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Results by year

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

Year Number of Results
1874 2
1886 1
1888 2
1889 1
1929 1
1967 2
1968 1
1970 2
1971 3
1972 2
1973 1
1974 1
1976 5
1977 9
1978 5
1979 2
1980 1
1981 4
1982 4
1983 6
1984 3
1985 5
1986 2
1987 3
1988 4
1989 1
1990 4
1991 7
1992 2
1993 3
1994 5
1995 4
1996 3
1997 1
1998 3
1999 3
2000 9
2001 4
2002 7
2003 4
2004 4
2005 8
2006 10
2007 5
2008 11
2009 14
2010 12
2011 10
2012 12
2013 14
2014 20
2015 18
2016 30
2017 41
2018 39
2019 25
2020 32
2021 44
2022 23
2023 30
2024 19

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Article type

Publication date

Search Results

486 results

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Page 1
Evolutionary routes and KRAS dosage define pancreatic cancer phenotypes.
Mueller S, Engleitner T, Maresch R, Zukowska M, Lange S, Kaltenbacher T, Konukiewitz B, Öllinger R, Zwiebel M, Strong A, Yen HY, Banerjee R, Louzada S, Fu B, Seidler B, Götzfried J, Schuck K, Hassan Z, Arbeiter A, Schönhuber N, Klein S, Veltkamp C, Friedrich M, Rad L, Barenboim M, Ziegenhain C, Hess J, Dovey OM, Eser S, Parekh S, Constantino-Casas F, de la Rosa J, Sierra MI, Fraga M, Mayerle J, Klöppel G, Cadiñanos J, Liu P, Vassiliou G, Weichert W, Steiger K, Enard W, Schmid RM, Yang F, Unger K, Schneider G, Varela I, Bradley A, Saur D, Rad R. Mueller S, et al. Among authors: strong a. Nature. 2018 Feb 1;554(7690):62-68. doi: 10.1038/nature25459. Epub 2018 Jan 24. Nature. 2018. PMID: 29364867 Free PMC article.
TOPORS as a novel causal gene for Joubert syndrome.
Strong A, Qu HQ, Cullina S, McManus ML, Zackai EH, Glessner J, Kenny EE, Hakonarson H. Strong A, et al. Am J Med Genet A. 2023 Aug;191(8):2156-2163. doi: 10.1002/ajmg.a.63303. Epub 2023 May 25. Am J Med Genet A. 2023. PMID: 37227088
A History of Flexible Gastrointestinal Endoscopy.
Ponsky JL, Strong AT. Ponsky JL, et al. Among authors: strong at. Surg Clin North Am. 2020 Dec;100(6):971-992. doi: 10.1016/j.suc.2020.08.013. Surg Clin North Am. 2020. PMID: 33128891 Review.
Genome editing in cardiovascular diseases.
Strong A, Musunuru K. Strong A, et al. Nat Rev Cardiol. 2017 Jan;14(1):11-20. doi: 10.1038/nrcardio.2016.139. Epub 2016 Sep 9. Nat Rev Cardiol. 2017. PMID: 27609628 Review.
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature.
Strong A, Rao S, von Hardenberg S, Li D, Cox LL, Lee PC, Zhang LQ, Awotoye W, Diamond T, Gold J, Gooch C, Gowans LJJ, Hakonarson H, Hing A, Loomes K, Martin N, Marazita ML, Mononen T, Piccoli D, Pfundt R, Raskin S, Scherer SW, Sobriera N, Vaccaro C, Wang X, Watson D, Weksberg R, Bhoj E, Murray JC, Lidral AC, Butali A, Buckley MF, Roscioli T, Koolen DA, Seaver LH, Prows CA, Stottmann RW, Cox TC. Strong A, et al. Am J Med Genet A. 2023 May;191(5):1227-1239. doi: 10.1002/ajmg.a.63130. Epub 2023 Feb 7. Am J Med Genet A. 2023. PMID: 36751037 Free PMC article.
Flexor Tendon Rupture Secondary to Gout.
Lynn JV, Strong AL, Chung KC. Lynn JV, et al. Among authors: strong al. Arch Plast Surg. 2023 Oct 5;50(5):492-495. doi: 10.1055/s-0043-1772756. eCollection 2023 Sep. Arch Plast Surg. 2023. PMID: 37808337 Free PMC article.
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
Brunet T, Zott B, Lieftüchter V, Lenz D, Schmidt A, Peters P, Kopajtich R, Zaddach M, Zimmermann H, Hüning I, Ballhausen D, Staufner C, Bianzano A, Hughes J, Taylor RW, McFarland R, Devlin A, Mihaljević M, Barišić N, Rohlfs M, Wilfling S, Sondheimer N, Hewson S, Marinakis NM, Kosma K, Traeger-Synodinos J, Elbracht M, Begemann M, Trepels-Kottek S, Hasan D, Scala M, Capra V, Zara F, van der Ven AT, Driemeyer J, Apitz C, Krämer J, Strong A, Hakonarson H, Watson D, Mayr JA, Prokisch H, Meitinger T, Borggraefe I, Spiegler J, Baric I, Paolini M, Gerstl L, Wagner M. Brunet T, et al. Among authors: strong a. Genet Med. 2024 Feb;26(2):101013. doi: 10.1016/j.gim.2023.101013. Epub 2023 Nov 1. Genet Med. 2024. PMID: 37924258
Ocular manifestations of ectodermal dysplasia.
Landau Prat D, Katowitz WR, Strong A, Katowitz JA. Landau Prat D, et al. Among authors: strong a. Orphanet J Rare Dis. 2021 May 1;16(1):197. doi: 10.1186/s13023-021-01824-2. Orphanet J Rare Dis. 2021. PMID: 33933124 Free PMC article.
486 results