HuGE Literature Finder
Records 1-5
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PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
PLoS genetics 2016 Oct 12 (10): e1006367. Kiando Soto Romuald, Tucker Nathan R, Castro-Vega Luis-Jaime, Katz Alexander, D'Escamard Valentina, Tréard Cyrielle, Fraher Daniel, Albuisson Juliette, Kadian-Dodov Daniella, Ye Zi, Austin Erin, Yang Min-Lee, Hunker Kristina, Barlassina Cristina, Cusi Daniele, Galan Pilar, Empana Jean-Philippe, Jouven Xavier, Gimenez-Roqueplo Anne-Paule, Bruneval Patrick, Hyun Kim Esther Soo, Olin Jeffrey W, Gornik Heather L, Azizi Michel, Plouin Pierre-François, Ellinor Patrick T, Kullo Iftikhar J, Milan David J, Ganesh Santhi K, Boutouyrie Pierre, Kovacic Jason C, Jeunemaitre Xavier, Bouatia-Naji Nabi |
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Spontaneous Bilateral Cervical Internal Carotid and Vertebral Artery Dissection in a Japanese Patient without Collagen Vascular Disease with Special Reference to Single-Nucleotide Polymorphisms.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2016 May . Abe Arata, Nito Chikako, Sakamoto Yuki, Nogami Akane, Hokama Hiroyuki, Takahashi Shiro, Kirita Kumiko, Ueda Masayuki, Ishimaru Yoshiro, Kimura Kazu |
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CO-43: Genetic study identifies common variation in phactr1 to associate with fibromuscular dysplasia.
Annales de cardiologie et d'ange?iologie 2015 Dec 64 Suppl 1 S20. Kiando S, Tucker N, Katz A, Tréard C, Desca-Mard V, Castro-Vega L, Barlasina C, Cusi D, Galan P, Empana J, Olin J, Gornik H, Plouin P, Kullo I, Milan D, Ganesh S, Boutouyrie P, Kovacic J, Jeunemaitre X, Bouatia-Naji |
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
Nature genetics 2015 Jan 47 (1): 78-83. Debette Stéphanie, Kamatani Yoichiro, Metso Tiina M, Kloss Manja, Chauhan Ganesh, Engelter Stefan T, Pezzini Alessandro, Thijs Vincent, Markus Hugh S, Dichgans Martin, Wolf Christiane, Dittrich Ralf, Touzé Emmanuel, Southerland Andrew M, Samson Yves, Abboud Shérine, Béjot Yannick, Caso Valeria, Bersano Anna, Gschwendtner Andreas, Sessa Maria, Cole John, Lamy Chantal, Medeiros Elisabeth, Beretta Simone, Bonati Leo H, Grau Armin J, Michel Patrik, Majersik Jennifer J, Sharma Pankaj, Kalashnikova Ludmila, Nazarova Maria, Dobrynina Larisa, Bartels Eva, Guillon Benoit, van den Herik Evita G, Fernandez-Cadenas Israel, Jood Katarina, Nalls Michael A, De Leeuw Frank-Erik, Jern Christina, Cheng Yu-Ching, Werner Inge, Metso Antti J, Lichy Christoph, Lyrer Philippe A, Brandt Tobias, Boncoraglio Giorgio B, Wichmann Heinz-Erich, Gieger Christian, Johnson Andrew D, Böttcher Thomas, Castellano Maurizio, Arveiler Dominique, Ikram M Arfan, Breteler Monique M B, Padovani Alessandro, Meschia James F, Kuhlenbäumer Gregor, Rolfs Arndt, Worrall Bradford B, , Ringelstein Erich-Bernd, Zelenika Diana, Tatlisumak Turgut, Lathrop Mark, Leys Didier, , Amouyel Philippe, Dallongeville Jean, |
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Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations.
Stroke; a journal of cerebral circulation 2012 Dec 43 (12): 3161-7. Bevan Steve, Traylor Matthew, Adib-Samii Poneh, Malik Rainer, Paul Nicola L M, Jackson Caroline, Farrall Martin, Rothwell Peter M, Sudlow Cathie, Dichgans Martin, Markus Hugh |
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- Page last updated:Jan 19, 2021
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