Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression von Pearson-Fuhrhop, Kristin M, Dunn, Erin C, Mortero, Sarah, Devan, William J, Falcone, Guido J, Lee, Phil, Holmes, Avram J, Hollinshead, Marisa O, Roffman, Joshua L, Smoller, Jordan W, Rosand, Jonathan, Cramer, Steven C

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Multicystic Dysplastic Kidney With Mass Effect in a Neonate Treated With Nephrectomy: Case Report von Pettit, Samuel M., Devan, William J., Chalmers, David J., Zanno, Allison

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Accuracy of imputation to infer unobserved APOE epsilon alleles in genome-wide genotyping data von Radmanesh, Farid, Devan, William J, Anderson, Christopher D, Rosand, Jonathan, Falcone, Guido J

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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage von Woo, Daniel, Falcone, Guido J., Devan, William J., Brown, W. Mark, Biffi, Alessandro, Howard, Timothy D., Anderson, Christopher D., Brouwers, H. Bart, Valant, Valerie, Battey, Thomas W.K., Radmanesh, Farid, Raffeld, Miriam R., Baedorf-Kassis, Sylvia, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Haverbusch, Mary, Moomaw, Charles J., Sun, Guangyun, Broderick, Joseph P., Flaherty, Matthew L., Martini, Sharyl R., Kleindorfer, Dawn O., Kissela, Brett, Comeau, Mary E., Jagiella, Jeremiasz M., Schmidt, Helena, Freudenberger, Paul, Pichler, Alexander, Enzinger, Christian, Hansen, Björn M., Norrving, Bo, Jimenez-Conde, Jordi, Giralt-Steinhauer, Eva, Elosua, Roberto, Cuadrado-Godia, Elisa, Soriano, Carolina, Roquer, Jaume, Kraft, Peter, Ayres, Alison M., Schwab, Kristin, McCauley, Jacob L., Pera, Joanna, Urbanik, Andrzej, Rost, Natalia S., Goldstein, Joshua N., Viswanathan, Anand, Stögerer, Eva-Maria, Tirschwell, David L., Selim, Magdy, Brown, Devin L., Silliman, Scott L., Worrall, Bradford B., Meschia, James F., Kidwell, Chelsea S., Montaner, Joan, Fernandez-Cadenas, Israel, Delgado, Pilar, Malik, Rainer, Dichgans, Martin, Greenberg, Steven M., Rothwell, Peter M., Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Langefeld, Carl D., Rosand, Jonathan

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17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage von Marini, Sandro, Devan, William J, Radmanesh, Farid, Miyares, Laura, Poterba, Timothy, Hansen, Björn M, Norrving, Bo, Jimenez-Conde, Jordi, Giralt-Steinhauer, Eva, Elosua, Roberto, Cuadrado-Godia, Elisa, Soriano, Carolina, Roquer, Jaume, Kourkoulis, Christina E, Ayres, Alison M, Schwab, Kristin, Tirschwell, David L, Selim, Magdy, Brown, Devin L, Silliman, Scott L, Worrall, Bradford B, Meschia, James F, Kidwell, Chelsea S, Montaner, Joan, Fernandez-Cadenas, Israel, Delgado, Pilar, Greenberg, Steven M, Lindgren, Arne, Matouk, Charles, Sheth, Kevin N, Woo, Daniel, Anderson, Christopher D, Rosand, Jonathan, Falcone, Guido J

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Statin Treatment and Functional Outcome After Ischemic Stroke: Case―Control and Meta-Analysis von BIFFI, Alessandro, DEVAN, William J, ANDERSON, Christopher D, CORTELLINI, Lynelle, FURIE, Karen L, ROSAND, Jonathan, ROST, Natalia S

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Unusual cause of Fournier’s gangrene: colorectal-genitourinary tract fistulae status post brachytherapy von Saleem, Nabil, Devan, William J, Pitts, Daniel R, VerLee, Graham T

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Integrative Mouse and Human Studies Implicate ANGPT1 and ZBTB7C as Susceptibility Genes to Ischemic Injury von Du, Rose, Zhou, Jing, Lorenzano, Svetlana, Liu, Wenming, Charoenvimolphan, Nareerat, Qian, Baogang, Xu, Jun, Wang, Jian, Zhang, Xinmu, Wang, Xin, Berndt, Annerose, Devan, William J, Valant, Valerie J, Wang, Jinyi, Furie, Karen L, Rosand, Jonathan, Rost, Natalia, Friedlander, Robert M, Paigen, Beverly, Weiss, Scott T

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Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke von Adib-Samii, Poneh, Devan, William, Traylor, Matthew, Lanfranconi, Silvia, Zhang, Cathy R, Cloonan, Lisa, Falcone, Guido J, Radmanesh, Farid, Fitzpatrick, Kaitlin, Kanakis, Allison, Rothwell, Peter M, Sudlow, Cathie, Boncoraglio, Giorgio B, Meschia, James F, Levi, Chris, Dichgans, Martin, Bevan, Steve, Rosand, Jonathan, Rost, Natalia S, Markus, Hugh S

