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- 2024
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Mark
Clarifying the relationship between physical injuries and risk for suicide attempt in a Swedish national sample
2024) In Acta Psychiatrica Scandinavica(
- Contribution to journal › Article
-
Mark
The genetic epidemiology of schizotypal personality disorder
2024) In Psychological Medicine(
- Contribution to journal › Article
- 2023
-
Mark
SAI-CH-6 : Development of a Short Form of the State Anxiety Inventory for Children At-Risk for Type 1 Diabetes
(
- Contribution to journal › Article
-
Mark
A large meta-analysis identifies genes associated with anterior uveitis
(
- Contribution to journal › Article
- 2022
-
Mark
The interaction between smoking and bladder cancer genetic variants on urothelial cancer risk by disease aggressiveness
(
- Contribution to journal › Article
-
Mark
The emotional well-being of parents with children at genetic risk for type 1 diabetes before and during participation in the POInT-study
(
- Contribution to journal › Article
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Mark
Genetic risk of type 2 diabetes modifies the effects of a lifestyle intervention aimed at the prevention of gestational and postpartum diabetes
(
- Contribution to journal › Article
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Mark
Is staff consistency important to parents' satisfaction in a longitudinal study of children at risk for type 1 diabetes : the TEDDY study
(
- Contribution to journal › Article
- 2021
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Mark
Adherence to oral glucose tolerance testing in children in stage 1 of type 1 diabetes : The TEDDY study
(
- Contribution to journal › Article
-
Mark
Selenium and Breast Cancer. Is It Protective? Epidemiologic Evidence Regarding Risk and Prognosis
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
- 2018
-
Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
- 2017
-
Mark
Barbara Fish and a Short History of the Neurodevelopmental Hypothesis of Schizophrenia
(
- Contribution to journal › Article
-
Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
-
Mark
The clinical features of alcohol use disorders in biological and step-fathers that predict risk for alcohol use disorders in offspring
(
- Contribution to journal › Article
-
Mark
Different DRB1*03 : 01-DQB1*02:01 haplotypes confer different risk for celiac disease
(
- Contribution to journal › Article
-
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
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
Lifestyle and glycaemic control before and after the onset of type 2 diabetes
2016)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
-
Mark
Genetic Determinants of Dyslipidemia
2016)(
- Thesis › Doctoral thesis (compilation)
- 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
-
Mark
Perceptions of genetic research and testing among members of families with an increased risk of malignant melanoma
(
- Contribution to journal › Article
- 2009
-
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
-
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
- 1995
-
Mark
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
(
- Contribution to journal › Article