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

Year Number of Results
1946 2
1947 1
1954 1
1956 1
1957 5
1958 1
1959 2
1960 5
1962 1
1963 1
1964 1
1966 1
1968 4
1970 1
1971 1
1972 3
1973 2
1974 1
1975 7
1976 2
1977 5
1978 5
1979 2
1980 5
1981 2
1982 1
1983 7
1984 4
1985 2
1986 6
1987 5
1988 5
1989 11
1990 9
1991 10
1992 6
1993 9
1994 3
1995 8
1996 8
1997 11
1998 5
1999 5
2000 8
2001 8
2002 6
2003 6
2004 8
2005 8
2006 18
2007 16
2008 19
2009 26
2010 21
2011 23
2012 27
2013 24
2014 27
2015 32
2016 35
2017 40
2018 36
2019 35
2020 55
2021 60
2022 67
2023 55
2024 49
2025 51
2026 5

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858 results

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Page 1
The cycling and aging mouse female reproductive tract at single-cell resolution.
Winkler I, Tolkachov A, Lammers F, Lacour P, Daugelaite K, Schneider N, Koch ML, Panten J, Grünschläger F, Poth T, Ávila BM, Schneider A, Haas S, Odom DT, Gonçalves Â. Winkler I, et al. Among authors: schneider n. Cell. 2024 Feb 15;187(4):981-998.e25. doi: 10.1016/j.cell.2024.01.021. Epub 2024 Feb 6. Cell. 2024. PMID: 38325365 Free article.
In Reply.
Schneider NC, Yarris LM, Coates WC. Schneider NC, et al. AEM Educ Train. 2018 Oct 7;2(4):343. doi: 10.1002/aet2.10129. eCollection 2018 Oct. AEM Educ Train. 2018. PMID: 30386847 Free PMC article. No abstract available.
RetiGene, a comprehensive gene atlas for inherited retinal diseases.
Rivolta C, Celik E, Kamdar D, Cancellieri F, Kaminska K, Ullah M, Barberán-Martínez P, Bouckaert M, Cortón M, Delanote E, Fernández-Caballero L, García García G, Holtes LK, Karali M, Lopez I, Peter VG, Schneider N, Vincke L, Ayuso C, Banfi S, Bocquet B, Coppieters F, Cremers FPM, Inglehearn CF, Iwata T, Kalatzis V, Koenekoop RK, Millán JM, Sharon D, Toomes C, Quinodoz M. Rivolta C, et al. Among authors: schneider n. Am J Hum Genet. 2025 Oct 2;112(10):2253-2265. doi: 10.1016/j.ajhg.2025.08.017. Epub 2025 Sep 16. Am J Hum Genet. 2025. PMID: 40961941 Free article. Review.
Four Core Genotypes mice harbour a 3.2MB X-Y translocation that perturbs Tlr7 dosage.
Panten J, Del Prete S, Cleland JP, Saunders LM, van Riet J, Schneider A, Ginno P, Schneider N, Koch ML, Chen X, Gerstung M, Stegle O, Arnold AP, Turner JMA, Heard E, Odom DT. Panten J, et al. Among authors: schneider n. Nat Commun. 2024 Oct 11;15(1):8814. doi: 10.1038/s41467-024-52640-8. Nat Commun. 2024. PMID: 39394207 Free PMC article.
Artificial intelligence in chemistry and drug design.
Brown N, Ertl P, Lewis R, Luksch T, Reker D, Schneider N. Brown N, et al. Among authors: schneider n. J Comput Aided Mol Des. 2020 Jul;34(7):709-715. doi: 10.1007/s10822-020-00317-x. J Comput Aided Mol Des. 2020. PMID: 32468207 No abstract available.
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Chen S, Abou-Khalil BW, Afawi Z, Ali QZ, Amadori E, Anderson A, Anderson J, Andrade DM, Annesi G, Arslan M, Auce P, Bahlo M, Baker MD, Balagura G, Balestrini S, Banks E, Barba C, Barboza K, Bartolomei F, Bass N, Baum LW, Baumgartner TH, Baykan B, Bebek N, Becker F, Bennett CA, Beydoun A, Bianchini C, Bisulli F, Blackwood D, Blatt I, Borggräfe I, Bosselmann C, Braatz V, Brand H, Brockmann K, Buono RJ, Busch RM, Caglayan SH, Canafoglia L, Canavati C, Castellotti B, Cavalleri GL, Cerrato F, Chassoux F, Cherian C, Cherny SS, Cheung CL, Chou IJ, Chung SK, Churchhouse C, Ciullo V, Clark PO, Cole AJ, Cosico M, Cossette P, Cotsapas C, Cusick C, Daly MJ, Davis LK, Jonghe P, Delanty N, Dennig D, Depondt C, Derambure P, Devinsky O, Di Vito L, Dickerson F, Dlugos DJ, Doccini V, Doherty CP, El-Naggar H, Ellis CA, Epstein L, Evans M, Faucon A, Feng YA, Ferguson L, Ferraro TN, Da Silva IF, Ferri L, Feucht M, Fields MC, Fitzgerald M, Fonferko-Shadrach B, Fortunato F, Franceschetti S, French JA, Freri E, Fu JM, Gabriel S, Gagliardi M, Gambardella A, Gauthier L, Giangregorio T, Gili T, Glauser TA, Goldberg E, Goldman A, Goldstein DB, Granata T, Grant R, Greenberg DA, Guerrini R, Gundogdu-Eken A, Gu… See abstract for full author list ➔ Chen S, et al. Among authors: schneider n. medRxiv [Preprint]. 2024 Sep 20:2023.02.22.23286310. doi: 10.1101/2023.02.22.23286310. medRxiv. 2024. Update in: Nat Neurosci. 2024 Oct;27(10):1864-1879. doi: 10.1038/s41593-024-01747-8. PMID: 36865150 Free PMC article. Updated. Preprint.
858 results