SwePub - search: WFRF:(Prince JA)

Enumeration	Reference	Cover	Find
1.	Murray, CJL, et al. (author) Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010 2012 In: Lancet (London, England). - 1474-547X. ; 380:9859, s. 2197-2223 Journal article (peer-reviewed)
2.	Vos, T, et al. (author) Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010 2012 In: Lancet (London, England). - 1474-547X. ; 380:9859, s. 2163-2196 Journal article (peer-reviewed)
3.	Niemi, MEK, et al. (author) 2021 swepub:Mat__t
4.	2021 swepub:Mat__t
5.	Bennet, AM, et al. (author) Interleukin-6 serum levels and genotypes influence the risk for myocardial infarction 2003 In: Atherosclerosis. - : Elsevier BV. - 0021-9150. ; 171:2, s. 359-367 Journal article (peer-reviewed)
6.	Bjork, BF, et al. (author) Positive association between risk for late-onset Alzheimer disease and genetic variation in IDE 2007 In: Neurobiology of aging. - : Elsevier BV. - 1558-1497 .- 0197-4580. ; 28:9, s. 1374-1380 Journal article (peer-reviewed)
7.	Brookes, AJ, et al. (author) Genetic association analysis: lessons from the study of Alzheimers disease 2005 In: Mutation research. - : Elsevier BV. - 0027-5107. ; 573:1-2, s. 152-159 Journal article (peer-reviewed)
8.	Buchanan, DD, et al. (author) Association of APOE with Parkinson disease age-at-onset in women 2007 In: Neuroscience letters. - : Elsevier BV. - 0304-3940. ; 411:3, s. 185-188 Journal article (peer-reviewed)
9.	Bullock, JM, et al. (author) Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease 2013 In: Neurobiology of aging. - : Elsevier BV. - 1558-1497 .- 0197-4580. ; 34:4, s. 1309.e1-7 Journal article (peer-reviewed)
10.	Chen, Q, et al. (author) OMICmAge: An integrative multi-omics approach to quantify biological age with electronic medical records 2023 In: bioRxiv : the preprint server for biology. Journal article (other academic/artistic)
11.	Chen, Y, et al. (author) Sphingolipid classes and the interrelationship with pediatric asthma and asthma risk factors 2023 In: Allergy. - 1398-9995. Journal article (peer-reviewed)
12.	Chen, YL, et al. (author) Sphingolipid classes and the interrelationship with pediatric asthma and asthma risk factors 2024 In: Allergy. - 1398-9995. ; 79:2, s. 404-418 Journal article (peer-reviewed)
13.	Culpan, D, et al. (author) Neither sequence variation in the IL-10 gene promoter nor presence of IL-10 protein in the cerebral cortex is associated with Alzheimer's disease 2006 In: Neuroscience letters. - : Elsevier BV. - 0304-3940. ; 408:2, s. 141-145 Journal article (peer-reviewed)
14.	Ekblom, J, et al. (author) A cell culture model of cerebral ischemia as a convenient system to screenfor neuroprotective drugs. 1998 In: J Neural Transm Suppl. ; 52, s. 93- Journal article (peer-reviewed)
15.	Emahazion, T, et al. (author) SNP association studies in Alzheimer's disease highlight problems for complex disease analysis 2001 In: Trends in genetics : TIG. - 0168-9525. ; 17:7, s. 407-413 Journal article (peer-reviewed)
16.	Eriksson, UK, et al. (author) Associations of gene sequence variation and serum levels of C-reactive protein and interleukin-6 with Alzheimer's disease and dementia 2011 In: Journal of Alzheimer's disease : JAD. - 1875-8908. ; 23:2, s. 361-369 Journal article (peer-reviewed)
17.	Ertekin-Taner, N, et al. (author) Analysis of Alzheimer's disease candidate genes on chromosome 10 2004 In: NEUROBIOLOGY OF AGING. - 0197-4580. ; 25, s. S501-S501 Conference paper (other academic/artistic)
18.	Feuk, L, et al. (author) apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease: finding of a positive association for a polymorphism in the TNFRSF6 gene 2000 In: Human genetics. - : Springer Science and Business Media LLC. - 0340-6717 .- 1432-1203. ; 107:4, s. 391-396 Journal article (peer-reviewed)
19.	Feuk, L, et al. (author) Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer disease 2003 In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 21:1, s. 53-60 Journal article (peer-reviewed)
20.	Feuk, L, et al. (author) Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's disease 2005 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. - : Wiley. - 1552-4841. ; 136B:1, s. 69-71 Journal article (peer-reviewed)
21.	Gigante, B, et al. (author) Retrospective analysis of coagulation factor II receptor (F2R) sequence variation and coronary heart disease in hypertensive patients 2007 In: Arteriosclerosis, thrombosis, and vascular biology. - 1524-4636. ; 28, s. 441-441 Journal article (peer-reviewed)
22.	Gu, HF, et al. (author) Quantitative trait loci near the insulin-degrading enzyme gene (IDE) contribute to variation in plasma insulin levels 2004 In: DIABETOLOGIA. - 0012-186X. ; 47, s. A137-A137 Conference paper (other academic/artistic)
23.	Gu, HF, et al. (author) Quantitative trait loci near the insulin-degrading enzyme (IDE) gene contribute to variation in plasma insulin levels 2004 In: Diabetes. - : American Diabetes Association. - 0012-1797 .- 1939-327X. ; 53:8, s. 2137-2142 Journal article (peer-reviewed)abstract Insulin-degrading enzyme (IDE) plays a principal role in the proteolysis of several peptides in addition to insulin and is encoded by IDE, which resides in a region of chromosome 10q that is linked to type 2 diabetes. Two recent studies presented genetic association data on IDE and type 2 diabetes (one positive and the other negative), but neither explored the fundamental question of whether polymorphism in IDE has a measurable influence on insulin levels in human populations. To address this possibility, 14 single nucleotide polymorphisms (SNPs) from a linkage disequilibrium block encompassing IDE have been genotyped in a sample of 321 impaired glucose tolerant and 403 nondiabetic control subjects. Analyses based on haplotypic genotypes (diplotypes), constructed with SNPs that differentiate common extant haplotypes extending across IDE, provided compelling evidence of association with fasting insulin levels (P = 0.0009), 2-h insulin levels (P = 0.0027), homeostasis model assessment of insulin resistance (P = 0.0001), and BMI (P = 0.0067), with effects exclusively evident in men. The strongest evidence for an effect of a single marker was obtained for rs2251101 (located near the 3′ untranslated region of IDE) on 2-h insulin levels (P = 0.000023). Diplotype analyses, however, suggest the presence of multiple interacting trait-modifying sequences in the region. Results indicate that polymorphism in/near IDE contributes to a large proportion of variance in plasma insulin levels and correlated traits, but questions of sex specificity and allelic heterogeneity will need to be taken into consideration as the molecular basis of the observed phenotypic effects unfolds.
24.	Hong, MG, et al. (author) Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease 2010 In: Journal of human genetics. - : Springer Science and Business Media LLC. - 1435-232X .- 1434-5161. ; 55:10, s. 707-709 Journal article (peer-reviewed)
25.	Hong, MG, et al. (author) Phenotype selection for detecting variable genes: a survey of cardiovascular quantitative traits and TNF locus polymorphism 2007 In: European journal of human genetics : EJHG. - : Springer Science and Business Media LLC. - 1018-4813 .- 1476-5438. ; 15:6, s. 685-693 Journal article (peer-reviewed)

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