Výsledky vyhledávání - Michael Ronemus

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  1. 1
    Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses

    Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses Autor Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup

    Vydáno 2011
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  2. 2
    Low load for disruptive mutations in autism genes and their biased transmission

    Low load for disruptive mutations in autism genes and their biased transmission Autor Ivan Iossifov, Dan Levy, Jeremy Allen, Kenny Ye, Michael Ronemus, Yoonha Lee, Boris Yamrom, Michael Wigler

    Vydáno 2015
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  3. 3
    Reducing INDEL calling errors in whole genome and exome sequencing data

    Reducing INDEL calling errors in whole genome and exome sequencing data Autor Han Fang, Yiyang Wu, Giuseppe Narzisi, Jason O'Rawe, Laura T. Jiménez Barrón, Julie Rosenbaum, Michael Ronemus, Ivan Iossifov, Michael C. Schatz, Gholson J. Lyon

    Vydáno 2014
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  4. 4
    Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

    Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders Autor Dan Levy, Michael Ronemus, Boris Yamrom, Yoonha Lee, Anthony Leotta, Jude Kendall, Steven C. Marks, B. Lakshmi, Deepa Pai, Kenny Ye, Andreas Buja, Abba Μ. Krieger, Seungtai Yoon, Jennifer Troge, Linda Rodgers, Ivan Iossifov, Michael Wigler

    Vydáno 2011
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  5. 5
    The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

    The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left hear... Autor Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane‐Yeboa, Wendy K. Chung, Lan Yu, Nancy Wong, Danielle Awad, Chih‐Yu Yu, Anthony Leotta, Jude Kendall, Boris Yamrom, Yoon-ha Lee, Michael Wigler, Dan Levy

    Vydáno 2013
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  6. 6
    Indel variant analysis of short-read sequencing data with Scalpel

    Indel variant analysis of short-read sequencing data with Scalpel Autor Han Fang, Ewa A. Bergmann, Kanika Arora, Vladimir Vacic, Michael C. Zody, Ivan Iossifov, Jason O'Rawe, Yiyang Wu, Laura T. Jiménez Barrón, Julie Rosenbaum, Michael Ronemus, Yoon-ha Lee, Zihua Wang, Esra Dikoglu, Vaidehi Jobanputra, Gholson J. Lyon, Michael Wigler, Michael C. Schatz, Giuseppe Narzisi

    Vydáno 2016
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  7. 7
    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 Autor 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

    Vydáno 2014
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  8. 8
    De Novo Gene Disruptions in Children on the Autistic Spectrum

    De Novo Gene Disruptions in Children on the Autistic Spectrum Autor Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoonha Lee, Giuseppe Narzisi, Anthony Leotta, Jude Kendall, Ewa Grabowska, Beicong Ma, Steven C. Marks, Linda Rodgers, Asya Stepansky, Jennifer Troge, Peter Andrews, Mitchell A. Bekritsky, Kith Pradhan, Elena Ghiban, Melissa Kramer, Jennifer Parla, Ryan Demeter, Lucinda Fulton, Robert S. Fulton, Vincent Magrini, Kenny Ye, Jennifer C. Darnell, Robert B. Darnell, Elaine R. Mardis, Richard K. Wilson, Michael C. Schatz, W. Richard McCombie, Michael Wigler

    Vydáno 2012
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  9. 9
    The contribution of de novo coding mutations to autism spectrum disorder

    The contribution of de novo coding mutations to autism spectrum disorder Autor Ivan Iossifov, Brian J. O’Roak, Stephan Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A.F. Stessman, Kali Witherspoon, Laura Vives, Karynne Patterson, Joshua D. Smith, Bryan Paeper, Deborah A. Nickerson, Jeanselle Dea, Shan Dong, Luis Eduardo González, Jeffrey D. Mandell, Shrikant Mane, Michael T. Murtha, Catherine Sullivan, Michael F. Walker, Zainulabedin Waqar, Liping Wei, A. Jeremy Willsey, Boris Yamrom, Yoonha Lee, Ewa Grabowska, Ertuğrul Dalkıç, Zihua Wang, Steven C. Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C. Schatz, Kenny Ye, W. Richard McCombie, Jay Shendure, Evan E. Eichler, Matthew W. State, Michael Wigler

    Vydáno 2014
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  10. 10
    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 Autor 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

    Vydáno 2015
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