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- 2024
-
Mark
Multimorbidity disease clusters are associated with venous thromboembolism : an extended cross-sectional national study
2024) In Journal of Thrombosis and Thrombolysis(
- Contribution to journal › Article
-
Mark
Increased risk of venous thromboembolism in young and middle-aged individuals with hereditary angioedema : a family study
2024) In Blood(
- Contribution to journal › Article
-
Mark
miR-145 and incident thromboembolism
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Association between changed self-rated health and the risk of venous thromboembolism in Malmö Preventive Program : a cohort study
2024) In Journal of Thrombosis and Thrombolysis(
- Contribution to journal › Article
-
Mark
The risk for venous thromboembolism and cardiometabolic disorders in offspring from thrombosis-prone pedigrees
2024) In Journal of Thrombosis and Haemostasis(
- Contribution to journal › Article
-
Mark
Mitochondria-DNA copy-number in osteoporosis and osteoarthritis among middle-aged women - A population-based cohort study
(
- Contribution to journal › Article
-
Mark
Rare-variant collapsing and bioinformatic analyses for different types of cardiac arrhythmias in the UK Biobank reveal novel susceptibility loci and candidate amyloid-forming proteins
(
- Contribution to journal › Article
-
Mark
Heritability of Atrial Fibrillation Among Swedish Adoptees
(
- Contribution to journal › Letter
-
Mark
SERPINH1 variants and thrombotic risk among middle-aged and older adults : a population-based cohort study
(
- Contribution to journal › Letter
- 2023
-
Mark
Sex-Specific Risk Factors for Deep Venous Thrombosis and Pulmonary Embolism in a Population-Based Historical Cohort Study of Middle-Aged and Older Individuals
(
- Contribution to journal › Article
-
Mark
Rare-variant collapsing analyses of arterial hypertension in the UK biobank
(
- Contribution to journal › Letter
-
Mark
Contribution of rare and common coding variants to haematological malignancies in the UK biobank
(
- Contribution to journal › Article
-
Mark
Familial Associations of Complete Atrioventricular Block : A National Family Study in Sweden
(
- Contribution to journal › Article
-
Mark
Familial risk of dilated and hypertrophic cardiomyopathy : a national family study in Sweden
(
- Contribution to journal › Article
-
Mark
Long-term ambient air pollution and venous thromboembolism in a population-based Swedish cohort
(
- Contribution to journal › Article
-
Mark
Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
(
- Contribution to journal › Letter
-
Mark
Multimorbidity can run in families - What are implications for clinical practice?
2023) In BMJ(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Familial aggregation of multimorbidity in Sweden: national explorative family study
(
- Contribution to journal › Article
-
Mark
A hypothesis - generating Swedish extended national cross-sectional family study of multimorbidity severity and venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Bioinformatic and rare-variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci
(
- Contribution to journal › Article
-
Mark
Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank
(
- Contribution to journal › Letter
-
Mark
The role of fibrinolysis in vascular diseases in UK biobank
(
- Contribution to journal › Letter
-
Mark
Lung function, respiratory symptoms and incident venous thromboembolism during a 44-year follow-up
(
- Contribution to journal › Article
-
Mark
“C1-inhibitor levels and Venous Thromboembolism : Results from a Mendelian Randomization Study”: comment from Grover et al
(
- Contribution to journal › Letter
-
Mark
Familial risk of vasospastic angina : a nationwide family study in Sweden
(
- Contribution to journal › Article
-
Mark
Heredity of pregnancy-related pelvic girdle pain in Sweden
(
- Contribution to journal › Article
-
Mark
Rare-variant collapsing and bioinformatic analyses for amyloidosis, dementia and Parkinson’s disease in the UK biobank reveal novel susceptibility loci
(
- Contribution to journal › Letter
- 2022
-
Mark
Air pollution and biomarkers of cardiovascular disease and inflammation in the Malmö Diet and Cancer cohort
(
- Contribution to journal › Article
-
Mark
Association between self-rated health and venous thromboembolism in Malmö Preventive Program : A cohort study
