Výsledky vyhledávání - Ivan Iossifov

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  1. 1
    Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network

    Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network Autor Ivan Iossifov, Tian Zheng, Miron Baron, T. Conrad Gilliam, Andrey Rzhetsky

    Vydáno 2008
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  2. 2
    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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  3. 3
    A comparative analysis of exome capture

    A comparative analysis of exome capture Autor Jennifer Parla, Ivan Iossifov, Ian Grabill, Mona S. Spector, Melissa Kramer, W. Richard McCombie

    Vydáno 2011
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  4. 4
    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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  5. 5
    Damaging de novo mutations diminish motor skills in children on the autism spectrum

    Damaging de novo mutations diminish motor skills in children on the autism spectrum Autor Andreas Buja, Natalia Volfovsky, Abba Μ. Krieger, Catherine Lord, Alex E. Lash, Michael Wigler, Ivan Iossifov

    Vydáno 2018
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  6. 6
    Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk

    Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk Autor Stephane E. Castel, Alejandra Cervera, Pejman Mohammadi, François Aguet, Ferrán Reverter, Aaron Wolman, Roderic Guigó, Ivan Iossifov, Ana Vasileva, Tuuli Lappalainen

    Vydáno 2018
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  7. 7
    Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction

    Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction Autor Xi Shi, Congyi Lu, Alba Corman, Alexandria Nikish, Yang Zhou, R. Platt, Ivan Iossifov, Feng Zhang, Jen Q. Pan, Neville E. Sanjana

    Vydáno 2023
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  8. 8
    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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  9. 9
    Accurate de novo and transmitted indel detection in exome-capture data using microassembly

    Accurate de novo and transmitted indel detection in exome-capture data using microassembly Autor Giuseppe Narzisi, Jason O'Rawe, Ivan Iossifov, Han Fang, Yoon-ha Lee, Zihua Wang, Yiyang Wu, Gholson J. Lyon, Michael Wigler, Michael C. Schatz

    Vydáno 2014
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  10. 10
    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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  11. 11
    Analysis of <i>Drosophila</i> Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer

    Analysis of <i>Drosophila</i> Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer Autor Jiang Liu, Murad Ghanim, Lei Xue, Christopher D. Brown, Ivan Iossifov, César Angeletti, Sujun Hua, Nicolas Nègre, Michael Ludwig, Thomas Stricker, Hikmat Al‐Ahmadie, Maria Tretiakova, Robert L. Camp, Montse Perera-Alberto, David L. Rimm, Tian Xu, Andrey Rzhetsky, K White

    Vydáno 2009
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  12. 12
    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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  13. 13
    Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA

    Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA Autor Tychele N. Turner, Fereydoun Hormozdiari, Michael H. Duyzend, Sarah A. McClymont, Paul W. Hook, Ivan Iossifov, Archana N. Raja, Carl Baker, Kendra Hoekzema, Holly A.F. Stessman, Michael C. Zody, Bradley J. Nelson, John Huddleston, Richard Sandstrom, Joshua D. Smith, D. Hanna, James M. Swanson, Elaine M. Faustman, Michael J. Bamshad, J Stamatoyannopoulos, Deborah A. Nickerson, Andrew S. McCallion, Robert B. Darnell, Evan E. Eichler

    Vydáno 2015
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  14. 14
    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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  15. 15
    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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  16. 16
    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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  17. 17
    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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  18. 18
    De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

    De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms Autor Sandra Jansen, Ilse van der Werf, A. Micheil Innes, Alexandra Afenjar, Pankaj B. Agrawal, Ilse J. Anderson, Paldeep S. Atwal, Ellen van Binsbergen, Marie-José van den Boogaard, Lucia Castiglia, Zeynep Coban‐Akdemir, Anke Van Dijck, Diane Doummar, Albertien M. van Eerde, Anthonie J. van Essen, Koen L.I. van Gassen, María J. Guillen Sacoto, Mieke M. van Haelst, Ivan Iossifov, Jessica L. Jackson, Elizabeth Judd, Charu Kaiwar, Boris Keren, Eric W. Klee, Jolien S. Klein Wassink‐Ruiter, Marije Meuwissen, Kristin G. Monaghan, Sonja A. de Munnik, Caroline Nava, Charlotte W. Ockeloen, Rosa Pettinato, Hilary Racher, Tuula Rinne, Corrado Romano, Victoria R. Sanders, Rhonda E. Schnur, Eric J. Smeets, Alexander P.A. Stegmann, Asbjørg Stray‐Pedersen, David A. Sweetser, Paulien A. Terhal, Kristian Tveten, Grace E. VanNoy, Petra F. de Vries, Jessica L. Waxler, Marcia Willing, Rolph Pfundt, Joris A. Veltman, R. Frank Kooy, Lisenka E.L.M. Vissers, Bert B.A. de Vries

    Vydáno 2019
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