HuGE Literature Finder
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Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies. Journal of hypertension and management 2018 3 3 (1): . Do Anh N, Zhao Wei, Srinivasasainagendra Vinodh, Aslibekyan Stella, Tiwari Hemant K, Limdi Nita, Shah Sanjiv J, Zhi Degui, Broeckel Uli, Gu C Charles, Rao D C, Schwander Karen, Smith Jennifer A, Kardia Sharon L R, Arnett Donna K, Irvin Marguerite |
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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