Zobrazeno 1 - 10
of 563
pro vyhledávání: '"Meschia JF"'
Autor:
Jaworek, T, Xu, H, Gaynor, BJ, Cole, JW, Rannikmae, K, Stanne, TM, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, ND, Attia, J, Bell, S, Benavente, OR, Boncoraglio, GB, Butterworth, A, Cervical Artery Dissections and Ischemic Stroke Patients (CADSIP) Consortium, Carcel-Marquez, J, Chen, Z, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, DJ, Durda, JP, Engstrom, G, Enzinger, C, Faul, JD, Fecteau, NS, Fernandez-Cadenas, I, Gieger, C, Giese, A-K, Grewal, RP, Grittner, U, Havulinna, AS, Heitsch, L, Hochberg, MC, Holliday, E, Hu, J, Ilinca, A, INVENT Consortium, Irvin, MR, Jackson, RD, Jacob, MA, Janssen, RR, Jimenez-Conde, J, Johnson, JA, Kamatani, Y, Kardia, SL, Koido, M, Kubo, M, Lange, L, Lee, J-M, Lemmens, R, Levi, CR, Li, J, Li, L, Lin, K, Lopez, H, Luke, S, Maguire, J, McArdle, PF, McDonough, CW, Meschia, JF, Metso, T, Muller-Nurasyid, M, O'Connor, TD, O'Donnell, M, Peddareddygari, LR, Pera, J, Perry, JA, Peters, A, Putaala, J, Ray, D, Rexrode, K, Ribases, M, Rosand, J, Rothwell, PM, Rundek, T, Ryan, KA, Sacco, RL, Salomaa, V, Sanchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, JA, Smith, NL, Wassertheil-Smoller, S, Soederholm, M, Stine, OC, Strbian, D, Sudlow, CL, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, NP, Tregouet, D-A, Tuladhar, AM, Veldink, JH, Walters, RG, Weir, DR, Woo, D, Worrall, BB, Hong, CC, Ross, O, Zand, R, Leeuw, F-ED, Lindgren, AG, Pare, G, Anderson, CD, Markus, HS, Jern, C, Malik, R, Dichgans, M, Mitchell, BD, Kittner, SJ, Early Onset Stroke Genetics Consortium of the International Stroke Genetics Consortium (ISGC)
BACKGROUND AND OBJECTIVES: Current genome-wide association studies of ischemic stroke have focused primarily on late onset disease. As a complement to these studies, we sought to identifythe contribution of common genetic variants to risk of early on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______363::7825182351d7ba24c5edcdcb648740f2
https://hdl.handle.net/10453/164004
https://hdl.handle.net/10453/164004
Autor:
Traylor, M, Persyn, E, Tomppo, L, Klasson, S, Abedi, V, Bakker, MK, Torres, N, Li, LX, Bell, S, Rutten-Jacobs, L, Tozer, DJ, Griessenauer, CJ, Zhang, YF, Pedersen, A, Sharma, P, Jimenez-Conde, J, Rundek, T, Grewal, RP, Lindgren, A, Meschia, JF, Salomaa, V, Havulinna, A, Kourkoulis, C, Crawford, K, Marini, S, Mitchell, BD, Kittner, SJ, Rosand, J, Dichgans, M, Jern, C, Strbian, D, Fernandez-Cadenas, I, Zand, R, Ruigrok, Y, Rost, N, Lemmens, R, Rothwell, PM, Anderson, CD, Wardlaw, J, Lewis, CM, Markus, HS, Helsinki Stroke Study, Dutch Parelsnoer Inst Cerebrovasc, Natl Inst Neurological Disorders, UK DNA Lacunar Stroke Study, Int Stroke Genetics Consortium
Publikováno v:
