Bibliografia UJ CM

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Tatiana Foroud, Dongbing Lai, Daniel Koller, Femke van't Hof, Mitja I. Kurki, Craig S. Anderson, Robert D. Brown Jr, Edward Sander Connolly, Johan G. Eriksson, Matthew Flaherty, Myriam Fornage, Mikael von und zu Fraunberg, Emilia I. Gaal, Aki Laakso, Juha Hernesniemi, John Huston, Juha E. Jaaskelainen, Lambertus A. Kiemeney, Riku Kivisaari, Dawn Kleindorfer, Nerissa Ko, Hanna Lehto, Jason Mackey, Irene Meissner, Charles J. Moomaw, Thomas H. Mosley, Marek Moskala, Mika Niemela, Aarno Palotie, Joanna Pera, Gabriel Rinkel, Stephan Ripke, Guy Rouleau, Ynte Ruigrok, Laura Sauerbeck, Agnieszka Słowik, Sita H. Vermeulen, Daniel Woo, Bradford B. Worrall, Joseph Broderick.
Genome-Wide Association Study of Intracranial Aneurysm Identifies a New Association on Chromosome 7.
Stroke
2014 : Vol. 45, nr 11, s. 3194-3199, il., bibliogr. 30 poz.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 5.723
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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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