Family history of stroke and severity of neurologic deficit after stroke

Por Meschia, J.F., Case, L.D., Worrall, B.B., Brown, R.D., Brott, T.G., Frankel, M., Silliman, S., Rich, S.S.
Publicado em 2006

The impact of privacy protections on recruitment in a multicenter stroke genetics study

Por Chen, D.T., Worrall, B.B., Brown, R.D., Brott, T.G., Kissela, B.M., Olson, T.S., Rich, S.S., Meschia, J.F.
Publicado em 2005

Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk

Por Hsu, F.-C., Sides, E.G., Mychaleckyj, J.C., Worrall, B.B., Elias, G.A., Liu, Y., Chen, W.-M., Coull, B.M., Toole, J.F., Rich, S.S., Furie, K.L., Sale, M.M.
Publicado em 2011

White matter hyperintensity volume is increased in small vessel stroke subtypes

Por Rost, N.S., Rahman, R.M., Biffi, A., Smith, E.E., Kanakis, A., Fitzpatrick, K., Lima, F., Worrall, B.B., Meschia, J.F., Brown, R.D., Brott, T.G., Sorensen, A.G., Greenberg, S.M., Furie, K.L., Rosand, J.
Publicado em 2010

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

Por Hannibal, M C., Ruzzo, E K., Miller, L R., Betz, B, Buchan, J G., Knutzen, D M., Barnett, K, Landsverk, M L., Brice, A, LeGuern, E, Bedford, H M., Worrall, B B., Lovitt, S, Appel, S H., Andermann, E, Bird, T D., Chance, P F.
Publicado em 2009

Genetic variation at CR1 increases risk of cerebral amyloid angiopathy

Por Biffi, A., Shulman, J.M., Jagiella, J.M., Cortellini, L., Ayres, A.M., Schwab, K., Brown, D.L., Silliman, S.L., Selim, M., Worrall, B.B., Meschia, J.F., Slowik, A., De Jager, P.L., Greenberg, S.M., Schneider, J.A., Bennett, D.A., Rosand, J.
Publicado em 2012

Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N=112 151) and 24 GWAS consortia

Por Hagenaars, S P, Harris, S E, Davies, G, Hill, W D, Liewald, D C M, Ritchie, S J, Marioni, R E, Fawns-Ritchie, C, Cullen, B, Malik, R, Worrall, B B, Sudlow, C L M, Wardlaw, J M, Gallacher, J, Pell, J, McIntosh, A M, Smith, D J, Gale, C R, Deary, I J
Publicado no Mol Psychiatry (2016)

The Causative Classification of Stroke system: An international reliability and optimization study

Por Arsava, E.M., Ballabio, E., Benner, T., Cole, J.W., Delgado-Martinez, M.P., Dichgans, M., Fazekas, F., Furie, K.L., Illoh, K., Jood, K., Kittner, S., Lindgren, A.G., Majersik, J.J., Macleod, M.J., Meurer, W.J., Montaner, J., Olugbodi, A.A., Pasdar, A., Redfors, P., Schmidt, R., Sharma, P., Singhal, A.B., Sorensen, A.G., Sudlow, C., Thijs, V., Worrall, B.B., Rosand, J., Ay, H.
Publicado em 2010

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

Por Zhou, Q., Yang, D., Ombrello, A.K., Zavialov, Andrey V., Toro, C., Zavialov, Anton V., Stone, D.L., Chae, J.J., Rosenzweig, S.D., Bishop, K., Barron, K.S., Kuehn, H.S., Hoffmann, P., Negro, A., Tsai, W.L., Cowen, E.W., Pei, W., Milner, J.D., Silvin, C., Heller, T., Chin, D.T., Patronas, N.J., Barber, J.S., Lee, C.-C.R., Wood, G.M., Ling, A., Kelly, S.J., Kleiner, D.E., Mullikin, J.C., Ganson, N.J., Kong, H.H., Hambleton, S., Candotti, F., Quezado, M.M., Calvo, K.R., Alao, H., Barham, B.K., Jones, A., Meschia, J.F., Worrall, B.B., Kasner, S.E., Rich, S.S., Goldbach-Mansky, R., Abinun, M., Chalom, E., Gotte, A.C., Punaro, M., Pascual, V., Verbsky, J.W., Torgerson, T.R., Singer, N.G., Gershon, T.R., Ozen, S., Karadag, O., Fleisher, T.A., Remmers, E.F., Burgess, S.M., Moir, S.L., Gadina, M., Sood, R., Hershfield, M.S., Boehm, M., Kastner, D.L., Aksentijevich, I.
Publicado em 2014