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- 2017
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Mark
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
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- Contribution to journal › Article
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Mark
Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction
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- Contribution to journal › Article
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Mark
Novel APC gene mutations associated with protein alteration in diffuse type gastric cancer
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- Contribution to journal › Article
- 2016
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Mark
Association of CD247 (CD3ζ) gene polymorphisms with T1D and AITD in the population of northern Sweden
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- Contribution to journal › Article
- 2015
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Mark
Genes involved in muscle contractility and nutrient signaling pathways within celiac disease risk loci show differential mRNA expression
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- Contribution to journal › Article
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Mark
Physical activity, smoking, and genetic predisposition to obesity in people from Pakistan: the PROMIS study.
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- Contribution to journal › Article
- 2014
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Mark
The chromosome 9p21 variant interacts with vegetable and wine intake to influence the risk of cardiovascular disease : a population based cohort study
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- Contribution to journal › Article
- 2013
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Mark
Heterozygous FA2H mutations in autism spectrum disorders
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- Contribution to journal › Article
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Mark
Investigating highly replicated asthma genes as candidate genes for allergic rhinitis
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- Contribution to journal › Article
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Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
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- Contribution to journal › Article
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Mark
A genetic variant of the atrial natriuretic peptide gene is associated with left ventricular hypertrophy in a non-diabetic population - the Malmo preventive project study
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- Contribution to journal › Article
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Mark
DNA methylation of the glucagon-like peptide 1 receptor (GLP1R) in human pancreatic islets.
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- Contribution to journal › Article
- 2012
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Mark
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
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- Contribution to journal › Article
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Mark
Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
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- Contribution to journal › Article
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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
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- Contribution to journal › Article
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Mark
Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
(
- Contribution to journal › Article
- 2011
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Mark
A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study
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- Contribution to journal › Article
- 2009
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Mark
Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels
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- Contribution to journal › Article
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Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
(
- Contribution to journal › Article
- 2008
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Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
(
- Contribution to journal › Article
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Mark
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72
(
- Contribution to journal › Article
- 2007
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Mark
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
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Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
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- Contribution to journal › Article
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Mark
CT60 genotype does not affect CTLA-4 isoform expression despite association to TID and AITD in northern Sweden
(
- Contribution to journal › Article
- 2006
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Mark
Multilevel analysis of systolic blood pressure and ACE gene I/D polymorphism in 438 Swedish families - a public health perspective
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- Contribution to journal › Article