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

Year Number of Results
1965 4
1966 3
1968 7
1969 4
1970 10
1971 17
1972 13
1973 12
1974 12
1975 30
1976 24
1977 27
1978 14
1979 18
1980 8
1981 9
1982 15
1983 22
1984 25
1985 29
1986 31
1987 21
1988 40
1989 32
1990 32
1991 33
1992 30
1993 40
1994 35
1995 36
1996 43
1997 59
1998 76
1999 73
2000 107
2001 139
2002 162
2003 151
2004 211
2005 166
2006 213
2007 247
2008 341
2009 329
2010 268
2011 277
2012 251
2013 286
2014 293
2015 510
2016 602
2017 611
2018 609
2019 676
2020 822
2021 978
2022 1165
2023 993
2024 279

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10,002 results

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Page 1
Immune Dysregulation in Autism Spectrum Disorder: What Do We Know about It?
Robinson-Agramonte MLA, Noris García E, Fraga Guerra J, Vega Hurtado Y, Antonucci N, Semprún-Hernández N, Schultz S, Siniscalco D. Robinson-Agramonte MLA, et al. Int J Mol Sci. 2022 Mar 11;23(6):3033. doi: 10.3390/ijms23063033. Int J Mol Sci. 2022. PMID: 35328471 Free PMC article. Review.
Autism spectrum disorder.
Campisi L, Imran N, Nazeer A, Skokauskas N, Azeem MW. Campisi L, et al. Br Med Bull. 2018 Sep 1;127(1):91-100. doi: 10.1093/bmb/ldy026. Br Med Bull. 2018. PMID: 30215678 Review.
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X, Feliciano P, Shu C, Wang T, Astrovskaya I, Hall JB, Obiajulu JU, Wright JR, Murali SC, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey WT, Nishida A, O'Roak BJ, Geschwind DH; SPARK Consortium; Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK. Zhou X, et al. Nat Genet. 2022 Sep;54(9):1305-1319. doi: 10.1038/s41588-022-01148-2. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982159 Free PMC article.
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Fu JM, et al. Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982160 Free PMC article.
10,002 results
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