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

Year Number of Results
2002 1
2003 1
2004 1
2005 1
2006 2
2007 2
2010 2
2011 2
2012 4
2013 6
2014 5
2015 9
2016 14
2017 5
2018 16
2019 22
2020 31
2021 29
2022 24
2023 21
2024 30
2025 41
2026 7

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249 results

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Page 1
YTHDF1/RNF7/p27 axis promotes prostate cancer progression.
Shi Y, Liu B, Zhang Y, Zhao S, Zuo L, Pu J, Zhai H, Mu D, Du J, Cheng Y, Yang C, Chen Y. Shi Y, et al. Among authors: zhao s. Cell Death Dis. 2025 Apr 18;16(1):314. doi: 10.1038/s41419-025-07648-3. Cell Death Dis. 2025. PMID: 40251202 Free PMC article.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Dermaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Pérez Baca MDR, et al. Am J Hum Genet. 2024 Mar 7;111(3):509-528. doi: 10.1016/j.ajhg.2024.01.013. Epub 2024 Feb 26. Am J Hum Genet. 2024. PMID: 38412861 Free PMC article.
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: zhao s. J Clin Invest. 2024 Jan 16;134(2):e168783. doi: 10.1172/JCI168783. J Clin Invest. 2024. PMID: 37962965 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: zhao s. 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
Clinical validation of RNA sequencing for Mendelian disorder diagnostics.
Zhao S, Macakova K, Sinson JC, Dai H, Rosenfeld J, Zapata GE, Li S, Ward PA, Wang C, Qu C, Maywald B; Undiagnosed Diseases Network; Lee B, Eng C, Liu P. Zhao S, et al. Am J Hum Genet. 2025 Apr 3;112(4):779-792. doi: 10.1016/j.ajhg.2025.02.006. Epub 2025 Mar 4. Am J Hum Genet. 2025. PMID: 40043707 Free PMC article.
Genome-wide cell-free DNA methylation analyses improve accuracy of non-invasive diagnostic imaging for early-stage breast cancer.
Liu J, Zhao H, Huang Y, Xu S, Zhou Y, Zhang W, Li J, Ming Y, Wang X, Zhao S, Li K, Dong X, Ma Y, Qian T, Chen X, Xing Z, Zhang Y, Chen H, Liu Z, Pang D, Zhou M, Wu Z, Wang X, Wang X, Wu N, Su J. Liu J, et al. Among authors: zhao s. Mol Cancer. 2021 Feb 19;20(1):36. doi: 10.1186/s12943-021-01330-w. Mol Cancer. 2021. PMID: 33608029 Free PMC article.
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine.
Zhao S, Zhao H, Zhao L, Cheng X, Zheng Z, Wu M, Wen W, Wang S, Zhou Z, Xie H, Ruan D, Li Q, Liu X, Ou C, Li G, Zhao Z, Chen G, Niu Y, Yin X, Hu Y, Zhang X; Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study; Liu P, Qiu G, Liu W, Zhao C, Wu Z, Zhang J, Wu N. Zhao S, et al. Nat Commun. 2024 Feb 6;15(1):1125. doi: 10.1038/s41467-024-45442-5. Nat Commun. 2024. PMID: 38321032 Free PMC article.
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: zhao s. 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.
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.
Liu F, Liang C, Li Z, Zhao S, Yuan H, Yao R, Qin Z, Shangguan S, Zhang S, Zou LP, Chen Q, Gao Z, Wen S, Peng J, Yin F, Chen F, Qiu X, Luo J, Xie Y, Lu D, Zhang Y, Xie H, Li G, Zhang TJ, Luan P, Wang H, Cui X, Huang H, Liu R, Sun X, Chen C, Wu N, Wang J, Liu C, Shen Y, Gusella JF, Chen X. Liu F, et al. Among authors: zhao s. Brain. 2023 Aug 1;146(8):3347-3363. doi: 10.1093/brain/awad071. Brain. 2023. PMID: 36869767
249 results