Association of stroke risk biomarkers with stroke symptoms: the Reasons for Geographic and Racial Differences in Stroke cohort von Landry, K. K., Alexander, K. S., Zakai, N. A., Judd, S. E., Kleindorfer, D. O., Howard, V. J., Howard, G., Cushman, M.

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Migraine-associated common genetic variants confer greater risk of posterior vs. anterior circulation ischemic stroke von Frid, P., Xu, H., Mitchell, B.D., Drake, M., Wasselius, J., Gaynor, B., Ryan, K., Giese, A.K., Schirmer, M., Donahue, K.L., Irie, R., Bouts, M.J.R.J., McIntosh, E.C., Mocking, S.J.T., Dalca, A.V., Giralt-Steinhauer, E., Holmegaard, L., Jood, K., Roquer, J., Cole, J.W., McArdle, P.F., Broderick, J.P., Jimenez-Conde, J., Jern, C., Kissela, B.M., Kleindorfer, D.O., Lemmens, R., Meschia, J.F., Rosand, J., Rundek, T., Sacco, R.L., Schmidt, R., Sharma, P., Slowik, A., Thijs, V., Woo, D., Worrall, B.B., Kittner, S.J., Petersson, J., Golland, P., Wu, O., Rost, N.S., Lindgren, A.

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Migraine-Associated Common Genetic Variants Confer Greater Risk of Posterior vs. Anterior Circulation Ischemic Stroke von Frid, P, Xu, H, Mitchell, B.D, Drake, M, Wasselius, J, Gaynor, B, Ryan, K, Giese, A.K, Schirmer, M, Donahue, K.L, Irie, R, Bouts, M.J.R.J, McIntosh, E.C, Mocking, S.J.T, Dalca, A.V, Giralt-Steinhauer, E, Holmegaard, L, Jood, K, Roquer, J, Cole, J.W, McArdle, P.F, Broderick, J.P, Jimenez-Conde, J, Jern, C, Kissela, B.M, Kleindorfer, D.O, Lemmens, R, Meschia, J.F, Rosand, J, Rundek, T, Sacco, R.L, Schmidt, R, Sharma, P, Slowik, A, Thijs, V, Woo, D, Worrall, B.B, Kittner, S.J, Petersson, J, Golland, P, Wu, O, Rost, N.S, Lindgren, A

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Detailed phenotyping of posterior vs. anterior circulation ischemic stroke: a multi-center MRI study von Frid, Petrea, Drake, Mattias, Giese, A.K, Wasselius, J, Schirmer, M.D, Donahue, K.L, Cloonan, L, Irie, R, Bouts, M.J.R.J, McIntosh, E.C, Mocking, S.J.T, Dalca, A.V, Sridharan, R, Xu, H, Giralt-Steinhauer, E, Holmegaard, L, Jood, K, Roquer, J, Cole, J.W, McArdle, P.F, Broderick, J.P, Jimenez-Conde, J, Jern, C, Kissela, B.M, Kleindorfer, D.O, Lemmens, R, Meschia, J.F, Rundek, T, Sacco, R.L, Schmidt, R, Sharma, P, Slowik, A, Thijs, V, Woo, D, Worrall, B.B, Kittner, S.J, Mitchell, B.D, Petersson, J, Rosand, J, Golland, P, Wu, O, Rost, N.S, Lindgren, A

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Intravenous Fibrinolysis Eligibility: A Survey of Stroke Clinicians' Practice Patterns and Review of the Literature von De Los Rios, Felipe, MD, Kleindorfer, Dawn O., MD, Guzik, Amy, MD, Ortega-Gutierrez, Santiago, MD, MSc, Sangha, Navdeep, MD, Kumar, Gyanendra, MD, Grotta, James C., MD, Lee, Jin-Moo, MD, PhD, Meyer, Brett C., MD, Schwamm, Lee H., MD, Khatri, Pooja, MD

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Design and rationale for examining neuroimaging genetics in ischemic stroke: The MRI-GENIE study von Giese, A.K., Schirmer, M.D., Donahue, K.L., Cloonan, L., Irie, R., Winzeck, S., Bouts, M.J.R.J., McIntosh, E.C., Mocking, S.J., Dalca, A.V., Sridharan, R., Xu, H., Frid, P., Giralt-Steinhauer, E., Holmegaard, L., Wasselius, J., Roquer, J., McArdle, P.F., Cole, J.W., Jimenez-Conde, J., Broderick, J.P., Kissela, B.M., Jern, C., Lemmens, R., Kleindorfer, D.O., Meschia, J.F., Lindgren, A., Sacco, R.L., Rundek, T., Sharma, P., Schmidt, R., Woo, D., Worrall, B.B., Slowik, A., Thijs, V., Rosand, J., Golland, P., Kittner, S.J., Mitchell, B.D., Wu, O., Rost, N.S.

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes von Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Rutten-Jacobs, L., Laan, S.W. van der, Anderson, C.D., Chong, M., Adams, H.H.H., Ago, T., Amouyel, P., Ay, H., Boncoraglio, G.B., Brown, R.D., Carrera, C., Carty, C.L., Chasman, D.I., Chen, W.M., Cole, J.W., Danesh, J., Duan, Q., Engelter, S.T., Gudnason, V., Gustafsson, S., Haessler, J., Havulinna, A.S., Howard, G., Hyacinth, H.I., Ikram, M.A., Jian, X.Q., Johnson, J.A., Kanai, M., Keene, K.L., Kissela, B.M., Kleindorfer, D.O., Kooperberg, C., Kubo, M., Lange, L.A., Launer, L.J., Leys, D., Lindgren, A.G., Lorentzen, E., Magnusson, P.K., Maguire, J., Meschia, J.F., Mosley, T.H., Nalls, M.A., Ninomiya, T., O'Donnell, M.J., Pulit, S.L., Rannikmae, K., Rexrode, K.M., Ridker, P.M., Rost, N.S., Rundek, T., Sacco, R.L., Sakaue, S., Sale, M.M., Schmidt, R., Schminke, U., Slowik, A., Sudlow, C.L.M., Tanislav, C., Thorsteinsdottir, U., Tzourio, C., Duijn, C.M. van, Walters, M., Wareham, N.J., Wiggins, K.L., Yang, Q., Yusuf, S., Ruusalepp, A., Schadt, E.E., Koplev, S., Smith, N.L., Lubitz, S.A., Ellinor, P.T., Tai, E.S., He, J., Harst, P. van der, Elliott, P., Chambers, J.C., Takeuchi, F., Sanghera, D.K., Jern, C., Strbian, D., Longstreth, W.T., Hata, J., Woo, D., Rosand, J., Pare, G., Hopewell, J.C., Saleheen, D., Stefansson, K., Kittner, S.J., Fornage, M., Markus, H.S., Howson, J.M.M., Kamatani, Y., Dichgans, M.

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In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease von Kleindorfer, Dawn Olson, Dlouhy, Stephen R., Pratt, Victoria M., Jones, Marylin C., Trofatter, James A., Hodes, M. E.

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