Peter Almgren
Titel
Biostatistiker
Organisation
+4640391234
Peter [dot] Almgren [at] med [dot] lu [dot] se
Publikationer (hämtat ur Lunds universitets publikationsdatabas)
författare
- 2013
- 2012
- A common variant upstream of the PAX6 gene influences islet function in man.
- A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
- Genetic Polymorphisms for Estimating Risk of Atrial Fibrillation in the General Population: A Prospective Study
- Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.
- Genetic prediction of postpartum diabetes in women with gestational diabetes mellitus
- Impact of an Exercise Intervention on DNA Methylation in Skeletal Muscle From First-Degree Relatives of Patients With Type 2 Diabetes.
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
- Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
- Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
- Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality.
- Prediction of Blood Pressure Changes Over Time and Incidence of Hypertension by a Genetic Risk Score in Swedes.
- Reduced Insulin Exocytosis in Human Pancreatic β-cells With Gene Variants Linked to Type 2 Diabetes.
- Secreted frizzled-related protein 4 reduces insulin secretion and is overexpressed in type 2 diabetes.
- Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases
- The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
- The Triglyceride Content in Skeletal Muscle Is Associated with Hepatic But Not Peripheral Insulin Resistance in Elderly Twins.
- The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
- Vasoactive Peptides with Angiogenesis-Regulating Activity Predict Cancer Risk in Males.
- 2011
- A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
- A functional variant of the NEDD4L gene is associated with beneficial treatment response with β-blockers and diuretics in hypertensive patients.
- Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
- Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study.
- Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.
- Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
- 2010
- A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study
- A gene score of nine LDL and HDL regulating genes is associated with fluvastatin induced cholesterol changes in women.
- An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA.
- Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation.
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
- Genome wide association analysis for free fatty acid levels in DGI
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior
- Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes.
- Hundreds of variants clustered in genomic loci and biological pathways affect human height
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
- NordicDB: a Nordic pool and portal for genome-wide control data
- Plasma copeptin and the risk of diabetes mellitus.
- Prediction of postpartum diabetes in women with gestational diabetes mellitus
- The Association of Mitochondrial Content with Prevalent and Incident Type 2 Diabetes.
- The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes.
- 2009
- Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
- Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs
- Homozygosity for the EPHX2 K55R Polymorphism Increases the Long-Term Risk of Ischemic Stroke in Men: A Study in Swedes
- Novel and conventional biomarkers for prediction of incident cardiovascular events in the community.
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
- The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
- 2008
- Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscle.
- Clinical risk factors, DNA variants, and the development of type 2 diabetes.
- Common variants in MODY genes and future risk of type 2 diabetes.
- Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes
- Determinants of kidney function in Swedish families. Role of heritable factors
- Determinants of kidney function in Swedish families: role of heritable factors.
- Functional polymorphism of the NEDD4L gene strongly influences cardiovascular outcome in hypertensive patients treated with beta-blockers and diuretics
- Functional variation of the NEDD4L gene predicts ischemic stroke
- Interaction Between Renal Function and Microalbuminuria for Cardiovascular Risk in Hypertension The Nordic Diltiazem Study
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
- Molecular correlates for maximal oxygen uptake (VO2max) and type 1 fibers.
- Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
- The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of cardiovascular risk factors and coronary events in patients with hypertension
- 2007
- Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.
- Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes
- Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes
- Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle
- Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
- Impact of the peroxisome proliferator activated receptor-gamma coactivator-1 beta (PGC-1 beta) Ala203Pro polymorphism on in vivo metabolism, PGC-1 beta expression and fibre type composition in human skeletal muscle
- Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
- Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion
- The Environmental Determinats of Diabetes in the Y
- The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
- Variants in the FFAR1 Gene Are Associated with Beta Cell Function
- Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
- 2006
- 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 Swedes.
- 24-hour Ambulatory Blood Pressure is Linked to Chromosome 18q21-22 and Genetic Variation of NEDD4L Associates with Cross-Sectional and Longitudinal Blood Pressure in Swedes.
- Authors' reply.
- Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
- Common variants in HNF-1 alpha and risk of type 2 diabetes.
- Common variants in MODY genes increase the risk of gestational diabetes mellitus.
- Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity
- Haplotype structures and large-scale association testing of the 5 ' AMP-activated protein kinase genes PRK4A2, PRKAB1, and PRK4B1 with type 2 diabetes
- High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people
- Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
- The Kruppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people
- 2005
- A male-specific quantitative trait locus on 1p21 controlling human stature
- Association of common variation in the HNF1 alpha gene region with risk of type 2 diabetes
- Association of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus.
- Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people
- Association testing of variants in the hepatocyte nuclear factor 4 alpha gene with risk of type 2 diabetes in 7,883 people
- Diabetes-associated HLA genotypes affect birthweight in the general population.
- Dipping and variability of blood pressure and heart rate at night are heritable traits.
- Genetic and Nongenetic Regulation of CAPN10 mRNA Expression in Skeletal Muscle.
- Genetic prediction of future type 2 diabetes
- Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
- Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes.
- 2004
- Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes
- Contribution of insulin-stimulated glucose uptake and basal hepatic insulin sensitivity to surrogate measures of insulin sensitivity.
- Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region.
- Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
- Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins.
- The FOXC2 C-512T Polymorphism Is Associated with Obesity and Dyslipidemia.
- 2003
- A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity.
- A genome wide scan for early onset primary hypertension in Scandinavians.
- A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
- Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
- 2002
- A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
- Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
- Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
- 2001
- Cardiovascular morbidity and mortality associated with the metabolic syndrome
- Characterization of the annexin I gene and evaluation of its role in type 2 diabetes
- Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes
- The metabolic syndrome influences the risk of chronic complications in patients with type II diabetes
- 2000
- 1999
