Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: PRICKLE1[original query] |
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Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach. Diabetes 2009 Jun 58 (6): 1463-7. Perry John R B, McCarthy Mark I, Hattersley Andrew T, Zeggini Eleftheria, , Weedon Michael N, Frayling Timothy |
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects. Human mutation 2011 Dec 32 (12): 1371-5. Bosoi Ciprian M, Capra Valeria, Allache Redouane, Trinh Vincent Quoc-Huy, De Marco Patrizia, Merello Elisa, Drapeau Pierre, Bassuk Alexander G, Kibar Zo |
Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study. Pharmacogenetics and genomics 2014 Nov 24 (11): 556-63. Sørensen Izel F, Vazquez Ana I, Irvin Marguerite R, Sørensen Peter, Davis Barry R, Ford Charles E, Boerwinkle Eric, Eckfeldt John H, Arnett Donna |
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.
Gastroenterology 2018 Dec . Lu Yingchang, Kweon Sun-Seog, Tanikawa Chizu, Jia Wei-Hua, Xiang Yong-Bing, Cai Qiuyin, Zeng Chenjie, Schmit Stephanie L, Shin Aesun, Matsuo Keitaro, Jee Sun Ha, Kim Dong-Hyun, Kim Jeongseon, Wen Wanqing, Shi Jiajun, Guo Xingyi, Li Bingshan, Wang Nan, Zhang Ben, Li Xinxiang, Shin Min-Ho, Li Hong-Lan, Ren Zefang, Oh Jae Hwan, Oze Isao, Ahn Yoon-Ok, Jung Keum Ji, Conti David V, Schumacher Fredrick R, Rennert Gad, Jenkins Mark A, Campbell Peter T, Hoffmeister Michael, Casey Graham, Gruber Stephen B, Gao Jing, Gao Yu-Tang, Pan Zhi-Zhong, Kamatani Yoichiro, Zeng Yi-Xin, Shu Xiao-Ou, Long Jirong, Matsuda Koichi, Zheng W |
Paediatric-onset and adult-onset Graves' disease share multiple genetic risk factors. Clinical endocrinology 2019 Feb 90 (2): 320-327. Ku? Aleksander, Radziszewski Miko?aj, Glina Aleksandra, Szyma?ski Konrad, Jurecka-Lubieniecka Beata, Pawlak-Adamska Edyta, Kula Dorota, Wawrusiewicz-Kurylonek Natalia, Ku? Joanna, Mi?kiewicz Piotr, P?oski Rafa?, Bolanowski Marek, Daroszewski Jacek, Jarz?b Barbara, Bossowski Artur, Bednarczuk Toma |
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders. Human mutation 2022 8 43 (12): 1795-1807. Lieberwirth Johann Kaspar, Büttner Benjamin, Klöckner Chiara, Platzer Konrad, Popp Bernt, Abou Jamra Ra |
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- Page last updated:Apr 22, 2024
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