Resultats de la cerca - Jason D. Merker

Refinar resultats
  1. 1
    Next-generation sequencing of acute myeloid leukemia identifies the significance of TP53, U2AF1, ASXL1, and TET2 mutations

    Next-generation sequencing of acute myeloid leukemia identifies the significance of TP53, U2AF1, ASXL1, and TET2 mutations per Robert S. Ohgami, Lisa Ma, Jason D. Merker, Jason Gotlib, Iris Schrijver, James L. Zehnder, Daniel A. Arber

    Publicat 2014
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  2. 2
    Intricate and Cell Type-Specific Populations of Endogenous Circular DNA (eccDNA) in <i>Caenorhabditis elegans</i> and <i>Homo sapiens</i>

    Intricate and Cell Type-Specific Populations of Endogenous Circular DNA (eccDNA) in <i>Caenorhabditis elegans</i> and <i>Homo sapiens</i> per Massa J. Shoura, Idan Gabdank, Loren Hansen, Jason D. Merker, Jason Gotlib, Stephen D. Levene, Andrew Fire

    Publicat 2017
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  3. 3
    A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing

    A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing per Eric J. Duncavage, Haley Abel, Jason D. Merker, John B. Bodner, Qin Zhao, Karl V. Voelkerding, John D. Pfeifer

    Publicat 2016
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  4. 4
    Diagnosis of a Critical Respiratory Illness Caused by Human Metapneumovirus by Use of a Pan-Virus Microarray

    Diagnosis of a Critical Respiratory Illness Caused by Human Metapneumovirus by Use of a Pan-Virus Microarray per Charles Y. Chiu, Ash A. Alizadeh, Silvi Rouskin, Jason D. Merker, Elaine Yeh, Shigeo Yagi, David Schnurr, Bruce K. Patterson, Don Ganem, Joseph L. DeRisi

    Publicat 2007
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  5. 5
    Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms

    Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms per Stephen T. Oh, Erin F. Simonds, Carol D. Jones, Matthew B. Hale, Yury Goltsev, Kenneth D. Gibbs, Jason D. Merker, James L. Zehnder, Garry P. Nolan, Jason Gotlib

    Publicat 2010
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  6. 6
    A study of the mutational landscape of pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma

    A study of the mutational landscape of pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma per Michael G. Ozawa, Aparna Bhaduri, Karen M. Chisholm, Steven Andrew Baker, Lisa Ma, James L. Zehnder, Sandra Luna‐Fineman, Michael P. Link, Jason D. Merker, Daniel A. Arber, Robert S. Ohgami

    Publicat 2016
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  7. 7
    Microarray Detection of Human Parainfluenzavirus 4 Infection Associated with Respiratory Failure in an Immunocompetent Adult

    Microarray Detection of Human Parainfluenzavirus 4 Infection Associated with Respiratory Failure in an Immunocompetent Adult per Charles Y. Chiu, Silvi Rouskin, Anita A. Koshy, Anatoly Urisman, Kael F. Fischer, Shigeo Yagi, David Schnurr, Paul B. Eckburg, Lucy S. Tompkins, Brian G. Blackburn, Jason D. Merker, Bruce K. Patterson, Don Ganem, Joseph L. DeRisi

    Publicat 2006
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  8. 8
    College of American Pathologists' Laboratory Standards for Next-Generation Sequencing Clinical Tests

    College of American Pathologists' Laboratory Standards for Next-Generation Sequencing Clinical Tests per Nazneen Aziz, Qin Zhao, Lynn Bry, Denise K. Driscoll, Birgit Funke, Jane S. Gibson, Wayne W. Grody, Madhuri Hegde, Gerald A. Hoeltge, Debra G. B. Leonard, Jason D. Merker, Rakesh Nagarajan, Linda A. Palicki, Ryan S. Robetorye, Iris Schrijver, Karen E. Weck, Karl V. Voelkerding

    Publicat 2014
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  9. 9
    Measurement and Clinical Monitoring of Human Lymphocyte Clonality by Massively Parallel V-D-J Pyrosequencing

    Measurement and Clinical Monitoring of Human Lymphocyte Clonality by Massively Parallel V-D-J Pyrosequencing per Scott D. Boyd, Eleanor L. Marshall, Jason D. Merker, Jay M. Maniar, Lyndon N. Zhang, Bita Sahaf, Carol D. Jones, Birgitte B. Simen, Bozena Hanczaruk, Khoa D. Nguyen, Kari C. Nadeau, Michael D. Miller, David B. Miklos, James L. Zehnder, Andrew Fire

    Publicat 2009
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  10. 10
    The impact of rare variation on gene expression across tissues

