检索结果 - Akash Kamandula

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    Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers

    Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers 由 Yile Chen, Kyoungyeul Lee, Junwoo Woo, Dong Wook Kim, Changwon Keum, Giulia Babbi, Rita Casadio, Pier Luigi Martelli, Castrense Savojardo, Matteo Manfredi, Yang Shen, Yuanfei Sun, Panagiotis Katsonis, Olivier Lichtarge, Vikas Pejaver, David J. Seward, Akash Kamandula, Constantina Bakolitsa, Steven E. Brenner, Predrag Radivojac, Anne O’Donnell‐Luria, Sean D. Mooney, Shantanu Jain

    出版 2025
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  2. 2
    Predicting the impact of rare variants on RNA splicing in CAGI6

    Predicting the impact of rare variants on RNA splicing in CAGI6 由 Jenny Lord, Carolina Jaramillo Oquendo, Htoo A. Wai, Andrew G. L. Douglas, David J. Bunyan, Yaqiong Wang, Zhiqiang Hu, Zishuo Zeng, Daniel Daniš, Panagiotis Katsonis, Amanda M. Williams, Olivier Lichtarge, Yu‐Chen Chang, Richard D. Bagnall, Stephen M. Mount, Brynja Matthiasardottir, Chiao‐Feng Lin, Thomas van Overeem Hansen, Raphaël Leman, Alexandra Martins, Claude Houdayer, Sophie Krieger, Constantina Bakolitsa, Yisu Peng, Akash Kamandula, Predrag Radivojac, Diana Baralle

    出版 2024
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  3. 3
    Critical assessment of missense variant effect predictors on disease-relevant variant data

    Critical assessment of missense variant effect predictors on disease-relevant variant data 由 Ruchir Rastogi, Ryan Chung, Sindy Li, Chang Li, Kyoungyeul Lee, Junwoo Woo, Dongwook Kim, Changwon Keum, Giulia Babbi, Pier Luigi Martelli, Castrense Savojardo, Rita Casadio, Kirsley Chennen, Thomas Weber, Olivier Poch, François Ancien, Gabriel Cia, Fabrizio Pucci, Daniele Raimondi, Wim Vranken, Marianne Rooman, Céline Marquet, Tobias Olenyi, Burkhard Rost, Gaia Andreoletti, Akash Kamandula, Yisu Peng, Constantina Bakolitsa, Matthew Mort, D.N. Cooper, Timothy Bergquist, Vikas Pejaver, Xiaoming Liu, Predrag Radivojac, Steven E. Brenner, Nilah M. Ioannidis

    出版 2025
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  4. 4
    Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project

    Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project 由 Sarah L. Stenton, Melanie O’Leary, Gabrielle Lemire, Grace E. VanNoy, Stephanie DiTroia, Vijay Ganesh, Emily Groopman, Emily O’Heir, Brian Mangilog, Ikeoluwa Osei‐Owusu, Lynn Pais, Jillian Serrano, Moriel Singer‐Berk, Ben Weisburd, Michael W. Wilson, Christina Austin‐Tse, Marwa Abdelhakim, Azza Althagafi, Giulia Babbi, Riccardo Bellazzi, Samuele Bovo, Maria Giulia Carta, Rita Casadio, Pieter-Jan Coenen, Federica De Paoli, Matteo Floris, Manavalan Gajapathy, Robert Hoehndorf, Julius O.B. Jacobsen, Thomas Joseph, Akash Kamandula, Panagiotis Katsonis, Cyrielle Kint, Olivier Lichtarge, Ivan Limongelli, Yulan Lu, Paolo Magni, Tarun Karthik Kumar Mamidi, Pier Luigi Martelli, M. Mulargia, Giovanna Nicora, Keith Nykamp, Vikas Pejaver, Yisu Peng, Thi Hong Cam Pham, Maurizio Podda, Aditya Rao, Ettore Rizzo, Vangala G. Saipradeep, Castrense Savojardo, Peter Schols, Yang Shen, Naveen Sivadasan, Damian Smedley, Dorian Soru, Rajgopal Srinivasan, Yuanfei Sun, Uma Sunderam, Wuwei Tan, Naina Tiwari, Xiao Wang, Yaqiong Wang, Amanda M. Williams, Elizabeth A. Worthey, Rujie Yin, Yuning You, Daniel Zeiberg, Susanna Zucca, Constantina Bakolitsa, Steven E. Brenner, Stephanie M. Fullerton, Predrag Radivojac, Heidi L. Rehm, Anne O’Donnell‐Luria

    出版 2024
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