检索结果 - Chimene Kesserwan

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  1. 1
    Li‐Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition

    Li‐Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition 由 Jessica M. Valdez, Kim E. Nichols, Chimene Kesserwan

    出版 2016
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    Revisão
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  2. 2
    Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase–deficient severe combined immune deficiency

    Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase–deficient severe combined immune deficiency 由 Chimene Kesserwan, Robert Sokolic, Edward W. Cowen, Elizabeth Garabedian, Kerstin Heselmeyer‐Haddad, Chyi‐Chia Richard Lee, Stefania Pittaluga, Clarymar Ortiz, Kristin Baird, Dolores López‐Terrada, Julia A. Bridge, Alan S. Wayne, Fabio Candotti

    出版 2011
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    Artigo
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  3. 3
    Integrating next‐generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics

    Integrating next‐generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics 由 Liza‐Marie Johnson, Jessica M. Valdez, Emily A. Quinn, April Sykes, Rose B. McGee, Regina Nuccio, Stacy J. Hines‐Dowell, Justin N. Baker, Chimene Kesserwan, Kim E. Nichols, Belinda N. Mandrell

    出版 2017
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    Artigo
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  4. 4
    The genomic landscape of pediatric myelodysplastic syndromes

    The genomic landscape of pediatric myelodysplastic syndromes 由 Jason R. Schwartz, Jing Ma, Tamara Lamprecht, Michael Walsh, Shuoguo Wang, Victoria Bryant, Guangchun Song, Gang Wu, John Easton, Chimene Kesserwan, Kim E. Nichols, Charles G. Mullighan, Raul C. Ribeiro, Jeffery M. Klco

    出版 2017
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    Artigo
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  5. 5
    Genomic and transcriptomic analyses identify a prognostic gene signature and predict response to therapy in pleural and peritoneal mesothelioma

    Genomic and transcriptomic analyses identify a prognostic gene signature and predict response to therapy in pleural and peritoneal mesothelioma 由 Nishanth Ulhas Nair, Qun Jiang, Jun S. Wei, Vikram Misra, Betsy Morrow, Chimene Kesserwan, Leandro C. Hermida, Joo Sang Lee, Idrees Mian, Jingli Zhang, Alexandra Lebensohn, Markku Miettinen, Manjistha Sengupta, Javed Khan, Eytan Ruppin, Raffit Hassan

    出版 2023
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    Artigo
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  6. 6
    Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome

    Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome 由 Jason R. Schwartz, S Wang, Jing Ma, Tamara Lamprecht, Michael F. Walsh, Guangchun Song, S C Raimondi, Gang Wu, Michael F. Walsh, Rose B. McGee, Chimene Kesserwan, Kim E. Nichols, Brian Cauff, Raul C. Ribeiro, Marcin W. Włodarski, Jeffery M. Klco

    出版 2017
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    Carta
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  7. 7
    Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes

    Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes 由 Michael F. Walsh, Deborah Ritter, Chimene Kesserwan, Dmitriy Sonkin, Debyani Chakravarty, Elizabeth Chao, Rajarshi Ghosh, Yelena Kemel, Gang Wu, Kristy Lee, Shashikant Kulkarni, Dale J. Hedges, Diana Mandelker, Ozge Ceyhan‐Birsoy, Minjie Luo, Michael W. Drazer, Liying Zhang, Kenneth Offit, Sharon E. Plon

    出版 2018
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    Artigo
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  8. 8
    The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute

    The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute 由 Kelvin C. de Andrade, Elaine E. Lee, Elise M. Tookmanian, Chimene Kesserwan, James J. Manfredi, Jessica N. Hatton, Jennifer K. Loukissas, Jiří Zavadil, Lei Zhou, Magali Olivier, Megan N. Frone, Owais Shahzada, William J.R. Longabaugh, Christian P. Kratz, David Malkin, Pierre Hainaut, Sharon A. Savage

    出版 2022
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    Artigo
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  9. 9
    Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants

    Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants 由 Michael N. Edmonson, Aman Patel, Dale J. Hedges, Zhaoming Wang, Evadnie Rampersaud, Chimene Kesserwan, Xin Zhou, Yanling Liu, Scott Newman, Michael Rusch, Clay McLeod, Mark R. Wilkinson, Stephen V. Rice, Thierry Soussi, J. Paul Taylor, Michael Benatar, Jared Becksfort, Kim E. Nichols, Leslie L. Robison, James R. Downing, Jinghui Zhang

    出版 2019
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    Artigo
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  10. 10
    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 由 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

    出版 2018
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  11. 11
    ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants

    ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants 由 Xi Luo, Simone Feurstein, Shruthi Mohan, Christopher C. Porter, Sarah A. Jackson, Sioḃán Keel, Michael C. Chicka, Anna Brown, Chimene Kesserwan, Anupriya Agarwal, Minjie Luo, Zejuan Li, Justyne Ross, Panagiotis Baliakas, Daniel Pineda‐Alvarez, Courtney D. DiNardo, Alison A. Bertuch, Nikita Mehta, Tom Vulliamy, Ying Wang, Kim E. Nichols, Luca Malcovati, Michael F. Walsh, Lesley Rawlings, Shannon K. McWeeney, Jean Soulier, Anna Raimbault, Mark J. Routbort, Liying Zhang, Gabriella Ryan, Nancy A. Speck, Sharon E. Plon, David Wu, Lucy A. Godley

    出版 2019
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  12. 12
    Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans

    Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans 由 Fabio Candotti, Kit L. Shaw, Linda Muul, Denise A. Carbonaro, Robert Sokolic, Christopher Choi, Shepherd H. Schurman, Elizabeth Garabedian, Chimene Kesserwan, G. Jayashree Jagadeesh, Pei-Yu Fu, Eric H. Gschweng, Aaron Cooper, John F. Tisdale, Kenneth I. Weinberg, Gay M. Crooks, Neena Kapoor, Ami J. Shah, Hisham Abdel‐Azim, Xiao-Jin Yu, Monika Smogorzewska, Alan S. Wayne, Howard M. Rosenblatt, Carla M. Davis, Celine Hanson, Radha Rishi, Xiaoyan Wang, David W. Gjertson, Otto O. Yang, Arumugam Balamurugan, Gerhard Bauer, Joanna A. Ireland, Barbara C. Engel, Gregory M. Podsakoff, Michael S. Hershfield, R. Michael Blaese, Robertson Parkman, Donald B. Kohn

    出版 2012
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    Artigo
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  13. 13
    Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

    Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer 由 Zhaoming Wang, Carmen L. Wilson, John Easton, Andrew Thrasher, Heather L. Mulder, Qi Liu, Dale J. Hedges, Shuoguo Wang, Michael Rusch, Michael N. Edmonson, Shawn Levy, Jennifer Q. Lanctot, Eric Caron, Kyla Shelton, Kelsey Currie, Matthew Lear, Aman Patel, Celeste Rosencrance, Ying Shao, Bhavin Vadodaria, Donald Yergeau, Yadav Sapkota, Russell J. Brooke, Wonjong Moon, Evadnie Rampersaud, Xiaotu Ma, Ti-Cheng Chang, Stephen V. Rice, Cynthia Pepper, Xin Zhou, Xiang Chen, Wenan Chen, Angela Jones, Braden Boone, Matthew J. Ehrhardt, Matthew J. Krasin, Rebecca M. Howell, Nicholas S. Phillips, Courtney Lewis, Deo Kumar Srivastava, Ching‐Hon Pui, Chimene Kesserwan, Gang Wu, Kim E. Nichols, James R. Downing, Melissa M. Hudson, Yutaka Yasui, Leslie L. Robison, Jinghui Zhang

    出版 2018
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    Artigo
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  14. 14
    Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing

    Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing 由 Scott Newman, Joy Nakitandwe, Chimene Kesserwan, Elizabeth M. Azzato, David A. Wheeler, Michael Rusch, Sheila Shurtleff, Dale J. Hedges, Kayla V. Hamilton, Scott G. Foy, Michael N. Edmonson, Andrew Thrasher, Armita Bahrami, Brent A. Orr, Jeffery M. Klco, Jiali Gu, Lynn W. Harrison, Lu Wang, Michael R. Clay, Annastasia Ouma, Antonina Silkov, Yanling Liu, Zhaojie Zhang, Yu Liu, Samuel W. Brady, Xin Zhou, Ti‐Cheng Chang, Manjusha Pande, Eric M. Davis, Jared Becksfort, Aman Patel, Mark R. Wilkinson, Delaram Rahbarinia, Manish Kubal, Jamie L. Maciaszek, Víctor Manuel López Pastor, Jay Knight, Alexander M. Gout, Jian Wang, Zhaohui Gu, Charles G. Mullighan, Rose B. McGee, Emily A. Quinn, Regina Nuccio, Roya Mostafavi, Elsie L. Gerhardt, Leslie M. Taylor, Jessica M. Valdez, Stacy J. Hines‐Dowell, Alberto S. Pappo, Giles Robinson, Liza‐Marie Johnson, Ching‐Hon Pui, David W. Ellison, James R. Downing, Jinghui Zhang, Kim E. Nichols

    出版 2021
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