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- 2024
-
Mark
The HLA region in ANCA-associated vasculitis : characterisation of genetic associations in a Scandinavian patient population
(
- Contribution to journal › Article
- 2023
-
Mark
Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome
(
- Contribution to journal › Article
-
Mark
Role of Mannose-binding Lectin and Association with Microbial Sensitization in a Cohort of Patients with Atopic Dermatitis
(
- Contribution to journal › Article
-
Mark
Caveolin-1 genotypes as predictor for locoregional recurrence and contralateral disease in breast cancer
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
(
- Contribution to journal › Article
-
Mark
A large meta-analysis identifies genes associated with anterior uveitis
(
- Contribution to journal › Article
- 2022
-
Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
(
- Contribution to journal › Article
-
Mark
Factors associated with clinical progression to severe COVID-19 in people with cystic fibrosis: A global observational study
(
- Contribution to journal › Article
-
Mark
APOE in the bullseye of neurodegenerative diseases : impact of the APOE genotype in Alzheimer’s disease pathology and brain diseases
(
- Contribution to journal › Scientific review
-
Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
- 2021
-
Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
(
- Contribution to journal › Article
-
Mark
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
(
- Contribution to journal › Article
- 2020
-
Mark
Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Evaluating drug targets through human loss-of-function genetic variation
(
- Contribution to journal › Article
-
Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
(
- Contribution to journal › Article
-
Mark
Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting
(
- Contribution to journal › Article
- 2019
-
Mark
Gene transfer by interspecific hybridization in bryophytes
2019)(
- Thesis › Doctoral thesis (compilation)
-
Mark
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Atrial Fibrillation in Long QT Syndrome by Genotype
(
- Contribution to journal › Article
-
Mark
Genotyping and serotyping profiles showed weak Jka presentation for previously typed as Jknull donors
(
- Contribution to journal › Article
-
Mark
Noninvasive fetal RHD genotyping to guide targeted anti-D prophylaxis–an external quality assessment workshop
(
- Contribution to journal › Article
-
Mark
SSD1 suppresses phenotypes induced by the lack of Elongator-dependent tRNA modifications
(
- Contribution to journal › Article
- 2018
-
Mark
TSC-associated neuropsychiatric disorders (TAND) : findings from the TOSCA natural history study
(
- Contribution to journal › Article
-
Mark
Differential distribution of IgA-protease genotypes in mucosal and invasive isolates of Haemophilus influenzae in Sweden
(
- Contribution to journal › Article
-
Mark
Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers with Normal QTc Interval : The Value of Sex, T-Wave Morphology, and Mutation Type
(
- Contribution to journal › Article
-
Mark
ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies
(
- Contribution to journal › Article
-
Mark
Contrasting results from GWAS and QTL mapping on wing length in great reed warblers
(
- Contribution to journal › Article
- 2017
-
Mark
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
(
- Contribution to journal › Article
-
Mark
ECG-derived spatial QRS-T angle is strongly associated with hypertrophic cardiomyopathy
(
- Contribution to journal › Article
-
Mark
Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD
(
- Contribution to journal › Article
-
Mark
Identification of new disease mechanisms and treatments for type 2 diabetes based on genetic variants and gene expression networks
2017)(
- Thesis › Doctoral thesis (compilation)
-
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
-
Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
(
- Contribution to journal › Article
-
Mark
The P1 histo-blood group antigen is present on human red blood cell glycoproteins
2017) 27th Regional Congress of the International Society of Blood Transfusion, ISBT 2017 In Vox Sanguinis 112(S1). p.25-25(
- Contribution to journal › Published meeting abstract
-
Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
-
Mark
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
(
- Contribution to journal › Article
-
Mark
Identification of shared and unique serum lipid profiles in diabetes mellitus and myocardial infarction
(
- Contribution to journal › Article
-
Mark
Genetic variants in CETP increase risk of intracerebral hemorrhage
(
- Contribution to journal › Article
-
Mark
CYP1A2 genotype affects carbamazepine pharmacokinetics in children with epilepsy
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
-
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
Effector-driven marker development and cloning of resistance genes against Phytophthora infestans in potato breeding clone SW93-1015
(
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
- 2015
-
Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
-
Mark
Tracking Parkinson's : Study Design and Baseline Patient Data
(
- Contribution to journal › Article
-
Mark
Genetic variation in caveolin-1 correlates with long-term pancreas transplant function
(
- Contribution to journal › Article
-
Mark
Early and exudative age-related macular degeneration is associated with increased plasma levels of soluble TNF receptor II
(
- Contribution to journal › Article
-
Mark
Fell-Muir Lecture : Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour
(
- Contribution to journal › Scientific review
-
Mark
Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis
