Search Results - Radmanesh, Farid

Translational Genomics in Neurocritical Care: a Review by Myserlis, Pavlos, Radmanesh, Farid, Anderson, Christopher D.

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Congenital spinal tumor in a patient with encephalocele and hydrocephalus: a case report by Radmanesh, Farid, Nejat, Farideh, Mahjoub, Fatemeh, El Khashab, Mostafa

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Severe cerebral involvement in adult-onset hemophagocytic lymphohistiocytosis by Radmanesh, Farid, Rodriguez-Pla, Alicia, Pincus, Michael D., Burns, Joseph D.

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

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Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities by Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar, Kaya, Dobyns, William B., Zaki, Maha S., Gunel, Murat, Gleeson, Joseph G.

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Risk Factors for CT Angiography Spot Sign in Deep and Lobar Intracerebral Hemorrhage are Shared by Radmanesh, Farid, Falcone, Guido J., Anderson, Christopher D., Battey, Thomas W. K., Ayres, Alison M., Vashkevich, Anastasia, McNamara, Kristen A., Schwab, Kristin, Romero, Javier M., Viswanathan, Anand, Greenberg, Steven M., Goldstein, Joshua N., Rosand, Jonathan, Brouwers, H. Bart

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Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke by 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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A genome-wide association study of outcome from traumatic brain injury by Kals, Mart, Kunzmann, Kevin, Parodi, Livia, Radmanesh, Farid, Wilson, Lindsay, Izzy, Saef, Anderson, Christopher D., Puccio, Ava M., Okonkwo, David O., Temkin, Nancy, Steyerberg, Ewout W., Stein, Murray B., Manley, Geoff T., Maas, Andrew I.R., Richardson, Sylvia, Diaz-Arrastia, Ramon, Palotie, Aarno, Ripatti, Samuli, Rosand, Jonathan, Menon, David K.

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Association of Traumatic Brain Injury With the Risk of Developing Chronic Cardiovascular, Endocrine, Neurological, and Psychiatric Disorders by Izzy, Saef, Chen, Patrick M., Tahir, Zabreen, Grashow, Rachel, Radmanesh, Farid, Cote, David J., Yahya, Taha, Dhand, Amar, Taylor, Herman, Shih, Shirley L., Albastaki, Omar, Rovito, Craig, Snider, Samuel B., Whalen, Michael, Nathan, David M., Miller, Karen K., Speizer, Frank E., Baggish, Aaron, Weisskopf, Marc G., Zafonte, Ross

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Rare Coding Variation and Risk of Intracerebral Hemorrhage by 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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COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls by Rannikmäe, Kristiina, Sivakumaran, Vhinoth, Millar, Henry, Malik, Rainer, Anderson, Christopher D., Chong, Mike, Dave, Tushar, Falcone, Guido J., Fernandez-Cadenas, Israel, Jimenez-Conde, Jordi, Lindgren, Arne, Montaner, Joan, O'Donnell, Martin, Paré, Guillaume, Radmanesh, Farid, Rost, Natalia S., Slowik, Agnieszka, Söderholm, Martin, Traylor, Matthew, Pulit, Sara L., Seshadri, Sudha, Worrall, Brad B., Woo, Daniel, Markus, Hugh S., Mitchell, Braxton D., Dichgans, Martin, Rosand, Jonathan, Sudlow, Cathie L.M.

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Genome-Wide Association Study (GWAS) and Genome-Wide Environment Interaction Study (GWEIS) of Depressive Symptoms in African American and Hispanic/Latina Women by Dunn, Erin C., Wiste, Anna, Radmanesh, Farid, Almli, Lynn M., Gogarten, Stephanie M., Sofer, Tamar, Faul, Jessica D., Kardia, Sharon L.R., Smith, Jennifer A., Weir, David R., Zhao, Wei, Soare, Thomas W., Mirza, Saira S., Hek, Karin, Tiemeier, Henning W., Goveas, Joseph S., Sarto, Gloria E., Snively, Beverly M., Cornelis, Marilyn, Koenen, Karestan C., Kraft, Peter, Purcell, Shaun, Ressler, Kerry J., Rosand, Jonathan, Wassertheil-Smoller, Sylvia, Smoller, Jordan W.