Traylor, M, Persyn, E, Tomppo, L, Klasson, S, Abedi, V, Bakker, M K, Torres, N, Li, L, Bell, S, Rutten-jacobs, L, Tozer, D J, Griessenauer, C J, Zhang, Y, Pedersen, A, Sharma, P, Jimenez-conde, J, Rundek, T, Grewal, R P, Lindgren, A, Meschia, J F, Salomaa, V, Havulinna, A, Kourkoulis, C, Crawford, K, Marini, S, Mitchell, B D, Kittner, S J, Rosand, J, Dichgans, M, Jern, C, Strbian, D, Fernandez-cadenas, I, Zand, R, Ruigrok, Y, Rost, N, Lemmens, R, Rothwell, P M, Anderson, C D, Wardlaw, J, Lewis, C M & Markus, H S 2021, ' Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies ', The Lancet Neurology . https://doi.org/10.1016/S1474-4422(21)00031-4
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
LANCET NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
LANCET NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Funding: This work, including collection and genotyping of the UK Young Lacunar Stroke DNA Study 2 (DNA Lacunar 2), was supported by a British Heart Foundation Programme Grant (RG/16/4/32218). Background: The genetic basis of lacunar stroke is poorly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae82b522dab9b3a9045561873aaf949
Autor:
Malik, R, Chauhan, G, Traylor, M, Sargurupremraj, M, Okada, Y, Mishra, A, Rutten-Jacobs, L, Giese, A-K, Van der Laan, SW, Gretarsdottir, S, Anderson, CD, Chong, M, Adams, HHH, Ago, T, Almgren, P, Amouyel, P, Ay, H, Bartz, TM, Benavente, OR, Bevan, S, Boncoraglio, GB, Brown, RD, Butterworth, AS, Carrera, C, Carty, CL, Chasman, DI, Chen, W-M, Cole, JW, Correa, A, Cotlarciuc, I, Cruchaga, C, Danesh, J, De Bakker, PIW, DeStefano, AL, Den Hoed, M, Duan, Q, Engelter, ST, Falcone, GJ, Gottesman, RF, Grewal, RP, Gudnason, V, Gustafsson, S, Haessler, J, Harris, TB, Hassan, A, Havulinna, AS, Heckbert, SR, Holliday, EG, Howard, G, Hsu, F-C, Hyacinth, IH, Ikram, MA, Ingelsson, E, Irvin, MR, Jian, X, Jimenez-Conde, J, Johnson, JA, Jukema, JW, Kanai, M, Keene, KL, Kissela, BM, Kleindorfer, DO, Kooperberg, C, Kubo, M, Lange, LA, Langefeld, CD, Langenberg, C, Launer, LJ, Lee, J-M, Lemmens, R, Leys, D, Lewis, CM, Lin, W-Y, Lindgren, AG, Lorentzen, E, Magnusson, PK, Maguire, J, Manichaikul, A, McArdle, PF, Meschia, JF, Mitchell, BD, Mosley, TH, Nalls, MA, Ninomiya, T, O'Donnell, MJ, Psaty, BM, Pulit, SL, Rannikmae, K, Reiner, AP, Rexrode, KM, Rice, K, Rich, SS, Ridker, PM, Rost, NS, Rothwell, PM, Rotter, JI, Rundek, T, Sacco, RL, Sakaue, S, Sale, MM, Salomaa, V, Sapkota, BR, Schmidt, R, Schmidt, CO, Schminke, U, Sharma, P, Slowik, A, Sudlow, CLM, Tanislav, C, Tatlisumak, T, Taylor, KD, Thijs, VNS, Thorleifsson, G, Thorsteinsdottir, U, Tiedt, S, Trompet, S, Tzourio, C, Van Duijn, CM, Walters, M, Wareham, NJ, Wassertheil-Smoller, S, Wilson, JG, Wiggins, KL, Yang, Q, Yusuf, S, Bis, JC, Pastinen, T, Ruusalepp, A, Schadt, EE, Koplev, S, Bjorkegren, JLM, Codoni, V, Civelek, M, Smith, NL, Tregouet, DA, Christophersen, IE, Roselli, C, Lubitz, SA, Ellinor, PT, Tai, ES, Kooner, JS, Kato, N, He, J, Van der