Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: ATP2C2[original query] |
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A high-density association screen of 155 ion transport genes for involvement with common migraine. Human molecular genetics 2008 Nov 17 (21): 3318-31. Nyholt Dale R, LaForge K Steven, Kallela Mikko, Alakurtti Kirsi, Anttila Verneri, Färkkilä Markus, Hämaläinen Eija, Kaprio Jaakko, Kaunisto Mari A, Heath Andrew C, Montgomery Grant W, Göbel Hartmut, Todt Unda, Ferrari Michel D, Launer Lenore J, Frants Rune R, Terwindt Gisela M, de Vries Boukje, Verschuren W M Monique, Brand Jan, Freilinger Tobias, Pfaffenrath Volker, Straube Andreas, Ballinger Dennis G, Zhan Yiping, Daly Mark J, Cox David R, Dichgans Martin, van den Maagdenberg Arn M J M, Kubisch Christian, Martin Nicholas G, Wessman Maija, Peltonen Leena, Palotie Aar |
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior genetics 2011 Jan 41 (1): 90-104. Newbury D F, Paracchini S, Scerri T S, Winchester L, Addis L, Richardson Alex J, Walter J, Stein J F, Talcott J B, Monaco A |
DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biological psychiatry 2011 Aug 70 (3): 237-45. Scerri Tom S, Morris Andrew P, Buckingham Lyn-Louise, Newbury Dianne F, Miller Laura L, Monaco Anthony P, Bishop Dorothy V M, Paracchini Silv |
Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders. Autism research : official journal of the International Society for Autism Research 2015 Apr 8 (2): 229-34. Eicher John D, Gruen Jeffrey |
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR. Brain and behavior 2017 11 7 (11): e00851. Müller Bent, Schaadt Gesa, Boltze Johannes, Emmrich Frank, , Skeide Michael A, Neef Nicole E, Kraft Indra, Brauer Jens, Friederici Angela D, Kirsten Holger, Wilcke Arn |
Surfactant protein D is a causal risk factor for COPD: results of Mendelian randomisation. The European respiratory journal 2017 11 50 (5): . Obeidat Ma'en, Li Xuan, Burgess Stephen, Zhou Guohai, Fishbane Nick, Hansel Nadia N, Bossé Yohan, Joubert Philippe, Hao Ke, Nickle David C, van den Berge Maarten, Timens Wim, Cho Michael H, Hobbs Brian D, de Jong Kim, Boezen Marike, Hung Rayjean J, Rafaels Nicholas, Mathias Rasika, Ruczinski Ingo, Beaty Terri H, Barnes Kathleen C, Paré Peter D, Sin Don D, |
Genome-wide association meta-analysis of age at first cannabis use.
Addiction (Abingdon, England) 2018 Jul . Minic? Camelia C, Verweij Karin J H, van der Most Peter J, Mbarek Hamdi, Bernard Manon, van Eijk Kristel R, Lind Penelope A, Liu Meng Zhen, Maciejewski Dominique F, Palviainen Teemu, Sánchez-Mora Cristina, Sherva Richard, Taylor Michelle, Walters Raymond K, Abdellaoui Abdel, Bigdeli Timothy B, Branje Susan J T, Brown Sandra A, Casas Miguel, Corley Robin P, Davey-Smith George, Davies Gareth E, Ehli Erik A, Farrer Lindsay, Fedko Iryna O, Garcia-Martínez Iris, Gordon Scott D, Hartman Catharina A, Heath Andrew C, Hickie Ian B, Hickman Matthew, Hopfer Christian J, Hottenga Jouke Jan, Kahn René S, Kaprio Jaakko, Korhonen Tellervo, Kranzler Henry R, Krauter Ken, van Lier Pol A C, Madden Pamela A F, Medland Sarah E, Neale Michael C, Meeus Wim H J, Montgomery Grant W, Nolte Ilja M, Oldehinkel Albertine J, Pausova Zdenka, Ramos-Quiroga Josep A, Richarte Vanesa, Rose Richard J, Shin Jean, Stallings Michael C, Wall Tamara L, Ware Jennifer J, Wright Margaret J, Zhao Hongyu, Koot Hans M, Paus Tomas, Hewitt John K, Ribasés Marta, Loukola Anu, Boks Marco P, Snieder Harold, Munafò Marcus R, Gelernter Joel, Boomsma Dorret I, Martin Nicholas G, Gillespie Nathan A, Vink Jacqueline M, Derks Eske |
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Human molecular genetics 2021 4 30 (12): 1160-1171. Martinelli Angela, Rice Mabel L, Talcott Joel B, Diaz Rebeca, Smith Shelley, Raza Muhammad Hashim, Snowling Margaret J, Hulme Charles, Stein John, Hayiou-Thomas Marianna E, Hawi Ziarih, Kent Lindsey, Pitt Samantha J, Newbury Dianne F, Paracchini Silv |
A genome-wide association study of bronchodilator response in participants of European and African ancestry from six independent cohorts. ERJ open research 2022 Apr 8 (2): . Gereige Jessica D, Xu Hanfei, Ortega Victor E, Cho Michael H, Liu Ming, Sakornsakolpat Phuwanat, Silverman Edwin K, Beaty Terri H, Miller Bruce E, Bakke Per, Gulsvik Amund, Hersh Craig P, Morrow Jarrett D, , Ampleford Elizabeth J, Hawkins Gregory A, Bleecker Eugene R, Meyers Deborah A, Peters Stephen P, Celedón Juan C, Tantisira Kelan, Li Jiang, Dupuis Josée, O'Connor George |
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- Page last updated:Apr 22, 2024
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