Bibliografia UJ CM

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Kristiina Rannikmae, Vhinoth Sivakumaran, Henry Millar, Rainer Malik, Christopher D. Anderson, Mike Chong, Tushar Dave, Guido J. Falcone, Israel Fernandez-Cadenas, Jordi Jimenez-Conde, Arne Lindgren, Joan Montaner, Martin O'Donnell, Guillaume Paré, Farid Radmanesh, Natalia S. Rost, Agnieszka Slowik, Martin Soderholm, Matthew Traylor, Sara L. Pulit, Sudha Seshadri, Brad B. Worrall, Daniel Woo, Hugh S. Markus, Braxton D. Mitchell, Martin Dichgans, Jonathan Rosand, Cathie L.M. Sudlow.
COL4A2 is associated with lacunar ischemic stroke and deep ICH.
Neurology
2017 : Vol. 89, nr 17, s. 1829-1839
Autor korespondencyjny: Cathie L.M. Sudlow.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.055
BB: PubMed ; Web of Science Core Collection
PubMed; Web of Science Core Collection
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2/6
Matthew Traylor, Rainer Malik, Mike A. Nalls, Ioana Cotlarciuc, Farid Radmanesh, Gudmar Thorleifsson, Ken B. Hanscombe, Carl Langefeld, Danish Saleheen, Natalia S. Rost, Idil Yet, Tim D. Spector, Jordana T. Bell, Eilis Hannon, Jonathan Mill, Ganesh Chauhan, Stephanie Debette, Joshua C. Bis, W.T. Longstreth Jr, M. Arfan Ikram, Lenore J. Launer, Sudha Seshadri, Monica Anne Hamilton-Bruce, Jordi Jimenez-Conde, John W. Cole, Reinhold Schmidt, Agnieszka Słowik, Robin Lemmens, Arne Lindgren, Olle Melander, Raji P. Grewal, Ralph L. Sacco, Tatjana Rundek, Kathryn Rexrode, Donna K. Arnett, Julie A. Johnson, Oscar R. Benavente, Sylvia Wasssertheil- Smolle, Jin-Moo Lee, Sara L. Pulit, Quenna Wong, Stephen S. Rich, Paul I.W. de Bakker, Patrick F. McArdle, Daniel Woo, Christopher D. Anderson, Huichun Xu, Laura Heitsch, Myriam Fornage, Christina Jern, Kari Stefansson, Unnur Thorsteinsdottir, Solveig Gretarsdottir, Cathryn M. Lewis, Pankaj Sharma, Cathie L.M. Sudlow, Peter M. Rothwell, Giorgio B. Boncoraglio, Vincent Thijs, Chris Levi, James F. Meschia, Jonathan Rosand, Steven J. Kittner, Braxton D. Mitchell, Martin Dichgans, Bradford B. Worrall, Hugh S. Markus.
Genetic Variation at 16q24.2 is associated with small vessel stroke.
Annals of Neurology
2017 : Vol. 81, nr 3, s. 383-394, il., bibliogr. 51 poz., abstr.
Autor korespondencyjny: Matthew Traylor.
Open Access Creative Commons Attribution License CC-BY 4.0.
Data udostępnienia w sposób otwarty: 2016-12-20
p-ISSN: 0364-5134
AZ
ORG
AIF
IF: 10.244
BB: PubMed ; Scopus ; Web of Science Core Collection
PubMed; Scopus; Web of Science Core Collection
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Christopher D. Anderson, Guido J. Falcone, Chia-Ling Phuah, Farid Radmanesh, H. Bart Brouwers, Thomas W. K. Battey, Alessandro Biffi, Gina M. Peloso, Dajiang J. Liu, Alison M. Ayres, Joshua N. Goldstein, Anand Viswanathan, Steven M. Greenberg, Magdy Selim, James F. Meschia, Devin L. Brown, Bradford B. Worrall, Scott L. Silliman, David L. Tirschwell, Matthew L. Flaherty, Peter Kraft, Jeremiasz M. Jagiella, Helena Schmidt, Bjorn M. Hansen, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano, Koen M. van Nieuwenhuizen, Catharina J. M. Klijn, Kristiina Rannikmae, Neshika Samarasekera, Rustam Al-Shahi Salman, Catherine L. Sudlow, Ian J. Deary, Andrea Morotti, Alessandro Pezzini, Joana Pera, Andrzej Urbanik, Alexander Pichler, Christian Enzinger, Bo Norrving, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Chelsea S. Kidwell, Steven J. Kittner, Salina P. Waddy, Carl D. Langefeld, Goncalo Abecasis, Cristen J. Willer, Sekar Kathiresan, Daniel Woo, Jonathan Rosand.