(
- Contribution to journal › Article
-
Mark
Familial Mortality Risks in Patients with Ischemic Stroke : A Swedish Sibling Study
(
- Contribution to journal › Article
-
Mark
Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
-
Mark
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
-
Mark
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
(
- Contribution to journal › Letter
-
Mark
Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study
(
- Contribution to journal › Article
-
Mark
Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study
(
- Contribution to journal › Article
- 2021
-
Mark
Effect of mindfulness on physical activity in primary healthcare patients : a randomised controlled trial pilot study
(
- Contribution to journal › Article
-
Mark
Risk Factors for Syncope Associated With Multigenerational Relatives With a History of Syncope
(
- Contribution to journal › Article
-
Mark
Familial Segregation of Venous Thromboembolism in Sweden: A Nationwide Family Study of Heritability and Complex Segregation Analysis
(
- Contribution to journal › Article
-
Mark
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study
(
- Contribution to journal › Letter
-
Mark
Reactome Pathway Analysis of Venous Thromboembolism, Peripheral Artery Disease, Stroke, and Coronary Artery Disease
(
- Contribution to journal › Letter
-
Mark
Mitochondria-DNA copy-number and incident venous thromboembolism among middle-aged women : a population-based cohort study
(
- Contribution to journal › Article
- 2020
-
Mark
Mortality risks associated with sibling heart failure
(
- Contribution to journal › Article
-
Mark
Self-rated health and venous thromboembolism among middle-aged women : a population-based cohort study
(
- Contribution to journal › Article
-
Mark
Risk of Stroke in Patients With Atrial Fibrillation Is Associated With Stroke in Siblings : A Nationwide Study
(
- Contribution to journal › Article
-
Mark
Neighborhood socioeconomic status and aortic stenosis : A Swedish study based on nationwide registries and an echocardiographic screening cohort
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
- 2019
-
Mark
New functional test for the TFPIα cofactor activity of Protein S working in synergy with FV-Short
(
- Contribution to journal › Article
-
Mark
Cardiovascular Risk Factors Associated with Venous Thromboembolism
(
- Contribution to journal › Article
-
Mark
Association of Genetic vs Environmental Factors in Swedish Adoptees with Clinically Significant Tinnitus
(
- Contribution to journal › Article
-
Mark
Familial association of attention-deficit hyperactivity disorder with autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Association of Short-Term Mortality of Venous Thromboembolism with Family History of Venous Thromboembolism and Charlson Comorbidity Index
(
- Contribution to journal › Article
-
Mark
Association of recurrent venous thromboembolism and circulating microRNAs
(
- Contribution to journal › Article
-
Mark
Outcomes associated with dual antiplatelet therapy after myocardial infarction in patients with aortic stenosis
2019) In International Journal of Cardiology(
- Contribution to journal › Article
-
Mark
J-curve association between alcohol intake and varicose veins in Japan : The Shimane CoHRE Study
(
- Contribution to journal › Article
-
Mark
Next-Generation Sequencing of 17 Genes Associated with Venous Thromboembolism Reveals a Deficit of Non-Synonymous Variants in Procoagulant Genes
(
- Contribution to journal › Article
-
Mark
Heritability of glomerulonephritis : A Swedish adoption study
(
- Contribution to journal › Article
-
Mark
Genetics of venous thromboembolism revised
(
- Contribution to journal › Debate/Note/Editorial
- 2018
-
Mark
Evaluation of Expression Level of Apolipoprotein M as a Diagnostic Marker for Primary Venous Thromboembolism
(
- Contribution to journal › Article
-
Mark
Heritability of End-Stage Renal Disease : A Swedish Adoption Study
(
- Contribution to journal › Article
-
Mark
Perinatal and familial risk factors for irritable bowel syndrome in a Swedish national cohort
(
- Contribution to journal › Article
-
Mark
Family history of diabetes and its relationship with insulin secretion and insulin sensitivity in Iraqi immigrants and native Swedes : a population-based cohort study