Harst, P, Elliott, P, Chambers, JC, Takeuchi, F, Johnson, AD, Sanghera, DK, Melander, O, Jern, C, Strbian, D, Fernandez-Cadenas, I, Longstreth, WT, Rolfs, A, Hata, J, Woo, D, Rosand, J, Pare, G, Hopewell, JC, Saleheen, D, Stefansson, K, Worrall, BB, Kittner, SJ, Seshadri, S, Fornage, M, Markus, HS, Howson, JMM, Kamatani, Y, Debette, S, Dichgans, M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::baa55c97f47572e79f07ce720e55419e
http://hdl.handle.net/10044/1/72119
http://hdl.handle.net/10044/1/72119
Autor:
Chung, J, Marini, S, Pera, J, Norrving, B, Jimenez-Conde, J, Roquer, J, Fernandez-Cadenas, I, Tirschwell, DL, Selim, M, Brown, DL, Silliman, SL, Worrall, BB, Meschia, JF, Demel, S, Greenberg, SM, Slowik, A, Lindgren, A, Schmidt, R, Traylor, M, Sargurupremraj, M, Tiedt, S, Malik, R, Debette, S, Dichgans, M, Langefeld, CD, Woo, D, Rosand, J, Anderson, CD, Int Stroke Genetics Consortium
Publikováno v:
BRAIN
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Intracerebral haemorrhage and small vessel ischaemic stroke (SVS) are the most acute manifestations of cerebral small vessel disease, with no established preventive approaches beyond hypertension management. Combined genome-wide association study (GW
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::1a1bf05a1d2ad372fbf33e86ad260da3
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=2379
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=2379
Autor:
Larsson, SC, Traylor, M, Burgess, S, Boncoraglio, GB, Jern, C, Michaëlsson, K, Markus, HS, Malik, R, Chauhan, G, Sargurupremraj, M, Okada, Y, Mishra, A, Rutten-Jacobs, L, Giese, AK, Van Der Laan, SW, Gretarsdottir, S, Anderson, CD, Chong, M, Adams, HHH, Ago, T, Almgren, P, Amouyel, P, Ay, H, Bartz, RM, Benavente, OR, Bevan, S, Brown, RD, Butterworth, AS, Carrera, C, Carty, CL, Chasman, DI, Chen, WM, Cole, JW, Correa, A, Cotlarciuc, I, Cruchaga, C, Danesh, J, De Bakker, PIW, Destefano, AL, Hoed, MD, Duan, Q, Engelter, ST, Falcone, GJ, Gottesman, RF, Grewal, RP, Gudnason, V, Gustafsson, S, Haessler, J, Harris, TB, Hassan, A, Havulinna, AS, Heckbert, SR, Holliday, EG, Howard, G, Hsu, FC, Hyacinth, HI, Ikram, MA, Ingelsson, E, Irvin, MR, Jian, X, Jiménez-Conde, J, Johnson, JA, Jukema, JW, Kanai, M, Keene, KL, Kissela, BM, Kleindorfer, DO, Kooperberg, C, Kubo, M, Lange, LA, Langefeld, CD, Langenberg, C, Launer, LJ, Lee, JM, Lemmens, R, Leys, D, Lewis, CM, Lin, WY, Lindgren, AG, Lorentzen, E, Magnusson, PK, Maguire, J, Manichaikul, A, McArdle, PF, Meschia, JF, Mitchell, BD, Mosley, TH, Nalls, MA, Ninomiya, T, O'Donnell, MJ, Psaty, BM, Pulit, SL, Rannikmäe, K, Reiner, AP, Rexrode, KM, Rice, K, Rich, SS, Ridker, PM, Rost, NS, Rothwell, PM
© 2019 American Academy of Neurology. ObjectiveTo determine whether serum magnesium and calcium concentrations are causally associated with ischemic stroke or any of its subtypes using the mendelian randomization approach.MethodsAnalyses were conduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______363::4517fe7d66d52dc93f4f6ecf30beabe5
