Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype

- Rutten-Jacobs, Loes C. A., Traylor, Matthew, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Bevan, Steve, Markus, Hugh S., Adib-Samii, Ppneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Meschia, James, Maguire, Jane

Genetic associations with white matter hyperintensities confer risk of lacunar stroke

- Traylor, Matthew, Rutten-Jacobs, Loes C. A., Dichgans, Martin, Markus, Hugh S., Thijs, Vincent, Holliday, Elizabeth G., Levi, Chris, Bevan, Steve, Malik, Rainer, Boncoraglio, Giorgio, Sudlow, Cathie, Rothwell, Peter M.

Common NOTCH3 variants and cerebral small-vessel disease

- Rutten-Jacobs, Loes C. A., Traylor, Matthew, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Markus, Hugh S., Adib-Samii, Poneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Bevan, Steve, Meschia, James

Genetic overlap between diagnostic subtypes of ischemic stroke

- Holliday, Elizabeth G., Traylor, Matthew, Boncoraglio, Giorgio B., Clarke, Robert, Cole, John W., Fornage, Myriam, Furie, Karen L., Ikram, M. Arfan, Jannes, Jim, Kittner, Steven J., Lincz, Lisa F., Maguire, Jane M., Malik, Rainer, Oldmeadow, Christopher, Scott, Rodney J., Levi, Christopher, Attia, John, Bevan, Steve, Falcone, Guido, Hopewell, Jemma C., Cheng, Yu-Ching, Cotlarciuc, Ioana, Bis, Joshua C., Boerwinkle, Eric