(
- Contribution to journal › Article
- 2014
-
Mark
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
(
- Contribution to journal › Article
-
Mark
Norovirus epidemiology in community and health care settings and association with patient age, Denmark
(
- Contribution to journal › Article
- 2013
-
Mark
The occurrence of noncoagulating milk and the association of bovine milk coagulation properties with genetic variants of the caseins in 3 Scandinavian dairy breeds
(
- Contribution to journal › Article
-
Mark
The CamPaIGN study of Parkinson's disease : 10-year outlook in an incident population-based cohort
(
- Contribution to journal › Article
-
Mark
Age-related macular degeneration is associated with increased proportion of CD56(+) T cells in peripheral blood
(
- Contribution to journal › Article
-
Mark
Short communication : HIV type 1 transmitted drug resistance and evidence of transmission clusters among recently infected antiretroviral-naive individuals from Ugandan fishing communities of Lake Victoria
(
- Contribution to journal › Article
- 2012
-
Mark
Exposure and toxic effects of elemental mercury in gold-mining activities in Ecuador
(
- Contribution to journal › Article
-
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
Large-scale replication and heterogeneity in Parkinson disease genetic loci
(
- Contribution to journal › Article
-
Mark
Diversity and zoonotic potential of rotaviruses in swine and cattle across Europe
(
- Contribution to journal › Article
-
Mark
Isolation of Coxsackievirus A24 variant from patients with hemorrhagic conjunctivitis in Cuba, 2008-2009
(
- Contribution to journal › Article
-
Mark
Paranoid potato : phytophthora-resistant genotype shows constitutively activated defense
(
- Contribution to journal › Article
-
Mark
On the roles and regulation of chondroitin sulfate and heparan sulfate in zebrafish pharyngeal cartilage morphogenesis
(
- Contribution to journal › Article
-
Mark
ANKRD55 and DHCR7 are novel multiple sclerosis risk loci
(
- Contribution to journal › Article
-
Mark
CRYAB-650 C>G (rs2234702) affects susceptibility to Type 1 diabetes and IAA-positivity in Swedish population
(
- Contribution to journal › Article
- 2011
-
Mark
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers
(
- Contribution to journal › Article
-
Mark
Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer
(
- Contribution to journal › Article
-
Mark
Polymorphic variation in the androgen receptor gene : association with risk of testicular germ cell cancer and metastatic disease
(
- Contribution to journal › Article
-
Mark
Clinical effect of point mutations in myelodysplastic syndromes
(
- Contribution to journal › Article
-
Mark
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Clinical and virological features of enterovirus 71 infections in Denmark, 2005 to 2008
(
- Contribution to journal › Article
-
Mark
Efficacy and safety of imatinib on top of BFM-like chemotherapy in pediatric patients with Ph+/BCR-ABL+ acute lymphoblastic leukemia (Ph+ALL). the EsPhALL study
(
- Contribution to journal › Published meeting abstract
- 2010
-
Mark
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : implications for risk prediction
(
- Contribution to journal › Article
-
Mark
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
(
- Contribution to journal › Article
-
Mark
Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk
(
- Contribution to journal › Article
-
Mark
Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood
(
- Contribution to journal › Article
-
Mark
MicroRNAs are necessary for vascular smooth muscle growth, differentiation, and function
(
- Contribution to journal › Article
-
Mark
Incidence, diversity, and molecular epidemiology of sapoviruses in swine across Europe
(
- Contribution to journal › Article
- 2009
-
Mark
Transmission af hepatitis E i Danmark
(
- Contribution to journal › Article
-
Mark
Genetic diversity of sapovirus infections in Danish children 2005-2007
(
- Contribution to journal › Article
- 2008
-
Mark
Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles
(
- Contribution to journal › Article
-
Mark
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis
(
- Contribution to journal › Article
-
Mark
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis : the GENOMOS study
(
- Contribution to journal › Article
- 2007
-
Mark
Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.
(
- Contribution to journal › Article
-
Mark
Personalised nutrition : status and perspectives
(
- Contribution to journal › Scientific review
-
Mark
The benefit of molecular characterization during a measles upsurge in Denmark
(
- Contribution to journal › Article
-
Mark
Host genetic resistance to symptomatic norovirus (GGII.4) infections in Denmark
(
- Contribution to journal › Article
- 2006
-
Mark
The association between common vitamin D receptor gene variations and osteoporosis : a participant-level meta-analysis
(
- Contribution to journal › Article
-
Mark
Chromosomal aberrations and SCEs as biomarkers of cancer risk
(
- Contribution to journal › Article
-
Mark
Analysis of the interleukin-1 and interleukin-6 polymorphisms in patients with chronic periodontitis. A pilot study
(
- Contribution to journal › Article
-
Mark
Maeslinger hos to børn og en voksen--udbrud med maeslingevirus genotype B3
(
- Contribution to journal › Article
-
Mark
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes : the GENOMOS study
(
- Contribution to journal › Article
-
Mark
Ablation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethality
(
- Contribution to journal › Article
-
Mark
Why do inhibitors develop? Principles of and factors influencing the risk for inhibitor development in haemophilia.
