Risultati della ricerca - Bradley P. Coe

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  1. 1
    Genome structural variation discovery and genotyping

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

    Pubblicazione 2011
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  2. 2
    The genetic variability and commonality of neurodevelopmental disease

    The genetic variability and commonality of neurodevelopmental disease di Bradley P. Coe, Santhosh Girirajan, Evan E. Eichler

    Pubblicazione 2012
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  3. 3
    A genetic model for neurodevelopmental disease

    A genetic model for neurodevelopmental disease di Bradley P. Coe, Santhosh Girirajan, Evan E. Eichler

    Pubblicazione 2012
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  4. 4
    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 di Raj Chari, Bradley P. Coe, Emily A. Vucic, William W. Lockwood, Wan L. Lam

    Pubblicazione 2010
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  5. 5
    Estimates of penetrance for recurrent pathogenic copy-number variations

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

    Pubblicazione 2012
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  6. 6
    Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications

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

    Pubblicazione 2017
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  7. 7
    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. di Bryan Chi, Ronald J. deLeeuw, Bradley P. Coe, Calum MacAulay, Wan L. Lam

    Pubblicazione 2004
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  8. 8
    Brain white matter structure and <i>COMT</i> gene are linked to second-language learning in adults

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

    Pubblicazione 2016
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  9. 9
    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 di Roland Hubaux, Kelsie L. Thu, Bradley P. Coe, Calum MacAulay, Stephen Lam, Wan L. Lam

    Pubblicazione 2013
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  10. 10
    Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV

    Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV di Michael H. Duyzend, Xander Nuttle, Bradley P. Coe, Carl Baker, Deborah A. Nickerson, Raphael Bernier, Evan E. Eichler

    Pubblicazione 2015
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  11. 11
    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 di Sébastien Jacquemont, Bradley P. Coe, Micha Hersch, Michael H. Duyzend, Niklas Krumm, Sven Bergmann, J. Beckmann, Jill A. Rosenfeld, Evan E. Eichler

    Pubblicazione 2014
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  12. 12
    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 di Bradley P. Coe, Kelsie L. Thu, Sarit Aviel‐Ronen, Emily A. Vucic, Adi F. Gazdar, Stephen Lam, Ming‐Sound Tsao, Wan L. Lam

    Pubblicazione 2013
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  13. 13
    DNA amplification is a ubiquitous mechanism of oncogene activation in lung and other cancers

    DNA amplification is a ubiquitous mechanism of oncogene activation in lung and other cancers di William W. Lockwood, Raj Chari, Bradley P. Coe, Luc Girard, Calum MacAulay, Stephen Lam, Adi F. Gazdar, John D. Minna, Wan L. Lam

    Pubblicazione 2008
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  14. 14
    Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer

    Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer di Bradley P. Coe, William W. Lockwood, Luc Girard, Raj Chari, Calum MacAulay, Alfred K. Lam, Adi F. Gazdar, John D. Minna, Wan L. Lam

    Pubblicazione 2006
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  15. 15
    Copy number variation detection and genotyping from exome sequence data

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

    Pubblicazione 2012
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  16. 16
    Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar features

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

    Pubblicazione 2008
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  17. 17
    Copy-Number Variation and False Positive Prenatal Aneuploidy Screening Results

    Copy-Number Variation and False Positive Prenatal Aneuploidy Screening Results di Matthew W. Snyder, LaVone E. Simmons, Jacob O. Kitzman, Bradley P. Coe, Jessica M. Henson, Riza M. Daza, Evan E. Eichler, Jay Shendure, Hilary S. Gammill

    Pubblicazione 2015
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  18. 18
    Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity

    Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity di Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, Madeleine R. Geisheker, Trygve E. Bakken, Allison M. Lake, Joseph D. Dougherty, Ed S. Lein, Fereydoun Hormozdiari, Raphael Bernier, Evan E. Eichler

    Pubblicazione 2018
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  19. 19
    Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

    Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder di Santhosh Girirajan, Megan Y. Dennis, Carl Baker, Maika Malig, Bradley P. Coe, Colin Campbell, Kenneth M. K. Mark, Tiffany Vu, Can Alkan, Ze Cheng, Leslie G. Biesecker, Raphael Bernier, Evan E. Eichler

    Pubblicazione 2013
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  20. 20
    Genomic Patterns of De Novo Mutation in Simplex Autism

    Genomic Patterns of De Novo Mutation in Simplex Autism di Tychele N. Turner, Bradley P. Coe, Diane E. Dickel, Kendra Hoekzema, Bradley J. Nelson, Michael C. Zody, Zev Kronenberg, Fereydoun Hormozdiari, Archana N. Raja, L Pennacchio, Robert B. Darnell, Evan E. Eichler

    Pubblicazione 2017
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