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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 34
2025 53
2026 19

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556 results

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Page 1
Did you mean trong a[au] (1 results)?
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.
Advancing precision care in pregnancy through a treatable fetal findings list.
Cohen JL, Duyzend M, Adelson SM, Yeo J, Fleming M, Ganetzky R, Hale R, Mitchell DM, Morton SU, Reimers R, Roberts A, Strong A, Tan W, Thiagarajah JR, Walker MA, Green RC, Gold NB. Cohen JL, et al. Among authors: strong a. Am J Hum Genet. 2025 Jun 5;112(6):1251-1269. doi: 10.1016/j.ajhg.2025.03.011. Epub 2025 Apr 9. Am J Hum Genet. 2025. PMID: 40209713 Free PMC article. Review.
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants.
Saeidian AH, March ME, Youssefian L, Watson DJ, Bhandari E, Wang X, Zhao X, Owen NM, Strong A, Harr MH; CAG Secondary Finding Consortium; Bhoj E, Zackai E, Vahidnezhad H, Gudjonsson JE, Cederbaum SD, Deignan JL, Glessner J, Grody WW, Hakonarson H. Saeidian AH, et al. Among authors: strong a. Genet Med. 2024 Nov;26(11):101225. doi: 10.1016/j.gim.2024.101225. Epub 2024 Jul 31. Genet Med. 2024. PMID: 39096151 Free article.
2024 Canadian Surgery Forum: Sept. 25-28, 2024.
Li C, Guo M, Karimuddin A, Guo M, Li C, Karimuddin A, Sutherland J, Huo B, McKechnie T, Ortenzi M, Lee Y, Antoniou S, Mayol J, Ahmed H, Boudreau V, Ramji K, Eskicioglu C, de Jager P, Urbach D, Poole M, Abbad A, Al-Shamali H, Al-Faraj Z, Wen C, Pescarus R, Bechara R, Hong D, Park LJ, Marcucci M, Ofori S, Bogach J, Serrano PE, Simunovic M, Yang I, Cadeddu M, Marcaccio MJ, Borges FK, Nenshi R, Devereaux PJ, Urbanellis P, Douglas J, Nemeth E, Ellsmere J, Spence R, Cunningham J, Falk R, Skinner T, Ebert N, Galbraith L, Prins M, Joharifard S, Joos E, Orovec A, Lethbridge L, Spence R, Hoogerboord M, Stuart H, Bergeron AM, Yang I, Bogach J, Nguyen L, Reade C, Eiriksson L, Morais M, Hanley G, Mah S, Brar K, Seymour KA, Eckhouse SR, Sudan R, Greenberg JA, Portenier D, Jung JJ, Light A, Dingley B, Delisle M, Apte S, Mallick R, Hamilton T, Stuart H, Talbot M, McKinnon G, Jost E, Thiboutot E, Nessim C, Katote N, Drohan A, Spence R, Neumann K, Shi G, Leung R, Lim C, Van Oirschot M, Grant A, Knowles S, Van Koughnett JA, Brousseau K, Monette L, McIsaac D, Wherrett C, Mallick R, Workneh A, Ramsay T, Tinmouth A, Shaw J, Carrier FM, Fergusson D, Martel G, Cornacchia M, Ivankovic V, Mamalchi SA, Choi… See abstract for full author list ➔ Li C, et al. Among authors: strong a. Can J Surg. 2024 Nov 28;67(6suppl2):S77-S108. doi: 10.1503/cjs.012624. Print 2024 Nov-Dec. Can J Surg. 2024. PMID: 39609036 Free PMC article. No abstract available.
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes.
Smal N, Majdoub F, Janssens K, Reyniers E, Meuwissen MEC, Ceulemans B, Northrup H, Hill JB, Liu L, Errichiello E, Gana S, Strong A, Rohena L, Franciskovich R, Murali CN, Huybrechs A, Sulem T, Fridriksdottir R, Sulem P, Stefansson K, Bai Y, Rosenfeld JA, Lalani SR, Streff H; Undiagnosed Diseases Network; Kooy RF, Weckhuysen S. Smal N, et al. Among authors: strong a. Eur J Hum Genet. 2024 Nov;32(11):1378-1386. doi: 10.1038/s41431-024-01661-4. Epub 2024 Jul 4. Eur J Hum Genet. 2024. PMID: 38965372 Free PMC article.
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome.
Strong A, March ME, Cardinale CJ, Liu Y, Battig MR, Finoti LS, Matsuoka LS, Watson D, Sridhar S, Jarrett JF, Cannon I, Li D, Bhoj E, Zackai EH, Rand EB, Wenger T, Lerman BB, Shikany A, Weaver KN, Hakonarson H. Strong A, et al. Genet Med. 2024 Oct;26(10):101222. doi: 10.1016/j.gim.2024.101222. Epub 2024 Jul 20. Genet Med. 2024. PMID: 39045790 Free PMC article.
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.
556 results