Common genetic variation indicates separate causes for periventricular and deep 
white matter hyperintensities

Armstrong, Nicola J.; Mather, Karen A.; Sargurupremraj, Muralidharan; Knol, Maria J.; Malik, Rainer; Satizabal, Claudia L.; Yanek, Lisa R.; Wen, Wei; Gudnason, Vilmundur G.; Dueker, Nicole D.; Elliott, Lloyd T.; Hofer, Edith; Bis, Joshua; Jahanshad, Neda; Li, Shuo; Logue, Mark A.; Luciano, Michelle; Scholz, Markus; Smith, Albert V.; Trompet, Stella; Vojinovic, Dina; Xia, Rui; Alfaro-Almagro, Fidel; Ames, David; Amin, Najaf; Amouyel, Philippe; Beiser, Alexa S.; Brodaty, Henry; Deary, Ian J.; Fennema-Notestine, Christine; Gampawar, Piyush G.; Gottesman, Rebecca; Griffanti, Ludovica; Jack, Clifford R.; Jenkinson, Mark; Jiang, Jiyang; Kral, Brian G.; Kwok, John B.; Lampe, Leonie; C.M. Liewald, David; Maillard, Pauline; Marchini, Jonathan; Bastin, Mark E.; Mazoyer, Bernard; Pirpamer, Lukas; Rafael Romero, José; Roshchupkin, Gennady V.; Schofield, Peter R.; Schroeter, Matthias L.; Stott, David J.; Thalamuthu, Anbupalam; Trollor, Julian; Tzourio, Christophe; van der Grond, Jeroen; Vernooij, Meike W.; Witte, A. Veronica; Wright, Margaret J.; Yang, Qiong; Morris, Zoe; Siggurdsson, Siggi; Psaty, Bruce; Villringer, Arno; Schmidt, Helena; Haberg, Asta K.; van Duijn, Cornelia M.; Jukema, J. Wouter; Dichgans, Martin; Sacco, Ralph L.; Wright, Clinton B.; Kremen, William S.; Becker, Lewis C.; Thompson, Paul M.; Mosley, Thomas H.; Wardlaw, Joanna M.; Ikram, M. Arfan; Adams, Hieab H.H.; Seshadri, Sudha; Sachdev, Perminder S.; Smith, Stephen M.; Launer, Lenore; Longstreth, William; DeCarli, Charles; Schmidt, Reinhold; Fornage, Myriam; Debette, Stephanie; Nyquist, Paul A.

doi:10.1161/STROKEAHA.119.027544

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Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities

MPS-Authors

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Lampe, Leonie
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Schroeter, Matthias L.
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Witte, A. Veronica
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Villringer, Arno
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Armstrong, N. J., Mather, K. A., Sargurupremraj, M., Knol, M. J., Malik, R., Satizabal, C. L., et al. (2020). Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities. Stroke, 51(7), 2111-2121. doi:10.1161/STROKEAHA.119.027544.

Cite as: https://hdl.handle.net/21.11116/0000-0006-D2ED-2

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