Bibliografia UJ CM

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Thomas Jaworek, Huichun Xu, Brady J. Gaynor, John W. Cole, Kristiina Rannikmae, Tara M. Stanne, Liisa Tomppo, Vida Abedi, Philippe Amouyel, Nicole D. Armstrong, John Attia, Steven Bell, Oscar R. Benavente, Giorgio B. Boncoraglio, Adam Butterworth, Jara Carcel-Marquez, Zhengming Chen, Michael Chong, Carlos Cruchaga, Mary Cushman, John Danesh, Stephanie Debette, David J. Duggan, Jon Peter Durda, Gunnar Engstrom, Chris Enzinger, Jessica D. Faul, Natalie S. Fecteau, Israel Fernandez-Cadenas, Christian Gieger, Anne-Katrin Giese, Raji P. Grewal, Ulrike Grittner, Aki S. Havulinna, Laura Heitsch, Marc C. Hochberg, Elizabeth Holliday, Jie Hu, Andreea Ilinca, Marguerite R. Irvin, Rebecca D. Jackson, Mina A. Jacob, Raquel Rabionet, Jordi Jimenez-Conde, Julie A. Johnson, Yoichiro Kamatani, Sharon L.R. Kardia, Masaru Koido, Michiaki Kubo, Leslie Lange, Jin-Moo Lee, Robin Lemmens, Christopher R. Levi, Jiang Li, Liming Li, Kuang Lin, Haley Lopez, Sothear Luke, Jane Maguire, Patrick F. McArdle, Caitrin W. McDonough, James F. Meschia, Tiina Metso, Martina Muller-Nurasyid, Timothy D. O'Connor, Martin O'Donnell, Leema R. Peddareddygari, Joanna Pera, James A. Perry, Annette Peters, Jukka Putaala, Debashree Ray, Kathryn Rexrode, Marta Ribases, Jonathan Rosand, Peter M. Rothwell, Tatjana Rundek, Kathleen A. Ryan, Ralph L. Sacco, Veikko Salomaa, Cristina Sanchez-Mora, Reinhold Schmidt, Pankaj Sharma, Agnieszka Slowik, Jennifer A. Smith, Nicholas L. Smith, Sylvia Wassertheil-Smoller, Martin Soderholm, O. Colin Stine, Daniel Strbian, Cathie L.M. Sudlow, Turgut Tatlisumak, Chikashi Terao, Vincent Thijs, Nuria P. Torres-Aguila, David-Alexandre Tregouet, Anil M. Tuladhar, Jan H. Veldink, Robin G. Walters, David R. Weir, Daniel Woo, Bradford B. Worrall, Charles C. Hong, Owen A. Ross, Ramin Zand, Frank-Erik de Leeuw, Arne G. Lindgren, Guillaume Pare, Christopher D. Anderson, Hugh S. Markus, Christina Jern, Rainer Malik, Martin Dichgans, Braxton D. Mitchell, Steven J. Kittner.
Contribution of common genetic variants to risk of early-onset ischemic stroke.
Neurology
2022 : Vol. 99, nr 16, s. e1738-e1754, il., bibliogr. 41 poz., abstr.
Autor korespondencyjny: Braxton D. Mitchell.
Online First 2022-08-31
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 0028-3878
e-ISSN: 1526-632X
AZ
ORG
AIF
IF: 9.900
Adres url:
Streszczenie w PubMed:
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Mark K. Bakker, Rick A.A. van der Spek, Wouter van Rheenen, Sandrine Morel, Romain Bourcier, Isabel C. Hostettler, Varinder S. Alg, Kristel R. van Eijk, Masaru Koido, Masato Akiyama, Chikashi Terao, Koichi Matsuda, Robin G. Walters, Kuang Lin, Liming Li, Iona Y. Millwood, Zhengming Chen, Guy A. Rouleau, Sirui Zhou, Kristiina Rannikmae, Cathie L.M. Sudlow, Henry Houlden, Leonard H. van den Berg, Christian Dina, Olivier Naggara, Jean-Christophe Gentric, Eimad Shotar, François Eugene, Hubert Desal, Bendik S. Winsvold, Sigrid Borte, Marianne Bakke Johnsen, Ben M. Brumpton, Marie Softeland Sandvei, Cristen J. Willer, Kristian Hveem, John-Anker Zwart, W. M. Monique Verschuren, Christoph M. Friedrich, Sven Hirsch, Sabine Schilling, Jérôme Dauvillier, Olivier Martin, HUNT All-In Stroke, China Kadoorie Biobank Collaborative Group, BioBank Japan Project Consortium, The ICAN Study Group, CADISP Group, Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigator, International Stroke Genetics Consortium (ISGC), Gregory T. Jones, Matthew J. Bown, Nerissa U. Ko, Helen Kim, Jonathan R.I. Coleman, Gerome Breen, Jonathan G. Zaroff, Catharina J.M. Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Philippe Amouyel, Stéphanie Debette, Gabriel J.E. Rinkel, Bradford B. Worrall, Joanna Pera, Agnieszka Slowik, Emília I. Gaál-Paavola, Mika Niemela, Juha E. Jaaskelainen, Mikael von und zu Fraunberg, Antti Lindgren, Joseph P. Broderick, David J. Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan H. Veldink, Ynte M. Ruigrok.