https://hdl.handle.net/10453/135706
https://hdl.handle.net/10453/135706
Autor:
Malik, R, Chauhan, G, Traylor, M, Sargurupremraj, M, Okada, Y, Mishra, A, Rutten-Jacobs, L, Giese, AK, van der Laan, SW, Gretarsdottir, S, Anderson, CD, Chong, M, Adams, HHH, Ago, T, Almgren, P, Amouyel, P, Ay, H, Bartz, TM, Benavente, OR, Bevan, S, Boncoraglio, GB, Brown, RD, Butterworth, AS, Carrera, C, Carty, CL, Chasman, DI, Chen, WM, Cole, JW, Correa, A, Cotlarciuc, I, Cruchaga, C, Danesh, J, de Bakker, PIW, Destefano, AL, Den Hoed, M, Duan, Q, Engelter, ST, Falcone, GJ, Gottesman, RF, Grewal, RP, Gudnason, V, Gustafsson, S, Haessler, J, Harris, TB, Hassan, A, Havulinna, AS, Heckbert, SR, Holliday, EG, Howard, G, Hsu, FC, Hyacinth, HI, Arfan Ikram, M, Ingelsson, E, Irvin, MR, Jian, X, Jiménez-Conde, J, Johnson, JA, Wouter Jukema, J, Kanai, M, Keene, KL, Kissela, BM, Kleindorfer, DO, Kooperberg, C, Kubo, M, Lange, LA, Langefeld, CD, Langenberg, C, Launer, LJ, Lee, JM, Lemmens, R, Leys, D, Lewis, CM, Lin, WY, Lindgren, AG, Lorentzen, E, Magnusson, PK, Maguire, J, Manichaikul, A, McArdle, PF, Meschia, JF, Mitchell, BD, Mosley, TH, Nalls, MA, Ninomiya, T, O’donnell, MJ, Psaty, BM, Pulit, SL, Rannikmäe, K, Reiner, AP, Rexrode, KM, Rice, K, Rich, SS, Ridker, PM, Rost, NS, Rothwell, PM, Rotter, JI, Rundek, T, Sacco, RL, Sakaue, S, Sale, MM
© 2019, Nature Publishing Group. All rights reserved. In the HTML version of this article initially published, the author groups ‘AFGen Consortium’, ‘Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium’, ‘Inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______363::c7b7886f24595c2b38a3afc81ed525f1
https://hdl.handle.net/10453/135681
https://hdl.handle.net/10453/135681
Autor:
Traenka, C, Dougoud, D, Simonetti, B, Metso, T, Debette, S, Pezzini, A, Kloss, M, Grond Ginsbach, C, Majersik, J, Worrall, B, Leys, D, Baumgartner, R, Caso, V, Béjot, Y, Compter, A, Reiner, P, Thijs, V, Southerland, A, Bersano, A, Brandt, T, Gensicke, H, Touzé, E, Martin, J, Chabriat, H, Tatlisumak, T, Lyrer, P, Arnold, M, Engelter, ST, Abboud S, Pandolfo M, Bodenant M, Louillet F, Mas JL, Leder S, Léger A, Deltour S, Crozier S, Méresse I, Canaple S, Godefroy O, Giroud M, Decavel P, Medeiros E, Montiel P, Moulin T, Vuillier F, Amouyel P, Wiest T, Werner I, Arnold ML, Santos MD, Dichgans M, Thomas Feles C, Weber R, Del Zotto E, Giossi A, Volonghi I, Padovani A, Poli L, Morotti A, Lanfranconi S, Baron P, Beretta S, Giacolone G, Fluri F, Hatz F, Gisler D, Bonati, Amort M, Markus H, Meschia JF, Cole J, Kittner S, Buffon F, Mawet J, Heldner MR, Mattle HP, Gralla J., FERRARESE, CARLO
