Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: WNT7B[original query] |
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Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2008 Apr 23 (4): 499-506. Sims Anne-Marie, Shephard Neil, Carter Kim, Doan Tracy, Dowling Alison, Duncan Emma L, Eisman John, Jones Graeme, Nicholson Geoffrey, Prince Richard, Seeman Ego, Thomas Gethin, Wass John A, Brown Matthew |
Wnt signaling and Dupuytren's disease.
The New England journal of medicine 2011 Jul 365 (4): 307-17. Dolmans Guido H, Werker Paul M, Hennies Hans C, Furniss Dominic, Festen Eleonora A, Franke Lude, Becker Kerstin, van der Vlies Pieter, Wolffenbuttel Bruce H, Tinschert Sigrid, Toliat Mohammad R, Nothnagel Michael, Franke Andre, Klopp Norman, Wichmann H-Erich, Nürnberg Peter, Giele Henk, Ophoff Roel A, Wijmenga Cisca, , , , |
a-Actinin-3 deficiency is associated with reduced bone mass in human and mouse. Bone 2011 Oct 49 (4): 790-8. Yang Nan, Schindeler Aaron, McDonald Michelle M, Seto Jane T, Houweling Peter J, Lek Monkol, Hogarth Marshall, Morse Alyson R, Raftery Joanna M, Balasuriya Dominic, MacArthur Daniel G, Berman Yemima, Quinlan Kate G R, Eisman John A, Nguyen Tuan V, Center Jacqueline R, Prince Richard L, Wilson Scott G, Zhu Kathy, Little David G, North Kathryn |
Beta-catenin in schizophrenia: Possibly deleterious novel mutation. Psychiatry research 2015 Aug 228 (3): 843-8. Levchenko Anastasia, Davtian Stepan, Freylichman Olga, Zagrivnaya Maria, Kostareva Anna, Malashichev Yeg |
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.
Nature communications 2015 6 6689. Miyake Masahiro, Yamashiro Kenji, Tabara Yasuharu, Suda Kenji, Morooka Satoshi, Nakanishi Hideo, Khor Chiea-Chuen, Chen Peng, Qiao Fan, Nakata Isao, Akagi-Kurashige Yumiko, Gotoh Norimoto, Tsujikawa Akitaka, Meguro Akira, Kusuhara Sentaro, Polasek Ozen, Hayward Caroline, Wright Alan F, Campbell Harry, Richardson Andrea J, Schache Maria, Takeuchi Masaki, Mackey David A, Hewitt Alex W, Cuellar Gabriel, Shi Yi, Huang Luling, Yang Zhenglin, Leung Kim Hung, Kao Patrick Y P, Yap Maurice K H, Yip Shea Ping, Moriyama Muka, Ohno-Matsui Kyoko, Mizuki Nobuhisa, MacGregor Stuart, Vitart Veronique, Aung Tin, Saw Seang-Mei, Tai E-Shyong, Wong Tien Yin, Cheng Ching-Yu, Baird Paul N, Yamada Ryo, Matsuda Fumihiko, , Yoshimura Nagahi |
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.
Human molecular genetics 2016 11 25 (22): 5035-5045. Gao Xiaoyi, Nannini Drew R, Corrao Kristen, Torres Mina, Chen Yii-Der I, Fan Bao J, Wiggs Janey L, , Taylor Kent D, Gauderman W James, Rotter Jerome I, Varma Roh |
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.
Investigative ophthalmology & visual science 2018 May 59 (6): 2495-2502. Fan Bao Jian, Chen Xueli, Sondhi Nisha, Sharmila P Ferdinamarie, Soumittra Nagasamy, Sripriya Sarangapani, Sacikala Srinivasan, Asokan Rashima, Friedman David S, Pasquale Louis R, Gao X Raymond, Vijaya Lingam, Cooke Bailey Jessica, Vitart Veronique, MacGregor Stuart, Hammond Christopher J, Khor Chiea Chuen, Haines Jonathan L, George Ronnie, Wiggs Janey L, |
Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin. Archives of dermatological research 2019 May . Assarsson Malin, Söderman Jan, Duvetorp Albert, Mrowietz Ulrich, Skarstedt Marita, Seifert Oliv |
Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke. CNS neuroscience & therapeutics 2020 9 27 (1): 71-81. Ta Song, Rong Xianfang, Guo Zhen-Ni, Jin Hang, Zhang Peng, Li Fenge, Li Zhihuan, Lin Lilong, Zheng Chenqing, Gu Qingquan, Zhang Yuan, Liu Wenlan, Yang Yi, Chang Junl |
Association of WNT7B and RSPO1 with Axial Length in School Children. Investigative ophthalmology & visual science 2020 Aug 61 (10): 11. Lu Shi Yao, Tang Shu Min, Li Fen Fen, Kam Ka Wai, Tam Pancy O S, Yip Wilson W K, Young Alvin L, Tham Clement C, Pang Chi Pui, Yam Jason C, Chen Li J |
Corneal curvature-associated MTOR variant differentiates mild myopia from high myopia in Han Chinese population. Ophthalmic genetics 2021 5 42 (4): 446-457. Yuan Xiang-Ling, Zhang Riping, Zheng Yuqian, Sun Lixia, Wang Geng, Chen Shaowan, Xu Yanxuan, Chen Shao-Lang, Qiu Kunliang, Ng Tsz K |
A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor.
PLoS genetics 2021 6 17 (6): e1009577. Green Harry D, Jones Alistair, Evans Jonathan P, Wood Andrew R, Beaumont Robin N, Tyrrell Jessica, Frayling Timothy M, Smith Christopher, Weedon Michael |
A shared genetic architecture between adhesive capsulitis and Dupuytren disease. Journal of shoulder and elbow surgery 2022 Aug . Kim Stuart K, Khan Condor, Ladd Amy L, Tashjian Robert |
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- Page last updated:Apr 29, 2024
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