Author Correction : Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Nature Genetics
2021 : Vol. 53, s. 254
Autor korespondencyjny: Mark K. Bakker.
p-ISSN: 1061-4036
KOR
Adres url:
Streszczenie w PubMed:
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Mark K. Bakker, Rick A.A. van der Spek, Wouter van Rheenen, Sandrine Morel, Romain Bourcier, Isabel C. Hostettler, Varinder S. Alg, Kristel R. van Eijk, Masaru Koido, Masato Akiyama, Chikashi Terao, Koichi Matsuda, Robin G. Walters, Kuang Lin, Liming Li, Iona Y. Millwood, Zhengming Chen, Guy A. Rouleau, Sirui Zhou, Kristiina Rannikmae, Cathie L.M. Sudlow, Henry Houlden, Leonard H. van den Berg, Christian Dina, Olivier Naggara, Jean-Christophe Gentric, Eimad Shotar, François Eugene, Hubert Desal, Bendik S. Winsvold, Sigrid Borte, Marianne Bakke Johnsen, Ben M. Brumpton, Marie Softeland Sandvei, Cristen J. Willer, Kristian Hveem, John-Anker Zwart, W. M. Monique Verschuren, Christoph M. Friedrich, Sven Hirsch, Sabine Schilling, Jérôme Dauvillier, Olivier Martin, HUNT All-In Stroke, China Kadoorie Biobank Collaborative Group, BioBank Japan Project Consortium, The ICAN Study Group, CADISP Group, Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigator, International Stroke Genetics Consortium (ISGC), Gregory T. Jones, Matthew J. Bown, Nerissa U. Ko, Helen Kim, Jonathan R.I. Coleman, Gerome Breen, Jonathan G. Zaroff, Catharina J.M. Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Philippe Amouyel, Stéphanie Debette, Gabriel J.E. Rinkel, Bradford B. Worrall, Joanna Pera, Agnieszka Slowik, Emília I. Gaál-Paavola, Mika Niemela, Juha E. Jaaskelainen, Mikael von und zu Fraunberg, Antti Lindgren, Joseph P. Broderick, David J. Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan H. Veldink, Ynte M. Ruigrok.
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Nature Genetics
2020 : Vol. 52, nr 12, s. 1303-1313, il., bibliogr. 56 poz.
Autor korespondencyjny: Mark K. Bakker.
p-ISSN: 1061-4036
e-ISSN: 1546-1718
AZ
ORG
AIF
IF: 38.330
Adres url:
Streszczenie w PubMed:
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Hylke M. Blauw, Ammar Al-Chalabi, Peter M. Andersen, Paul W.J. Vught, van, Frank P. Diekstra, Michael A. Es, van, Christian G.J. Saris, Ewout J.N. Groen, Wouter Rheenen, van, Max Koppers, Ruben van't Slot, Eric Strengman, Karol Estrada, Fernando Rivadeneira, Albert Hofman, Andre G. Uitterlinden, Lambertus A. Kiemeney, Sita H.M. Vermeulen, Anna Birve, Stefan Waibel, Thomas Meyer, Simon Cronin, Russell L. McLaughlin, Orla Hardiman, Peter C. Sapp, Martin D. Tobin, Louise V. Wain, Barbara Tomik, Agnieszka Slowik, Robin Lemmens, Dan Rujescu, Claudia Schulte, Tomasz Gasser, Robert H. Brown, Jr., John E. Landers, Wim Robberecht, Albert C. Ludolph, Roel A. Ophoff, Jan H. Veldink, Leonard H. Berg, van den.
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Human Molecular Genetics
2010 : Vol. 19, nr 20, s. 4091-4099, il., bibliogr. 52 poz.
p-ISSN: 0964-6906
AZ
ORG
AIF
IF: 8.058
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Michael A. Es, van, Jan H. Veldink, Christian G.J. Saris, Hylke M. Blauw, Paul W.J. Vught, van, Anna Birve, Robin Lemmens, Helenius J. Schelhaas, Ewout J.N. Groen, Mark H.B. Huisman, Anneke J. Kooi, van der, Marianne Visser, de, Caroline Dahlberg, Karol Estrada, Fernando Rivadeneira, Albert Hofman, Maciel J. Zwarts, Perry T.C. Doormaal, van, Dan Rujescu, Eric Strengman, Ina Giegling, Pierandrea Muglia, Barbara Tomik, Agnieszka Slowik, Andre G. Uitterlinden, Corinna Hendrich, Stefan Waibel, Thomas Meyer, Albert C. Ludolph, Jonathan D. Glass, Shaun Purcell, Sven Cichon, Markus M. Nothen, H.-Erich Wichmann, Stefan Schreiber, Sita H.H.M. Vermeulen, Lambertus A. Kiemeney, John H.J. Wokke, Simon Cronin, Russell L. McLaughlin, Orla Hardiman, Katsumi Fumoto, R. Jeroen Pasterkamp, Vincent Meininger, Judith Melki, P. Nigel Leigh, Christopher E. Shaw, John E. Landers, Ammar Al-Chalabi, Robert H. Brown Jr, Wim Robberecht, Peter M. Andersen, Roel A. Ophoff, Leonard H. Berg, van den.
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
Nature Genetics
2009 : Vol. 41, nr 10, s. 1083-1087, il., bibliogr. 33 poz.
p-ISSN: 1061-4036
AZ
ORG
AIF
IF: 30.259
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