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APOE ε variants increase risk of warfarin-related intracerebral hemorrhage by 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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17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage by 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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Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease by 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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Genetic variants in CETP increase risk of intracerebral hemorrhage by Anderson, Christopher D., Falcone, Guido J., Phuah, Chia‐Ling, Radmanesh, Farid, Brouwers, H. Bart, Battey, Thomas W. K., Biffi, Alessandro, Peloso, Gina M., Liu, Dajiang J., Ayres, Alison M., 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., Kraft, Peter, Jagiella, Jeremiasz M., Schmidt, Helena, Hansen, Björn M., Jimenez‐Conde, Jordi, Giralt‐Steinhauer, Eva, Elosua, Roberto, Cuadrado‐Godia, Elisa, Soriano, Carolina, van Nieuwenhuizen, Koen M., Klijn, Catharina J. M., Rannikmae, Kristiina, Samarasekera, Neshika, Salman, Rustam Al‐Shahi, Sudlow, Catherine L., Deary, Ian J., Morotti, Andrea, Pezzini, Alessandro, Pera, Joanna, Urbanik, Andrzej, Pichler, Alexander, Enzinger, Christian, Norrving, Bo, Montaner, Joan, Fernandez‐Cadenas, Israel, Delgado, Pilar, Roquer, Jaume, Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Kidwell, Chelsea S., Kittner, Steven J., Waddy, Salina P., Langefeld, Carl D., Abecasis, Goncalo, Willer, Cristen J., Kathiresan, Sekar, Woo, Daniel, Rosand, Jonathan

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Genetic variation at 16q24.2 is associated with small vessel stroke by Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W.T., Ikram, M. Arfan, Launer, Lenore J., Seshadri, Sudha, Hamilton‐Bruce, Monica Anne, Jimenez‐Conde, Jordi, Cole, John W., Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P., Sacco, Ralph L., Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K., Johnson, Julie A., Benavente, Oscar R., Wasssertheil‐Smoller, Sylvia, Lee, Jin‐Moo, Pulit, Sara L., Wong, Quenna, Rich, Stephen S., de Bakker, Paul I.W., McArdle, Patrick F., Woo, Daniel, Anderson, Christopher D., Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M., Sharma, Pankaj, Sudlow, Cathie L.M., Rothwell, Peter M., Boncoraglio, Giorgio B., Thijs, Vincent, Levi, Chris, Meschia, James F., Rosand, Jonathan, Kittner, Steven J., Mitchell, Braxton D., Dichgans, Martin, Worrall, Bradford B., Markus, Hugh S.

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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage by 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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Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval by Lin, Honghuang, van Setten, Jessica, Smith, Albert V, Bihlmeyer, Nathan A, Warren, Helen R., Brody, Jennifer A, Radmanesh, Farid, Hall, Leanne, Grarup, Niels, Müller-Nurasyid, Martina, Boutin, Thibaud, Verweij, Niek, Lin, Henry J., Li-Gao, Ruifang, van den Berg, Marten E., Marten, Jonathan, Weiss, Stefan, Prins, Bram, Haessler, Jeffrey, Lyytikäinen, Leo-Pekka, Mei, Hao, Harris, Tamara B., Launer, Lenore J., Li, Man, Alonso, Alvaro, Soliman, Elsayed Z, Connell, John M., Huang, Paul L, Weng, Lu-Chen, Jameson, Heather S, Hucker, William, Hanley, Alan, Tucker, Nathan R, Chen, Yii-Der Ida, Bis, Joshua C., Rice, Kenneth M., Sitlani, Colleen M., Kors, Jan A., Xie, Zhijun, Wen, Chengping, Magnani, Jared W, Nelson, Christopher P, Kanters, Jørgen K., Sinner, Moritz F., Strauch, Konstantin, Peters, Annette, Waldenberger, Melanie, Meitinger, Thomas, Bork-Jensen, Jette, Pedersen, Oluf, Linneberg, Allan, Rudan, Igor, de Boer, Rudolf A., van der meer, Peter, Yao, Jie, Guo, Xiuqing, Taylor, Kent D., Sotoodehnia, Nona, Rotter, Jerome I., Mook-Kanamori, Dennis O., Trompet, Stella, Rivadeneira, Fernando, Uitterlinden, André, Eijgelsheim, Mark, Padmanabhan, Sandosh, Smith, Blair H., Völzke, Henry, Felix, Stephan B., Homuth, Georg, Völker, Uwe, Mangino, Massimo, Spector, Timothy D, Bots, Michiel L., Perez, Marco, Kähönen, Mika, Raitakari, Olli T., Gudnason, Vilmundur, Arking, Dan E, Munroe, Patricia B, Psaty, Bruce M, van Duijn, Cornelia M., Benjamin, Emelia J., Rosand, Jonathan, Samani, Nilesh J, Hansen, Torben, Kääb, Stefan, Polasek, Ozren, van der Harst, Pim, Heckbert, Susan R., Jukema, J. Wouter, Stricker, Bruno H, Hayward, Caroline, Dörr, Marcus, Jamshidi, Yalda, Asselbergs, Folkert W., Kooperberg, Charles, Lehtimäki, Terho, Wilson, James G., Ellinor, Patrick T., Lubitz, Steven A., Isaacs, Aaron

