Resultats de la cerca - Paras Garg

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  1. 1
    A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome

    A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome per Paras Garg, Ricky S. Joshi, Corey T. Watson, Andrew J. Sharp

    Publicat 2018
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  2. 2
    Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease

    Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease per Corey T. Watson, Panos Roussos, Paras Garg, Daniel Ho, Nidha Azam, Pavel Katsel, Vahram Haroutunian, Andrew J. Sharp

    Publicat 2016
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  3. 3
    Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure

    Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure per Corey T. Watson, Henrietta Szutorisz, Paras Garg, Qammarah Martin, Joseph A. Landry, Andrew J. Sharp, Yasmin L. Hurd

    Publicat 2015
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  4. 4
    DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation

    DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation per Neeta Bala Tannan, Manisha Brahmachary, Paras Garg, Christelle Borel, Randah Alnefaie, Corey T. Watson, N. Simon Thomas, Andrew J. Sharp

    Publicat 2013
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  5. 5
    Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans

    Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans per Javier Quilez, Audrey Guilmatre, Paras Garg, Gareth Highnam, Melissa Gymrek, Yaniv Erlich, Ricky S. Joshi, David Mittelman, Andrew J. Sharp

    Publicat 2016
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  6. 6
    Dynamics of DNA Methylation in Recent Human and Great Ape Evolution

    Dynamics of DNA Methylation in Recent Human and Great Ape Evolution per Irene Hernando-Herraez, Javier Prado-Martinez, Paras Garg, Marcos Fernández-Callejo, Holger Heyn, Christina Hvilsom, Arcadi Navarro, Manel Esteller, Andrew J. Sharp, Tomàs Marquès‐Bonet

    Publicat 2013
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  7. 7
    Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains

    Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains per Jimmy Huynh, Paras Garg, Tin Htwe Thin, Seungyeul Yoo, Ranjan Dutta, Bruce D. Trapp, Vahram Haroutunian, Jun Zhu, Michael Donovan, Andrew J. Sharp, Patrizia Casaccia

    Publicat 2013
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  8. 8
    A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

    A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions per Paras Garg, Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain, Sofie Metsu, Hugh E. Olsen, Benedict Paten, Beate Ritz, R. Frank Kooy, Jozef Gécz, Andrew J. Sharp

    Publicat 2020
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  9. 9
    DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition

    DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition per Cyril Peter, Laura Fischer, Marija Kundaković, Paras Garg, Mira Jakovcevski, Aslihan Dincer, Ana C. Amaral, Edward I. Ginns, Marzena Galdzicka, Cyralene P. Bryce, Chana Ratner, Deborah P. Waber, David J. Mokler, Gayle Medford, Frances A. Champagne, Douglas L. Rosene, Jill McGaughy, Andrew J. Sharp, Janina R. Galler, Schahram Akbarian

    Publicat 2016
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  10. 10
    Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

    Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles per Alejandro Martin-Trujillo, Nihir Patel, Felix Richter, Bharati Jadhav, Paras Garg, Sarah U. Morton, David McKean, Steven R. DePalma, Elizabeth Goldmuntz, Dorota Gruber, Richard Kim, Jane W. Newburger, George A. Porter, Anna Giardini, Daniel Bernstein, Martin Tristani‐Firouzi, Jonathan G. Seidman, Christine E. Seidman, Wendy K. Chung, Bruce D. Gelb, Andrew J. Sharp

    Publicat 2020
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  11. 11
    Identification of rare de novo epigenetic variations in congenital disorders

    Identification of rare de novo epigenetic variations in congenital disorders per Mafalda Barbosa, Ricky S. Joshi, Paras Garg, Alejandro Martin-Trujillo, Nihir Patel, Bharati Jadhav, Corey T. Watson, William T. Gibson, Kelsey Chetnik, Chloé Tessereau, Hui Mei, Silvia De Rubeis, Jennifer Reichert, Fátima Lopes, Lisenka E.L.M. Vissers, Tjitske Kleefstra, Dorothy E. Grice, Lisa Edelmann, Gabriela Soares, Patrı́cia Maciel, Han G. Brunner, Joseph D. Buxbaum, Bruce D. Gelb, Andrew J. Sharp

    Publicat 2018
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  12. 12
    Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

    Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype per Michael S. Breen, Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa, Anne B. Arnett, Evangeline C. Kurtz‐Nelson, Emanuele Agolini, Agatino Battaglia, Andreas G. Chiocchetti, Christine M. Freitag, Alicia García-Alcón, Paola Grammatico, Irva Hertz‐Picciotto, Yunin Ludena‐Rodriguez, Carmen Moreno, Antonio Novelli, Mara Parellada, Giulia Pascolini, Flora Tassone, Dorothy E. Grice, Daniele Di Marino, Raphael Bernier, Alexander Kolevzon, Andrew J. Sharp, Joseph D. Buxbaum, Paige M. Siper, Silvia De Rubeis

    Publicat 2020
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  13. 13
    Increased frequency of repeat expansion mutations across different populations

    Increased frequency of repeat expansion mutations across different populations per Kristina Ibáñez, Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini, Paras Garg, Alejandro Martin-Trujillo, Scott J Gies, Valentina Galassi Deforie, Anupriya Dalmia, Davina J. Hensman Moss, Jana Vandrovcová, Clarissa Rocca, Loukas Moutsianas, Chiara Marini‐Bettolo, Helen Walker, Chris Turner, Maryam Shoai, Jeffrey D. Long, Pietro Fratta, Douglas R. Langbehn, Sarah J. Tabrizi, Mark J. Caulfield, Andrea Cortese, Valentina Escott‐Price, John Hardy, Henry Houlden, Andrew J. Sharp, Arianna Tucci

    Publicat 2024
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  14. 14
    DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

    DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome per Ricky S. Joshi, Paras Garg, Noah Zaitlen, Tuuli Lappalainen, Corey T. Watson, Nidha Azam, Daniel Ho, Xin Li, Stylianos E. Antonarakis, Han G. Brunner, Karin Buiting, Sau Wai Cheung, Bradford Coffee, Thomas Eggermann, David Francis, Joep Geraedts, Giorgio Gimelli, Samuel G. Jacobson, Cédric Le Caignec, Nicole de Leeuw, Thomas Liehr, Deborah Mackay, Stephen B. Montgomery, Alistair T. Pagnamenta, Peter Papenhausen, David Robinson, Claudia Ruivenkamp, Charles E. Schwartz, Bernhard Steiner, David A. Stevenson, Urvashi Surti, Thomas H. Wassink, Andrew J. Sharp

    Publicat 2016
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