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Daniela C Zarnescu

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  • Calculated based on no. of publications stored in Pure and citations from Scopus
19982021

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  • Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)

    Jin, S. C., Lewis, S. A., Bakhtiari, S., Zeng, X., Sierant, M. C., Shetty, S., Nordlie, S. M., Elie, A., Corbett, M. A., Norton, B. Y., van Eyk, C. L., Haider, S., Guida, B. S., Magee, H., Liu, J., Pastore, S., Vincent, J. B., Brunstrom-Hernandez, J., Papavasileiou, A., Fahey, M. C. & 57 others, Berry, J. G., Harper, K., Zhou, C., Zhang, J., Li, B., Zhao, H., Heim, J., Webber, D. L., Frank, M. S. B., Xia, L., Xu, Y., Zhu, D., Zhang, B., Sheth, A. H., Knight, J. R., Castaldi, C., Tikhonova, I. R., López-Giráldez, F., Keren, B., Whalen, S., Buratti, J., Doummar, D., Cho, M., Retterer, K., Millan, F., Wang, Y., Waugh, J. L., Rodan, L., Cohen, J. S., Fatemi, A., Lin, A. E., Phillips, J. P., Feyma, T., MacLennan, S. C., Vaughan, S., Crompton, K. E., Reid, S. M., Reddihough, D. S., Shang, Q., Gao, C., Novak, I., Badawi, N., Wilson, Y. A., McIntyre, S. J., Mane, S. M., Wang, X., Amor, D. J., Zarnescu, D. C., Lu, Q., Xing, Q., Zhu, C., Bilguvar, K., Padilla-Lopez, S., Lifton, R. P., Gecz, J., MacLennan, A. H. & Kruer, M. C., Mar 2021, In: Nature Genetics. 53, 3, p. 412 1 p.

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6

    Lehmkuhl, E. M., Loganathan, S., Alsop, E., Blythe, A. D., Kovalik, T., Mortimore, N. P., Barrameda, D., Kueth, C., Eck, R. J., Siddegowda, B. B., Joardar, A., Ball, H., Macias, M. E., Bowser, R., Van Keuren-Jensen, K. & Zarnescu, D. C., Dec 2021, In: Acta neuropathologica communications. 9, 1, 52.

    Research output: Contribution to journal › Article › peer-review

    Open Access

  • The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease

    Bakkar, N., Starr, A., Rabichow, B. E., Lorenzini, I., McEachin, Z. T., Kraft, R., Chaung, M., Macklin-Isquierdo, S., Wingfield, T., Carhart, B., Zahler, N., Chang, W. H., Bassell, G. J., Betourne, A., Boulis, N., Alworth, S. V., Ichida, J. K., August, P. R., Zarnescu, D. C., Sattler, R. & 1 others, Bowser, R., Feb 2021, In: Neurobiology of Disease. 149, 105228.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    1 Scopus citations

  • Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    Jin, S. C., Lewis, S. A., Bakhtiari, S., Zeng, X., Sierant, M. C., Shetty, S., Nordlie, S. M., Elie, A., Corbett, M. A., Norton, B. Y., van Eyk, C. L., Haider, S., Guida, B. S., Magee, H., Liu, J., Pastore, S., Vincent, J. B., Brunstrom-Hernandez, J., Papavasileiou, A., Fahey, M. C. & 56 others, Berry, J. G., Harper, K., Zhou, C., Zhang, J., Li, B., Heim, J., Webber, D. L., Frank, M. S. B., Xia, L., Xu, Y., Zhu, D., Zhang, B., Sheth, A. H., Knight, J. R., Castaldi, C., Tikhonova, I. R., López-Giráldez, F., Keren, B., Whalen, S., Buratti, J., Doummar, D., Cho, M., Retterer, K., Millan, F., Wang, Y., Waugh, J. L., Rodan, L., Cohen, J. S., Fatemi, A., Lin, A. E., Phillips, J. P., Feyma, T., MacLennan, S. C., Vaughan, S., Crompton, K. E., Reid, S. M., Reddihough, D. S., Shang, Q., Gao, C., Novak, I., Badawi, N., Wilson, Y. A., McIntyre, S. J., Mane, S. M., Wang, X., Amor, D. J., Zarnescu, D. C., Lu, Q., Xing, Q., Zhu, C., Bilguvar, K., Padilla-Lopez, S., Lifton, R. P., Gecz, J., MacLennan, A. H. & Kruer, M. C., Oct 1 2020, In: Nature Genetics. 52, 10, p. 1046-1056 11 p.

    Research output: Contribution to journal › Article › peer-review

    29 Scopus citations

  • Think globally, act locally: Centrosome-localized mRNAs ensure mitotic fidelity

    Zarnescu, D. C., Dec 7 2020, In: Journal of Cell Biology. 219, 12, e202010172.

    Research output: Contribution to journal › Article › peer-review

    Open Access
View all 49 Research outputs