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

Year Number of Results
2002 2
2003 3
2004 3
2007 2
2008 2
2009 3
2010 2
2011 2
2012 3
2013 9
2014 10
2015 8
2016 11
2017 20
2018 26
2019 32
2020 9
2021 11
2022 14
2023 12
2024 7

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172 results

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Page 1
Vitamin C epigenetically controls osteogenesis and bone mineralization.
Thaler R, Khani F, Sturmlechner I, Dehghani SS, Denbeigh JM, Zhou X, Pichurin O, Dudakovic A, Jerez SS, Zhong J, Lee JH, Natarajan R, Kalajzic I, Jiang YH, Deyle DR, Paschalis EP, Misof BM, Ordog T, van Wijnen AJ. Thaler R, et al. Among authors: jiang yh. Nat Commun. 2022 Oct 6;13(1):5883. doi: 10.1038/s41467-022-32915-8. Nat Commun. 2022. PMID: 36202795 Free PMC article.
IRF2BPL Is Associated with Neurological Phenotypes.
Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Graham JM Jr, Ortiz D, Infante E, Steyaert W, Dermaut B, Poppe B, Chung HL, Zuo Z, Lee PT, Kanca O, Xia F, Yang Y, Smith EC, Jasien J, Kansagra S, Spiridigliozzi G, El-Dairi M, Lark R, Riley K, Koeberl DD, Golden-Grant K; Program for Undiagnosed Diseases (UD-PrOZA); Undiagnosed Diseases Network; Yamamoto S, Wangler MF, Mirzaa G, Hemelsoet D, Lee B, Nelson SF, Goldstein DB, Bellen HJ, Pena LDM. Marcogliese PC, et al. Am J Hum Genet. 2018 Aug 2;103(2):245-260. doi: 10.1016/j.ajhg.2018.07.006. Epub 2018 Jul 26. Am J Hum Genet. 2018. PMID: 30057031 Free PMC article.
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Frésard L, Smail C, Ferraro NM, Teran NA, Li X, Smith KS, Bonner D, Kernohan KD, Marwaha S, Zappala Z, Balliu B, Davis JR, Liu B, Prybol CJ, Kohler JN, Zastrow DB, Reuter CM, Fisk DG, Grove ME, Davidson JM, Hartley T, Joshi R, Strober BJ, Utiramerur S; Undiagnosed Diseases Network; Care4Rare Canada Consortium; Lind L, Ingelsson E, Battle A, Bejerano G, Bernstein JA, Ashley EA, Boycott KM, Merker JD, Wheeler MT, Montgomery SB. Frésard L, et al. Nat Med. 2019 Jun;25(6):911-919. doi: 10.1038/s41591-019-0457-8. Epub 2019 Jun 3. Nat Med. 2019. PMID: 31160820 Free PMC article.
Novel epigenetic molecular therapies for imprinting disorders.
Wang SE, Jiang YH. Wang SE, et al. Among authors: jiang yh. Mol Psychiatry. 2023 Aug;28(8):3182-3193. doi: 10.1038/s41380-023-02208-7. Epub 2023 Aug 25. Mol Psychiatry. 2023. PMID: 37626134 Free PMC article. Review.
Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years.
Zhou H, Xu X, Yan W, Zou X, Wu L, Luo X, Li T, Huang Y, Guan H, Chen X, Mao M, Xia K, Zhang L, Li E, Ge X, Zhang L, Li C, Zhang X, Zhou Y, Ding D, Shih A, Fombonne E, Zheng Y, Han J, Sun Z, Jiang YH, Wang Y; LATENT-NHC Study Team. Zhou H, et al. Among authors: jiang yh. Neurosci Bull. 2020 Sep;36(9):961-971. doi: 10.1007/s12264-020-00530-6. Epub 2020 Jun 30. Neurosci Bull. 2020. PMID: 32607739 Free PMC article.
Epigenetic therapy of Prader-Willi syndrome.
Kim Y, Wang SE, Jiang YH. Kim Y, et al. Among authors: jiang yh. Transl Res. 2019 Jun;208:105-118. doi: 10.1016/j.trsl.2019.02.012. Epub 2019 Mar 5. Transl Res. 2019. PMID: 30904443 Free PMC article. Review.
Therapeutic approaches for shankopathies.
Wang X, Bey AL, Chung L, Krystal AD, Jiang YH. Wang X, et al. Among authors: jiang yh. Dev Neurobiol. 2014 Feb;74(2):123-35. doi: 10.1002/dneu.22084. Epub 2013 Oct 11. Dev Neurobiol. 2014. PMID: 23536326 Free PMC article. Review.
Brain-wide electrical dynamics encode individual appetitive social behavior.
Mague SD, Talbot A, Blount C, Walder-Christensen KK, Duffney LJ, Adamson E, Bey AL, Ndubuizu N, Thomas GE, Hughes DN, Grossman Y, Hultman R, Sinha S, Fink AM, Gallagher NM, Fisher RL, Jiang YH, Carlson DE, Dzirasa K. Mague SD, et al. Among authors: jiang yh. Neuron. 2022 May 18;110(10):1728-1741.e7. doi: 10.1016/j.neuron.2022.02.016. Epub 2022 Mar 15. Neuron. 2022. PMID: 35294900 Free PMC article.
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.
Yang-Li D, Fei-Hong L, Hui-Wen Z, Ming-Sheng M, Xiao-Ping L, Li L, Yi W, Qing Z, Yong-Hui J, Chao-Chun Z; PWS Cooperation Group of Rare Diseases Branch of Chinese Pediatric Society; Zhejiang Expert Group for PWS. Yang-Li D, et al. Among authors: yong hui j. Orphanet J Rare Dis. 2022 Jun 13;17(1):221. doi: 10.1186/s13023-022-02302-z. Orphanet J Rare Dis. 2022. PMID: 35698200 Free PMC article. Review.
172 results