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- 2024
-
Mark
Oxidative stress-related genetic variation and antioxidant vitamin intake in intact and ruptured abdominal aortic aneurysm : a Swedish population-based retrospective cohort study
(
- Contribution to journal › Article
-
Mark
OMICs Signatures Linking Persistent Organic Pollutants to Cardiovascular Disease in the Swedish Mammography Cohort
(
- Contribution to journal › Article
-
Mark
Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes
(
- 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
Proteomic analysis shows decreased type I fibers and ectopic fat accumulation in skeletal muscle from women with PCOS
(
- Contribution to journal › Article
-
Mark
A genomic mutational constraint map using variation in 76,156 human genomes
(
- Contribution to journal › Article
- 2023
-
Mark
The impact of sex, age at onset, recurrence, mode of ascertainment and medical complications on the family genetic risk score profiles for alcohol use disorder
(
- Contribution to journal › Article
-
Mark
Genetic liability to suicide attempt, suicide death, and psychiatric and substance use disorders on the risk for suicide attempt and suicide death : A Swedish national study
(
- Contribution to journal › Article
-
Mark
Genetic insights into resting heart rate and its role in cardiovascular disease
(
- Contribution to journal › Article
-
Mark
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
(
- Contribution to journal › Article
-
Mark
Genetic mechanisms underlying arrhythmogenic mitral valve prolapse : Current and future perspectives
(
- Contribution to journal › Scientific review
-
Mark
Mosaic Loss of Chromosome Y Is Associated With Functional Outcome After Ischemic Stroke
(
- Contribution to journal › Article
-
Mark
How Well do Polygenic Risk Scores Identify Men at High Risk for Prostate Cancer? Systematic Review and Meta-Analysis
(
- Contribution to journal › Article
-
Mark
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
(
- Contribution to journal › Article
-
Mark
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
(
- Contribution to journal › Article
-
Mark
Obesity-associated changes in molecular biology of primary breast cancer
(
- Contribution to journal › Article
-
Mark
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
(
- Contribution to journal › Article
-
Mark
Clonal haematopoiesis and risk of chronic liver disease
(
- Contribution to journal › Article
-
Mark
Life is pain : Fibromyalgia as a nexus of multiple liability distributions
2023) In American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 192(7-8). p.171-182(
- Contribution to journal › Article
-
Mark
Oxidative stress-related factors in abdominal aortic aneurysm: potential clinical implications
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetics of diabetes-associated microvascular complications
(
- Contribution to journal › Scientific review
-
Mark
Genetically proxied impaired GIPR signaling and risk of 6 cancers
(
- Contribution to journal › Article
-
Mark
Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patients
2023) In Gut(
- Contribution to journal › Article
-
Mark
Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B
(
- Contribution to journal › Article
-
Mark
Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome
(
- Contribution to journal › Article
-
Mark
The etiology of Parkinson's disease. Genetic and non-genetic risk factors for a multifactorial disease
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
The moderation of the genetic risk for alcohol and drug use disorders in a Swedish national sample by the genetic aptitude for educational attainment
(
- Contribution to journal › Article
-
Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
(
- Contribution to journal › Article
-
Mark
Contribution of rare and common coding variants to haematological malignancies in the UK biobank
(
- Contribution to journal › Letter
-
Mark
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
(
- Contribution to journal › Article
-
Mark
Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes : A genetic association study in Europeans
(
- Contribution to journal › Article
-
Mark
HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
(
- Contribution to journal › Article
-
Mark
Birth Weight Is Associated With Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Outcomes in Adulthood
(
- 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
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project
(
- Contribution to journal › Article
-
Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
(
- Contribution to journal › Article
-
Mark
Revisiting Diagnosis and Treatment of Hypertrophic Cardiomyopathy : Current Practice and Novel Perspectives
(
- Contribution to journal › Scientific review
-
Mark
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
(
- Contribution to journal › Article
-
Mark
A large meta-analysis identifies genes associated with anterior uveitis
(
- Contribution to journal › Article
-
Mark
Differences in genetic risk score profiles for drug use disorder, major depression, and ADHD as a function of sex, age at onset, recurrence, mode of ascertainment, and treatment
(