(
- Contribution to journal › Article
- 2005
-
Mark
Genetic influences on the retention of inorganic mercury.
(
- Contribution to journal › Article
-
Mark
Genetic basis of the K phenotype in the Swedish population.
(
- Contribution to journal › Article
-
Mark
Blood group genotype analysis for the quality improvement of reagent test red blood cells
(
- Contribution to journal › Article
-
Mark
Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A
(
- Contribution to journal › Article
-
Mark
A population-based cohort study of KIR genes and genotypes in relation to cervical intraepithelial neoplasia
(
- Contribution to journal › Article
-
Mark
Polymorphisms of the CLCN7 gene are associated with BMD in women
(
- Contribution to journal › Article
- 2004
-
Mark
Association of the Collagen Type 1 (COL1A 1) Sp1 Binding Site Polymorphism to Femoral Neck Bone Mineral Density and Wrist Fracture in 1044 Elderly Swedish Women.
(
- Contribution to journal › Article
-
Mark
Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes
(
- Contribution to journal › Article
-
Mark
Methylenetetrahydrofolate reductase polymorphism interacts with riboflavin intake to influence bone mineral density
(
- Contribution to journal › Article
-
Mark
Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Heparan sulfate synthesized by mouse embryonic stem cells deficient in NDST1 and NDST2 is 6-O-sulfated but contains no N-sulfate groups
(
- Contribution to journal › Article
- 2003
-
Mark
Genes and erectile function
(
- Contribution to journal › Scientific review
-
Mark
Discrete gene loci regulate neurodegeneration, lymphocyte infiltration, and major histocompatibility complex class II expression in the CNS
2003) In The Journal of Neuroscience : the official journal of the Society for Neuroscience 23(30). p.23-9817(
- Contribution to journal › Article
-
Mark
Finnish and Swedish genotypes and risk of cancer in Sweden
(
- Contribution to journal › Letter
- 2002
-
Mark
HLA-DQ genotypes in classic type 1 diabetes and in latent autoimmune diabetes of the adult.
(
- Contribution to journal › Article
-
Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
-
Mark
Thrifty genotypes and phenotypes in the pathogenesis of early-onset obesity.
(
- Contribution to journal › Letter
-
Mark
Genetic variability in hepatitis B viruses.
(
- Contribution to journal › Scientific review
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
Genetic links between the acute-phase response and arthritis development in rats.
(
- Contribution to journal › Article
-
Mark
Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
(
- Contribution to journal › Article
-
Mark
Effects of harvest time and storage on dietary fibre components in various cultivars of white cabbage (Brassica oleracea var capitata)
(
- Contribution to journal › Article
-
Mark
Food-borne outbreak of gastroenteritis associated with genogroup I calicivirus.
(
- Contribution to journal › Article
-
Mark
Multiple endocrine neoplasia type 1 polymorphism D418D is associated with sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2001
-
Mark
CYP gene polymorphisms and early menarche
(
- Contribution to journal › Article
-
Mark
Genetic factors related to racial variation in plasma levels of insulin-like growth factor-1: implications for premenopausal breast cancer risk
(
- Contribution to journal › Article
-
Mark
Gene-expression profiles in hereditary breast cancer
(
- Contribution to journal › Article
-
Mark
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden--an evolutionary advantage?
(
- Contribution to journal › Letter
-
Mark
Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
2001)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
(
- Contribution to journal › Article
-
Mark
Prediction of osteoporotic fractures by bone densitometry and COLIA1 genotyping : a prospective, population-based study in men and women
(
- Contribution to journal › Article
-
Mark
COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss
(
- Contribution to journal › Article
-
Mark
Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
(
- Contribution to journal › Article
-
Mark
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2000
-
Mark
Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
(
- Contribution to journal › Article
- 1999
-
Mark
Prenatal diagnosis of haemophilia
(
- Contribution to journal › Scientific review
-
Mark
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
(
- Contribution to journal › Article
-
Mark
The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels
(
- Contribution to journal › Article
-
Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
(
- Contribution to journal › Article
- 1998
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
(
- Contribution to journal › Article
-
Mark
Inverse relationship between GAD65 antibody levels and severe retinopathy in younger type 1 diabetic patients
(
- Contribution to journal › Article
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
-
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
(
- Contribution to journal › Letter
-
Mark
Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women
(
- Contribution to journal › Article
- 1997
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
(
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
-
Mark
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
(
- Contribution to journal › Article
- 1996
-
Mark
HLA-DQB1*0201/0302 is associated with severe retinopathy in patients with IDDM
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
(
- Contribution to journal › Article
- 1995
-
Mark
Hepatitis C superinfection in hepatitis C virus (HCV)-infected patients transplanted with an HCV-infected kidney
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
- 1994
-
Mark
Typing of hepatitis C virus isolates by DNA enzyme immunoassay
(
- Contribution to journal › Article