Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: FBN2[original query] |
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Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm. Journal of human genetics 2003 48 (6): 309-14. Yoneyama Taku, Kasuya Hidetoshi, Onda Hideaki, Akagawa Hiroyuki, Jinnai Nobuyoshi, Nakajima Toshiaki, Hori Tomokatsu, Inoue Itu |
Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries. Molecular human reproduction 2009 Dec 15 (12): 829-41. Prodoehl Mark J, Hatzirodos Nicholas, Irving-Rodgers Helen F, Zhao Zhen Z, Painter Jodie N, Hickey Theresa E, Gibson Mark A, Rainey William E, Carr Bruce R, Mason Helen D, Norman Robert J, Montgomery Grant W, Rodgers Raymond |
Association analysis of genes involved in the maintenance of the integrity of the extracellular matrix with intracranial aneurysms in a Japanese cohort. Cerebrovascular diseases (Basel, Switzerland) 2009 28 (2): 131-4. Ruigrok Ynte M, Rinkel Gabriel J E, Wijmenga Cisca, Kasuya Hidetoshi, Tajima Atsushi, Takahashi Tomoko, Hata Akira, Inoue Ituro, Krischek Bor |
GWAS of 972 autologous stem cell recipients with multiple myeloma identifies 11 genetic variants associated with chemotherapy-induced oral mucositis. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 2015 Mar 23 (3): 841-9. Coleman Elizabeth Ann, Lee Jeannette Y, Erickson Stephen W, Goodwin Julia A, Sanathkumar Naveen, Raj Vinay R, Zhou Daohong, McKelvey Kent D, Apewokin Senu, Stephens Owen, Enderlin Carol A, Vangsted Annette Juul, Reed Patty J, Anaissie Elias |
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human molecular genetics 2014 Nov 23 (21): 5827-37. Ratnapriya Rinki, Zhan Xiaowei, Fariss Robert N, Branham Kari E, Zipprer David, Chakarova Christina F, Sergeev Yuri V, Campos Maria M, Othman Mohammad, Friedman James S, Maminishkis Arvydas, Waseem Naushin H, Brooks Matthew, Rajasimha Harsha K, Edwards Albert O, Lotery Andrew, Klein Barbara E, Truitt Barbara J, Li Bingshan, Schaumberg Debra A, Morgan Denise J, Morrison Margaux A, Souied Eric, Tsironi Evangelia E, Grassmann Felix, Fishman Gerald A, Silvestri Giuliana, Scholl Hendrik P N, Kim Ivana K, Ramke Jacqueline, Tuo Jingsheng, Merriam Joanna E, Merriam John C, Park Kyu Hyung, Olson Lana M, Farrer Lindsay A, Johnson Matthew P, Peachey Neal S, Lathrop Mark, Baron Robert V, Igo Robert P, Klein Ronald, Hagstrom Stephanie A, Kamatani Yoichiro, Martin Tammy M, Jiang Yingda, Conley Yvette, Sahel Jose-Alan, Zack Donald J, Chan Chi-Chao, Pericak-Vance Margaret A, Jacobson Samuel G, Gorin Michael B, Klein Michael L, Allikmets Rando, Iyengar Sudha K, Weber Bernhard H, Haines Jonathan L, Léveillard Thierry, Deangelis Margaret M, Stambolian Dwight, Weeks Daniel E, Bhattacharya Shomi S, Chew Emily Y, Heckenlively John R, Abecasis Gonçalo R, Swaroop Ana |
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Human molecular genetics 2014 Oct 23 (19): 5271-82. Buchan Jillian G, Alvarado David M, Haller Gabe E, Cruchaga Carlos, Harms Matthew B, Zhang Tianxiao, Willing Marcia C, Grange Dorothy K, Braverman Alan C, Miller Nancy H, Morcuende Jose A, Tang Nelson Leung-Sang, Lam Tsz-Ping, Ng Bobby Kin-Wah, Cheng Jack Chun-Yiu, Dobbs Matthew B, Gurnett Christina |
ELN and FBN2 gene variants as risk factors for two sports-related musculoskeletal injuries. International journal of sports medicine 2015 Apr 36 (4): 333-7. Khoury L El, Posthumus M, Collins M, van der Merwe W, Handley C, Cook J, Raleigh S |
Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration. PloS one 2016 11 (3): e0152047. Duvvari Maheswara R, van de Ven Johannes P H, Geerlings Maartje J, Saksens Nicole T M, Bakker Bjorn, Henkes Arjen, Neveling Kornelia, Rosario Marisol Del, Westra Dineke, van den Heuvel Lambertus P W J, Schick Tina, Fauser Sascha, Boon Camiel J F, Hoyng Carel B, Jong Eiko K de, Hollander Anneke I d |
New Evidence Supporting the Role of FBN1 in the Development of Adolescent Idiopathic Scoliosis. Spine 2018 Jul . Sheng Fei, Xia Chao, Xu Leilei, Qin Xiaodong, Tang Nelson Leung-Sang, Qiu Yong, Cheng Jack Chun-Yiu, Zhu Zezha |
Femoral Artery Aneurysm Repair in a Patient With a Fibrillin-2 Mutation. Vascular and endovascular surgery 2018 5 52 (7): 583-586. Ratschiller Thomas, Müller Hannes, Schachner Thomas, Fellner Franz, Sulzbacher Gregor, Zierer Andre |
Gene polymorphisms of fibronectin rs2289202 and fibrillin 2 rs331069 associate with vascular disease, the TAMRISK study. Biomedical reports 2018 Jan 8 (1): 65-68. Kunnas Tarja, Solakivi Tiina, Nikkari Seppo |