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APOE ε variants increase risk of warfarin-related intracerebral hemorrhage von Falcone, Guido J, Radmanesh, Farid, Brouwers, H Bart, Battey, Thomas W.K, Devan, William J, Valant, Valerie, Raffeld, Miriam R, Chitsike, Lennox P, Ayres, Alison M, Schwab, Kristin, Goldstein, Joshua N, Viswanathan, Anand, Greenberg, Steven M, Selim, Magdy, Meschia, James F, Brown, Devin L, Worrall, Bradford B, Silliman, Scott L, Tirschwell, David L, Flaherty, Matthew L, Martini, Sharyl R, Deka, Ranjan, Biffi, Alessandro, Kraft, Peter, Woo, Daniel, Rosand, Jonathan, Anderson, Christopher D

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Burden of Blood Pressure―Related Alleles Is Associated With Larger Hematoma Volume and Worse Outcome in Intracerebral Hemorrhage von FALCONE, Guido J, BIFFI, Alessandro, VISWANATHAN, Anand, GREENBERG, Steven M, SELIM, Magdy, MESCHIA, James F, BROWN, Devin L, WORRALL, Bradford B, SILLIMAN, Scott L, TIRSCHWELL, David L, ROSAND, Jonathan, DEVAN, William J, BART BROUWERS, H, ANDERSON, Christopher D, VALANT, Valerie, AYRES, Alison M, SCHWAB, Kristin, ROST, Natalia S, GOLDSTEIN, Joshua N

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A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach von Traylor, Matthew, Mäkelä, Kari-Matti, Kilarski, Laura L, Holliday, Elizabeth G, Devan, William J, Nalls, Mike A, Wiggins, Kerri L, Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja, Malik, Rainer, Sudlow, Cathie, Bevan, Steve, Raitoharju, Emma, Oksala, Niku, Thijs, Vincent, Lemmens, Robin, Lindgren, Arne, Slowik, Agnieszka, Maguire, Jane M, Walters, Matthew, Algra, Ale, Sharma, Pankaj, Attia, John R, Boncoraglio, Giorgio B, Rothwell, Peter M, de Bakker, Paul I W, Bis, Joshua C, Saleheen, Danish, Kittner, Steven J, Mitchell, Braxton D, Rosand, Jonathan, Meschia, James F, Levi, Christopher, Dichgans, Martin, Lehtimäki, Terho, Lewis, Cathryn M, Markus, Hugh S

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Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage von ANDERSON, Christopher D, BIFFI, Alessandro, VISWANATHAN, Anand, WORRALL, Bradford B, BROTT, Thomas G, GOLDSTEIN, Joshua N, BROWN, Devin, BRODERICK, Joseph P, NORRVING, Bo, GREENBERG, Steven M, SILLIMAN, Scott L, HANSEN, Björn M, NALLS, Michael A, TIRSCHWELL, David L, LINDGREN, Arne, SLOWIK, Agnieszka, SCHMIDT, Reinhold, SELIM, Magdy, ROQUER, Jaume, MONTANER, Joan, SINGLETON, Andrew B, KIDWELL, Chelsea S, WOO, Daniel, DEVAN, William J, FURIE, Karen L, MESCHIA, James F, ROSAND, Jonathan, SCHWAB, Kristin, AYRES, Alison M, VALANT, Valerie, ROSS, Owen A, ROST, Natalia S, SAXENA, Richa

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Rare Coding Variation and Risk of Intracerebral Hemorrhage von Radmanesh, Farid, Falcone, Guido J, Anderson, Christopher D, McWilliams, David, Devan, William J, Brown, W Mark, Battey, Thomas W.K, Ayres, Alison M, Raffeld, Miriam R, Schwab, Kristin, Sun, Guangyun, Deka, Ranjan, Viswanathan, Anand, Goldstein, Joshua N, Greenberg, Steven M, Tirschwell, David L, Silliman, Scott L, Selim, Magdy, Meschia, James F, Brown, Devin L, Worrall, Bradford B, Langefeld, Carl D, Woo, Daniel, Rosand, Jonathan

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TOMM40 in Cerebral Amyloid Angiopathy Related Intracerebral Hemorrhage: Comparative Genetic Analysis with Alzheimer’s Disease von Valant, Valerie, Keenan, Brendan T., Anderson, Christopher D., Shulman, Joshua M., Devan, William J., Ayres, Alison M., Schwab, Kristin, Goldstein, Joshua N., Viswanathan, Anand, Greenberg, Steven M., Bennett, David A., De Jager, Philip L., Rosand, Jonathan, Biffi, Alessandro