(
- Contribution to journal › Article
-
Mark
Fat mass and obesity-associated gene rs9939609 polymorphism is a potential biomarker of recurrent venous thromboembolism in male but not in female patients
(
- Contribution to journal › Article
-
Mark
Association of irritable bowel syndrome and venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Polymorphisms in PARK2 and MRPL37 are associated with higher risk of recurrent venous thromboembolism in a sex-specific manner
(
- Contribution to journal › Article
-
Mark
Identification of novel diagnostic biomarkers for deep venous thrombosis
(
- Contribution to journal › Article
-
Mark
Dementia and Alzheimer's disease risks in patients with autoimmune disorders
(
- Contribution to journal › Article
-
Mark
Postoperative Joint Replacement Complications in Swedish Patients With a Family History of Venous Thromboembolism
(
- Contribution to journal › Article
-
Mark
Alpha 2-macroglobulin 5 bp insertion/deletion polymorphism increases the risk of recurrent venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Familial Mortality Risks in Patients With Heart Failure : A Swedish Sibling Study
(
- Contribution to journal › Article
-
Mark
Characteristics and prognosis of healthy severe obesity (HSO) subjects - The Malmo Preventive Project
(
- Contribution to journal › Article
-
Mark
Familial Risks of Glaucoma in the Population of Sweden
(
- Contribution to journal › Article
-
Mark
Prevalence and in silico analysis of missense mutations in the PROS1 gene in the Swedish population : The SweGen dataset
(
- Contribution to journal › Letter
-
Mark
Hospitalization rate of paroxysmal supraventricular tachycardia in Sweden
(
- Contribution to journal › Article
-
Mark
Pilot study on increased adherence to physical activity on prescription (PAP) through mindfulness : Study protocol 11 Medical and Health Sciences 1117 Public Health and Health Services
(
- Contribution to journal › Article
-
Mark
A swedish nationwide adoption study of the heritability of heart failure
(
- Contribution to journal › Article
-
Mark
Factor V Leiden paradox in a middle-aged Swedish population : A prospective study
(
- Contribution to journal › Article
- 2017
-
Mark
A sibling based design to quantify genetic and shared environmental effects of venous thromboembolism in Sweden
(
- Contribution to journal › Article
-
Mark
Cardiovascular fitness in young males and risk of unprovoked venous thromboembolism in adulthood
(
- Contribution to journal › Article
-
Mark
Family history of venous thromboembolism and mortality after venous thromboembolism : a Swedish population-based cohort study
(
- Contribution to journal › Article
-
Mark
Seasonal variation of pulmonary embolism and age dependence
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Heritability of Mitral Regurgitation : Observations From the Framingham Heart Study and Swedish Population
(
- Contribution to journal › Article
-
Mark
Quantification of mitochondrial DNA copy number in suspected cancer patients by a well optimized ddPCR method
(
- Contribution to journal › Article
-
Mark
Body Height and Incident Risk of Venous Thromboembolism : A Cosibling Design
(
- Contribution to journal › Article
-
Mark
Risk of pulmonary embolism and deep venous thrombosis in patients with asthma : A nationwide case-control study from Sweden
(
- Contribution to journal › Article
-
Mark
Identification of Genetic Aberrations in Thrombomodulin Gene in Patients with Recurrent Venous Thromboembolism
(
- Contribution to journal › Article
-
Mark
Association between TLR9 rs5743836 polymorphism and risk of recurrent venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Familial Aggregation of Aortic Valvular Stenosis : A Nationwide Study of Sibling Risk
(
- Contribution to journal › Article
-
Mark
Risk of ocular manifestations in patients with giant cell arteritis : a nationwide study in Sweden
(
- Contribution to journal › Article
-
Mark
Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register study
(
- Contribution to journal › Article
-
Mark
A Swedish national adoption study of risk of irritable bowel syndrome (IBS)
(
- Contribution to journal › Article
- 2016
-
Mark
Neighbourhood Deprivation, Individual-Level and Familial-Level Socio-demographic Factors and Risk of Congenital Heart Disease: A Nationwide Study from Sweden.