Genetic variants in CETP increase risk of intracerebral hemorrhage.
Annals of Neurology
2016 : Vol. 80, nr 5, s. 730-740, il., bibliogr. 47 poz.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 0364-5134
AZ
ORG
AIF
IF: 9.890
BB: PubMed ; Scopus ; Web of Science Core Collection
PubMed; Scopus; Web of Science Core Collection
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4/6
Matthew Traylor, Cathy R. Zhang, Poneh Adib-Samii, William J. Devan, Owen E. Parsons, Silvia Lanfranconi, Sarah Gregory, Lisa Cloonan, Guido J. Falcone, Farid Radmanesh, Kaitlin Fitzpatrick, Allison Kanakis, Thomas R. Barrick, Barry Moynihan, Cathryn M. Lewis, Giorgio B. Boncoraglio, Robin Lemmens, Vincent Thijs, Cathie Sudlow, Joanna Wardlaw, Peter M. Rothwell, James F. Meschia, Bradford B. Worrall, Christopher Levi, Steve Bevan, Karen L. Furie, Martin Dichgans, Jonathan Rosand, Hugh S. Markus, Natalia Rost, International Stroke Genetics Consortium.
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology
2016 : Vol. 86, nr 2, s. 146-153, il., bibliogr. 30 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.320
Adres url:
Streszczenie w PubMed:
5/6
Kristiina Rannikmae, Pippa A. Thomson, Steve Bevan, William J. Devan, Guido J. Falcone, Matthew Traylor, Christopher D. Anderson, Thomas W.K. Battey, Farid Radmanesh, Ranjan Deka, Jessica G. Woo, Lisa J. Martin, Jordi Jimenez-Conde, Magdy Selim, Devin L. Brown, Scott L. Silliman, Chelsea S. Kidwell, Joan Montaner, Carl D. Langefeld, Agnieszka Slowik, Bjorn M. Hansen, Arne G. Lindgren, James F. Meschia, Myriam Fornage, Joshua C. Bis, Stephanie Debette, Mohammad A. Ikram, Will T. Longstreth, Reinhold Schmidt, Cathy R. Zhang, Qiong Yang, Pankaj Sharma, Steven J. Kittner, Braxton D. Mitchell, Elizabeth G. Holliday, Christopher R. Levi, John Attia, Peter M. Rothwell, Deborah L. Poole, Giorgio B. Boncoraglio, Bruce M. Psaty, Rainer Malik, Natalia Rost, Bradford B. Worrall, Martin Dichgans, Tom Van Agtmael, Daniel Woo, Hugh S. Markus, Sudha Seshadri, Jonathan Rosand, Cathie L.M. Sudlow.
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.
Neurology
2015 : Vol. 84, nr 9, s. 918-926, il., bibliogr. 36 poz., abstr.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
6/6
Daniel Woo, Guido J. Falcone, William J. Devan, W. Mark Brown, Alessandro Biffi, Timothy D. Howard, Christopher D. Anderson, H. Bart Brouwers, Valerie Valant, Thomas W.K. Battey, Farid Radmanesh, Miriam R. Raffeld, Sylvia Baedorf-Kassis, Ranjan Deka, Jessica G. Woo, Lisa J. Martin, Mary Haverbusch, Charles J. Moomaw, Guangyun Sun, Joseph P. Broderick, Matthew L. Flaherty, Sharyl L. Martini, Dawn O. Kleindorfer, Brett Kissela, Mary E. Comeau, Jeremiasz M. Jagiella, Helena Schmidt, Paul Freudenberger, Alexander Pichler, Christian Enzinger, Bjorn M. Hansen, Bo Norrving, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano, Jaime Roquer, Peter Kraft, Alison M. Ayres, Kristian Schwab, Jacob L. McCauley, Joanna Pera, Andrzej Urbanik, Natalia S. Rost, Joshua N. Goldstein, Anand Viswanathan, Eva-Maria Stogerer, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Rainer Malik, Martin Dichgans, Steven M. Greenberg, Peter M. Rothwell, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Carl D. Langefeld, Jonathan Rosand.
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
American Journal of Human Genetics
2014 : Vol. 94, nr 4, s. 511-521
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.931
Adres url:
DOI:
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