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- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
- 2016
-
Mark
Lifestyle and glycaemic control before and after the onset of type 2 diabetes
2016)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic Determinants of Dyslipidemia
2016)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Heterozygous PINK1 p.G411S mutation increases risk for Parkinson's disease (PD)
2016) 20th International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 31(Suppl. S2). p.282-282(
- Contribution to journal › Published meeting abstract
-
Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
- 2012
-
Mark
Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes
(
- Contribution to journal › Article
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Mark
Perceptions of genetic research and testing among members of families with an increased risk of malignant melanoma
(
- Contribution to journal › Article
- 2009
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Mark
Unwanted pregnancy as a risk factor for offspring schizophrenia-spectrum and affective disorders in adulthood: a prospective high-risk study.
(
- Contribution to journal › Article
- 2007
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Mark
Two insulin gene single nucleotide polymorphisms associated with type 1 diabetes risk in the Finnish and Swedish populations
(
- Contribution to journal › Article
- 1998
-
Mark
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families [3]
(
- Contribution to journal › Letter