    The impact of rare variation on gene expression across tissues per Xin Li, Yungil Kim, Emily K. Tsang, Joe R. Davis, Farhan N. Damani, Colby Chiang, Gaelen T. Hess, Zachary Zappala, Benjamin J. Strober, Alexandra J. Scott, Amy Li, Andrea Ganna, Michael C. Bassik, Jason D. Merker, Ira M. Hall, Alexis Battle, Stephen B. Montgomery

    Publicat 2017
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  11. 11
    Long-read genome sequencing identifies causal structural variation in a Mendelian disease

    Long-read genome sequencing identifies causal structural variation in a Mendelian disease per Jason D. Merker, Aaron M. Wenger, Tam P. Sneddon, Megan E. Grove, Zachary Zappala, Laure Frésard, Daryl Waggott, Sowmi Utiramerur, Yanli Hou, Kevin S. Smith, Stephen B. Montgomery, Matthew T. Wheeler, Jillian G. Buchan, Christine Lambert, Kevin Eng, Luke Hickey, Jonas Korlach, James M. Ford, Euan A. Ashley

    Publicat 2017
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  12. 12
    Circulating Tumor DNA Analysis in Patients With Cancer: American Society of Clinical Oncology and College of American Pathologists Joint Review

    Circulating Tumor DNA Analysis in Patients With Cancer: American Society of Clinical Oncology and College of American Pathologists Joint Review per Jason D. Merker, Geoffrey R. Oxnard, Carolyn C. Compton, Maximilian Diehn, Patricia A. Hurley, Alexander J. Lazar, Neal Lindeman, Christina M. Lockwood, J. Alex, Richard L. Schilsky, Apostolia M. Tsimberidou, Patricia Vasalos, Brooke L. Billman, Thomas K. Oliver, Suanna S. Bruinooge, Daniel F. Hayes, Nicholas C. Turner

    Publicat 2018
    Obtenir text complet
    Revisão
    Afegir a favorits
    Guardat en:
  13. 13
    ESMO recommendations on the use of circulating tumour DNA assays for patients with cancer: a report from the ESMO Precision Medicine Working Group

    ESMO recommendations on the use of circulating tumour DNA assays for patients with cancer: a report from the ESMO Precision Medicine Working Group per Javier Pascual, Gerhardt Attard, François‐Clément Bidard, Giuseppe Curigliano, Leticia De Mattos‐Arruda, Maximilian Diehn, Antoîne Italiano, Johan Lindberg, Jason D. Merker, Clara Montagut, Nicola Normanno, Klaus Pantel, George Pentheroudakis, Sanjay Popat, Jorge S. Reis‐Filho, Jeanne Tie, Joan Seoane, N. Tarazona, Takayuki Yoshino, Nicholas C. Turner

    Publicat 2022
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  14. 14
    Individual Variation in the Germline Ig Gene Repertoire Inferred from Variable Region Gene Rearrangements

    Individual Variation in the Germline Ig Gene Repertoire Inferred from Variable Region Gene Rearrangements per Scott D. Boyd, Bruno Gaëta, Katherine Jackson, Andrew Fire, Eleanor L. Marshall, Jason D. Merker, Jay M. Maniar, Lyndon N. Zhang, Bita Sahaf, Carol D. Jones, Birgitte B. Simen, Bozena Hanczaruk, Khoa D. Nguyen, Kari C. Nadeau, Michael D. Miller, David B. Miklos, James L. Zehnder, Andrew M. Collins

    Publicat 2010
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  15. 15
    Impact of somatic and germline mutations on the outcome of systemic mastocytosis

    Impact of somatic and germline mutations on the outcome of systemic mastocytosis per Javier I. Muñoz‐González, María Jara‐Acevedo, Iván Álvarez‐Twöse, Jason D. Merker, Cristina Teodósio, Yanli Hou, Ana Henriques, Krishna M. Roskin, Laura Sánchez‐Muñoz, Albert G. Tsai, Carolina Caldas, Almudena Matito, José I. Sánchez-Gallego, Andrea Mayado, Noelia Dasilva, Jason Gotlib, Luís Escribano, Alberto Órfão, Andrés C. García‐Montero

    Publicat 2018
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  16. 16
    A randomized phase II/III study of paclitaxel/carboplatin/metformin versus paclitaxel/carboplatin/placebo as initial therapy for measurable stage III or IVA, stage IVB, or recurrent endometrial cancer: An NRG oncology/GOG study

    A randomized phase II/III study of paclitaxel/carboplatin/metformin versus paclitaxel/carboplatin/placebo as initial therapy for measurable stage III or IVA, stage IVB, or recurren... per Victoria Bae‐Jump, Michael W. Sill, Paola A. Gehrig, Jason D. Merker, David L. Corcoran, Adam D. Pfefferle, Michele C. Hayward, Joan L. Walker, Andrea R. Hagemann, Steven Waggoner, Roisin E. O’Cearbhaill, Megan McDonald, Mitchell I. Edelson, Paul DiSilvestro, Amy McNally, Aimee C. Fleury, Ramey D. Littell, Frederick R. Ueland, Heather A. Lankes, Carol Aghajanian