Joint Association Analysis Identified 18 New Loci for Bone Mineral Density.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 Jan . Pei Yu-Fang, Liu Lu, Liu Tao-Le, Yang Xiao-Lin, Zhang Hong, Wei Xin-Tong, Feng Gui-Juan, Hai Rong, Ran Shu, Zhang L |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jan . Renner Sina, Schüler Helke, Alawi Malik, Kolbe Verena, Rybczynski Meike, Woitschach Rixa, Sheikhzadeh Sara, Stark Veronika C, Olfe Jakob, Roser Elke, Seggewies Friederike Sophia, Mahlmann Adrian, Hempel Maja, Hartmann Melanie J, Hillebrand Mathias, Wieczorek Dagmar, Volk Alexander Erich, Kloth Katja, Koch-Hogrebe Margarete, Abou Jamra Rami, Mitter Diana, Altmüller Janine, Wey-Fabrizius Alexandra, Petersen Christine, Rau Isabella, Borck Guntram, Kubisch Christian, Mir Thomas S, von Kodolitsch Yskert, Kutsche Kerstin, Rosenberger Geo |
A novel pathogenic mutation in FBN2 associated with congenital contractural arachnodactyly for preimplantation genetic diagnosis. Journal of genetics and genomics = Yi chuan xue bao 2020 8 47 (5): 281-284. Li Jiaxin, Wang Yuqian, Zhu Xiaohui, Nie Yanli, Kuo Ying, Guan Shuo, Huang Jin, Lian Ying, Zhao Yangyu, Li Rong, Wei Yuan, Qiao Jie, Yan Liyi |
Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population.
Arthritis research & therapy 2020 Aug 22 (1): 185. Tangtanatakul Pattarin, Thumarat Chisanu, Satproedprai Nusara, Kunhapan Punna, Chaiyasung Tassamonwan, Klinchanhom Siriwan, Wang Yong-Fei, Wei Wei, Wongshinsri Jeerapat, Chiewchengchol Direkrit, Rodsaward Pongsawat, Ngamjanyaporn Pintip, Suangtamai Thanitta, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Hirankarn Natti |
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome. European journal of medical genetics 2020 7 63 (10): 104008. Maya Idit, Kahana Sarit, Agmon-Fishman Ifaat, Klein Cochava, Matar Reut, Berger Racheli, Shohat Mordechai, Basel-Salmon Lina, Sharony Reuven, Sagi-Dain Le |
[Pathological variant of FBN2 gene identified in a pedigree affected with congenital contracture arachnodactyly]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 4 37 (5): 497-500. Wang Jieqiong, Xia Yanjie, Wang Yanan, Yang Fan, Kong Xiangdo |
Risk score based on expression of five novel genes predicts survival in soft tissue sarcoma. Aging 2020 2 12 (4): 3807-3827. Gu Hui-Yun, Zhang Chao, Guo Jia, Yang Min, Zhong Hou-Cheng, Jin Wei, Liu Yang, Gao Li-Ping, Wei Ren-Xio |
99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population. BioMed research international 2020 2020 7857043. Wang Zanxin, Zhuang Xianmian, Chen Bailang, Wen Junmin, Peng Fang, Liu Xiling, Wei Minx |
Recurrent germline mutations as genetic markers for aortic root dilatation in bicuspid aortic valve patients. Heart and vessels 2020 Oct . Wu Boting, Li Jun, Wang Yongshi, Cheng Yunfeng, Wang Chunsheng, Shu Xianho |
[A novel splicing acceptor variant of the FBN2 gene contributes to a case of congenital contractural arachnodactyly]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 5 39 (5): 522-525. Tan Xiaolan, Leng Xiangyou, Tao Dachang, Yang Yuan, Liu Yunqia |
Genetic variations in relation to bleeding and pharmacodynamics of dabigatran in Chinese patients with nonvalvular atrial fibrillation: A nationwide multicentre prospective cohort study. Clinical and translational medicine 2022 12 12 (12): e1104. Xiang Qian, Xie Qiufen, Liu Zhiyan, Mu Guangyan, Zhang Hanxu, Zhou Shuang, Wang Zhe, Wang Zining, Zhang Yatong, Zhao Zinan, Yuan Dongdong, Guo Liping, Wang Na, Xiang Jing, Song Hongtao, Sun Jianjun, Jiang Jie, Cui Yim |
Assessment of fibrillin-2 and elastin gene polymorphisms in patients with a traumatic Achilles tendon rupture: Is Achilles tendon rupture a genetic disease? Acta orthopaedica et traumatologica turcica 2023 5 . Jan Poszepczy?ski, Micha? Pietrusi?ski, Maciej Borowiec, Marcin Edward Dom?als |
Impact of mini-driver genes in the prognosis and tumor features of colorectal cancer samples: a novel perspective to support current biomarkers. PeerJ 2023 5 11 e15410. Anthony Vladimir Campos Segura, Mariana Belén Velásquez Sotomayor, Ana Isabel Flor Gutiérrez Román, César Alexander Ortiz Rojas, Alexis Germán Murillo Carras |
Utility of whole-exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population. Molecular genetics & genomic medicine 2023 2 e2160. Hsu Rai-Hseng, Lee Chen-Hao, Chien Yin-Hsiu, Lin Shuan-Pei, Hung Miao-Zi, Chen Nai-Chi, Lin Yi-Lin, Hwu Wuh-Liang, Lee Ni-Chu |
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- Page last updated:Mar 25, 2024
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