Objective:In a cohort of patients diagnosed with cervical artery dissection (CeAD), to determine the proportion of patients aged ≥60 years and compare the frequency of characteristics (presenting symptoms, risk factors, and outcome) in patients age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed372425219cbf6429228ef272694857
Autor:
Traylor, M, Zhang, Cr, Adib Samii, P, Devan, Wj, Parsons, Oe, Lanfranconi, S, Gregory, S, Cloonan, L, Falcone, Gj, Radmanesh, F, Fitzpatrick, K, Kanakis, A, Barrick, Tr, Moynihan, B, Lewis, Cm, Boncoraglio, Gb, Lemmens, R, Thijs, V, Sudlow, C, Wardlaw, J, Rothwell, Pm, Meschia, Jf, Worrall, Bb, Levi, C, Bevan, S, Furie, Kl, Dichgans, M, Rosand, J, Markus, Hs, Rost, N, Smoller, S, Sorkin, J, Wang, X, Selim, M, Pikula, A, Wolf, P, Debette, S, Seshadri, S, de Bakker, P, Chasman, D, Rexrode, K, Chen, I, Rotter, J, Luke, M, Sale, M, Lee, Th, Chang, Kc, Elkind, M, Goldstein, L, James, Ml, Breteler, M, O'Donnell, C, Leys, D, Carty, C, Kidwell, C, Olesen, J, Sharma, P, Rich, S, Tatlisumak, T, Happola, O, Bijlenga, P, Soriano, C, Giralt, E, Roquer, J, Jimenez Conde, J, Cotlarcius, I, Hardy, J, Korostynski, M, Boncoraglio, G, Ballabio, E, Parati, E, Mateusz, A, Urbanik, A, Dziedzic, T, Jagiella, J, Gasowski, J, Wnuk, M, Olszanecki, R, Pera, J, Slowik, A, Juchniewicz, Kj, Nyquist, P, Cendes, I, Cabral, N, Franca, P, Goncalves, A, Keller, L, Crisby, M, Kostulas, K, Ahmadi, K, Opherk, C, Duering, M, Malik, R, Gonik, M, Staals, J, Melander, O, Burri, P, Sadr Nabavi, A, Romero, J, Biffi, A, Anderson, C, Falcone, G, Brouwers, B, Du, R, Kourkoulis, C, Battey, T, Lubitz, S, Mueller Myhsok, B, Meschia, J, Brott, T, Pare, G, Pichler, A, Enzinger, C, Schmidt, H, Schmidt, R, Seiler, S, Blanton, S, Yamada, Y, Bersano, A, Rundek, T, Sacco, R, Yvonne Chan, Yf, Gschwendtner, A, Deng, Z, Barr, T, Gwinn, K, Corriveau, R, Singleton, A, Waddy, S, Launer, L, Chen, C, Ke, Le, Lee, Wl, Tan, Ek, Olugbodi, A, Rothwell, P, Schilling, S, Mok, V, Lebedeva, E, Jern, C, Jood, K, Olsson, S, Kim, H, Lee, C, Kilarski, L, Markus, H, Peycke, J, Sheu, W, Chiou, Hy, Chern, J, Giraldo, E, Taqi, M, Jain, V, Lam, O, Howard, G, Woo, D, Kittner, S, Mitchell, B, Cole, J, O'Connell, J, Milewicz, D, Illoh, K, Worrall, B, Stine, C, Karaszewski, B, Werring, D, Sofat, R, Smalley, J, Lindgren, A, Hansen, B, Norrving, B, Smith, G, Martín, Jj, Klijn, K, Van't Hof, F, Algra, A, Macleod, M, Perry, R, Arnett, D, Pezzini, Alessandro, Padovani, Alessandro, Cramer, S, Fisher, M, Saleheen, D, Broderick, J, Kissela, B, Doney, A, Rannikmae, K, Silliman, S, Mcdonough, C, Walters, M, Pedersen, A, Nakagawa, K, Chang, C, Dobbins, M, Mcardle, P, Chang, Yc, Brown, R, Brown, D, Holliday, E, Kalaria, R, Maguire, J, Attia, J, Farrall, M, Giese, Ak, Fornage, M, Majersik, J, Cushman, M, Keene, K, Bennett, S, Tirschwell, D, Psaty, B, Reiner, A, Longstreth, W, Spence, D, Montaner, J, Fernandez Cadenas, I, Langefeld, C, Bushnell, C, Heitsch, L, Lee, Jm, Sheth, K.