    Publicat 2025
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  17. 17
    Clinical Interpretation and Implications of Whole-Genome Sequencing

    Clinical Interpretation and Implications of Whole-Genome Sequencing per Frederick E. Dewey, Megan E. Grove, Cuiping Pan, Benjamin A. Goldstein, Jonathan A. Bernstein, Hassan Chaı̈b, Jason D. Merker, Rachel L. Goldfeder, Gregory M. Enns, Sean P. David, Neda Pakdaman, Kelly E. Ormond, Colleen Caleshu, Kerry Kingham, Teri E. Klein, Michelle Whirl‐Carrillo, Kenneth Sakamoto, Matthew T. Wheeler, Atul J. Butte, James M. Ford, Linda M. Boxer, John P. A. Ioannidis, Alan C. Yeung, Russ B. Altman, Themistocles L. Assimes, M Snyder, Euan A. Ashley, Thomas Quertermous

    Publicat 2014
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  18. 18
    Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts

    Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts per Laure Frésard, Craig Smail, Nicole M. Ferraro, Nicole A. Teran, Xin Li, Kevin S. Smith, Devon Bonner, Kristin D. Kernohan, Shruti Marwaha, Zachary Zappala, Brunilda Balliu, Joe R. Davis, Boxiang Liu, Cameron J. Prybol, Jennefer N. Kohler, Diane B. Zastrow, Chloe M. Reuter, Dianna G. Fisk, Megan E. Grove, Jean M. Davidson, Taila Hartley, Ruchi Joshi, Benjamin J. Strober, Sowmithri Utiramerur, Lars Lind, Erik Ingelsson, Alexis Battle, Gill Bejerano, Jonathan A. Bernstein, Euan A. Ashley, Kym M. Boycott, Jason D. Merker, Matthew T. Wheeler, Stephen B. Montgomery

    Publicat 2019
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  19. 19
    Assuring the quality of next-generation sequencing in clinical laboratory practice

    Assuring the quality of next-generation sequencing in clinical laboratory practice per Amy S. Gargis, Lisa V. Kalman, Meredith W Berry, David Bick, David Dimmock, Tina Hambuch, Fei Lu, Elaine Lyon, Karl V. Voelkerding, Barbara A. Zehnbauer, Richa Agarwala, Sarah F Bennett, Bin Chen, Ephrem Chin, John G. Compton, Soma Das, Daniel H. Farkas, Matthew J. Ferber, Birgit Funke, Manohar R. Furtado, Lilia Ganova‐Raeva, Ute Geigenmüller, Sandra J. Gunselman, Madhuri Hegde, Philip L. Johnson, Andrew Kasarskis, Shashikant Kulkarni, Thomas Lenk, C S Jonathan Liu, Megan Manion, Teri A. Manolio, Elaine R. Mardis, Jason D. Merker, Mangalathu S. Rajeevan, Martin G. Reese, Heidi L. Rehm, Birgitte B. Simen, Joanne M. Yeakley, Justin M. Zook, Ira M. Lubin

    Publicat 2012
    Obtenir text complet
    Carta
    Afegir a favorits
    Guardat en:
  20. 20
    Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

    Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consort... per Peter Horak, Malachi Griffith, Arpad Danos, Beth A. Pitel, Subha Madhavan, Xue‐Lu Liu, Cynthia Chow, Heather Williams, Leigh Carmody, Lisa Barrow-Laing, Damian Rieke, Simon Kreutzfeldt, Albrecht Stenzinger, David Tamborero, Manuela Benary, Padma Sheila Rajagopal, Cristiane M. Ida, Harry Lesmana, Laveniya Satgunaseelan, Jason D. Merker, Michael Tolstorukov, Paulo Vidal Campregher, Jeremy L. Warner, Shruti Rao, Maya Natesan, Haolin Shen, Jeffrey M. Venstrom, Somak Roy, Kayoko Tao, Rashmi Kanagal‐Shamanna, Xinjie Xu, Deborah Ritter, Kym Pagel, Kilannin Krysiak, Adrian M. Dubuc, Yassmine Akkari, Xuan Shirley Li, Jennifer Lee, Ian King, Gordana Raca, Alex H. Wagner, Marylin M. Li, Sharon E. Plon, Shashikant Kulkarni, Obi L. Griffith, Debyani Chakravarty, Dmitriy Sonkin

    Publicat 2022
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:

Eines de cerca: