نتائج البحث - Jason Homsy

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  1. 1
    Drosophila AP-1: lessons from an invertebrate

    Drosophila AP-1: lessons from an invertebrate حسب Lutz Kockel, Jason Homsy, Dirk Bohmann

    منشور في 2001
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    Revisão
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  2. 2
    Interpreting <i>de novo</i> Variation in Human Disease Using denovolyzeR

    Interpreting <i>de novo</i> Variation in Human Disease Using denovolyzeR حسب James S. Ware, Kaitlin E. Samocha, Jason Homsy, Mark J. Daly

    منشور في 2015
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    Artigo
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  3. 3
    CANOES: detecting rare copy number variants from whole exome sequencing data

    CANOES: detecting rare copy number variants from whole exome sequencing data حسب Daniel Backenroth, Jason Homsy, Laura Rodriguez Murillo, Joseph Glessner, Edwin Lin, Martina Brueckner, Richard P. Lifton, Elizabeth Goldmuntz, Wendy K. Chung, Yufeng Shen

    منشور في 2014
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    Artigo
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  4. 4
    Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells

    Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells حسب Luhan Yang, Dennis Grishin, Gang Wang, John Aach, Cheng‐Zhong Zhang, Raj Chari, Jason Homsy, Xuyu Cai, Yue Zhao, Jian‐Bing Fan, Christine E. Seidman, Jonathan G. Seidman, William T. Pu, George M. Church

    منشور في 2014
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    Artigo
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  5. 5
    Single-Cell Resolution of Temporal Gene Expression during Heart Development

    Single-Cell Resolution of Temporal Gene Expression during Heart Development حسب Daniel M. DeLaughter, Alexander G. Bick, Hiroko Wakimoto, David McKean, Joshua M. Gorham, Irfan S. Kathiriya, J. Travis Hinson, Jason Homsy, Jesse Gray, William T. Pu, Benoit G. Bruneau, Jonathan G. Seidman, Christine E. Seidman

    منشور في 2016
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    Artigo
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  6. 6
    Loss of RNA expression and allele-specific expression associated with congenital heart disease

    Loss of RNA expression and allele-specific expression associated with congenital heart disease حسب David McKean, Jason Homsy, Hiroko Wakimoto, Neil Patel, Joshua M. Gorham, Steven R. DePalma, James S. Ware, Samir Zaidi, Wenji Ma, Nihir Patel, Richard P. Lifton, Wendy K. Chung, Richard Kim, Yufeng Shen, Martina Brueckner, Elizabeth Goldmuntz, Andrew J. Sharp, Christine E. Seidman, Bruce D. Gelb

    منشور في 2016
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    Artigo
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  7. 7
    Robust identification of mosaic variants in congenital heart disease

    Robust identification of mosaic variants in congenital heart disease حسب Kathryn B. Manheimer, Felix Richter, Lisa Edelmann, Sunita L. D’Souza, Lisong Shi, Yufeng Shen, Jason Homsy, Marko T. Boskovski, Angela C. Tai, Joshua M. Gorham, Christopher Yasso, Elizabeth Goldmuntz, Martina Brueckner, Richard P. Lifton, Wendy K. Chung, Christine E. Seidman, J. G. Seidman, Bruce D. Gelb

    منشور في 2018
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    Artigo
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  8. 8
    Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

    Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy حسب J. Travis Hinson, Anant Chopra, Navid A. Nafissi, William J. Polacheck, Craig C Benson, Sandra Swist, Joshua M. Gorham, Luhan Yang, Sebastian Schäfer, Calvin C. Sheng, Alireza Haghighi, Jason Homsy, Norbert Hübner, George M. Church, Stuart A. Cook, Wolfgang A. Linke, Christopher S. Chen, J. G. Seidman, Christine E. Seidman

    منشور في 2015
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    Artigo
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  9. 9
    Paternal-age-related de novo mutations and risk for five disorders

    Paternal-age-related de novo mutations and risk for five disorders حسب Jacob Taylor, Jean-Christophe Debost, Sarah U. Morton, Emilie M. Wigdor, Henrike Heyne, Dennis Lal, Daniel P. Howrigan, Alex Bloemendal, Janne Tidselbak Larsen, Jack A. Kosmicki, Daniel J. Weiner, Jason Homsy, Jonathan G. Seidman, Christine E. Seidman, Esben Agerbo, John J. McGrath, Preben Bo Mortensen, Liselotte Petersen, Mark J. Daly, Elise Robinson

    منشور في 2019
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    Artigo
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  10. 10
    Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

    Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data حسب Joseph Glessner, Alexander G. Bick, Kaoru Ito, Jason Homsy, Laura Rodriguez‐Murillo, Menachem Fromer, Erica Mazaika, Badri N. Vardarajan, Michael J. Italia, Jeremy Leipzig, Steven R. DePalma, Ryan Golhar, Stephan Sanders, Boris Yamrom, Michael Ronemus, Ivan Iossifov, A. Jeremy Willsey, Matthew W. State, Jonathan R. Kaltman, Peter S. White, Yufeng Shen, Dorothy Warburton, Martina Brueckner, Christine E. Seidman, Elizabeth Goldmuntz, Bruce D. Gelb, Richard P. Lifton, Jonathan G. Seidman, Hákon Hákonarson, Wendy K. Chung

    منشور في 2014
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    Artigo
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  11. 11
    Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency

    Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency حسب Tarsha Ward, Warren Tai, Sarah U. Morton, Francis Impens, Petra Van Damme, Delphi Van Haver, Evy Timmerman, Gabriela Venturini, Kehan Zhang, Min Young Jang, Jon A. L. Willcox, Alireza Haghighi, Bruce D. Gelb, Wendy K. Chung, Elizabeth Goldmuntz, George A. Porter, Richard P. Lifton, Martina Brueckner, H. Joseph Yost, Benoit G. Bruneau, Joshua M. Gorham, Yuri Kim, Alexandre C. Pereira, Jason Homsy, Craig C Benson, Steven R. DePalma, Sylvia Varland, Christopher S. Chen, Thomas Arnesen, Kris Gevaert, Christine E. Seidman, Jonathan G. Seidman

    منشور في 2021
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    Artigo
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  12. 12
    De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease

    De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease حسب Marko T. Boskovski, Jason Homsy, Meena Nathan, Lynn A. Sleeper, Sarah U. Morton, Kathryn B. Manheimer, Angela C. Tai, Joshua M. Gorham, Matthew Lewis, Michael F. Swartz, George M. Alfieris, Emile Bacha, Mohsen Karimi, David Meyer, Khanh Nguyen, Daniel Bernstein, Angela Romano-Adesman, George A. Porter, Elizabeth Goldmuntz, Wendy K. Chung, Deepak Srivastava, Jonathan R. Kaltman, Martin Tristani‐Firouzi, Richard P. Lifton, Amy E. Roberts, J. William Gaynor, Bruce D. Gelb, Richard Kim, Jonathan G. Seidman, Martina Brueckner, John E. Mayer, Jane W. Newburger, Christine E. Seidman

    منشور في 2020
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    Artigo
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  13. 13
    Genomic analyses implicate noncoding de novo variants in congenital heart disease

    Genomic analyses implicate noncoding de novo variants in congenital heart disease حسب Felix Richter, Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen, Jian Zhou, Hongjian Qi, Nihir Patel, Steven R. DePalma, Michael Parfenov, Jason Homsy, Joshua M. Gorham, Kathryn B. Manheimer, Matthew Velinder, Andrew Farrell, Gábor Marth, Eric E. Schadt, Jonathan R. Kaltman, Jane W. Newburger, Anna Giardini, Elizabeth Goldmuntz, Martina Brueckner, Richard Kim, George A. Porter, Daniel Bernstein, Wendy K. Chung, Deepak Srivastava, Martin Tristani‐Firouzi, Olga G. Troyanskaya, Diane E. Dickel, Yufeng Shen, Jonathan G. Seidman, Christine E. Seidman, Bruce D. Gelb

    منشور في 2020
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    Artigo
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  14. 14
    De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

    De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies حسب Jason Homsy, Samir Zaidi, Yufeng Shen, James S. Ware, Kaitlin E. Samocha, Konrad J. Karczewski, Steven R. DePalma, David McKean, Hiroko Wakimoto, Josh Gorham, Sheng Chih Jin, John Deanfield, Anna Giardini, George A. Porter, Richard Kim, Kaya Bilgüvar, Francesc López‐Giráldez, Irina Tikhonova, Shrikant Mane, Angela Romano-Adesman, Hongjian Qi, Badri N. Vardarajan, Lijiang Ma, Mark J. Daly, Amy E. Roberts, Mark W. Russell, Seema Mital, Jane W. Newburger, J. William Gaynor, Roger E. Breitbart, Ivan Iossifov, Michael Ronemus, Stephan Sanders, Jonathan R. Kaltman, Jonathan G. Seidman, Martina Brueckner, Bruce D. Gelb, Elizabeth Goldmuntz, Richard P. Lifton, Christine E. Seidman, Wendy K. Chung

    منشور في 2015
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    Artigo
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  15. 15
    Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

    Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands حسب Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah U. Morton, Steven R. DePalma, Xue Zeng, Hongjian Qi, Wen-I Chang, Michael C. Sierant, Wei-Chien Hung, Shozeb Haider, Junhui Zhang, James Knight, Robert Bjornson, Christopher Castaldi, Irina R Tikhonoa, Kaya Bilgüvar, Shrikant Mane, Stephan Sanders, Seema Mital, Mark W. Russell, J. William Gaynor, John Deanfield, Anna Giardini, George A. Porter, Deepak Srivastava, Cecilia Lo, Yufeng Shen, W. Scott Watkins, Mark Yandell, H. Joseph Yost, Martin Tristani‐Firouzi, Jane W. Newburger, Amy E. Roberts, Richard Kim, Hongyu Zhao, Jonathan R. Kaltman, Elizabeth Goldmuntz, Wendy K. Chung, Jonathan G. Seidman, Bruce D. Gelb, Christine E. Seidman, Richard P. Lifton, Martina Brueckner

    منشور في 2017
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    Artigo
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