(
- Contribution to journal › Article
-
Mark
Cognitive ability in Swedish conscripts and future risk of venous thromboembolism: A co-relative prospective national study.
2016) In European Journal of Internal Medicine(
- Contribution to journal › Article
-
Mark
Thrombomodulin gene c.1418C>T polymorphism and risk of recurrent venous thromboembolism.
(
- Contribution to journal › Article
-
Mark
Epidemiology of Familial Aggregation of Venous Thromboembolism
(
- Contribution to journal › Scientific review
-
Mark
Diagnostic potential of plasma microRNA signatures in patients with deep-vein thrombosis
(
- Contribution to journal › Article
-
Mark
Familial Transmission of Hospital-Treated Varicose Veins in Adoptees : A Swedish Family Study
(
- Contribution to journal › Article
-
Mark
Identification of polymorphisms in Apolipoprotein M gene and their relationship with risk of recurrent venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Sibling risk of hospitalization for heart failure – A nationwide study
(
- Contribution to journal › Article
-
Mark
A nationwide family study of venous thromboembolism and risk of arterial vascular disease
(
- Contribution to journal › Article
-
Mark
Venous thromboembolism does not share familial susceptibility with retinal vascular occlusion or glaucoma : a nationwide family study
(
- Contribution to journal › Article
-
Mark
Risk of solid tumors and hematological malignancy in persons with Turner and Klinefelter syndromes : A national cohort study
(
- Contribution to journal › Article
-
Mark
Familial risks of glomerulonephritis : a nationwide family study in Sweden
(
- Contribution to journal › Article
-
Mark
High Risk of Venous Thromboembolism in Klinefelter Syndrome
(
- Contribution to journal › Article
- 2015
-
Mark
Family history of venous thromboembolism as a risk factor and genetic research tool.
(
- Contribution to journal › Article
-
Mark
Perinatal risk factors for premature ischaemic heart disease in a Swedish national cohort.
(
- Contribution to journal › Article
-
Mark
Plasminogen activator inhibitor-1 4G/5G polymorphism, factor V Leiden, prothrombin mutations and the risk of VTE recurrence.
(
- Contribution to journal › Article
-
Mark
Genetic aspects of thrombotic disease
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Familial transmission of chronic obstructive pulmonary disease in adoptees: a Swedish nationwide family study.
(
- Contribution to journal › Article
-
Mark
Family history of venous thromboembolism is a risk factor for venous thromboembolism in combined oral contraceptive users: a nationwide case-control study.
(
- Contribution to journal › Article
-
Mark
Role of family history of venous thromboembolism (VTE) and thrombophilia as predictors of VTE recurrence: a prospective follow-up study.
(
- Contribution to journal › Article
-
Mark
Neighbourhood deprivation and lung cancer incidence and mortality: a multilevel analysis from Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of irritable bowel syndrome in first-degree, second-degree and thirddegree relatives of affected individuals: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of breast cancer among patients with bioprosthetic or mechanical valve replacement: a population-based study in Sweden.
(
- Contribution to journal › Article
-
Mark
Circulating HER2 is associated with hyperglycaemia and insulin resistance.
(
- Contribution to journal › Article
-
Mark
Alcohol use disorders are associated with venous thromboembolism.
(
- Contribution to journal › Article
-
Mark
Family history of venous thromboembolism and risk of hospitalized thromboembolism in cancer patients: A nationwide family study.
(
- Contribution to journal › Article
-
Mark
Soluble urokinase plasminogen activator receptor and incidence of venous thromboembolism.