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Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease von Rannikmäe, Kristiina, Davies, Gail, Thomson, Pippa A, Bevan, Steve, Devan, William J, Falcone, Guido J, Traylor, Matthew, Anderson, Christopher D, Battey, Thomas W.K, Radmanesh, Farid, Deka, Ranjan, Woo, Jessica G, Martin, Lisa J, Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L, Silliman, Scott L, Kidwell, Chelsea S, Montaner, Joan, Langefeld, Carl D, Slowik, Agnieszka, Hansen, Björn M, Lindgren, Arne G, Meschia, James F, Fornage, Myriam, Bis, Joshua C, Debette, Stéphanie, Ikram, Mohammad A, Longstreth, Will T, Schmidt, Reinhold, Zhang, Cathy R, Yang, Qiong, Sharma, Pankaj, Kittner, Steven J, Mitchell, Braxton D, Holliday, Elizabeth G, Levi, Christopher R, Attia, John, Rothwell, Peter M, Poole, Deborah L, Boncoraglio, Giorgio B, Psaty, Bruce M, Malik, Rainer, Rost, Natalia, Worrall, Bradford B, Dichgans, Martin, Van Agtmael, Tom, Woo, Daniel, Markus, Hugh S, Seshadri, Sudha, Rosand, Jonathan, Sudlow, Cathie L.M

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Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke von Traylor, Matthew, Zhang, Cathy R, Adib-Samii, Poneh, Devan, William J, Parsons, Owen E, Lanfranconi, Silvia, Gregory, Sarah, Cloonan, Lisa, Falcone, Guido J, Radmanesh, Farid, Fitzpatrick, Kaitlin, Kanakis, Allison, Barrick, Thomas R, Moynihan, Barry, Lewis, Cathryn M, Boncoraglio, Giorgio B, Lemmens, Robin, Thijs, Vincent, Sudlow, Cathie, Wardlaw, Joanna, Rothwell, Peter M, Meschia, James F, Worrall, Bradford B, Levi, Christopher, Bevan, Steve, Furie, Karen L, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S, Rost, Natalia

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Common variants at 6p21.1 are associated with large artery atherosclerotic stroke von Holliday, Elizabeth G, Maguire, Jane M, Evans, Tiffany-Jane, Koblar, Simon A, Jannes, Jim, Sturm, Jonathan W, Hankey, Graeme J, Baker, Ross, Golledge, Jonathan, Parsons, Mark W, Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D, Lincz, Lisa F, Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Bevan, Steve, Bis, Joshua C, Boerwinkle, Eric, Boncoraglio, Giorgio B, Brott, Thomas G, Brown, Robert D, Cheng, Yu-Ching, Cole, John W, Cotlarciuc, Ioana, Devan, William J, Fornage, Myriam, Furie, Karen L, Grétarsdóttir, Sólveig, Gschwendtner, Andreas, Ikram, M Arfan, Longstreth, W T, Meschia, James F, Mitchell, Braxton D, Mosley, Thomas H, Nalls, Michael A, Parati, Eugenio A, Psaty, Bruce M, Sharma, Pankaj, Stefansson, Kari, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Traylor, Matthew, Verhaaren, Benjamin F J, Wiggins, Kerri L, Worrall, Bradford B, Sudlow, Cathie, Rothwell, Peter M, Farrall, Martin, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S, Scott, Rodney J, Levi, Christopher, Attia, John

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Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case-Control and Prospective Cohort Studies von MALIK, Rainer, BEVAN, Steve, DE STEFANO, Anita L, FORNAGE, Myriam, PSATY, Bruce M, IKRAM, M. Arfan, LAUNER, Lenore J, VAN DUIJN, Cornelia M, SHARMA, Pankaj, MITCHELL, Braxton D, ROSAND, Jonathan, MESCHIA, James F, NALLS, Michael A, LEVI, Christopher, ROTHWELL, Peter M, SUDLOW, Cathie, MARKUS, Hugh S, SESHADRI, Sudha, DICHGANS, Martin, HOLLIDAY, Elizabeth G, DEVAN, William J, CHENG, Yu-Ching, IBRAHIM-VERBAAS, Carla A, VERHAAREN, Benjamin F. J, BIS, Joshua C, JOON, Aron Y

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Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage von DEVAN, William J, FALCONE, Guido J, AYRES, Alison M, SCHWAB, Kristin, BAEDORF KASSIS, Sylvia, VALANT, Valerie, PERA, Joanna, URBANIK, Andrzej, VISWANATHAN, Anand, ROST, Natalia S, GOLDSTEIN, Joshua N, FREUDENBERGER, Paul, ANDERSON, Christopher D, STÖGERER, Eva-Maria, NORRVING, Bo, TIRSCHWELL, David L, SELIM, Magdy, BROWN, Devin L, SILLIMAN, Scott L, WORRALL, Bradford B, MESCHIA, James F, KIDWELL, Chelsea S, MONTANER, Joan, JAGIELLA, Jeremiasz M, FERNANDEZ-CADENAS, Israel, DELGADO, Pilar, GREENBERG, Steven M, ROQUER, Jaume, LINDGREN, Arne, SLOWIK, Agnieszka, SCHMIDT, Reinhold, WOO, Daniel, ROSAND, Jonathan, BIFFI, Alessandro, SCHMIDT, Helena, HANSEN, Björn M, JIMENEZ-CONDE, Jordi, GIRALT-STEINHAUER, Eva, CUADRADO-GODIA, Elisa, SORIANO, Carolina

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