- Contribution to journal › Article
- 2022
-
Mark
Differential Activation of Immune Effector Processes in Mature Compared to Immature Sacrococcygeal Teratomas
(
- Contribution to journal › Article
-
Mark
Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study
(
- Contribution to journal › Article
-
Mark
The genetic contribution to hand osteoarthritis
(
- Contribution to journal › Article
-
Mark
Origin and evolution of animal multicellularity in the light of phylogenomics and cancer genetics
(
- Contribution to journal › Article
-
Mark
Applicability of polygenic risk scores in endometriosis clinical presentation
(
- Contribution to journal › Article
-
Mark
Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization
(
- Contribution to journal › Article
-
Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
(
- Contribution to journal › Article
-
Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
(
- Contribution to journal › Article
-
Mark
Birthweight, BMI in adulthood and latent autoimmune diabetes in adults : a Mendelian randomisation study
(
- Contribution to journal › Article
-
Mark
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
(
- Contribution to journal › Article
-
Mark
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
(
- Contribution to journal › Article
-
Mark
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
(
- Contribution to journal › Article
-
Mark
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women
(
- Contribution to journal › Article
-
Mark
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
(
- Contribution to journal › Article
-
Mark
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
(
- Contribution to journal › Article
-
Mark
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
(
- Contribution to journal › Article
-
Mark
Phenotypic and genetic classification of diabetes
(
- Contribution to journal › Scientific review
-
Mark
Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium
(
- Contribution to journal › Article
-
Mark
Genotype-phenotype correlation in arrhythmogenic right ventricular cardiomyopathy-risk of arrhythmias and heart failure
(
- Contribution to journal › Article
-
Mark
Genetic Predisposition to Sporadic and Familial Multiple Myeloma
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Rare germline copy number variants (CNVs) and breast cancer risk
(
- Contribution to journal › Article
-
Mark
Familial Mortality Risks in Patients with Ischemic Stroke : A Swedish Sibling Study
(
- Contribution to journal › Article
-
Mark
RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts
(
- 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
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
(
- Contribution to journal › Article
-
Mark
Genetically identical twins show comparable tau PET load and spatial distribution
(
- Contribution to journal › Article
-
Mark
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
(
- Contribution to journal › Article
-
Mark
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk
(
- Contribution to journal › Article
-
Mark
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
(
- Contribution to journal › Article
-
Mark
ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma
(
- Contribution to journal › Article
-
Mark
A saturated map of common genetic variants associated with human height
(
- Contribution to journal › Article
-
Mark
Sugar-Coated. The role of sugar intake and cardiovascular disease development in the context of nutritional recommendations
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
-
Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
-
Mark
Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study
(
- Contribution to journal › Article
- 2021
-
Mark
Adult-onset type 1 diabetic patients with less severe clinical manifestation have less risk DR-DQ genotypes than childhood-onset patients
(
- Contribution to journal › Article
-
Mark
Precision oncology of high-grade ovarian cancer defined through targeted sequencing
(
- Contribution to journal › Article
-
Mark
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study
(
- Contribution to journal › Letter
-
Mark
Genotype–Phenotype Relations for the Atypical Parkinsonism Genes : MDSGene Systematic Review
(
- Contribution to journal › Scientific review
-
Mark
Novel Reclassification of Adult Diabetes Is Useful to Distinguish Stages of β-Cell Function Linked to the Risk of Vascular Complications : The DOLCE Study From Northern Ukraine
(
- Contribution to journal › Article
-
Mark
“Omics” in traumatic brain injury : novel approaches to a complex disease
(
- Contribution to journal › Scientific review
-
Mark
Causal effect of adiposity measures on blood pressure traits in 2 urban swedish cohorts : A mendelian randomization study
(
- Contribution to journal › Article
-
Mark
Cancer risk and predisposition in families with childhood cancer
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series 2021(
- Thesis › Doctoral thesis (monograph)
-
Mark
The heritability of doctor-diagnosed traumatic and degenerative meniscus tears
(
- Contribution to journal › Article
-
Mark
The genomics of heart failure : design and rationale of the HERMES consortium
(
- Contribution to journal › