Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

MyNCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

232 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Multiple common variants for celiac disease influencing immune gene expression.
Dubois PC, Trynka G, Franke L, Hunt KA, Romanos J, Curtotti A, Zhernakova A, Heap GA, Adány R, Aromaa A, Bardella MT, van den Berg LH, Bockett NA, de la Concha EG, Dema B, Fehrmann RS, Fernández-Arquero M, Fiatal S, Grandone E, Green PM, Groen HJ, Gwilliam R, Houwen RH, Hunt SE, Kaukinen K, Kelleher D, Korponay-Szabo I, Kurppa K, MacMathuna P, Mäki M, Mazzilli MC, McCann OT, Mearin ML, Mein CA, Mirza MM, Mistry V, Mora B, Morley KI, Mulder CJ, Murray JA, Núñez C, Oosterom E, Ophoff RA, Polanco I, Peltonen L, Platteel M, Rybak A, Salomaa V, Schweizer JJ, Sperandeo MP, Tack GJ, Turner G, Veldink JH, Verbeek WH, Weersma RK, Wolters VM, Urcelay E, Cukrowska B, Greco L, Neuhausen SL, McManus R, Barisani D, Deloukas P, Barrett JC, Saavalainen P, Wijmenga C, van Heel DA. Dubois PC, et al. Among authors: Grandone E. Nat Genet. 2010 Apr;42(4):295-302. doi: 10.1038/ng.543. Epub 2010 Feb 28. Nat Genet. 2010. PMID: 20190752 Free PMC article.
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.
Zhernakova A, Stahl EA, Trynka G, Raychaudhuri S, Festen EA, Franke L, Westra HJ, Fehrmann RS, Kurreeman FA, Thomson B, Gupta N, Romanos J, McManus R, Ryan AW, Turner G, Brouwer E, Posthumus MD, Remmers EF, Tucci F, Toes R, Grandone E, Mazzilli MC, Rybak A, Cukrowska B, Coenen MJ, Radstake TR, van Riel PL, Li Y, de Bakker PI, Gregersen PK, Worthington J, Siminovitch KA, Klareskog L, Huizinga TW, Wijmenga C, Plenge RM. Zhernakova A, et al. Among authors: Grandone E. PLoS Genet. 2011 Feb;7(2):e1002004. doi: 10.1371/journal.pgen.1002004. Epub 2011 Feb 24. PLoS Genet. 2011. PMID: 21383967 Free PMC article.
Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.
Cotlarciuc I, Marjot T, Khan MS, Hiltunen S, Haapaniemi E, Metso TM, Putaala J, Zuurbier SM, Brouwer MC, Passamonti SM, Bucciarelli P, Pappalardo E, Patel T, Costa P, Colombi M, Canhão P, Tkach A, Santacroce R, Margaglione M, Favuzzi G, Grandone E, Colaizzo D, Spengos K, Arauz A, Hodge A, Ditta R, Debette S, Zedde M, Pare G, Ferro JM, Thijs V, Pezzini A, Majersik JJ, Martinelli I, Coutinho JM, Tatlisumak T, Sharma P; ISGC (International Stroke Genetics Consortium) and BEAST investigators. Cotlarciuc I, et al. Among authors: Grandone E. BMJ Open. 2016 Nov 22;6(11):e012351. doi: 10.1136/bmjopen-2016-012351. BMJ Open. 2016. PMID: 27881526 Free PMC article.
Antithrombotic treatment of splanchnic vein thrombosis: results of an international registry.
Ageno W, Riva N, Schulman S, Bang SM, Sartori MT, Grandone E, Beyer-Westendorf J, Barillari G, Di Minno MN, Dentali F; IRSVT study group. Ageno W, et al. Among authors: Grandone E. Semin Thromb Hemost. 2014 Feb;40(1):99-105. doi: 10.1055/s-0033-1363473. Epub 2013 Dec 31. Semin Thromb Hemost. 2014. PMID: 24381147 Clinical Trial.
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis.
Colaizzo D, Amitrano L, Guardascione MA, Favuzzi G, Tiscia GL, D'Andrea G, Santacroce R, Grandone E, Margaglione M. Colaizzo D, et al. Among authors: Grandone E. Thromb Haemost. 2015 Jun;113(6):1381-2. doi: 10.1160/TH14-12-1055. Epub 2015 Mar 12. Thromb Haemost. 2015. PMID: 25761617 No abstract available.
Fatal pulmonary thromboembolism. A retrospective autopsy study: searching for genetic thrombophilias (Factor V Leiden (G1691A) and FII (G20210A) gene variants) and dating the thrombus.
Fineschi V, Bafunno V, Bello S, De Stefano F, Margaglione M, Neri M, Riezzo I, Turillazzi E, Bonsignore A, Vecchione G, Ventura F, Grandone E. Fineschi V, et al. Among authors: Grandone E. Forensic Sci Int. 2012 Jan 10;214(1-3):152-8. doi: 10.1016/j.forsciint.2011.07.046. Epub 2011 Aug 26. Forensic Sci Int. 2012. PMID: 21871746
Lack of association between genetic variants in the mannose-binding lectin 2 (MBL2) gene and HPV infection.
Parrella P, Seripa D, Matera MG, Rinaldi M, Signori E, Gravina C, Gallo AP, Prencipe M, Grandone E, Mariani L, Cordiali P, Di Carlo A, Stentella P, Pachì A, Fazio VM. Parrella P, et al. Among authors: Grandone E. Eur J Epidemiol. 2007;22(3):159-62. doi: 10.1007/s10654-007-9111-8. Epub 2007 Feb 15. Eur J Epidemiol. 2007. PMID: 17380431
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study.
Aucella F, Margaglione M, Grandone E, Vigilante M, Gatta G, Forcella M, Ktena M, De Min A, Salatino G, Procaccini DA, Stallone C, Gesualdo L; Genetic Polymorphisms in Dialysis Study Group. Aucella F, et al. Among authors: Grandone E. Nephrol Dial Transplant. 2005 Feb;20(2):382-6. doi: 10.1093/ndt/gfh620. Epub 2004 Dec 23. Nephrol Dial Transplant. 2005. PMID: 15618240 Clinical Trial.
232 results
Jump to page
Feedback