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

Year Number of Results
1799 1
1848 1
1854 1
1858 1
1885 1
1888 1
1889 2
1890 2
1893 1
1895 1
1896 1
1898 1
1901 2
1902 1
1903 5
1904 9
1905 9
1906 3
1907 4
1908 2
1909 2
1910 11
1911 12
1912 4
1913 9
1914 8
1915 13
1916 8
1917 4
1918 10
1919 13
1920 11
1921 8
1922 8
1923 15
1924 5
1925 5
1926 14
1927 9
1928 12
1929 10
1930 15
1931 11
1932 25
1933 21
1934 14
1935 18
1936 10
1937 5
1938 8
1939 4
1940 1
1941 8
1942 12
1943 7
1944 11
1945 13
1946 12
1947 13
1948 22
1949 15
1950 23
1951 35
1952 58
1953 41
1954 26
1955 14
1956 30
1957 32
1958 38
1959 53
1960 48
1961 48
1962 65
1963 64
1964 102
1965 72
1966 45
1967 69
1968 79
1969 85
1970 80
1971 84
1972 73
1973 104
1974 107
1975 250
1976 244
1977 243
1978 275
1979 273
1980 319
1981 351
1982 396
1983 507
1984 587
1985 739
1986 888
1987 1689
1988 3066
1989 3285
1990 3683
1991 3792
1992 3862
1993 4267
1994 4411
1995 4739
1996 5084
1997 5254
1998 5270
1999 5845
2000 6850
2001 8054
2002 8875
2003 9834
2004 11338
2005 13112
2006 14460
2007 15771
2008 17524
2009 18733
2010 20325
2011 22514
2012 25724
2013 29127
2014 36405
2015 42569
2016 46329
2017 49431
2018 54608
2019 59244
2020 69172
2021 38974
2022 2
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Search Results

613,395 results
Results by year
Filters applied: . Clear all The following term was not found in PubMed: Shangqian
Page 1
Did you mean shangin ma (1 results)?
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
Guo H, Wang T, Wu H, Long M, Coe BP, Li H, Xun G, Ou J, Chen B, Duan G, Bai T, Zhao N, Shen Y, Li Y, Wang Y, Zhang Y, Baker C, Liu Y, Pang N, Huang L, Han L, Jia X, Liu C, Ni H, Yang X, Xia L, Chen J, Shen L, Li Y, Zhao R, Zhao W, Peng J, Pan Q, Long Z, Su W, Tan J, Du X, Ke X, Yao M, Hu Z, Zou X, Zhao J, Bernier RA, Eichler EE, Xia K. Guo H, et al. Mol Autism. 2018 Dec 13;9:64. doi: 10.1186/s13229-018-0247-z. eCollection 2018. Mol Autism. 2018. PMID: 30564305 Free PMC article.
Prospective investigation of FOXP1 syndrome.
Siper PM, De Rubeis S, Trelles MDP, Durkin A, Di Marino D, Muratet F, Frank Y, Lozano R, Eichler EE, Kelly M, Beighley J, Gerdts J, Wallace AS, Mefford HC, Bernier RA, Kolevzon A, Buxbaum JD. Siper PM, et al. Mol Autism. 2017 Oct 24;8:57. doi: 10.1186/s13229-017-0172-6. eCollection 2017. Mol Autism. 2017. PMID: 29090079 Free PMC article.
Autism prevalence in China is comparable to Western prevalence.
Sun X, Allison C, Wei L, Matthews FE, Auyeung B, Wu YY, Griffiths S, Zhang J, Baron-Cohen S, Brayne C. Sun X, et al. Mol Autism. 2019 Feb 28;10:7. doi: 10.1186/s13229-018-0246-0. eCollection 2019. Mol Autism. 2019. PMID: 30858963 Free PMC article.
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.
Earl RK, Turner TN, Mefford HC, Hudac CM, Gerdts J, Eichler EE, Bernier RA. Earl RK, et al. Mol Autism. 2017 Oct 5;8:54. doi: 10.1186/s13229-017-0173-5. eCollection 2017. Mol Autism. 2017. PMID: 29034068 Free PMC article.
Savant syndrome has a distinct psychological profile in autism.
Hughes JEA, Ward J, Gruffydd E, Baron-Cohen S, Smith P, Allison C, Simner J. Hughes JEA, et al. Mol Autism. 2018 Oct 12;9:53. doi: 10.1186/s13229-018-0237-1. eCollection 2018. Mol Autism. 2018. PMID: 30344992 Free PMC article.
613,395 results
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