Bagnat, M. and R. S. Gray (2020). "Development of a straight vertebrate body axis." Development 147(21).
Baschal, E. E., E. A. Terhune, C. I. Wethey, R. M. Baschal, K. D. Robinson, M. T. Cuevas, S. Pradhan, B. S. Sutphin, M. R. G. Taylor, K. Gowan, C. G. Pearson, L. A. Niswander, K. L. Jones and N. H. Miller (2018). "Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology." G3 (Bethesda) 8(8): 2663-2672.
Baschal, E. E., C. I. Wethey, K. Swindle, R. M. Baschal, K. Gowan, N. L. Tang, D. M. Alvarado, G. E. Haller, M. B. Dobbs, M. R. Taylor, C. A. Gurnett, K. L. Jones and N. H. Miller (2014). "Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis." G3 (Bethesda) 5(2): 167-174.
Borovina, A., S. Superina, D. Voskas and B. Ciruna (2010). "Vangl2 directs the posterior tilting and asymmetric localization of motile primary cilia." Nat Cell Biol 12(4): 407-412.
Boswell, C. W. and B. Ciruna (2017). "Understanding Idiopathic Scoliosis: A New Zebrafish School of Thought." Trends Genet 33(3): 183-196.
Buchan, J. G., D. M. Alvarado, G. E. Haller, C. Cruchaga, M. B. Harms, T. Zhang, M. C. Willing, D. K. Grange, A. C. Braverman, N. H. Miller, J. A. Morcuende, N. L. Tang, T. P. Lam, B. K. Ng, J. C. Cheng, M. B. Dobbs and C. A. Gurnett (2014). "Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis." Hum Mol Genet 23(19): 5271-5282.
Buchan, J. G., R. S. Gray, J. M. Gansner, D. M. Alvarado, L. Burgert, J. D. Gitlin, C. A. Gurnett and M. I. Goldsmith (2014). "Kinesin family member 6 (kif6) is necessary for spine development in zebrafish." Dev Dyn 243(12): 1646-1657.
Cantaut-Belarif, Y., J. R. Sternberg, O. Thouvenin, C. Wyart and P. L. Bardet (2018). "The Reissner Fiber in the Cerebrospinal Fluid Controls Morphogenesis of the Body Axis." Curr Biol 28(15): 2479-2486.e2474.
Cheng, J. C., R. M. Castelein, W. C. Chu, A. J. Danielsson, M. B. Dobbs, T. B. Grivas, C. A. Gurnett, K. D. Luk, A. Moreau, P. O. Newton, I. A. Stokes, S. L. Weinstein and R. G. Burwell (2015). "Adolescent idiopathic scoliosis." Nat Rev Dis Primers 1: 15030.
Einarsdottir, E., A. Grauers, J. Wang, H. Jiao, S. A. Escher, A. Danielsson, A. Simony, M. Andersen, S. B. Christensen, K. Akesson, I. Kou, A. M. Khanshour, A. Ohlin, C. Wise, S. Ikegawa, J. Kere and P. Gerdhem (2017). "CELSR2 is a candidate susceptibility gene in idiopathic scoliosis." PLoS One 12(12): e0189591.
Gao, W., C. Chen, T. Zhou, S. Yang, B. Gao, H. Zhou, C. Lian, Z. Wu, X. Qiu, X. Yang, E. Alattar, W. Liu, D. Su, S. Sun, Y. Chen, K. M. C. Cheung, Y. Song, K. K. D. Luk, D. Chan, P. C. Sham, C. Xing, C. C. Khor, G. Liu, J. Yang, Y. Deng, D. Hao, D. Huang, Q. Z. Li, C. Xu and P. Su (2017). "Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis." Hum Mutat 38(11): 1500-1510.
Gao, Y., C. Zhang, L. Yuan, Y. Ling, X. Wang, C. Liu, Y. Pan, X. Zhang, X. Ma, Y. Wang, Y. Lu, K. Yuan, W. Ye, J. Qian, H. Chang, R. Cao, X. Yang, L. Ma, Y. Ju, L. Dai, Y. Tang, G. Zhang and S. Xu (2020). "PGG.Han: the Han Chinese genome database and analysis platform." Nucleic Acids Res 48(D1): D971-d976.
Grimes, D. T., C. W. Boswell, N. F. Morante, R. M. Henkelman, R. D. Burdine and B. Ciruna (2016). "Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature." Science 352(6291): 1341-1344.
Grimes, D. T. and R. D. Burdine (2017). "Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis." Trends Genet 33(9): 616-628.
Hadley Miller, N. (2000). "Spine update: genetics of familial idiopathic scoliosis." Spine (Phila Pa 1976) 25(18): 2416-2418.
Haller, G., D. Alvarado, K. McCall, P. Yang, C. Cruchaga, M. Harms, A. Goate, M. Willing, J. A. Morcuende, E. Baschal, N. H. Miller, C. Wise, M. B. Dobbs and C. A. Gurnett (2016). "A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis." Hum Mol Genet 25(1): 202-209.
Haller, G., K. McCall, S. Jenkitkasemwong, B. Sadler, L. Antunes, M. Nikolov, J. Whittle, Z. Upshaw, J. Shin, E. Baschal, C. Cruchaga, M. Harms, C. Raggio, J. A. Morcuende, P. Giampietro, N. H. Miller, C. Wise, R. S. Gray, L. Solnica-Krezel, M. Knutson, M. B. Dobbs and C. A. Gurnett (2018). "A missense variant in SLC39A8 is associated with severe idiopathic scoliosis." Nat Commun 9(1): 4171.
Hayes, M., X. Gao, L. X. Yu, N. Paria, R. M. Henkelman, C. A. Wise and B. Ciruna (2014). "ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease." Nat Commun 5: 4777.
Jiang, H., S. Liang, K. He, J. Hu, E. Xu, T. Lin, Y. Meng, J. Zhao, J. Ma, R. Gao, C. Wang, F. Yang and X. Zhou (2020). "Exome sequencing analysis identifies frequent oligogenic involvement and FLNB variants in adolescent idiopathic scoliosis." J Med Genet 57(6): 405-413.
Kamiya, R. and T. Yagi (2014). "Functional diversity of axonemal dyneins as assessed by in vitro and in vivo motility assays of Chlamydomonas mutants." Zoolog Sci 31(10): 633-644.
Karner, C. M., F. Long, L. Solnica-Krezel, K. R. Monk and R. S. Gray (2015). "Gpr126/Adgrg6 deletion in cartilage models idiopathic scoliosis and pectus excavatum in mice." Hum Mol Genet 24(15): 4365-4373.
Knowles, M. R., L. A. Daniels, S. D. Davis, M. A. Zariwala and M. W. Leigh (2013). "Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease." Am J Respir Crit Care Med 188(8): 913-922.
Konjikusic, M. J., P. Yeetong, C. W. Boswell, C. Lee, E. C. Roberson, R. Ittiwut, K. Suphapeetiporn, B. Ciruna, C. A. Gurnett, J. B. Wallingford, V. Shotelersuk and R. S. Gray (2018). "Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development." PLoS Genet 14(11): e1007817.
Kou, I., Y. Takahashi, T. A. Johnson, A. Takahashi, L. Guo, J. Dai, X. Qiu, S. Sharma, A. Takimoto, Y. Ogura, H. Jiang, H. Yan, K. Kono, N. Kawakami, K. Uno, M. Ito, S. Minami, H. Yanagida, H. Taneichi, N. Hosono, T. Tsuji, T. Suzuki, H. Sudo, T. Kotani, I. Yonezawa, D. Londono, D. Gordon, J. A. Herring, K. Watanabe, K. Chiba, N. Kamatani, Q. Jiang, Y. Hiraki, M. Kubo, Y. Toyama, T. Tsunoda, C. A. Wise, Y. Qiu, C. Shukunami, M. Matsumoto and S. Ikegawa (2013). "Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis." Nat Genet 45(6): 676-679.
Li, W., Y. Li, L. Zhang, H. Guo, D. Tian, Y. Li, Y. Peng, Y. Zheng, Y. Dai, K. Xia, X. Lan, B. Wang and Z. Hu (2016). "AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis." J Med Genet 53(7): 488-493.
Liu, C., R. Cao, Y. Xu, T. Li, F. Li, S. Chen, R. Xu and K. Sun (2018). "Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects." Genome Med 10(1): 40.
Liu, Z. and R. S. Gray (2018). Animal Models of Idiopathic Scoliosis. The Genetics and Development of Scoliosis. K. Kusumi and S. L. Dunwoodie. Cham, Springer International Publishing: 107-138.
Lu, H., A. Shagirova, J. L. Goggi, H. L. Yeo and S. Roy (2020). "Reissner fibre-induced urotensin signalling from cerebrospinal fluid-contacting neurons prevents scoliosis of the vertebrate spine." Biol Open 9(5).
Mi, H., A. Muruganujan, X. Huang, D. Ebert, C. Mills, X. Guo and P. D. Thomas (2019). "Protocol Update for large-scale genome and gene function analysis with the PANTHER classification system (v.14.0)." Nat Protoc 14(3): 703-721.
Munoz, R. I., T. Kahne, H. Herrera, S. Rodriguez, M. M. Guerra, K. Vio, R. Hennig, E. Rapp and E. Rodriguez (2019). "The subcommissural organ and the Reissner fiber: old friends revisited." Cell Tissue Res 375(2): 507-529.
Myster, S. H., J. A. Knott, E. O'Toole and M. E. Porter (1997). "The Chlamydomonas Dhc1 gene encodes a dynein heavy chain subunit required for assembly of the I1 inner arm complex." Mol Biol Cell 8(4): 607-620.
Ogura, Y., I. Kou, S. Miura, A. Takahashi, L. Xu, K. Takeda, Y. Takahashi, K. Kono, N. Kawakami, K. Uno, M. Ito, S. Minami, I. Yonezawa, H. Yanagida, H. Taneichi, Z. Zhu, T. Tsuji, T. Suzuki, H. Sudo, T. Kotani, K. Watanabe, N. Hosogane, E. Okada, A. Iida, M. Nakajima, A. Sudo, K. Chiba, Y. Hiraki, Y. Toyama, Y. Qiu, C. Shukunami, Y. Kamatani, M. Kubo, M. Matsumoto and S. Ikegawa (2015). "A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis." Am J Hum Genet 97(2): 337-342.
Patten, S. A., P. Margaritte-Jeannin, J. C. Bernard, E. Alix, A. Labalme, A. Besson, S. L. Girard, K. Fendri, N. Fraisse, B. Biot, C. Poizat, A. Campan-Fournier, K. Abelin-Genevois, V. Cunin, C. Zaouter, M. Liao, R. Lamy, G. Lesca, R. Menassa, C. Marcaillou, M. Letexier, D. Sanlaville, J. Berard, G. A. Rouleau, F. Clerget-Darpoux, P. Drapeau, F. Moldovan and P. Edery (2015). "Functional variants of POC5 identified in patients with idiopathic scoliosis." J Clin Invest 125(3): 1124-1128.
Rose, C. D., D. Pompili, K. Henke, J. L. M. Van Gennip, A. Meyer-Miner, R. Rana, S. Gobron, M. P. Harris, M. Nitz and B. Ciruna (2020). "SCO-Spondin Defects and Neuroinflammation Are Conserved Mechanisms Driving Spinal Deformity across Genetic Models of Idiopathic Scoliosis." Curr Biol 30(12): 2363-2373.e2366.
Schindelin, J., I. Arganda-Carreras, E. Frise, V. Kaynig, M. Longair, T. Pietzsch, S. Preibisch, C. Rueden, S. Saalfeld, B. Schmid, J. Y. Tinevez, D. J. White, V. Hartenstein, K. Eliceiri, P. Tomancak and A. Cardona (2012). "Fiji: an open-source platform for biological-image analysis." Nat Methods 9(7): 676-682.
Sharma, S., D. Londono, W. L. Eckalbar, X. Gao, D. Zhang, K. Mauldin, I. Kou, A. Takahashi, M. Matsumoto, N. Kamiya, K. K. Murphy, R. Cornelia, J. A. Herring, D. Burns, N. Ahituv, S. Ikegawa, D. Gordon and C. A. Wise (2015). "A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females." Nat Commun 6: 6452.
Takahashi, Y., I. Kou, A. Takahashi, T. A. Johnson, K. Kono, N. Kawakami, K. Uno, M. Ito, S. Minami, H. Yanagida, H. Taneichi, T. Tsuji, T. Suzuki, H. Sudo, T. Kotani, K. Watanabe, K. Chiba, N. Hosono, N. Kamatani, T. Tsunoda, Y. Toyama, M. Kubo, M. Matsumoto and S. Ikegawa (2011). "A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis." Nat Genet 43(12): 1237-1240.
Thisse, C. and B. Thisse (2008). "High-resolution in situ hybridization to whole-mount zebrafish embryos." Nat Protoc 3(1): 59-69.
Troutwine, B. R., P. Gontarz, M. J. Konjikusic, R. Minowa, A. Monstad-Rios, D. S. Sepich, R. Y. Kwon, L. Solnica-Krezel and R. S. Gray (2020). "The Reissner Fiber Is Highly Dynamic In Vivo and Controls Morphogenesis of the Spine." Curr Biol 30(12): 2353-2362.e2353.
Vesque, C., I. Anselme, G. Pezeron, Y. Cantaut-Belarif, A. Eschstruth, M. Djebar, D. L. Santos, H. L. Ribeuz, A. Jenett, H. Khoury, J. Véziers, C. Parmentier and S. Schneider-Maunoury (2019). "Loss of the Reissner Fiber and increased URP neuropeptide signaling underlie scoliosis in a zebrafish ciliopathy mutant." bioRxiv: 2019.2012.2019.882258.
Wise, C. A., X. Gao, S. Shoemaker, D. Gordon and J. A. Herring (2008). "Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood." Curr Genomics 9(1): 51-59.
Wu, R. S., Lam, II, H. Clay, D. N. Duong, R. C. Deo and S. R. Coughlin (2018). "A Rapid Method for Directed Gene Knockout for Screening in G0 Zebrafish." Dev Cell 46(1): 112-125.e114.
Yılmaz, H., C. Zateri, A. Kusvuran Ozkan, G. Kayalar and H. Berk (2020). "Prevalence of adolescent idiopathic scoliosis in Turkey: an epidemiological study." Spine J 20(6): 947-955.
Zhang, H., C. Guo, M. Tang, S. Liu, J. Li, Q. Guo, L. Chen, Y. Zhu and S. Zhao (2015). "Prevalence of scoliosis among primary and middle school students in Mainland China: a systematic review and meta-analysis." Spine (Phila Pa 1976) 40(1): 41-49.
Zhang, X., S. Jia, Z. Chen, Y. L. Chong, H. Xie, D. Feng, X. Wu, D. Z. Song, S. Roy and C. Zhao (2018). "Cilia-driven cerebrospinal fluid flow directs expression of urotensin neuropeptides to straighten the vertebrate body axis." Nat Genet 50(12): 1666-1673.
Zhu, Z., L. Xu, N. Leung-Sang Tang, X. Qin, Z. Feng, W. Sun, W. Zhu, B. Shi, P. Liu, S. Mao, J. Qiao, Z. Liu, X. Sun, F. Li, J. Chun-Yiu Cheng and Y. Qiu (2017). "Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis." Hum Mol Genet 26(8): 1577-1583.
Zukas, R., A. J. Chang, M. Rice and A. L. Springer (2012). "Structural analysis of flagellar axonemes from inner arm dynein knockdown strains of Trypanosoma brucei." Biocell 36(3): 133-141.