Search Results - Paras Garg

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  1. 1

    Comment on "genomic hypomethylation in the human germline associates with selective structural mutability in the human genome". by Corey T Watson, Paras Garg, Andrew J Sharp

    Published in PLoS Genetics (2013-01-01)
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  2. 2

    Is evaluation of non-HDL-C better than calculated LDL-C in CAD patients? MMIMSR experiences by Gobardhan Kathariya, Jyoti Aggarwal, Paras Garg, Sonu Singh, Sajaad Manzoor

    Published in Indian Heart Journal (2020-05-01)
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  3. 3

    Automated Bone Marrow Cell Classification for Haematological Disease Diagnosis Using Siamese Neural Network by Balasundaram Ananthakrishnan, Ayesha Shaik, Shivam Akhouri, Paras Garg, Vaibhav Gadag, Muthu Subash Kavitha

    Published in Diagnostics (2022-12-01)
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  4. 4

    A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank by Celine A. Manigbas, Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Gabrielle Altman, Alejandro Martin-Trujillo, Andrew J. Sharp

    Published in Nature Communications (2024-12-01)
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  5. 5

    Comprehensive Analysis of the Genetic Variation in the <i>LPA</i> Gene from Short-Read Sequencing by Raphael O. Betschart, Georgios Koliopanos, Paras Garg, Linlin Guo, Massimiliano Rossi, Sebastian Schönherr, Stefan Blankenberg, Raphael Twerenbold, Tanja Zeller, Andreas Ziegler

    Published in BioMed (2024-06-01)
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  6. 6

    Dynamics of DNA methylation in recent human and great ape evolution. by Irene Hernando-Herraez, Javier Prado-Martinez, Paras Garg, Marcos Fernandez-Callejo, Holger Heyn, Christina Hvilsom, Arcadi Navarro, Manel Esteller, Andrew J Sharp, Tomas Marques-Bonet

    Published in PLoS Genetics (2013-01-01)
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  7. 7

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

    Published in PLoS Genetics (2020-11-01)
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