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

Year Number of Results
1957 1
1959 2
1960 2
1961 1
1962 3
1963 5
1964 6
1965 2
1966 1
1967 4
1968 1
1969 3
1970 1
1972 1
1973 1
1974 1
1975 3
1976 1
1977 2
1978 3
1979 7
1980 5
1981 11
1982 18
1983 9
1984 13
1985 15
1986 40
1987 32
1988 34
1989 39
1990 34
1991 38
1992 47
1993 55
1994 64
1995 77
1996 105
1997 95
1998 84
1999 96
2000 115
2001 145
2002 190
2003 203
2004 290
2005 354
2006 370
2007 425
2008 473
2009 574
2010 628
2011 776
2012 931
2013 1013
2014 1144
2015 1277
2016 1393
2017 1543
2018 1807
2019 1965
2020 2296
2021 1013
Text availability
Article attribute
Article type
Publication date

Search Results

17,891 results
Results by year
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Page 1
Biological functions of m6A methyltransferases.
Gu J, Zhan Y, Zhuo L, Zhang Q, Li G, Li Q, Qi S, Zhu J, Lv Q, Shen Y, Guo Y, Liu S, Xie T, Sui X. Gu J, et al. Among authors: shen y. Cell Biosci. 2021 Jan 11;11(1):15. doi: 10.1186/s13578-020-00513-0. Cell Biosci. 2021. PMID: 33431045 Free PMC article. Review.
Integrated Molecular Characterization of Fumarate Hydratase-deficient Renal Cell Carcinoma.
Sun G, Zhang X, Liang J, Pan X, Zhu S, Liu Z, Armstrong CM, Chen J, Lin W, Liao B, Lin T, Huang R, Zhang M, Zheng L, Yin X, Nie L, Shen P, Zhao J, Zhang H, Dai J, Shen Y, Li Z, Liu J, Chen J, Liu J, Wang Z, Zhu X, Ni Y, Qin D, Yang L, Chen Y, Wei Q, Li X, Zhou Q, Huang H, Yao J, Chen N, Zeng H. Sun G, et al. Among authors: shen y. Clin Cancer Res. 2021 Mar 15;27(6):1734-1743. doi: 10.1158/1078-0432.CCR-20-3788. Epub 2021 Jan 7. Clin Cancer Res. 2021. PMID: 33414138 Free article.
CNV profiles of Chinese pediatric patients with developmental disorders.
Yuan H, Shangguan S, Li Z, Luo J, Su J, Yao R, Zhang S, Liang C, Chen Q, Gao Z, Zhu Y, Zhang S, Li W, Lu W, Zhang Y, Xie H, Liu F, Wang Q, Lin Y, Liu L, Wang X, Liang L, Zhong J, Li H, Qiu H, Zhang H, Yan M, Mireguli M, Liu Y, Zhang D, Wang H, Lv H, Xie B, Gui C, Cui X, Zou L, Wang J, Gusella JF, Shen Y, Chen X. Yuan H, et al. Among authors: shen y. Genet Med. 2021 Apr;23(4):669-678. doi: 10.1038/s41436-020-01048-y. Epub 2021 Jan 5. Genet Med. 2021. PMID: 33402738
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.
Park J, Lucas AM, Zhang X, Chaudhary K, Cho JH, Nadkarni G, Dobbyn A, Chittoor G, Josyula NS, Katz N, Breeyear JH, Ahmadmehrabi S, Drivas TG, Chavali VRM, Fasolino M, Sawada H, Daugherty A, Li Y, Zhang C, Bradford Y, Weaver J, Verma A, Judy RL, Kember RL, Overton JD, Reid JG, Ferreira MAR, Li AH, Baras A, LeMaire SA, Shen YH, Naji A, Kaestner KH, Vahedi G, Edwards TL, Chen J, Damrauer SM, Justice AE, Do R, Ritchie MD, Rader DJ. Park J, et al. Among authors: shen yh. Nat Med. 2021 Jan;27(1):66-72. doi: 10.1038/s41591-020-1133-8. Epub 2021 Jan 11. Nat Med. 2021. PMID: 33432171
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