhoff, Kasmintan A. Schrader, Jennifer R. Brown, Ana Dutra-Clarke, Christopher Manschreck, Nichole Hansen, Rohini Rau‐Murthy, Kara Sarrel, Jennifer A. Przybylo, Sohela Shah, Srujana Cheguri, Zsofia K. Stadler, Liying Zhang, Ora Paltiel, Dina Ben‐Yehuda, Agnès Viale, Carol S. Portlock, David J. Straus, Steven M. Lipkin, Mortimer J. Lacher, Mark E. Robson, Robert J. Klein, Andrew D. Zelenetz, Kenneth Offit

    Foilsithe / Cruthaithe 2013
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  16. 16
    A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome

    A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome de réir Bari J. Ballew, Joseph Vijai, Saurav De, Grzegorz Sarek, Jean‐Baptiste Vannier, Travis H. Stracker, Kasmintan A. Schrader, Trudy N. Small, Richard O’Reilly, Chris Manschreck, Megan M. Harlan Fleischut, Liying Zhang, John Sullivan, Kelly Stratton, Meredith Yeager, Kevin B. Jacobs, Neelam Giri, Blanche P. Alter, Joseph F. Boland, Laurie Burdett, Kenneth Offit, Simon J. Boulton, Sharon A. Savage, John H.J. Petrini

    Foilsithe / Cruthaithe 2013
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  17. 17
    Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>CDH1</i> sequence variants

    Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>CDH1</i> sequence variants de réir Kristy Lee, Kate Krempely, Maegan E. Roberts, Michael J. Anderson, Fátima Carneiro, Elizabeth Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David G. Huntsman, Pardeep Kaurah, Chimene Kesserwan, Tyler Landrith, Shuwei Li, Arjen R. Mensenkamp, Carla Oliveíra, Carolina Pardo‐Díaz, Tina Pesaran, Matthew Richardson, Thomas P. Slavin, Amanda B. Spurdle, Mackenzie Trapp, Leora Witkowski, Charles Sunghoon Yi, Liying Zhang, Sharon E. Plon, Kasmintan A. Schrader, Rachid Karam

    Foilsithe / Cruthaithe 2018
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  18. 18
    The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

    The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk de réir Thomas P. Slavin, Kara N. Maxwell, Jenna Lilyquist, Joseph Vijai, Susan L. Neuhausen, Steven N. Hart, Vignesh Ravichandran, Tinu Thomas, Ann Maria, Danylo Villano, Kasmintan A. Schrader, Raymond M. Moore, Chunling Hu, Bradley Wubbenhorst, Brandon M. Wenz, Kurt D’Andrea, Mark E. Robson, Paolo Peterlongo, Bernardo Bonanni, James M. Ford, Judy E. Garber, Susan M. Domchek, Csilla I. Szabo, Kenneth Offit, Katherine L. Nathanson, Jeffrey N. Weitzel, Fergus J. Couch

    Foilsithe / Cruthaithe 2017
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  19. 19
    Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing

    Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing de réir My Linh Thibodeau, Kieran O’Neill, Katherine Dixon, Caralyn Reisle, Karen Mungall, Martin Krzywinski, Yaoqing Shen, Howard J. Lim, Dean Cheng, Kane Tse, Tina Wong, Eric Chuah, Alexandra Fok, Sophie Sun, Daniel J. Renouf, David F. Schaeffer, Carol Cremin, Stephen Chia, Sean Young, Pawan Pandoh, Stephen Pleasance, Erin Pleasance, Andrew J. Mungall, Richard A. Moore, Stephen Yip, Aly Karsan, Janessa Laskin, Marco A. Marra, Kasmintan A. Schrader, Steven J.M. Jones

    Foilsithe / Cruthaithe 2020
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  20. 20
    Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

    Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial de réir Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Raymond H. Kim, Sarah M. Muir, Lindsay Carlsson, Nancy N. Baxter, Adena Scheer, Christine Elser, Andrea Eisen, Seema Panchal, Tracy Graham, Melyssa Aronson, Carolyn Piccinin, Talia Mancuso, Kara Semotiuk, Michael F. Evans, June C. Carroll, Kenneth Offit, Mark E. Robson, Jada G. Hamilton, Emily Glogowski, Kasmintan A. Schrader, Raymond H. Kim, Jordan Lerner‐Ellis, Kevin E. Thorpe, Andreas Laupacis, Yvonne Bombard, Susan Randall Armel, Melyssa Aronson, Nancy N. Baxter, Ahmed M. Bayoumi, Kenneth Bond, June C. Carroll, Timothy Caulfield, Marc Clausen, Tammy Clifford, Iris Cohn, Irfan A. Dhalla, Craig C. Earle, Andrea Eisen, Christine Elser, M. Blair Evans, Tracy Graham, Emily Glogowski, Jada G. Hamilton, Wanrudee Isaranuwatchai, Monika Kastner, Raymond H. Kim, Andreas Laupacis, Jordan Lerner‐Ellis, Michelle Mujoomdar, Kenneth Offit, Seema Panchal, Mark E. Robson, Adena Scheer, Stephen W. Scherer, Kasmintan A. Schrader, Terrence Sullivan, Kevin E. Thorpe

    Foilsithe / Cruthaithe 2019
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