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- 2024
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Mark
Inflammation-related proteins in blood after dermal exposure to some common chemicals depend on the skin barrier gene filaggrin - a human experimental study
(
- Contribution to journal › Article
- 2023
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Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
(
- Contribution to journal › Article
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Mark
Low birthweight is associated with a higher incidence of type 2 diabetes over two decades independent of adult BMI and genetic predisposition
(
- Contribution to journal › Article
- 2022
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Mark
Nickel penetration into stratum corneum in FLG null carriers—A human experimental study
(
- Contribution to journal › Article
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Mark
Polygenic scores for low lung function and the future risk of adverse health outcomes
(
- Contribution to journal › Article
- 2021
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Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
- 2019
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Mark
Genetic variants of filaggrin are associated with occupational dermal exposure and blood DNA alterations in hairdressers
(
- Contribution to journal › Article
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Mark
Filaggrin variations are associated with PAH metabolites in urine and DNA alterations in blood
(
- Contribution to journal › Article
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Mark
Molecular determinants of disease severity in urinary tract infection
(
- Thesis › Doctoral thesis (compilation)
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Mark
Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region
(
- Contribution to journal › Article
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Mark
Autoimmune (type 1) diabetes
2019) p.769-787(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2018
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Mark
Toluene diisocyanate exposure and autotaxin–lysophosphatidic acid signalling
(
- Contribution to journal › Article
- 2017
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Mark
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3
(
- Contribution to journal › Article
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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
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Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
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Mark
Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study
(
- Contribution to journal › Article
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Mark
Oral contraceptive use and breast cancer risk: A cohort study of BRCA1 and BRCA2 mutation carriers
2017) American Association for Cancer Research (AACR) 108th Annual Meeting 2017 In Cancer Research 77(13 Suppl 1).(
- Contribution to journal › Published meeting abstract
- 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
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Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
- 2015
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Mark
Variation at ABO histo-blood group and FUT loci and diffuse and intestinal gastric cancer risk in a European population
(
- Contribution to journal › Article
- 2014
-
Mark
Polymorphisms of Helicobacter pylori signaling pathway genes and gastric cancer risk in the European Prospective Investigation into Cancer-Eurgast cohort
(
- Contribution to journal › Article
- 2013
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Mark
Vitamin C transporter gene (SLC23A1 and SLC23A2) polymorphisms, plasma vitamin C levels, and gastric cancer risk in the EPIC cohort
(
- Contribution to journal › Article
- 2012
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Mark
Prostate stem-cell antigen gene is associated with diffuse and intestinal gastric cancer in Caucasians: Results from the EPIC-EURGAST study
(
- Contribution to journal › Article
- 2009
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Mark
No association of the IRS1 and PAX4 genes with type I diabetes
(
- Contribution to journal › Article
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Mark
Novel Aspects Pertaining to the Relationship of Waldenstrom's Macroglobulinemia, IgM Monoclonal Gammopathy of Undetermined Significance, Polyclonal Gammopathy, and Hypoglobulinemia
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 2004
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Mark
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
(
- Contribution to journal › Article
- 2002
-
Mark
The combination of several polymorphic amino acid residues in the DQ alpha and DQ beta chains forms a domain structure pattern and is associated with insulin-dependent diabetes mellitus
(
- Contribution to journal › Article
- 1997
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Mark
Analysis of critical residues of HLA-DQ6 molecules in insulin-dependent diabetes mellitus
(
- Contribution to journal › Article
- 1996
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Mark
HLA and glutamic acid decarboxylase in human insulin-dependent diabetes mellitus
(
- Contribution to journal › Article
-
Mark
DR4 subtypes and their molecular properties in a population-based study of Swedish childhood diabetes
(
- Contribution to journal › Article
- 1995
-
Mark
Effects of the second HLA‐DQ haplotype on the association with childhood insulin‐dependent diabetes mellitus
(
- Contribution to journal › Article