Výsledky vyhledávání - Aaron Elliott

  • Zobrazuji výsledky 1 - 12 z 12
Upřesnit hledání
  1. 1
    Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection

    Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection Autor Phillip Gray, Charles Dunlop, Aaron Elliott

    Vydáno 2015
    Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  2. 2
    Rapid Detection of the ACMG/ACOG-Recommended 23 CFTR Disease-Causing Mutations Using Ion Torrent Semiconductor Sequencing

    Rapid Detection of the ACMG/ACOG-Recommended 23 CFTR Disease-Causing Mutations Using Ion Torrent Semiconductor Sequencing Autor Aaron Elliott, Joy Radecki, Bellal Moghis, Xiang Li, Anja Kammesheidt

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing

    Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing Autor Wenbo Mu, Hsiao‐Mei Lu, Jefferey Chen, Shuwei Li, Aaron Elliott

    Vydáno 2016
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia

    Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia Autor Felicia Hernandez, Robert Huether, Lester Carter, Tami Johnston, Jennifer Thompson, James R. Gossage, Elizabeth Chao, Aaron Elliott

    Vydáno 2015
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  5. 5
    Beyond DNA: An Integrated and Functional Approach for Classifying Germline Variants in Breast Cancer Genes

    Beyond DNA: An Integrated and Functional Approach for Classifying Germline Variants in Breast Cancer Genes Autor Tina Pesaran, Rachid Karam, Robert Huether, S. Li, Suzette Farber-Katz, Adam Chamberlin, Hansook Kim Chong, Holly LaDuca, Aaron Elliott

    Vydáno 2016
    Získat plný text Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  6. 6
    The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay

    The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay Autor Hansook Kim Chong, Tao Wang, Hsiao-Mei Lu, Sara Seidler, Hong Lu, Steven Keiles, Elizabeth Chao, Aaron J. Stuenkel, Xiang Li, Aaron Elliott

    Vydáno 2014
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing

    Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing Autor Hsiao‐Mei Lu, Shuwei Li, Mary Helen Black, Shela Lee, Robert Hoiness, Sitao Wu, Wenbo Mu, Robert Huether, Jefferey Chen, Srijani Sridhar, Yuan Tian, Rachel McFarland, Jill S. Dolinsky, Brigette Tippin Davis, Sharon Mexal, Charles Dunlop, Aaron Elliott

    Vydáno 2018
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  8. 8
    Somatic TP53 variants frequently confound germ-line testing results

    Somatic TP53 variants frequently confound germ-line testing results Autor Jeffrey N. Weitzel, Elizabeth Chao, Bita Nehoray, Lily R. Van Tongeren, Holly LaDuca, Kathleen R. Blazer, Thomas P. Slavin, Tina Pesaran, Christina Rybak, Ilana Solomon, Mariana Niell‐Swiller, Jill S. Dolinsky, Danielle Castillo, Aaron Elliott, Chia‐Ling Gau, Virginia Speare, Kory Jasperson

    Vydáno 2017
    Získat plný text Získat plný text
    Editorial
    Přidat do oblíbených
    Uloženo v:
  9. 9
    Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions

    Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions Autor Kelly D. Farwell, Layla Shahmirzadi, Dima El‐Khechen, Zöe Powis, Elizabeth Chao, Brigette Tippin Davis, Ruth M. Baxter, Wenqi Zeng, Cameron Mroske, Melissa Parra, Stephanie Gandomi, Ira Lu, Xiang Li, Hong Lu, Hsiao‐Mei Lu, David Salvador, David Ruble, Monica Lao, Soren Fischbach, Jennifer X. Wen, Shela Lee, Aaron Elliott, Charles Dunlop, Sha Tang

    Vydáno 2014
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  10. 10
    Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer

    Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer Autor Rachid Karam, Blair R. Conner, Holly LaDuca, Kelly McGoldrick, Kate Krempely, Marcy E. Richardson, Heather Zimmermann, Stephanie Gutierrez, Patrick Reineke, Lily Hoang, Kyle Allen, Amal Yussuf, Suzette Farber-Katz, Huma Q. Rana, Samantha Culver, John Lee, Sarah Nashed, Deborah Toppmeyer, Debra L. Collins, Ginger Haynes, Tina Pesaran, Jill S. Dolinsky, Brigette Tippin Davis, Aaron Elliott, Elizabeth Chao

    Vydáno 2019
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  11. 11
    Evidence for a role of Anopheles stephensi in the spread of drug- and diagnosis-resistant malaria in Africa

    Evidence for a role of Anopheles stephensi in the spread of drug- and diagnosis-resistant malaria in Africa Autor Tadele Emiru, Dejene Getachew, Maxwell Murphy, Luigi Sedda, Legesse Alamerie Ejigu, Mikiyas Gebremichael Bulto, Isabel Byrne, Mulugeta Demisse, Melat Abdo, Wakweya Chali, Aaron Elliott, Eric Neubauer Vickers, Andrés Aranda-Díaz, Lina Alemayehu, Sinknesh W. Behaksera, Gutema Jebessa, Hunduma Dinka, Tizita Tsegaye, Hiwot Teka, Sheleme Chibsa, Peter Mumba, Samuel Girma, Jimee Hwang, Melissa Yoshimizu, Alice Sutcliffe, Hiwot Solomon Taffese, Gudissa Aseffa Bayissa, Sarah Zohdy, Jon Eric Tongren, Chris Drakeley, Bryan Greenhouse, Teun Bousema, Fitsum G. Tadesse

    Vydáno 2023
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  12. 12
    Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes

    Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes Autor Tyler Landrith, Bing Li, Ashley Cass, Blair R. Conner, Holly LaDuca, Danielle McKenna, Kara N. Maxwell, Susan M. Domchek, Nichole A. Morman, Christopher Heinlen, Deborah Wham, Cathryn Koptiuch, Jennie Vagher, Ragene Rivera, Ann Bunnell, Gayle Patel, Jennifer L. Geurts, Morgan Depas, Shraddha Gaonkar, Sara Pirzadeh‐Miller, Rebekah C. Krukenberg, Meredith Seidel, Robert Pilarski, Meagan Farmer, Khateriaa Pyrtel, Kara J. Milliron, John Lee, Elizabeth Hoodfar, Deepika Nathan, Amanda Ganzak, Sitao Wu, Huy Gia Vuong, Dong Xu, Aarani Arulmoli, Melissa Parra, Lily Hoang, Bhuvan Molparia, Michele Fennessy, Susanne Fox, Sinead Charpentier, Julia Burdette, Tina Pesaran, Jessica Profato, Brandon Smith, Ginger Haynes, Emily Dalton, Joy Rae-Radecki Crandall, Ruth Baxter, Hsiao‐Mei Lu, Brigette Tippin‐Davis, Aaron Elliott, Elizabeth Chao, Rachid Karam

    Vydáno 2020
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: