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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 2
2004 2
2005 1
2006 1
2007 4
2008 5
2009 3
2010 3
2011 5
2012 8
2013 7
2014 8
2015 6
2016 5
2017 5
2018 6
2019 3
2020 4
2021 6
2022 2
2023 8
2024 7
2025 5

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99 results

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Page 1
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.
Wang X, Yue M, Cheung JPY, Cheung PWH, Fan Y, Wu M, Wang X, Zhao S, Khanshour AM, Rios JJ, Chen Z, Wang X, Tu W, Chan D, Yuan Q, Qin D, Qiu G, Wu Z, Zhang TJ, Ikegawa S, Wu N, Wise CA, Hu Y, Luk KDK, Song YQ, Gao B. Wang X, et al. Among authors: wise ca. J Clin Invest. 2024 Jan 16;134(2):e168783. doi: 10.1172/JCI168783. J Clin Invest. 2024. PMID: 37962965 Free PMC article.
Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis.
Charng WL, Haller G, Whittle J, Nikolov M, Avery A, Morcuende J, Giampietro P, Raggio C, Miller N, Justice AE, Strande NT, Seeley M, Bodian DL, Wise CA, Sepich DS, Dobbs MB, Gurnett CA. Charng WL, et al. Among authors: wise ca. J Med Genet. 2025 Jun 24;62(7):427-435. doi: 10.1136/jmg-2024-110586. J Med Genet. 2025. PMID: 40306904 Free PMC article.
EPHA4 signaling dysregulation links abnormal locomotion and the development of idiopathic scoliosis.
Wang L, Yang X, Zhao S, Zheng P, Wen W, Xu K, Cheng X, Li Q, Khanshour AM, Koike Y, Liu J, Fan X, Otomo N, Chen Z, Li Y, Li L, Xie H, Zhu P, Li X, Niu Y, Wang S, Liu S, Yuan S, Terao C, Li Z, Chen S, Zhao X, Liu P, Posey JE, Wu Z, Qiu G; DISCO study group (Deciphering Disorders Involving Scoliosis & COmorbidities); Ikegawa S, Lupski JR, Rios JJ, Wise CA, Zhang JT, Zhao C, Wu N. Wang L, et al. Among authors: wise ca. Elife. 2025 Jul 15;13:RP95324. doi: 10.7554/eLife.95324. Elife. 2025. PMID: 40662934 Free PMC article.
The cartilage matrisome in adolescent idiopathic scoliosis.
Wise CA, Sepich D, Ushiki A, Khanshour AM, Kidane YH, Makki N, Gurnett CA, Gray RS, Rios JJ, Ahituv N, Solnica-Krezel L. Wise CA, et al. Bone Res. 2020 Mar 9;8:13. doi: 10.1038/s41413-020-0089-0. eCollection 2020. Bone Res. 2020. PMID: 32195011 Free PMC article. Review.
Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities.
Moulton MJ, Atala K, Zheng Y, Dutta D, Grange DK, Lin WW, Wegner DJ, Wambach JA, Duker AL, Bober MB, Kratz L, Wise CA, Oxendine I, Khanshour A; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Cole FS, Rios J, Bellen HJ. Moulton MJ, et al. Among authors: wise ca. Genet Med. 2024 Sep;26(9):101174. doi: 10.1016/j.gim.2024.101174. Epub 2024 Jun 3. Genet Med. 2024. PMID: 38847193 Free PMC article.
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H, Khanshour AM, Ushiki A, Otomo N, Koike Y, Einarsdottir E, Fan Y, Antunes L, Kidane YH, Cornelia R, Sheng RR, Zhang Y, Pei J, Grishin NV, Evers BM, Cheung JPY, Herring JA, Terao C, Song YQ, Gurnett CA, Gerdhem P, Ikegawa S, Rios JJ, Ahituv N, Wise CA. Yu H, et al. Among authors: wise ca. Elife. 2024 Jan 26;12:RP89762. doi: 10.7554/eLife.89762. Elife. 2024. PMID: 38277211 Free PMC article.
99 results