Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: FLNB[original query] |
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Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2010 Jun 21 (6): 1009-20. Li G H Y, Kung A W C, Huang Q |
Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Dec 24 (12): 1989-97. Wilson Scott G, Jones Michelle R, Mullin Ben H, Dick Ian M, Richards J Brent, Pastinen Tomi M, Grundberg Elin, Ljunggren Osten, Surdulescu Gabriela L, Dudbridge Frank, Elliott Katherine S, Cervino Alessandra C L, Spector Timothy D, Prince Richard |
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. PloS one 2010 5 (7): e11493. Jugessur Astanand, Shi Min, Gjessing Håkon Kristian, Lie Rolv Terje, Wilcox Allen James, Weinberg Clarice Ring, Christensen Kaare, Boyles Abee Lowman, Daack-Hirsch Sandra, Nguyen Truc Trung, Christiansen Lene, Lidral Andrew Carl, Murray Jeffrey Cla |
Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal. BMC genetics 2013 14 (1): 107. Mullin Benjamin H, Mamotte Cyril, Prince Richard L, Spector Tim D, Dudbridge Frank, Wilson Scott |
Genetic association of ARHGAP21 gene variant with mandibular prognathism. Journal of dental research 2015 Apr 94 (4): 569-76. Perillo L, Monsurrò A, Bonci E, Torella A, Mutarelli M, Nigro |
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Genetic epidemiology 2015 Mar 39 (3): 207-16. Springelkamp Henriët, Mishra Aniket, Hysi Pirro G, Gharahkhani Puya, Höhn René, Khor Chiea-Chuen, Cooke Bailey Jessica N, Luo Xiaoyan, Ramdas Wishal D, Vithana Eranga, Koh Victor, Yazar Seyhan, Xu Liang, Forward Hannah, Kearns Lisa S, Amin Najaf, Iglesias Adriana I, Sim Kar-Seng, van Leeuwen Elisabeth M, Demirkan Ayse, van der Lee Sven, Loon Seng-Chee, Rivadeneira Fernando, Nag Abhishek, Sanfilippo Paul G, Schillert Arne, de Jong Paulus T V M, Oostra Ben A, Uitterlinden André G, Hofman Albert, , Zhou Tiger, Burdon Kathryn P, Spector Timothy D, Lackner Karl J, Saw Seang-Mei, Vingerling Johannes R, Teo Yik-Ying, Pasquale Louis R, Wolfs Roger C W, Lemij Hans G, Tai E-Shyong, Jonas Jost B, Cheng Ching-Yu, Aung Tin, Jansonius Nomdo M, Klaver Caroline C W, Craig Jamie E, Young Terri L, Haines Jonathan L, MacGregor Stuart, Mackey David A, Pfeiffer Norbert, Wong Tien-Yin, Wiggs Janey L, Hewitt Alex W, van Duijn Cornelia M, Hammond Christopher |
Exome sequencing analysis identifies frequent oligogenic involvement and FLNB variants in adolescent idiopathic scoliosis. Journal of medical genetics 2020 5 57 (6): 405-413. Jiang Heng, Liang Shulun, He Kai, Hu Jinghua, Xu Enjie, Lin Tao, Meng Yichen, Zhao Jianquan, Ma Jun, Gao Rui, Wang Ce, Yang Fu, Zhou Xuh |
Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion. Clinical orthopaedics and related research 2021 Sep . Quiggle Ashley, Charng Wu-Lin, Antunes Lilian, Nikolov Momchil, Bledsoe Xavier, Hecht Jacqueline T, Dobbs Matthew B, Gurnett Christina |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
The variants at FLNA and FLNB contribute to the susceptibility of hypertension and stroke with differentially expressed mRNA. The pharmacogenomics journal 2021 3 21 (4): 458-466. Liu Chunlan, Tang Wuzhuang, Zhao Hailong, Yang Song, Ren Zhanyun, Li Jie, Chen Yanchun, Zhao Xianghai, Xu Donghua, Zhao Yanping, Shen Cho |
Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Molecular genetics and genomics : MGG 2022 Jul . D?browska Justyna, Biedziak Barbara, Szponar-?urowska Anna, Budner Margareta, Jagodzi?ski Pawe? P, P?oski Rafa?, Mostowska Adrian |
A Necroptosis-Related lncRNA-Based Signature to Predict Prognosis and Probe Molecular Characteristics of Stomach Adenocarcinoma. Frontiers in genetics 2022 3 13 833928. Luo Lianghua, Li Leyan, Liu Li, Feng Zongfeng, Zeng Qingwen, Shu Xufeng, Cao Yi, Li Zhengro |
Innovative Family-Based Genetically Informed Series of Analyses of Whole-Exome Data Supports Likely Inheritance for Grammar in Children with Specific Language Impairment. Children (Basel, Switzerland) 2023 7 10 (7): . Erin M Andres, Kathleen Kelsey Earnest, Hao Xuan, Cuncong Zhong, Mabel L Rice, Muhammad Hashim Ra |
Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing. Journal of clinical medicine 2023 3 12 (5): . D?browska Justyna, Biedziak Barbara, Bogdanowicz Agnieszka, Mostowska Adrian |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
[Etiological analysis of a patient with multiple primary malignant neoplasms]. Zhonghua yi xue za zhi 2023 12 103 (47): 3848-3851. P J Shi, Y B Li, H P Xi |
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- Page last updated:Apr 16, 2024
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