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Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group.
Bennett ST, Wilson AJ, Esposito L, Bouzekri N, Undlien DE, Cucca F, Nisticò L, Buzzetti R, Bosi E, Pociot F, Nerup J, Cambon-Thomsen A, Pugliese A, Shield JP, McKinney PA, Bain SC, Polychronakos C, Todd JA. Bennett ST, et al. Among authors: shield jp. Nat Genet. 1997 Nov;17(3):350-2. doi: 10.1038/ng1197-350. Nat Genet. 1997. PMID: 9354805
Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6).
Merriman TR, Eaves IA, Twells RC, Merriman ME, Danoy PA, Muxworthy CE, Hunter KM, Cox RD, Cucca F, McKinney PA, Shield JP, Baum JD, Tuomilehto J, Tuomilehto-Wolf E, Ionesco-Tirgoviste C, Joner G, Thorsby E, Undlien DE, Pociot F, Nerup J, Ronningen KS, Bain SC, Todd JA. Merriman TR, et al. Among authors: shield jp. Hum Mol Genet. 1998 Mar;7(3):517-24. doi: 10.1093/hmg/7.3.517. Hum Mol Genet. 1998. PMID: 9467012
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.
Nakagawa Y, Kawaguchi Y, Twells RC, Muxworthy C, Hunter KM, Wilson A, Merriman ME, Cox RD, Merriman T, Cucca F, McKinney PA, Shield JP, Tuomilehto J, Tuomilehto-Wolf E, Ionesco-Tirgoviste C, Nisticò L, Buzzetti R, Pozzilli P, Joner G, Thorsby E, Undlien DE, Pociot F, Nerup J, Rönningen KS, Bain SC, Todd JA; Bart's-Oxford Family Study Group. Nakagawa Y, et al. Among authors: shield jp. Am J Hum Genet. 1998 Aug;63(2):547-56. doi: 10.1086/301974. Am J Hum Genet. 1998. PMID: 9683605 Free PMC article.
Parameters for reliable results in genetic association studies in common disease.
Dahlman I, Eaves IA, Kosoy R, Morrison VA, Heward J, Gough SC, Allahabadia A, Franklyn JA, Tuomilehto J, Tuomilehto-Wolf E, Cucca F, Guja C, Ionescu-Tirgoviste C, Stevens H, Carr P, Nutland S, McKinney P, Shield JP, Wang W, Cordell HJ, Walker N, Todd JA, Concannon P. Dahlman I, et al. Among authors: shield jp. Nat Genet. 2002 Feb;30(2):149-50. doi: 10.1038/ng825. Epub 2002 Jan 22. Nat Genet. 2002. PMID: 11799396
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases.
Merriman TR, Cordell HJ, Eaves IA, Danoy PA, Coraddu F, Barber R, Cucca F, Broadley S, Sawcer S, Compston A, Wordsworth P, Shatford J, Laval S, Jirholt J, Holmdahl R, Theofilopoulos AN, Kono DH, Tuomilehto J, Tuomilehto-Wolf E, Buzzetti R, Marrosu MG, Undlien DE, Rønningen KS, Ionesco-Tirgoviste C, Shield JP, Pociot F, Nerup J, Jacob CO, Polychronakos C, Bain SC, Todd JA. Merriman TR, et al. Among authors: shield jp. Diabetes. 2001 Jan;50(1):184-94. doi: 10.2337/diabetes.50.1.184. Diabetes. 2001. PMID: 11147786
Transient neonatal diabetes, a disorder of imprinting.
Temple IK, Shield JP. Temple IK, et al. Among authors: shield jp. J Med Genet. 2002 Dec;39(12):872-5. doi: 10.1136/jmg.39.12.872. J Med Genet. 2002. PMID: 12471198 Free PMC article. Review.
Ambulatory blood pressure measurements are related to albumin excretion and are predictive for risk of microalbuminuria in young people with type 1 diabetes.
Marcovecchio ML, Dalton RN, Schwarze CP, Prevost AT, Neil HA, Acerini CL, Barrett T, Cooper JD, Edge J, Shield J, Widmer B, Todd JA, Dunger DB. Marcovecchio ML, et al. Diabetologia. 2009 Jun;52(6):1173-81. doi: 10.1007/s00125-009-1327-6. Epub 2009 Mar 21. Diabetologia. 2009. PMID: 19305965 Free article.
185 results