Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysisSMITH, J. G; ALMGREN, P; ENGSTRÖM, G et al.Journal of internal medicine. 2012, Vol 272, Num 6, pp 573-582, issn 0954-6820, 10 p.Article

Diabetes-associated HLA genotypes affect birthweight in the general populationLARSSON, H. E; LYNCH, K; LERNMARK, B et al.Diabetologia (Berlin). 2005, Vol 48, Num 8, pp 1484-1491, issn 0012-186X, 8 p.Article

The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of strokeCARLSSON, M; ORHO-MELANDER, M; HEDENBRO, J et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 8, pp 2801-2804, issn 0021-972XArticle

A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia studyISOMAA, B; FORSEN, B; TUOMI, T et al.Diabetologia (Berlin). 2010, Vol 53, Num 8, pp 1709-1713, issn 0012-186X, 5 p.Article

Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscleRONN, T; POULSEN, P; LING, C et al.Diabetologia (Berlin). 2008, Vol 51, Num 7, pp 1159-1168, issn 0012-186X, 10 p.Article

The metabolic syndrome influences the risk of chronic complications in patients with Type II diabetesISOMAA, B; HENRICSSON, M; ALMGREN, P et al.Diabetologia (Berlin). 2001, Vol 44, Num 9, pp 1148-1154, issn 0012-186XArticle

Prediction of postpartum diabetes in women with gestational diabetes mellitusEKELUND, M; SHAAT, N; ALMGREN, P et al.Diabetologia (Berlin). 2010, Vol 53, Num 3, pp 452-457, issn 0012-186X, 6 p.Article

A male-specific quantitative trait locus on 1p21 controlling human statureSAMMALISTO, S; HIEKKALINNA, T; ALMGREN, P et al.Journal of medical genetics. 2005, Vol 42, Num 12, pp 932-939, issn 0022-2593, 8 p.Article

Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individualsSUVIOLAHTI, E; RIDDERSTRALE, M; ALMGREN, P et al.International journal of obesity. 2003, Vol 27, Num 10, pp 1204-1211, issn 0307-0565, 8 p.Article

Association between the human glycoprotein PC-1 gene and elevated glucose and insulin levels in a paired-sibling analysisGU, H. F; ALMGREN, P; LINDHOLM, E et al.Diabetes (New York, NY). 2000, Vol 49, Num 9, pp 1601-1603, issn 0012-1797Article

A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosisHAMREFORS, V; HEDBLAD, B; ENGSTRÖM, G et al.Journal of internal medicine. 2012, Vol 271, Num 3, pp 271-281, issn 0954-6820, 11 p.Article

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressureFAVA, C; MONTAGNANA, M; AURELL, M et al.Human molecular genetics (Print). 2008, Vol 17, Num 3, pp 413-418, issn 0964-6906, 6 p.Article

24-h ambulatory blood pressure is linked to chromosome 18q21-22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in SwedesFAVA, C; VON WOWERN, F; BERGLUND, G et al.Kidney international. 2006, Vol 70, Num 3, pp 562-569, issn 0085-2538, 8 p.Article

Genomewide search for type 2 diabetes mellitus susceptibility loci in finnish families: The Botnia studyLINDGREN, C. M; MAHTANI, M. M; ALMGREN, P et al.American journal of human genetics. 2002, Vol 70, Num 2, pp 509-516, issn 0002-9297Article

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Common variants in HNF-1 α and risk of type 2 diabetesHOLMKVIST, J; CERVIN, C; LINDGREN, C. M et al.Diabetologia (Berlin). 2006, Vol 49, Num 12, pp 2882-2891, issn 0012-186X, 10 p.Article

A paired-sibling analysis of the Xbal polymorphism in the muscle glycogen synthase geneORHO-MELANDER, M; ALMGREN, P; KANNINEN, T et al.Diabetologia (Berlin). 1999, Vol 42, Num 9, pp 1138-1145, issn 0012-186XArticle

Chronic complications in patients with slowly progressing autoimmune type 1 diabetes (LADA)ISOMAA, B; ALMGREN, P; HENRICSSON, M et al.Diabetes care. 1999, Vol 22, Num 8, pp 1347-1353, issn 0149-5992Conference Paper

Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia StudyALMGREN, P; LEHTOVIRTA, M; ISOMAA, B et al.Diabetologia (Berlin). 2011, Vol 54, Num 11, pp 2811-2819, issn 0012-186X, 9 p.Article

An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISACERVIN, C; AXLER, O; HOLMKVIST, J et al.Journal of internal medicine. 2010, Vol 267, Num 3, pp 316-321, issn 0954-6820, 6 p.Article

Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetesFLOREZ, J. C; SJÖGREN, M; ARDLIE, K. G et al.Diabetologia (Berlin). 2007, Vol 50, Num 6, pp 1209-1217, issn 0012-186X, 9 p.Article

Impact of the peroxisome proliferator activated receptor-γ coactivator-1β (PGC-1β) Ala203Pro polymorphism on in vivo metabolism, PGC-1β expression and fibre type composition in human skeletal muscleLING, C; WEGNER, L; ANDERSEN, G et al.Diabetologia (Berlin). 2007, Vol 50, Num 8, pp 1615-1620, issn 0012-186X, 6 p.Article

Polymorphisms in the gene encoding the voltage-dependent Ca²⁺ channel Ca_v2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretionHOLMKVIST, J; TOJJAR, D; ALMGREN, P et al.Diabetologia (Berlin). 2007, Vol 50, Num 12, pp 2467-2475, issn 0012-186X, 9 p.Article

Common variants in MODY genes increase the risk of gestational diabetes mellitusSHAAT, N; KARLSSON, E; LERNMARK, A et al.Diabetologia (Berlin). 2006, Vol 49, Num 7, pp 1545-1551, issn 0012-186X, 7 p.Article