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Results by year

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

Year Number of Results
1928 1
1929 1
1932 1
1939 1
1945 1
1946 4
1947 1
1948 1
1950 1
1951 1
1952 5
1953 5
1954 3
1955 1
1956 3
1957 1
1958 6
1959 1
1960 4
1961 5
1962 5
1963 7
1964 11
1965 12
1966 8
1967 8
1968 13
1969 11
1970 12
1971 18
1972 23
1973 15
1974 14
1975 26
1976 20
1977 21
1978 21
1979 26
1980 35
1981 44
1982 40
1983 44
1984 46
1985 52
1986 59
1987 65
1988 65
1989 71
1990 79
1991 61
1992 77
1993 75
1994 93
1995 91
1996 96
1997 91
1998 79
1999 95
2000 108
2001 80
2002 97
2003 89
2004 113
2005 92
2006 122
2007 123
2008 135
2009 142
2010 158
2011 210
2012 222
2013 228
2014 258
2015 249
2016 302
2017 241
2018 233
2019 216
2020 239
2021 266
2022 243
2023 239
2024 165

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5,681 results

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Page 1
The phenotypic spectrum of SCN2A-related epilepsy.
Reynolds C, King MD, Gorman KM. Reynolds C, et al. Among authors: king md. Eur J Paediatr Neurol. 2020 Jan;24:117-122. doi: 10.1016/j.ejpn.2019.12.016. Epub 2019 Dec 12. Eur J Paediatr Neurol. 2020. PMID: 31924505 Review.
Characterization of splice-altering mutations in inherited predisposition to cancer.
Casadei S, Gulsuner S, Shirts BH, Mandell JB, Kortbawi HM, Norquist BS, Swisher EM, Lee MK, Goldberg Y, O'Connor R, Tan Z, Pritchard CC, King MC, Walsh T. Casadei S, et al. Among authors: king mc. Proc Natl Acad Sci U S A. 2019 Dec 26;116(52):26798-26807. doi: 10.1073/pnas.1915608116. Epub 2019 Dec 16. Proc Natl Acad Sci U S A. 2019. PMID: 31843900 Free PMC article.
Targeted long-read sequencing identifies missing disease-causing variation.
Miller DE, Sulovari A, Wang T, Loucks H, Hoekzema K, Munson KM, Lewis AP, Fuerte EPA, Paschal CR, Walsh T, Thies J, Bennett JT, Glass I, Dipple KM, Patterson K, Bonkowski ES, Nelson Z, Squire A, Sikes M, Beckman E, Bennett RL, Earl D, Lee W, Allikmets R, Perlman SJ, Chow P, Hing AV, Wenger TL, Adam MP, Sun A, Lam C, Chang I, Zou X, Austin SL, Huggins E, Safi A, Iyengar AK, Reddy TE, Majoros WH, Allen AS, Crawford GE, Kishnani PS; University of Washington Center for Mendelian Genomics; King MC, Cherry T, Chong JX, Bamshad MJ, Nickerson DA, Mefford HC, Doherty D, Eichler EE. Miller DE, et al. Among authors: king mc. Am J Hum Genet. 2021 Aug 5;108(8):1436-1449. doi: 10.1016/j.ajhg.2021.06.006. Epub 2021 Jul 2. Am J Hum Genet. 2021. PMID: 34216551 Free PMC article.
Maintenance or Discontinuation of Antidepressants in Primary Care.
Lewis G, Marston L, Duffy L, Freemantle N, Gilbody S, Hunter R, Kendrick T, Kessler D, Mangin D, King M, Lanham P, Moore M, Nazareth I, Wiles N, Bacon F, Bird M, Brabyn S, Burns A, Clarke CS, Hunt A, Pervin J, Lewis G. Lewis G, et al. Among authors: king m. N Engl J Med. 2021 Sep 30;385(14):1257-1267. doi: 10.1056/NEJMoa2106356. N Engl J Med. 2021. PMID: 34587384 Clinical Trial.
How is quality of life defined and assessed in published research?
Costa DSJ, Mercieca-Bebber R, Rutherford C, Tait MA, King MT. Costa DSJ, et al. Among authors: king mt. Qual Life Res. 2021 Aug;30(8):2109-2121. doi: 10.1007/s11136-021-02826-0. Epub 2021 Apr 1. Qual Life Res. 2021. PMID: 33792834 Review.
The Molecular Mechanism of Transport by the Mitochondrial ADP/ATP Carrier.
Ruprecht JJ, King MS, Zögg T, Aleksandrova AA, Pardon E, Crichton PG, Steyaert J, Kunji ERS. Ruprecht JJ, et al. Among authors: king ms. Cell. 2019 Jan 24;176(3):435-447.e15. doi: 10.1016/j.cell.2018.11.025. Epub 2019 Jan 2. Cell. 2019. PMID: 30611538 Free PMC article.
NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Al Shehhi M, Forman EB, Fitzgerald JE, McInerney V, Krawczyk J, Shen S, Betts DR, Ardle LM, Gorman KM, King MD, Green A, Gallagher L, Lynch SA. Al Shehhi M, et al. Among authors: king md. Eur J Med Genet. 2019 Mar;62(3):204-209. doi: 10.1016/j.ejmg.2018.07.015. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031152
5,681 results