Publikováno v:
Neurology
Traylor, M, Zhang, C R, Adib-Samii, P, Devan, W J, Parsons, O E, Lanfranconi, S, Gregory, S, Cloonan, L, Falcone, G J, Radmanesh, F, Fitzpatrick, K, Kanakis, A, Barrick, T R, Moynihan, B, Lewis, C M, Boncoraglio, G B, Lemmens, R, Thijs, V, Sudlow, C, Wardlaw, J, Rothwell, P M, Meschia, J F, Worrall, B B, Levi, C, Bevan, S, Furie, K L, Dichgans, M, Rosand, J, Markus, H S & Rost, N 2016, ' Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke ', Neurology, vol. 86, no. 2, pp. 146-153 . https://doi.org/10.1212/WNL.0000000000002263
Traylor, M, Zhang, CR, Adib-samii, P, Devan, WJ, Parsons, OE, Lanfranconi, S, Gregory, S, Cloonan, L, Falcone, GJ, Radmanesh, F, Fitzpatrick, K, Kanakis, A, Barrick, T R, Moynihan, B, Lewis, CM, Boncoraglio, G, Lemmens, R, Thijs, V, Sudlow, C, Wardlaw, J, Rothwell, P M, Meschia, J F, Worrall, B B, Levi, C, Bevan, S, Furie, K L, Dichgans, M, Rosand, J & Markus, H S & Rost, NS 2016, ' Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke ', Neurology, vol. 86, pp. 146-153 . https://doi.org/10.1212/WNL.0000000000002263
Traylor, M, Zhang, C R, Adib-Samii, P, Devan, W J, Parsons, O E, Lanfranconi, S, Gregory, S, Cloonan, L, Falcone, G J, Radmanesh, F, Fitzpatrick, K, Kanakis, A, Barrick, T R, Moynihan, B, Lewis, C M, Boncoraglio, G B, Lemmens, R, Thijs, V, Sudlow, C, Wardlaw, J, Rothwell, P M, Meschia, J F, Worrall, B B, Levi, C, Bevan, S, Furie, K L, Dichgans, M, Rosand, J, Markus, H S & Rost, N 2016, ' Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke ', Neurology, vol. 86, no. 2, pp. 146-153 . https://doi.org/10.1212/WNL.0000000000002263
Traylor, M, Zhang, CR, Adib-samii, P, Devan, WJ, Parsons, OE, Lanfranconi, S, Gregory, S, Cloonan, L, Falcone, GJ, Radmanesh, F, Fitzpatrick, K, Kanakis, A, Barrick, T R, Moynihan, B, Lewis, CM, Boncoraglio, G, Lemmens, R, Thijs, V, Sudlow, C, Wardlaw, J, Rothwell, P M, Meschia, J F, Worrall, B B, Levi, C, Bevan, S, Furie, K L, Dichgans, M, Rosand, J & Markus, H S & Rost, NS 2016, ' Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke ', Neurology, vol. 86, pp. 146-153 . https://doi.org/10.1212/WNL.0000000000002263
Objective: For 3,670 stroke patients from the United Kingdom, United States, Australia, Belgium, and Italy, we performed a genome-wide meta-analysis of white matter hyperintensity volumes (WMHV) on data imputed to the 1000 Genomes reference dataset t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::80d26018f3faecf89869b04ff1142e32
http://hdl.handle.net/11379/485218
http://hdl.handle.net/11379/485218
Autor:
