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

Year Number of Results
1936 1
1940 2
1945 1
1946 1
1948 1
1949 1
1950 3
1951 2
1952 5
1953 5
1954 2
1955 4
1956 3
1957 7
1958 6
1959 3
1960 6
1961 4
1962 5
1963 5
1964 1
1965 5
1966 1
1967 4
1968 3
1969 4
1970 5
1971 3
1972 5
1973 5
1974 5
1975 9
1976 6
1977 8
1978 10
1979 4
1980 7
1981 7
1982 2
1983 3
1984 9
1985 3
1986 9
1987 8
1988 10
1989 4
1990 6
1991 5
1992 13
1993 15
1994 15
1995 20
1996 24
1997 31
1998 32
1999 29
2000 32
2001 45
2002 43
2003 48
2004 65
2005 63
2006 85
2007 115
2008 126
2009 184
2010 219
2011 283
2012 314
2013 327
2014 412
2015 454
2016 533
2017 580
2018 683
2019 764
2020 909
2021 985
2022 1173
2023 1185
2024 1220
2025 6

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10,114 results

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Page 1
Synaptic, transcriptional and chromatin genes disrupted in autism.
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimäki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK; DDD Study; Homozygosity Mapping Collaborative for Autism; UK10K Consortium; Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD. De Rubeis S, et al. Among authors: yu tw. Nature. 2014 Nov 13;515(7526):209-15. doi: 10.1038/nature13772. Epub 2014 Oct 29. Nature. 2014. PMID: 25363760 Free PMC article.
Reply.
Yen FS, Yu TS, Hsu CC, Hwu CM. Yen FS, et al. Among authors: yu ts. Clin Gastroenterol Hepatol. 2024 May;22(5):1143-1144.e1. doi: 10.1016/j.cgh.2023.09.017. Epub 2023 Sep 22. Clin Gastroenterol Hepatol. 2024. PMID: 37741301 No abstract available.
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Ceyhan-Birsoy O, Murry JB, Machini K, Lebo MS, Yu TW, Fayer S, Genetti CA, Schwartz TS, Agrawal PB, Parad RB, Holm IA, McGuire AL, Green RC, Rehm HL, Beggs AH; BabySeq Project Team. Ceyhan-Birsoy O, et al. Among authors: yu tw. Am J Hum Genet. 2019 Jan 3;104(1):76-93. doi: 10.1016/j.ajhg.2018.11.016. Am J Hum Genet. 2019. PMID: 30609409 Free PMC article.
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2.
Lai A, Soucy A, El Achkar CM, Barkovich AJ, Cao Y, DiStefano M, Evenson M, Guerrini R, Knight D, Lee YS, Mefford HC, Miller DT, Mirzaa G, Mochida G, Rodan LH, Patel M, Smith L, Spencer S, Walsh CA, Yang E, Yuskaitis CJ, Yu T, Poduri A; ClinGen Brain Malformation Variant Curation Expert Panel. Lai A, et al. Among authors: yu t. Genet Med. 2022 Nov;24(11):2240-2248. doi: 10.1016/j.gim.2022.07.020. Epub 2022 Aug 23. Genet Med. 2022. PMID: 35997716 Free PMC article.
Decoding and reconstructing disease relations between dry eye and depression: a multimodal investigation comprising meta-analysis, genetic pathways and Mendelian randomization.
Chang KJ, Wu HY, Chiang PH, Hsu YT, Weng PY, Yu TH, Li CY, Chen YH, Dai HJ, Tsai HY, Chang YJ, Wu YR, Yang YP, Li CT, Hsu CC, Chen SJ, Chen YC, Cheng CY, Hsieh AR, Chiou SH. Chang KJ, et al. Among authors: yu th. J Adv Res. 2024 Mar 27:S2090-1232(24)00115-2. doi: 10.1016/j.jare.2024.03.015. Online ahead of print. J Adv Res. 2024. PMID: 38548265 Free article.
10,114 results
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