(
- Contribution to journal › Article
- 2014
-
Mark
Venous thromboembolism and varicose veins share familial susceptibility: a nationwide family study in sweden.
(
- Contribution to journal › Article
-
Mark
Familial risks of kidney failure in sweden: a nationwide family study.
(
- Contribution to journal › Article
-
Mark
Morbidity and mortality risk among patients with screening-detected severe hypertension in the Malmo Preventive Project
(
- Contribution to journal › Article
-
Mark
Neighborhood deprivation and childhood autism: A nationwide study from Sweden.
(
- Contribution to journal › Article
-
Mark
Apolipoprotein M and the risk of unprovoked recurrent venous thromboembolism.
(
- Contribution to journal › Article
-
Mark
Transforming growth factor (TGF)-β levels and unprovoked recurrent venous thromboembolism.
(
- Contribution to journal › Article
-
Mark
Low degree of shared genetic susceptibility to coronary artery disease and venous thromboembolism.
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
The association between red cell distribution width and venous thromboembolism: A biochemical evaluation
(
- Contribution to journal › Letter
-
Mark
End stage renal disease risk and neighbourhood deprivation: A nationwide cohort study in Sweden.
(
- Contribution to journal › Article
-
Mark
Family history of venous thromboembolism (VTE) and risk of recurrent hospitalization for VTE: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
The association between apolipoprotein M and insulin resistance varies with country of birth.
(
- Contribution to journal › Article
-
Mark
Neighbourhood deprivation, individual-level familial and socio-demographic factors and diagnosed childhood obesity: a nationwide multilevel study from sweden.
(
- Contribution to journal › Article
-
Mark
Neighborhood, family, and childhood and adolescent epilepsy: A nationwide epidemiological study from Sweden.
(
- Contribution to journal › Article
-
Mark
Red cell distribution width and risk for venous thromboembolism: A population-based cohort study.
(
- Contribution to journal › Article
-
Mark
Familial transmission of prostate, breast and colorectal cancer in adoptees is related to cancer in biological but not in adoptive parents: A nationwide family study.
(
- Contribution to journal › Article
-
Mark
Gestational Age and Risk of Venous Thromboembolism From Birth Through Young Adulthood.
(
- Contribution to journal › Article
-
Mark
Familial Transmission of Venous Thromboembolism: A Cohort Study of 80,214 Swedish Adoptees Linked to Their Biological and Adoptive Parents.
(
- Contribution to journal › Article
-
Mark
Determination of 14 Circulating microRNAs in Swedes and Iraqis with and without Diabetes Mellitus Type 2.
(
- Contribution to journal › Article
- 2013
-
Mark
High Familial Risk of Atrial Fibrillation/Atrial Flutter in Multiplex Families: A Nationwide Family Study in Sweden
(
- Contribution to journal › Article
-
Mark
Familial risk of venous thromboembolism in first-, second- and third-degree relatives: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Age-and sex-specific seasonal variation of venous thromboembolism in patients with and without family history: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Mothers, places and risk of hospitalization for childhood asthma: a nationwide study from Sweden: Epidemiology of Allergic Disease.
(
- Contribution to journal › Article
-
Mark
Venous thromboembolism does not share strong familial susceptibility with pre-eclampsia/eclampsia: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Family history as a predictor of hospitalization for hypertension in Sweden.
(
- Contribution to journal › Article
-
Mark
Neighbourhood deprivation and hospitalization for atrial fibrillation in Sweden.
(
- Contribution to journal › Article
-
Mark
Occupational and socio-economic risk factors for giant cell arteritis: a nationwide study based on hospitalizations in Sweden.
(
- Contribution to journal › Article
-
Mark
Low prevalence of irritable bowel syndrome in primary health care in four Swedish counties.
(
- Contribution to journal › Article
-
Mark
Shared and non-shared familial susceptibility of coronary heart disease, ischemic stroke, peripheral artery disease and aortic disease.
