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Results by year

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

Year Number of Results
1976 4
1977 4
1978 3
1979 3
1980 1
1981 2
1982 2
1983 6
1984 1
1985 4
1986 2
1987 1
1988 5
1989 1
1991 1
1992 2
1993 3
1994 2
1995 2
1996 3
1997 3
1998 1
1999 1
2000 4
2001 1
2002 3
2003 1
2004 3
2005 3
2006 4
2007 12
2008 7
2009 14
2010 9
2011 4
2012 7
2013 9
2014 7
2015 15
2016 9
2017 7
2018 12
2019 7
2020 12
2021 12
2022 7
2023 10
2024 8

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Search Results

216 results

Results by year

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Page 1
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Liu JZ, van Sommeren S, Huang H, Ng SC, Alberts R, Takahashi A, Ripke S, Lee JC, Jostins L, Shah T, Abedian S, Cheon JH, Cho J, Dayani NE, Franke L, Fuyuno Y, Hart A, Juyal RC, Juyal G, Kim WH, Morris AP, Poustchi H, Newman WG, Midha V, Orchard TR, Vahedi H, Sood A, Sung JY, Malekzadeh R, Westra HJ, Yamazaki K, Yang SK; International Multiple Sclerosis Genetics Consortium; International IBD Genetics Consortium; Barrett JC, Alizadeh BZ, Parkes M, Bk T, Daly MJ, Kubo M, Anderson CA, Weersma RK. Liu JZ, et al. Nat Genet. 2015 Sep;47(9):979-986. doi: 10.1038/ng.3359. Epub 2015 Jul 20. Nat Genet. 2015. PMID: 26192919 Free PMC article.
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis.
Akhlaghpour M, Haritunians T, More SK, Thomas LS, Stamps DT, Dube S, Li D, Yang S, Landers CJ, Mengesha E, Hamade H, Murali R, Potdar AA, Wolf AJ, Botwin GJ, Khrom M; International IBD Genetics Consortium; Ananthakrishnan AN, Faubion WA, Jabri B, Lira SA, Newberry RD, Sandler RS, Sartor RB, Xavier RJ, Brant SR, Cho JH, Duerr RH, Lazarev MG, Rioux JD, Schumm LP, Silverberg MS, Zaghiyan K, Fleshner P, Melmed GY, Vasiliauskas EA, Ha C, Rabizadeh S, Syal G, Bonthala NN, Ziring DA, Targan SR, Long MD, McGovern DPB, Michelsen KS. Akhlaghpour M, et al. Gut. 2023 Nov;72(11):2068-2080. doi: 10.1136/gutjnl-2023-329689. Epub 2023 Apr 20. Gut. 2023. PMID: 37080587 Free article.
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study.
Cleynen I, Boucher G, Jostins L, Schumm LP, Zeissig S, Ahmad T, Andersen V, Andrews JM, Annese V, Brand S, Brant SR, Cho JH, Daly MJ, Dubinsky M, Duerr RH, Ferguson LR, Franke A, Gearry RB, Goyette P, Hakonarson H, Halfvarson J, Hov JR, Huang H, Kennedy NA, Kupcinskas L, Lawrance IC, Lee JC, Satsangi J, Schreiber S, Théâtre E, van der Meulen-de Jong AE, Weersma RK, Wilson DC; International Inflammatory Bowel Disease Genetics Consortium; Parkes M, Vermeire S, Rioux JD, Mansfield J, Silverberg MS, Radford-Smith G, McGovern DP, Barrett JC, Lees CW. Cleynen I, et al. Lancet. 2016 Jan 9;387(10014):156-67. doi: 10.1016/S0140-6736(15)00465-1. Epub 2015 Oct 18. Lancet. 2016. PMID: 26490195 Free PMC article.
Editor's Choice - Early Outcomes of a Novel Off the Shelf Preloaded Inner Branch Endograft for the Treatment of Complex Aortic Pathologies in the ItaliaN Branched Registry of E-nside EnDograft (INBREED).
Piazza M, Squizzato F, Pratesi G, Tshomba Y, Gaggiano A, Gatta E, Simonte G, Piffaretti G, Frigatti P, Veraldi GF, Silingardi R, Antonello M; INBREED Investigators. Piazza M, et al. Eur J Vasc Endovasc Surg. 2023 Jun;65(6):811-817. doi: 10.1016/j.ejvs.2023.02.076. Epub 2023 Mar 3. Eur J Vasc Endovasc Surg. 2023. PMID: 36871927 Free article.
MiR-216a: a link between endothelial dysfunction and autophagy.
Menghini R, Casagrande V, Marino A, Marchetti V, Cardellini M, Stoehr R, Rizza S, Martelli E, Greco S, Mauriello A, Ippoliti A, Martelli F, Lauro R, Federici M. Menghini R, et al. Among authors: ippoliti a. Cell Death Dis. 2014 Jan 30;5(1):e1029. doi: 10.1038/cddis.2013.556. Cell Death Dis. 2014. PMID: 24481443 Free PMC article.
C-peptide: A predictor of cardiovascular mortality in subjects with established atherosclerotic disease.
Cardellini M, Farcomeni A, Ballanti M, Morelli M, Davato F, Cardolini I, Grappasonni G, Rizza S, Guglielmi V, Porzio O, Pecchioli C, Menghini R, Ippoliti A, Federici M. Cardellini M, et al. Among authors: ippoliti a. Diab Vasc Dis Res. 2017 Sep;14(5):395-399. doi: 10.1177/1479164117710446. Epub 2017 May 31. Diab Vasc Dis Res. 2017. PMID: 28565926 Free article.
A Rare but Fatal Behçet Variant: The Hughes-Stovin Syndrome-Successful Case Report and New Evidence from Literature Review.
Ascoli Marchetti A, Belvivere L, Argirò R, Kroegler B, Oddi FM, Pennetta F, Giorgi A, Fazzini S, Morosetti D, Triggianese P, Greco E, D'Antonio A, Coccia I, Tesauro M, Sangiuolo F, Ippoliti A. Ascoli Marchetti A, et al. Among authors: ippoliti a. Aorta (Stamford). 2023 Aug;11(4):156-161. doi: 10.1055/s-0043-1777994. Epub 2024 Mar 26. Aorta (Stamford). 2023. PMID: 38531384 Free PMC article.
Thoracic Aneurysm Sac Endoleak. Not Only a Risk of Rupture.
Ascoli Marchetti A, Pompeo E, Ippoliti A. Ascoli Marchetti A, et al. Among authors: ippoliti a. Ann Vasc Surg. 2019 Apr;56:360-361. doi: 10.1016/j.avsg.2018.11.003. Epub 2018 Nov 23. Ann Vasc Surg. 2019. PMID: 30476596 No abstract available.
Endovascular Reconstruction for Total Aorto-Iliac Occlusion.
Piffaretti G, Fargion AT, Dorigo W, Pulli R, Ferri M, Antonello M, Bellosta R, Veraldi G, Benedetto F, Gargiulo M, Pratesi C; ILIACS Registry Group. Piffaretti G, et al. J Endovasc Ther. 2022 Aug;29(4):565-575. doi: 10.1177/15266028211059908. Epub 2021 Dec 1. J Endovasc Ther. 2022. PMID: 35112596
216 results