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ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals by Bihlmeyer, Nathan A., Brody, Jennifer A., Smith, Albert Vernon, Warren, Helen R., Lin, Honghuang, Isaacs, Aaron, Liu, Ching-Ti, Marten, Jonathan, Radmanesh, Farid, Hall, Leanne M., Grarup, Niels, Mei, Hao, Müller-Nurasyid, Martina, Huffman, Jennifer E., Verweij, Niek, Guo, Xiuqing, Yao, Jie, Li-Gao, Ruifang, van den Berg, Marten, Weiss, Stefan, Prins, Bram P., van Setten, Jessica, Haessler, Jeffrey, Lyytikäinen, Leo-Pekka, Li, Man, Alonso, Alvaro, Soliman, Elsayed Z., Bis, Joshua C., Austin, Tom, Chen, Yii-Der Ida, Psaty, Bruce M., Harrris, Tamara B., Launer, Lenore J., Padmanabhan, Sandosh, Dominiczak, Anna, Huang, Paul L., Xie, Zhijun, Ellinor, Patrick T., Kors, Jan A., Campbell, Archie, Murray, Alison D., Nelson, Christopher P., Tobin, Martin D., Bork-Jensen, Jette, Hansen, Torben, Pedersen, Oluf, Linneberg, Allan, Sinner, Moritz F., Peters, Annette, Waldenberger, Melanie, Meitinger, Thomas, Perz, Siegfried, Kolcic, Ivana, Rudan, Igor, de Boer, Rudolf A., van der Meer, Peter, Lin, Henry J., Taylor, Kent D., de Mutsert, Renée, Trompet, Stella, Jukema, J. Wouter, Maan, Arie C., Stricker, Bruno H.C., Rivadeneira, Fernando, Uitterlinden, André, Völker, Uwe, Homuth, Georg, Völzke, Henry, Felix, Stephan B., Mangino, Massimo, Spector, Timothy D., Bots, Michiel L., Perez, Marco, Raitakari, Olli T., Kähönen, Mika, Mononen, Nina, Gudnason, Vilmundur, Munroe, Patricia B., Lubitz, Steven A., van Duijn, Cornelia M., Newton-Cheh, Christopher H., Hayward, Caroline, Rosand, Jonathan, Samani, Nilesh J., Kanters, Jørgen K., Wilson, James G., Kääb, Stefan, Polasek, Ozren, van der Harst, Pim, Heckbert, Susan R., Rotter, Jerome I., Mook-Kanamori, Dennis O., Eijgelsheim, Mark, Dörr, Marcus, Jamshidi, Yalda, Asselbergs, Folkert W., Kooperberg, Charles, Lehtimäki, Terho, Arking, Dan E., Sotoodehnia, Nona

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