(
- Contribution to journal › Article
-
Mark
Shared and Nonshared Familial Susceptibility to Surgically Treated Inguinal Hernia, Femoral Hernia, Incisional Hernia, Epigastric Hernia, and Umbilical Hernia.
(
- Contribution to journal › Article
-
Mark
Time trends in pulmonary embolism: A matter of age and gender.
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Neighbourhood deprivation and risk of morbidity and mortality in people with lung cancer: A multilevel analysis from Sweden
2013) p.323-323(
- Contribution to conference › Poster
- 2012
-
Mark
Family history as a risk factor for recurrent hospitalization for lone atrial fibrillation: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of subsequent ischemic and hemorrhagic stroke in patients hospitalized for immune-mediated diseases: a nationwide follow-up study from Sweden
(
- Contribution to journal › Article
-
Mark
Risk of hospitalization for type 2 diabetes in first- and second-generation immigrants in Sweden: a nationwide follow-up study.
2012) In Journal of Diabetes and its Complications(
- Contribution to journal › Article
-
Mark
Small and large PROS1 deletions but no other types of rearrangements detected in patents with protein S deficiency
(
- Contribution to journal › Article
-
Mark
Risk of subsequent coronary heart disease in patients hospitalized for immune-mediated diseases: a nationwide follow-up study from sweden.
(
- Contribution to journal › Article
-
Mark
Neighborhood deprivation and risk of cervical cancer morbidity and mortality: A multilevel analysis from Sweden.
(
- Contribution to journal › Article
-
Mark
Occupational Risk Factors for Systemic Lupus Erythematosus: a Nationwide Study Based on Hospitalizations in Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of coronary heart disease in patients with cancer: A nationwide follow-up study from Sweden.
(
- Contribution to journal › Article
-
Mark
Family history and risk of hospital treatment for varicose veins in Sweden.
(
- Contribution to journal › Article
-
Mark
A nationwide family study of pulmonary embolism: Identification of high risk families with increased risk of hospitalized and fatal pulmonary embolism.
(
- Contribution to journal › Article
-
Mark
Risk of haemorrhagic and ischaemic stroke in patients with cancer: A nationwide follow-up study from Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of pulmonary embolism in patients with autoimmune disorders: a nationwide follow-up study from Sweden.
(
- Contribution to journal › Article
-
Mark
Risk of venous thromboembolism in first- and second-generation immigrants in Sweden.
(
- Contribution to journal › Article
-
Mark
Shared familial aggregation of susceptibility to different manifestations of venous thromboembolism: a nationwide family study in Sweden.
(
- Contribution to journal › Letter
-
Mark
Socioeconomic and occupational risk factors for venous thromboembolism in Sweden: A nationwide epidemiological study.
(
- Contribution to journal › Article
-
Mark
Increased Risks of Coronary Heart Disease and Stroke Among Spousal Caregivers of Cancer Patients.
(
- Contribution to journal › Article
-
Mark
Multiplex sibling history of coronary heart disease is a strong risk factor for coronary heart disease.
(
- Contribution to journal › Article
-
Mark
Neighborhood deprivation and hospitalization for venous thromboembolism in Sweden.
(
- Contribution to journal › Article
-
Mark
Stark ärftlighet för varicer bland svenskar, visar nationell studie
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Autoimmune diseases and venous thromboembolism : a review of the literature
(
- Contribution to journal › Article
- 2011
-
Mark
Age- and gender-specific familial risks for venous thromboembolism: a nationwide epidemiological study based on hospitalizations in sweden.
(
- Contribution to journal › Article
-
Mark
Parental history and venous thromboembolism: a nationwide study of age and sex-specific familial risks in Sweden.
(
- Contribution to journal › Article
-
Mark
Venous Thromboembolism Does Not Share Strong Familial Susceptibility with Ischemic Stroke: A Nationwide Family Study in Sweden.
