Resultados da busca - Nick Furlotte
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Fine Mapping in 94 Inbred Mouse Strains Using a High-Density Haplotype Resource por Andrew Kirby, Hyun Min Kang, Claire M. Wade, Chris Cotsapas, Emrah Kostem, Buhm Han, Nick Furlotte, Eun Yong Kang, Manuel A. Rivas, Molly A. Bogue, Kelly A. Frazer, F. M. Johnson, Erica Beilharz, David R. Cox, Eleazar Eskin, Mark J. Daly
Publicado em 2010Artigo -
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Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits por Anatole Ghazalpour, Christoph Rau, Charles R. Farber, Brian J. Bennett, Luz D. Orozco, Atila van Nas, Calvin Pan, Hooman Allayee, Simon W. Beaven, Mete Civelek, Richard C. Davis, Thomas A. Drake, Rick A. Friedman, Nick Furlotte, Simon T. Hui, J. David Jentsch, Emrah Kostem, Hyun Min Kang, Eun Yong Kang, Jong Wha J. Joo, Vyacheslav A. Korshunov, Rick E. Laughlin, Lisa Martin, Jeffrey D. Ohmen, Brian W. Parks, Matteo Pellegrini, Karen Reue, Desmond Smith, Sotirios Tetradis, Jessica Wang, Yibin Wang, James N. Weiss, Todd G. Kirchgessner, Peter S. Gargalovic, Eleazar Eskin, Aldons J. Lusis, Renee Leboeuf
Publicado em 2012Revisão -
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families por Padhraig Gormley, Mitja Kurki, Marjo Hiekkala, Kumar Veerapen, Paavo Häppölä, Adele A. Mitchell, Dennis Lal, Priit Palta, Ida Surakka, Mari Kaunisto, Eija Hämäläinen, Salli Vepsäläinen, Hannele Havanka, Hanna Harno, Matti Ilmavirta, M. Nissilä, Erkki Säkö, Marja‐Liisa Sumelahti, Jarmo Liukkonen, Matti Sillanpää, Liisa Metsähonkala, Seppo Koskinen, Terho Lehtimäki, Olli T. Raitakari, Minna Männikkö, Caroline Ran, Andrea Carmine Belin, Pekka Jousilahti, Verneri Anttila, Veikko Salomaa, Ville Artto, Martti Färkkilâ, Heiko Runz, Mark J. Daly, Benjamin M. Neale, Samuli Ripatti, Mikko Kallela, Maija Wessman, Aarno Palotie, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Joanna L. Mountain, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Verneri Anttila, Ville Artto, Andrea Carmine Belin, Dorret I. Boomsma, Sigrid Børte, Daniel I. Chasman, Lynn Cherkas, Anne Francke Christensen, Bru Cormand, Ester Cuenca-León, George Davey Smith, Martin Dichgans, Cornelia M. van Duijn, Tõnu Esko, Ann-Louise Esserlind, Michel D. Ferrari, Rune R. Frants, Tobias Freilinger, Nick Furlotte, Padhraig Gormley, Lyn R. Griffiths, Eija Hämäläinen, Thomas Hansen, Marjo Hiekkala, M. Arfan Ikram, Andrés Ingason, Marjo‐Riitta Järvelin, Risto Kajanne, Mikko Kallela, Jaakko Kaprio, Mari Kaunisto, Christian Kubisch, Mitja Kurki, Tobias Kurth, Lenore J. Launer, Terho Lehtimäki, Davor Lessel
Publicado em 2018Artigo
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Biology
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Single-nucleotide polymorphism
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Familial hemiplegic migraine
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Haplotype
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