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ISGC Publications List

 

The ISGC is a collaborative enterprise by researchers interested in the genetic basis of stroke. As such members pursue their own research as well as coming together under the ISGC banner to conduct larger, collaborative studies. Publications resulting from such studies, with the ISGC as an author, are listed here. Further details on the specific publications can be found by clicking on the links below. Links to individual researchers publications, in which the ISGC is not listed as an author, will not be listed here.

 

APOE Genotype and Extent of Bleeding and Outcome in Lobar Intracranial Haemorrhage: A Genetic Association Study

Biffi A, Anderson CD, Jagiella JM, Schmidt H, Kissela B, Hansen BM, Jimenez-Conde J, Pires CR, Ayers AM, Schwab K, Cortellini L, Pera J, Urbanik A, Romero JM, Rost NS, Goldstein JN, Viswanathan A, Pichler A, Enzinger C, Rabionet R, Norrving B, Tirschwell DL, Selim M, Brown DL, Silliman SL, Worrall BB, Meschia JF, Kidwell CS, Broderick JP, Greenberg SM, Roquer J, Lindgren A, Slowik A, Schmidt R, Woo D, Rosand J, Intermational Stroke Genetics Consortium.

Lancet Neurology 2011, 10:702-709.

 

Genetic Variant on Chromosome 12p13 Does not Show Association to Ischaemic Stroke in 3 Swedish Case-Control Studies

Olsson S, Melander O, Jood K, Smith JG, Lovkvist H, Sjogren M, Engstrom G, Norrving B, Lindgren A, Jern C, International Stroke Genetics Consortium.

Stroke 2011, 42:214-216.

 

Variants at APOE influence Risk of Deep and Lobar Intracerebral Hemorrhage

Biffi A, Sonni A, Anderson CD, Kissela B, Jagiella JM, Schmidt H, Jimenez-conde J, Hansen BM, Fernandez-Cadenas I, Cortellini L, Ayers A, Schwab K, Juchniewicz K, Urbanik A, Rost NS, Viswanathan A, Seifert-Held T, Stoegerer EM, Tomas M, Rabionet R, Estivill X, Brown DL, Silliman SL, Selim M, Worrall BB, Meschia JF, Montaner J, Lindgren A, Roquer J, Schmidt R, Greenberg SM, Slowik A, Broderick JP, Woo D, Rosand J, International Stroke Genetics Consortium

Annals of Neurology 2010; 68:934-943.

 

The Causative Classification of Stroke System. An International Reliability and Optimisation Study

Arsava EM, Ballabio E, Benner T, Cole JW, Delgado-Martinez MP, Dichgans M, Fazekas F, Furie KL, Illoh K, Jood K, Kittner S, Lindgren AG, Majersik JJ, Macleod MJ, Meurer WJ, Montaner J, Olugbodi AA, Pasdar A, Redfors P, Schmidt R, Sharma P, Singhal AB, Sorensen AG, Sudlow C, Thijs V, Worrall BB, Rosand J, Ay H; International Stroke Genetics Consortium.

Neurology 2010, 75:1277-1284.

 

Common Mitochondrial Sequence Variants in Ischaemic Stroke

Christopher D. Anderson, Alessandro Biffi, Rosanna Rahman, Owen A. Ross, Jeremiasz M. Jagiella, Brett Kissela, John W. Cole, Lynelle Cortellini, Natalia S. Rost, Yu-Ching Cheng, Steven M. Greenberg, Paul I.W. de Bakker, Robert D. Brown, Thomas G. Brott, Braxton D. Mitchell, Joseph P. Broderick, Bradford B. Worrall, Karen L. Furie, Steven J. Kittner, Daniel Woo, Agnieszka Slowik, James F. Meschia, Richa Saxena, Jonathan Rosand, on behalf of the International Stroke Genetics Consortium

Annals of Neurology 2010 - Advanced Online Publication

 

The Association of the 4q25 Susceptibility Variant for Atrial Fibrillation is Limited to Stroke of Cardioembolic Etiology

Lemmens R, Buysschaert I, Geelen V, Fernandez I, Montaner J, Schmidt H, Schmidt R, Attia J, Maguire J, Levi C, Jood K, Blomstrand C, Jern C, Wnuk M, Slowik A, Lambrechts D, Thijs V, International Stroke Genetics Consortium

Stroke 2010, 41: 1850-1857

 

Failure to Validate Associations Between 12p13 Variants and Ischaemic Stroke

International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2. Individual authors are listed in the supplementary information, available by clicking on the title link above.

NEJM 2010; 362:1547-1550

 

Sequence Variants on Chromosome 9p21.3 Confer Risk for Atherosclerotic Stroke

Andreas Gschwendtner, Steve Bevan, John W. Cole, Anna Plourde, Mar Matarin, Helen Ross-Adams, Thomas Meitinger, Erich Wichmann, Braxton D. Mitchell, Karen Furie, Agnieszka Slowik, Stephen S. Rich, Paul D. Syme, Mary J. MacLeod, James F. Meschia, Jonathan Rosand, Steve J. Kittner, Hugh S. Markus, Bertram Muller-Myhsok, Martin Dichgans, on behalf of the International Stroke Genetics Consortium

Ann Neurol 2009;65:531–539

 

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