(
- Contribution to journal › Article
-
Mark
Venous thromboembolism does not share strong familial susceptibility with coronary heart disease: a nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Familial risk factors shared by venous thromboembolism and cancer: A nationwide epidemiological study of Swedish families.
(
- Contribution to journal › Article
-
Mark
Determination of age-specific and sex-specific familial risks for the different manifestations of venous thromboembolism: A nationwide family study in Sweden.
(
- Contribution to journal › Article
-
Mark
Familial risks of unusual forms of venous thrombosis: a nationwide epidemiological study in Sweden.
(
- Contribution to journal › Article
- 2005
-
Mark
Large deletions of the PROS1 gene in a large fraction of mutationnegative patients with protein S deficiency
(
- Contribution to journal › Article
- 2004
-
Mark
Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.
(
- Contribution to journal › Article
- 2002
-
Mark
Naturally occurring mutations in the thrombomodulin gene leading to impaired expression and function
(
- Contribution to journal › Article
-
Mark
Genetic and phenotypic variability between families with hereditary protein S deficiency
(
- Contribution to journal › Article
- 2001
-
Mark
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden--an evolutionary advantage?
(
- Contribution to journal › Letter
- 1999
-
Mark
Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome
(
- Contribution to journal › Article
-
Mark
The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]
(
- Contribution to journal › Letter
-
Mark
Thrombophilia as a multigenic disease
(
- 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
(
- Contribution to journal › Letter
-
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
-
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
A new direct, fast and quantitative enzyme-linked ligandsorbent assay for measurement of free protein S antigen
(
- Contribution to journal › Article
-
Mark
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
(
- Contribution to journal › Article
- 1997
-
Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- Contribution to journal › Article
-
Mark
A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis
(
- Contribution to journal › Article
-
Mark
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
(
- Contribution to journal › Debate/Note/Editorial
-
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
The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- 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
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance due to a common factor V gene mutation is a major risk factor for venous thrombosis
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : Clinical implications
(
- Contribution to journal › Scientific review
- 1996
-
Mark
Elevated levels of prothrombin activation fragment 1 + 2 in plasma from patients with heterozygous Arg506 to Gln mutation in the factor V gene (APC-resistance) and/or inherited protein S deficiency
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C due to a factor V gene mutation : The most common inherited risk factor of thrombosis
(
- Contribution to journal › Article
-
Mark
Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
(
- Contribution to journal › Scientific review
-
Mark
High prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis.
(
- Contribution to journal › Letter
-
Mark
Inherited resistance to activated protein C caused by presence of the FV:Q506 allele as a basis of venous thrombosis
(
- Contribution to journal › Article
-
Mark
Factor V:Q506 mutation and anticardiolipin antibodies in systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
(
- Contribution to journal › Article
-
Mark
Familial thrombophilia : clinical and molecular analysis of Swedish families with inherited resistance to activated protein C or protein S deficiency
1996) In Scandinavian journal of clinical and laboratory investigation. Supplementum 56(226). p.19-46(
- Contribution to journal › Scientific review
-
Mark
Familial thrombophilia : Resistance to activated protein C and protein S deficiency
1996)(
- Thesis › Doctoral thesis (compilation)
- 1995
-
Mark
Resistance to activated protein C caused by a factor V gene mutation
(
- Contribution to journal › Article
-
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
-
Mark
Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
(
- Contribution to journal › Article
-
Mark
Methodological considerations on the determination of the APC response in plasma
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
-
Mark
Resistens mot aktiverat protein C. Vanlig genetisk riskfaktor för venös trombos
(
- Contribution to journal › Article
- 1994
-
Mark
Myocardial infarction associated with homozygous resistance to activated protein C
(
- Contribution to journal › Letter
-
Mark
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
(
- Contribution to journal › Article
-
Mark
Differential regulation of α and β chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein S
(
- Contribution to journal › Article
-
Mark
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
(
- Contribution to journal › Article
-
Mark
Differential regulation of alpha and beta chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein S
(
- Contribution to journal › Article