Arama Sonuçları - Coe, Bradley P.

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  1. 1
    A Genetic Model for Neurodevelopmental Disease

    A Genetic Model for Neurodevelopmental Disease Yazar: Coe, Bradley P., Girirajan, Santhosh, Eichler, Evan E.

    Baskı/Yayın Bilgisi 2012
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  2. 2
    Genome structural variation discovery and genotyping

    Genome structural variation discovery and genotyping Yazar: Alkan, Can, Coe, Bradley P., Eichler, Evan E.

    Baskı/Yayın Bilgisi 2011
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  3. 3
    The Genetic Variability and Commonality of Neurodevelopmental Disease

    The Genetic Variability and Commonality of Neurodevelopmental Disease Yazar: COE, BRADLEY P., GIRIRAJAN, SANTHOSH, EICHLER, EVAN E.

    Baskı/Yayın Bilgisi 2012
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  4. 4
    FACADE: a fast and sensitive algorithm for the segmentation and calling of high resolution array CGH data

    FACADE: a fast and sensitive algorithm for the segmentation and calling of high resolution array CGH data Yazar: Coe, Bradley P., Chari, Raj, MacAulay, Calum, Lam, Wan L.

    Baskı/Yayın Bilgisi 2010
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  5. 5
    An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer

    An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer Yazar: Chari, Raj, Coe, Bradley P, Vucic, Emily A, Lockwood, William W, Lam, Wan L

    Baskı/Yayın Bilgisi 2010
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  6. 6
    Estimates of penetrance for recurrent pathogenic copy-number variations

    Estimates of penetrance for recurrent pathogenic copy-number variations Yazar: Rosenfeld, Jill A., Coe, Bradley P., Eichler, Evan E., Cuckle, Howard, Shaffer, Lisa G.

    Baskı/Yayın Bilgisi 2013
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  7. 7
    Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications

    Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications Yazar: Wilfert, Amy B., Sulovari, Arvis, Turner, Tychele N., Coe, Bradley P., Eichler, Evan E.

    Baskı/Yayın Bilgisi 2017
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  8. 8
    SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data

    SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data Yazar: Chi, Bryan, deLeeuw, Ronald J, Coe, Bradley P, MacAulay, Calum, Lam, Wan L

    Baskı/Yayın Bilgisi 2004
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  9. 9
    Brain white matter structure and COMT gene are linked to second-language learning in adults

    Brain white matter structure and COMT gene are linked to second-language learning in adults Yazar: Mamiya, Ping C., Richards, Todd L., Coe, Bradley P., Eichler, Evan E., Kuhl, Patricia K.

    Baskı/Yayın Bilgisi 2016
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  10. 10
    EZH2 promotes E2F driven SCLC tumorigenesis through modulation of apoptosis and cell cycle regulation

    EZH2 promotes E2F driven SCLC tumorigenesis through modulation of apoptosis and cell cycle regulation Yazar: Hubaux, Roland, Thu, Kelsie L., Coe, Bradley P., MacAulay, Calum, Lam, Stephen, Lam, Wan L.

    Baskı/Yayın Bilgisi 2013
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  11. 11
    MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data

    MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data Yazar: Chi, Bryan, deLeeuw, Ronald J, Coe, Bradley P, Ng, Raymond T, MacAulay, Calum, Lam, Wan L

    Baskı/Yayın Bilgisi 2008
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  12. 12
    Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence

    Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence Yazar: Sapkota, Yadav, Ghosh, Sunita, Lai, Raymond, Coe, Bradley P., Cass, Carol E., Yasui, Yutaka, Mackey, John R., Damaraju, Sambasivarao

    Baskı/Yayın Bilgisi 2013
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  13. 13
    Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues

    Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues Yazar: Aviel-Ronen, Sarit, Qi Zhu, Chang, Coe, Bradley P, Liu, Ni, Watson, Spencer K, Lam, Wan L, Tsao, Ming Sound

    Baskı/Yayın Bilgisi 2006
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  14. 14
    A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

    A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders Yazar: Jacquemont, Sébastien, Coe, Bradley P., Hersch, Micha, Duyzend, Michael H., Krumm, Niklas, Bergmann, Sven, Beckmann, Jacques S., Rosenfeld, Jill A., Eichler, Evan E.

    Baskı/Yayın Bilgisi 2014
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  15. 15
    SIGMA: A System for Integrative Genomic Microarray Analysis of Cancer Genomes

    SIGMA: A System for Integrative Genomic Microarray Analysis of Cancer Genomes Yazar: Chari, Raj, Lockwood, William W, Coe, Bradley P, Chu, Anna, Macey, Devon, Thomson, Andrew, Davies, Jonathan J, MacAulay, Calum, Lam, Wan L

    Baskı/Yayın Bilgisi 2006
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  16. 16
    SIGMA(2): A system for the integrative genomic multi-dimensional analysis of cancer genomes, epigenomes, and transcriptomes

    SIGMA(2): A system for the integrative genomic multi-dimensional analysis of cancer genomes, epigenomes, and transcriptomes Yazar: Chari, Raj, Coe, Bradley P, Wedseltoft, Craig, Benetti, Marie, Wilson, Ian M, Vucic, Emily A, MacAulay, Calum, Ng, Raymond T, Lam, Wan L

    Baskı/Yayın Bilgisi 2008
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  17. 17
    Genomic Deregulation of the E2F/Rb Pathway Leads to Activation of the Oncogene EZH2 in Small Cell Lung Cancer

    Genomic Deregulation of the E2F/Rb Pathway Leads to Activation of the Oncogene EZH2 in Small Cell Lung Cancer Yazar: Coe, Bradley P., Thu, Kelsie L., Aviel-Ronen, Sarit, Vucic, Emily A., Gazdar, Adi F., Lam, Stephen, Tsao, Ming-Sound, Lam, Wan L.

    Baskı/Yayın Bilgisi 2013
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  18. 18
    Transcriptome Profiles of Carcinoma-in-Situ and Invasive Non-Small Cell Lung Cancer as Revealed by SAGE

    Transcriptome Profiles of Carcinoma-in-Situ and Invasive Non-Small Cell Lung Cancer as Revealed by SAGE Yazar: Lonergan, Kim M., Chari, Raj, Coe, Bradley P., Wilson, Ian M., Tsao, Ming-Sound, Ng, Raymond T., MacAulay, Calum, Lam, Stephen, Lam, Wan L.

    Baskı/Yayın Bilgisi 2010
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  19. 19
    Copy number variation detection and genotyping from exome sequence data

    Copy number variation detection and genotyping from exome sequence data Yazar: Krumm, Niklas, Sudmant, Peter H., Ko, Arthur, O'Roak, Brian J., Malig, Maika, Coe, Bradley P., Quinlan, Aaron R., Nickerson, Deborah A., Eichler, Evan E.

    Baskı/Yayın Bilgisi 2012
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  20. 20
    Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar features

    Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar features Yazar: Aviel-Ronen, Sarit, Coe, Bradley P., Lau, Suzanne K., da Cunha Santos, Gilda, Zhu, Chang-Qi, Strumpf, Dan, Jurisica, Igor, Lam, Wan L., Tsao, Ming-Sound

    Baskı/Yayın Bilgisi 2008
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