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

Year Number of Results
2002 5
2003 6
2004 5
2005 7
2006 9
2007 14
2008 14
2009 20
2010 13
2011 17
2012 24
2013 22
2014 22
2015 31
2016 15
2017 20
2018 22
2019 28
2020 34
2021 36
2022 49
2023 33
2024 26
2025 37

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456 results

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Page 1
Consensus Nomenclature for Reporting Neovascular Age-Related Macular Degeneration Data: Consensus on Neovascular Age-Related Macular Degeneration Nomenclature Study Group.
Spaide RF, Jaffe GJ, Sarraf D, Freund KB, Sadda SR, Staurenghi G, Waheed NK, Chakravarthy U, Rosenfeld PJ, Holz FG, Souied EH, Cohen SY, Querques G, Ohno-Matsui K, Boyer D, Gaudric A, Blodi B, Baumal CR, Li X, Coscas GJ, Brucker A, Singerman L, Luthert P, Schmitz-Valckenberg S, Schmidt-Erfurth U, Grossniklaus HE, Wilson DJ, Guymer R, Yannuzzi LA, Chew EY, Csaky K, Monés JM, Pauleikhoff D, Tadayoni R, Fujimoto J. Spaide RF, et al. Among authors: li x. Ophthalmology. 2020 May;127(5):616-636. doi: 10.1016/j.ophtha.2019.11.004. Epub 2019 Nov 14. Ophthalmology. 2020. PMID: 31864668 Free PMC article.
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.
Fan X, Zhao S, Yu C, Wu D, Yan Z, Fan L, Song Y, Wang Y, Li C, Ming Y, Gui B, Niu Y, Li X, Yang X, Luo S, Zhang Q, Zhao X, Pan H, Li M, Xia W, Qiu G, Liu P, Zhang S, Zhang J, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Lupski JR, Posey JE, Chen S, Gong C, Wu N. Fan X, et al. Among authors: li x. J Genet Genomics. 2021 May 20;48(5):396-402. doi: 10.1016/j.jgg.2021.02.008. Epub 2021 Mar 22. J Genet Genomics. 2021. PMID: 34006472
Phase 1 study of safety and preliminary efficacy of intranasal transplantation of human neural stem cells (ANGE-S003) in Parkinson's disease.
Jiang S, Wang H, Yang C, Feng F, Xu D, Zhang M, Xie M, Cui R, Zhu Z, Jia C, Liu L, Wang L, Yang X, Yang Y, Hao H, Liu Z, Wu Z, Leng L, Li X, Sun X, Zhao X, Xu J, Zhang Y, Wan X, Bao X, Wang R. Jiang S, et al. Among authors: li x. J Neurol Neurosurg Psychiatry. 2024 Nov 18;95(12):1102-1111. doi: 10.1136/jnnp-2023-332921. J Neurol Neurosurg Psychiatry. 2024. PMID: 38724232 Clinical Trial.
Hyperacute Outer Retinal Dysfunction.
Cheng Y, Liu X, Lu J, Ren J, Fei P, Chen M, Tang C, Zhang J, Zhang M, Yuan M, Sun L, Zhang L, Hou A, Jin Y, Lai Y, Wang Q, Yan W, Ke S, Li X, Ding X. Cheng Y, et al. Among authors: li x. JAMA Ophthalmol. 2025 Mar 1;143(3):222-229. doi: 10.1001/jamaophthalmol.2024.6372. JAMA Ophthalmol. 2025. PMID: 39946120
Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.
Feng X, Ye Y, Zhang J, Zhang Y, Zhao S, Mak JCW, Otomo N, Zhao Z, Niu Y, Yonezawa Y, Li G, Lin M, Li X, Cheung PWH, Xu K, Takeda K, Wang S, Xie J, Kotani T, Choi VNT, Song YQ, Yang Y, Luk KDK, Lee KS, Li Z, Li PS, Leung CYH, Lin X, Wang X, Qiu G; DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group; Watanabe K; Japanese Early Onset Scoliosis Research Group; Wu Z, Posey JE, Ikegawa S, Lupski JR, Cheung JPY, Zhang TJ, Gao B, Wu N. Feng X, et al. Among authors: li x. Proc Natl Acad Sci U S A. 2024 Apr 30;121(18):e2310283121. doi: 10.1073/pnas.2310283121. Epub 2024 Apr 26. Proc Natl Acad Sci U S A. 2024. PMID: 38669183 Free PMC article.
Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders.
Zhao S, Zhang Y, Hallgrimsdottir S, Zuo Y, Li X, Batkovskyte D, Liu S, Lindelöf H, Wang S, Hammarsjö A, Yang Y, Ye Y, Wang L, Yan Z, Lin J, Yu C, Chen Z, Niu Y, Wang H, Zhao Z, Liu P, Qiu G, Posey JE, Wu Z, Lupski JR, Micule I, Anderlid BM, Voss U, Sulander D, Kuchinskaya E, Nordgren A, Nilsson O; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Zhang TJ, Grigelioniene G, Wu N. Zhao S, et al. Among authors: li x. NPJ Genom Med. 2022 Feb 15;7(1):11. doi: 10.1038/s41525-021-00273-x. NPJ Genom Med. 2022. PMID: 35169139 Free PMC article.
Tocilizumab treatment in Felty's syndrome.
Li R, Wan Q, Chen P, Mao S, Wang Q, Li X, Yang Y, Dong L. Li R, et al. Among authors: li x. Rheumatol Int. 2020 Jul;40(7):1143-1149. doi: 10.1007/s00296-020-04588-3. Epub 2020 Apr 28. Rheumatol Int. 2020. PMID: 32347340 Review.
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis.
Wang L, Liu Z, Zhao S, Xu K, Aceves V, Qiu C, Feng HC, Bian F, He J, Song CJ, Troutwine B, Liu L, Ma S, Niu Y, Wang S, Yuan S, Li X, Zhao L, Liu X, Qiu G, Wu Z; Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study group; Zhang TJ, Gray RS, Wu N. Wang L, et al. Among authors: li x. Proc Natl Acad Sci U S A. 2025 Jan 28;122(4):e2313978121. doi: 10.1073/pnas.2313978121. Epub 2025 Jan 24. Proc Natl Acad Sci U S A. 2025. PMID: 39854231 Free PMC article.
456 results