Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: ADAMTS17[original query] |
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A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.
Blood 2012 Sep . Arning A, Hiersche M, Witten A, Kurlemann G, Kurnik K, Manner D, Stoll M, Nowak-Göttl U |
Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog. PloS one 2015 10 (10): e0140436. Oliver James A C, Forman Oliver P, Pettitt Louise, Mellersh Cathryn |
Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association Study.
JAMA ophthalmology 2019 Jun . Khawaja Anthony P, Rojas Lopez Karla E, Hardcastle Alison J, Hammond Chris J, Liskova Petra, Davidson Alice E, Gore Daniel M, Hafford Tear Nathan J, Pontikos Nikolas, Hayat Shabina, Wareham Nick, Khaw Kay-Tee, Tuft Stephen J, Foster Paul J, Hysi Pirro |
Polymorphisms of the BARX1 and ADAMTS17 Locus Genes in Individuals With Gastroesophageal Reflux Disease. Journal of neurogastroenterology and motility 2019 May . Argyrou Alexandra, Legaki Evangelia, Koutserimpas Christos, Gazouli Maria, Papaconstantinou Ioannis, Gkiokas George, Karamanolis Geor |
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome.
Nature communications 2019 03 10 (1): 1030. Wiberg Akira, Ng Michael, Schmid Annina B, Smillie Robert W, Baskozos Georgios, Holmes Michael V, Künnapuu K, Mägi R, Bennett David L, Furniss Domin |
Identification of 5 Gene Signatures in Survival Prediction for Patients with Lung Squamous Cell Carcinoma Based on Integrated Multiomics Data Analysis. BioMed research international 2020 6 2020 6427483. Ma Hongxia, Tong Lihong, Zhang Qian, Chang Wenjun, Li Fengs |
Investigation of the allele frequency of the G>A intron 10 ADAMTS17 mutation causing primary lens luxation in the Portuguese Podengo breed. Veterinary ophthalmology 2021 12 25 (1): 85-89. Tzouganakis Ioannis, Tsvetanova Agata, Jeanes Emily C, Mellersh Cathryn S, Gould David |
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome. Experimental eye research 2022 11 226 109307. Zhou Lin, Wang Xiaoli, An Jingqi, Zhang Yao, He Mengxia, Tang |
A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis. Scientific reports 2023 3 13 (1): 4900. Taniguchi Yuki, Akune Toru, Nishida Nao, Omori Go, Ha Kim, Ueno Kazuko, Saito Taku, Oichi Takeshi, Koike Asako, Mabuchi Akihiko, Oka Hiroyuki, Muraki Shigeyuki, Oshima Yasushi, Kawaguchi Hiroshi, Nakamura Kozo, Tokunaga Katsushi, Tanaka Sakae, Yoshimura Nori |
The role of ADAMTS6 and ADAMTS17 polymorphisms in susceptibility to lumbar disc herniation in Chinese Han population. European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society 2023 2 . Han Pengbo, Jiang Feng, Zhang L |
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- Page last updated:Apr 29, 2024
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