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- 2018
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
(
- Contribution to journal › Article
- 2016
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Mark
Gene variance in the nicotinic receptor cluster (CHRNA5-CHRNA3-CHRNB4) predicts death from cardiopulmonary disease and cancer in smokers.
(
- Contribution to journal › Article
- 2014
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Mark
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
(
- Contribution to journal › Article
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Mark
ASSOCIATION OF BTG2, CYR61, ZFP36, AND SCD GENE POLYMORPHISMS WITH GRAVES' DISEASE AND OPHTHALMOPATHY.
(
- Contribution to journal › Article
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Mark
Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö Diet and Cancer.
(
- Contribution to journal › Article
- 2013
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Mark
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
(
- Contribution to journal › Article
- 2012
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Mark
The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
(
- Contribution to journal › Article
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Mark
Prediction of Blood Pressure Changes Over Time and Incidence of Hypertension by a Genetic Risk Score in Swedes.
2012) In Hypertension(
- Contribution to journal › Article
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Mark
Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
(
- Contribution to journal › Article
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Mark
A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
(
- Contribution to journal › Article
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Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
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Mark
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
(
- Contribution to journal › Article
- 2011
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Mark
Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
2011) In Nutrition Metabolism and Cardiovascular Diseases(
- Contribution to journal › Article
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Mark
Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.
(
- Contribution to journal › Article
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Mark
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
- 2010
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Mark
Genetic loci influencing kidney function and chronic kidney disease
(
- Contribution to journal › Article
- 2008
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Mark
Genetics of Type 2 Diabetes and Metabolic Syndrome: From Genome Wide Linkage Scan and Candidate Genes to Genome Wide Association Studies
(
- Thesis › Doctoral thesis (compilation)
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Mark
A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population
(
- Contribution to journal › Article
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Mark
Is there a unifying genetic factor predisposing to the metabolic syndrome?
2008) 44th EASD Annual Meeting of the European Association for the Study of Diabetes In Diabetologia 51(S1). p.32-33(
- Contribution to journal › Published meeting abstract
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Mark
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
(
- Contribution to journal › Article