Holliday, EG, Maguire, JM, Evans, TJ, Koblar, SA, Jannes, J, Sturm, JW, Hankey, GJ, Baker, R, Golledge, J, Parsons, MW, Malik, R, McEvoy, M, Biros, E, Lewis, MD, Lincz, LF, Peel, R, Oldmeadow, C, Smith, W, Moscato, P, Barlera, S, Bevan, S, Bis, JC, Boerwinkle, E, Boncoraglio, GB, Brott, TG, Brown, RD, Cheng, YC, Cole, JW, Cotlarciuc, I, Devan, WJ, Fornage, M, Furie, KL, Grétarsdóttir, S, Gschwendtner, A, Ikram, MA, Longstreth, WT, Meschia, JF, Mitchell, BD, Mosley, TH, Nalls, MA, Parati, EA, Psaty, BM, Sharma, P, Stefansson, K, Thorleifsson, G, Thorsteinsdottir, U, Traylor, M, Verhaaren, BFJ, Wiggins, KL, Worrall, BB, Sudlow, C, Rothwell, PM, Farrall, M, Dichgans, M, Rosand, J, Markus, HS, Scott, RJ, Levi, C
Publikováno v:
Holliday, E G, Maguire, J M, Evans, T, Koblar, S A, Jannes, J, Sturm, J W, Hankey, G J, Baker, R, Golledge, J, Parsons, M W, Malik, R, Mcevoy, M, Biros, E, Lewis, M D, Lincz, L F, Peel, R, Oldmeadow, C, Smith, W, Moscato, P, Barlera, S, Bevan, S, Bis, J C, Boerwinkle, E, Boncoraglio, G B, Brott, T G, Brown, R D, Cheng, Y, Cole, J W, Cotlarciuc, I, Devan, W J, Fornage, M, Furie, K L, Grétarsdóttir, S, Gschwendtner, A, Ikram, M A, Longstreth, W T, Meschia, J F, Mitchell, B D, Mosley, T H, Nalls, M A, Parati, E A, Psaty, B M, Sharma, P, Stefansson, K, Thorleifsson, G, Thorsteinsdottir, U, Traylor, M, Verhaaren, B F J, Wiggins, K L, Worrall, B B, Sudlow, C, Rothwell, P M, Farrall, M, Dichgans, M, Rosand, J, Markus, H S, Scott, R J, Levi, C & Attia, J 2012, ' Common variants at 6p21.1 are associated with large artery atherosclerotic stroke ', Nature Genetics, vol. 44, no. 10, pp. 1147-1151 . https://doi.org/10.1038/ng.2397
Nature Genetics, 44(10), 1147-1151. Nature Publishing Group
Nature Genetics, 44(10), 1147-1151. Nature Publishing Group
Genome-wide association studies (GWAS) have not consistently detected replicable genetic risk factors for ischemic stroke, potentially due to etiological heterogeneity of this trait. We performed GWAS of ischemic stroke and a major ischemic stroke su
Autor:
Rosand, J, Mitchell, BD, Ay, H, de Bakker, PIW, Gwinn, K, Kittner, SJ, Lindgren, A, Meschia, JF, Pulit, SL, Sudlow, CLM, Thijs, V, Woo, D, Worrall, BB, Arnett, DK, Benavente, O, Cole, JW, Dichgans, M, Grewal, RP, Jern, C, Conde, JJ, Johnson, JA, Lee, J-M, Levi, C, Markus, HS, Melander, O, Rexrode, K, Rothwell, PM, Rundek, T, Sacco, RL, Schmidt, R, Sharma, P, Slowik, A, Wasssertheil-Smoller, S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______363::e5153c6d13ae8d2efc5200e9b1931dd0
https://hdl.handle.net/10453/116299
https://hdl.handle.net/10453/116299