Torthaí cuardaigh - Bharati Jadhav

  • 1 - 6 toradh as 6 á dtaispeáint
Beachtaigh na torthaí
  1. 1
    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 de réir 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

    Foilsithe / Cruthaithe 2020
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  2. 2
    Foxa2 identifies a cardiac progenitor population with ventricular differentiation potential

    Foxa2 identifies a cardiac progenitor population with ventricular differentiation potential de réir Evan Bardot, Damelys Calderon, Francis J. Santoriello, Songyan Han, Kakit Cheung, Bharati Jadhav, Ingo Burtscher, Stanley T Artap, Rajan Jain, Jonathan A. Epstein, Heiko Lickert, Valerie Gouon–Evans, Andrew J. Sharp, Nicole Dubois

    Foilsithe / Cruthaithe 2017
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  3. 3
    The GIAB genomic stratifications resource for human reference genomes

    The GIAB genomic stratifications resource for human reference genomes de réir Nathan Dwarshuis, Divya Kalra, Jennifer McDaniel, Philippe Sanio, Pilar Álvarez Jerez, Bharati Jadhav, Wenyu Huang, Ritwik Mondal, Ben Busby, Nathan D. Olson, Fritz J. Sedlazeck, Justin Wagner, Sina Majidian, Justin M. Zook

    Foilsithe / Cruthaithe 2024
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  4. 4
    Identification of rare de novo epigenetic variations in congenital disorders

    Identification of rare de novo epigenetic variations in congenital disorders de réir 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

    Foilsithe / Cruthaithe 2018
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  5. 5
    REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats

    REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats de réir Egor Dolzhenko, Ben Weisburd, Kristina Ibáñez, Indhu‐Shree Rajan‐Babu, Christine Anyansi, Mark F. Bennett, Kimberley J. Billingsley, Ashley Carroll, Samuel Clamons, Matt C. Danzi, Viraj Deshpande, Jinhui Ding, Sarah Fazal, Andreas Halman, Bharati Jadhav, Yunjiang Qiu, Phillip A. Richmond, Christopher T. Saunders, Konrad Scheffler, Joke J.F.A. van Vugt, Ramona R. A. J. Zwamborn, Samuel S. Chong, Jan M. Friedman, Arianna Tucci, Heidi L. Rehm, Michael A. Eberle

    Foilsithe / Cruthaithe 2022
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  6. 6
    Increased frequency of repeat expansion mutations across different populations

    Increased frequency of repeat expansion mutations across different populations de réir 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

    Foilsithe / Cruthaithe 2024
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