Результати пошуку - Clesson Turner

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  1. 1
    A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic Elements

    A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Geneti... за авторством Darrell L. Ellsworth, Clesson Turner, Rachel E. Ellsworth

    Опубліковано 2019
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  2. 2
    Management of Incidental Findings in the Era of Next-generation Sequencing

    Management of Incidental Findings in the Era of Next-generation Sequencing за авторством Heather L. Blackburn, Bradley W. Schroeder, Clesson Turner, Craig D. Shriver, Darrell L. Ellsworth, Rachel E. Ellsworth

    Опубліковано 2015
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  3. 3
    Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma

    Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma за авторством Andrew S. Brohl, Rajesh Patidar, Clesson Turner, Xinyu Wen, Young Song, Jun S. Wei, Kathleen A. Calzone, Javed Khan

    Опубліковано 2017
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  4. 4
    Genotype first: Clinical genomics research through a reverse phenotyping approach

    Genotype first: Clinical genomics research through a reverse phenotyping approach за авторством Caralynn M. Wilczewski, Justice Obasohan, Justin Paschall, Suiyuan Zhang, Sumeeta Singh, George L. Maxwell, Morgan Similuk, Tyra G. Wolfsberg, Clesson Turner, Leslie G. Biesecker, Alexander Katz

    Опубліковано 2023
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  5. 5
    <i>EIF2S3</i>Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO

    <i>EIF2S3</i>Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO за авторством Martina Škopková, Friederike Hennig, Byung‐Sik Shin, Clesson Turner, Daniela Staníková, Katarína Brennerová, Juraj Staník, Ute Fischer, Lyndal Henden, Ulrich Müller, Daniela Steinberger, Esther Leshinsky‐Silver, Armand Bottani, Tímea Kurdiová, Jozef Ukropec, Olga Nyitrayova, Miriam Kolníková, I Klimeś, Guntram Borck, Melanie Bahlo, Stefan A. Haas, Joo-Ran Kim, Leda E. Lotspeich-Cole, Daniela Gašperíková, Thomas Dever, Vera M. Kalscheuer

    Опубліковано 2017
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  6. 6
    Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair–targeted therapies

    Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair–targeted therapies за авторством Camille Tlemsani, Nobuyuki Takahashi, Lőrinc Sándor Pongor, Vinodh N. Rajapakse, Manoj Tyagi, Xinyu Wen, Grace‐Ann Fasaye, Keith T. Schmidt, Parth Desai, Chul Kim, Arun Rajan, Shannon Swift, Linda Sciuto, Rasa Vilimas, Santhana Webb, Samantha Nichols, William D. Figg, Yves Pommier, Kathleen A. Calzone, Seth M. Steinberg, Jun S. Wei, Udayan Guha, Clesson Turner, Javed Khan, Anish Thomas

    Опубліковано 2021
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  7. 7
    The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

    The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine за авторством Leslie G. Biesecker, James C. Mullikin, Flavia M. Facio, Clesson Turner, Praveen F. Cherukuri, Robert W. Blakesley, Gerard G. Bouffard, Peter S. Chines, Pedro Cruz, Nancy F. Hansen, Jamie K. Teer, Baishali Maskeri, Alice C. Young, Teri A. Manolio, Alexander F. Wilson, Toren Finkel, Paul M. Hwang, Andrew E. Arai, Alan T. Remaley, Vandana Sachdev, Robert D. Shamburek, Richard O. Cannon, Eric D. Green

    Опубліковано 2009
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  8. 8
    Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways

    Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways за авторством Anthony R. Soltis, Nicholas W. Bateman, Jianfang Liu, Trinh Mai Nguyen, Teri J. Franks, Xijun Zhang, Clifton L. Dalgard, Coralie Viollet, Stella Somiari, Chunhua Yan, Karen Zeman, William J. Skinner, Jerry Lee, Harvey B. Pollard, Clesson Turner, Emanuel F. Petricoin, Daoud Meerzaman, Thomas P. Conrads, Hai Hu, Rebecca Blackwell, Gauthaman Sukumar, Dagmar Bačíková, Camille Alba, Erinn McGrath, Sraavya Polisetti, Meila Tuck, Alden Chiu, G. A. Peterson, Caroline Larson, Leonid Kvecher, Brenda Deyarmin, J. Kane, Katie Miller, Kelly A. Conrads, Brian L. Hood, Sasha C. Makohon‐Moore, Tamara Abulez, Elisa Baldelli, Mariaelena Pierobon, Qing-rong Chen, Henry Rodriguez, Sean E. Hanlon, Anthony R. Soltis, Nicholas W. Bateman, Jianfang Liu, Trinh Mai Nguyen, Teri J. Franks, Xijun Zhang, Clifton L. Dalgard, Coralie Viollet, Stella Somiari, Chunhua Yan, Karen Zeman, William J. Skinner, Jerry Lee, Harvey B. Pollard, Clesson Turner, Emanuel F. Petricoin, Daoud Meerzaman, Thomas P. Conrads, Hai Hu, Craig D. Shriver, Christopher A. Moskaluk, Robert Browning, Matthew D. Wilkerson, Craig D. Shriver, Christopher A. Moskaluk, Robert Browning, Matthew D. Wilkerson

    Опубліковано 2022
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  9. 9
    De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia

    De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia за авторством Hanneke A. Haijes, Maria J.E. Koster, Holger Rehmann, Dong Li, Hákon Hákonarson, Gerarda Cappuccio, Miroslava Hančárová, Daphné Lehalle, William Reardon, G. Bradley Schaefer, Anna Lehman, Ingrid M.B.H. van de Laar, Coranne D. Tesselaar, Clesson Turner, Alice Goldenberg, Sophie Patrier, Julien Thévenon, Michele Pinelli, Nicola Brunetti‐Pierri, Darina Prchalová, Markéta Havlovicová, Markéta Vlčková, Zdeněk Sedláček, Elena Lopez‐Rangel, Vassilis Ragoussis, Alistair T. Pagnamenta, Usha Kini, Harmjan R. Vos, Robert M. van Es, Richard F.M.A. van Schaik, Ton A.J. van Essen, Maria Kibæk, Jenny C. Taylor, Jennifer A. Sullivan, Vandana Shashi, Slavé Petrovski, Christina Fagerberg, Donna M. Martin, Koen L.I. van Gassen, Rolph Pfundt, Marni J. Falk, Elizabeth M. McCormick, H. T. Marc Timmers, Peter M. van Hasselt

    Опубліковано 2019
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  10. 10
    De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome

    De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome за авторством Jung‐Hyun Kim, Deepali N. Shinde, Margot R.F. Reijnders, Natalie Hauser, Rebecca L. Belmonte, G. R. Wilson, Daniëlle G.M. Bosch, Paula A. Bubulya, Vandana Shashi, Slavé Petrovski, Joshua K. Stone, Eun Young Park, Joris A. Veltman, Margje Sinnema, Connie T. R. M. Stumpel, Jos Draaisma, Joost Nicolai, Helger G. Yntema, Kristin Lindstrom, Bert B.A. de Vries, Tamison Jewett, Stephanie L. Santoro, Julie Vogt, Kristine Bachman, Andrea Seeley, Alyson Krokosky, Clesson Turner, Luis Rohena, Maja Hempel, Fanny Kortüm, Davor Lessel, Axel Neu, Tim M. Strom, Dagmar Wieczorek, Nuria C. Bramswig, Franco Laccone, Jana Behunova, Helga Rehder, Christopher T. Gordon, Marlène Rio, Serge Romana, Sha Tang, Dima El‐Khechen, Megan T. Cho, Kirsty McWalter, Ganka Douglas, Berivan Baskin, Amber Begtrup, Tara Funari, Kelly Schoch, Alexander P.A. Stegmann, Servi J.C. Stevens, Dong‐Er Zhang, David Traver, Xu Yao, Daniel G. MacArthur, Han G. Brunner, Grazia M.S. Mancini, R Myers, Laurie B. Owen, Ssang‐Taek Lim, David L. Stachura, Lisenka E.L.M. Vissers, E. Ahn

    Опубліковано 2016
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