Kết quả tìm kiếm - Paras Garg
- Đang hiển thị 1 - 14 kết quả của 14
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Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease Bằng Corey T. Watson, Panos Roussos, Paras Garg, Daniel Ho, Nidha Azam, Pavel Katsel, Vahram Haroutunian, Andrew J. Sharp
Được phát hành 2016Artigo -
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Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure Bằng Corey T. Watson, Henrietta Szutorisz, Paras Garg, Qammarah Martin, Joseph A. Landry, Andrew J. Sharp, Yasmin L. Hurd
Được phát hành 2015Artigo -
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DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation Bằng Neeta Bala Tannan, Manisha Brahmachary, Paras Garg, Christelle Borel, Randah Alnefaie, Corey T. Watson, N. Simon Thomas, Andrew J. Sharp
Được phát hành 2013Artigo -
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Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans Bằng Javier Quilez, Audrey Guilmatre, Paras Garg, Gareth Highnam, Melissa Gymrek, Yaniv Erlich, Ricky S. Joshi, David Mittelman, Andrew J. Sharp
Được phát hành 2016Artigo -
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Dynamics of DNA Methylation in Recent Human and Great Ape Evolution Bằng 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
Được phát hành 2013Artigo -
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Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains Bằng 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
Được phát hành 2013Artigo -
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A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions Bằng 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
Được phát hành 2020Artigo -
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DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition Bằng 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
Được phát hành 2016Artigo -
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Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles Bằng 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
Được phát hành 2020Artigo -
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Identification of rare de novo epigenetic variations in congenital disorders Bằng 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
Được phát hành 2018Artigo -
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Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype Bằng 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
Được phát hành 2020Artigo -
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Increased frequency of repeat expansion mutations across different populations Bằng 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
Được phát hành 2024Artigo -
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome Bằng 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
Được phát hành 2016Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
DNA methylation
Gene expression
Epigenetics
Genome
Methylation
Computational biology
Medicine
DNA
Human genome
Neuroscience
Phenotype
Psychology
Bioinformatics
Computer science
CpG site
Disease
Environmental health
Epigenomics
Evolutionary biology
Human genetics
Operating system
Pathology
Population
Profiling (computer programming)
Promoter
Allele
Allele frequency