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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

S. Mukherjee, T. Cassini, N. Hu, T. Yang, B. Li, W. Shen, C. Moth, D. Rinker, J. Sheehan, J. Cogan, J. Newman, R. Hamid, R. Macdonald, D. Roden, J. Meiler, G. Kuenze, J. Phillips, and J. Capra. Human Genetics and Genomics Advances, 3 (4): 100131 (2022)
DOI: https://doi.org/10.1016/j.xhgg.2022.100131

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Predicting the functional impact of KCNQ1 variants with artificial neural networksS. Phul, G. Kuenze, C. Vanoye, C. Sanders, A. George, Jr, and J. Meiler. PLoS Comput. Biol., 18 (4): e1010038 (April 2022)Docking cholesterol to integral membrane proteins with RosettaB. Marlow, G. Kuenze, J. Meiler, and J. Koehler Leman. PLoS Comput. Biol., 19 (3): e1010947 (March 2023)Predicting the functional impact of KCNQ1 variants with artificial neural networksS. Phul, G. Kuenze, C. Vanoye, C. Sanders, A. George, and J. Meiler. PLOS Computational Biology, 18 (4): e1010038 (April 2022)Ensuring scientific reproducibility in bio-macromolecular modeling via extensive, automated benchmarksJ. Koehler Leman, S. Lyskov, S. Lewis, J. Adolf-Bryfogle, R. Alford, K. Barlow, Z. Ben-Aharon, D. Farrell, J. Fell, W. Hansen and 40 other author(s). Nat. Commun., 12 (1): 6947 (November 2021)Predicting the Functional Impact of KCNQ1 Variants with Artificial Neural NetworksS. Phul, G. Kuenze, C. Vanoye, C. Sanders, A. George, and J. Meiler. (December 2021)Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variantsS. Mukherjee, T. Cassini, N. Hu, T. Yang, B. Li, W. Shen, C. Moth, D. Rinker, J. Sheehan, J. Cogan and 8 other author(s). Human Genetics and Genomics Advances, 3 (4): 100131 (2022)

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Disambiguation of "Kuenze, Georg"

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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

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Disambiguation of "Kuenze, Georg"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants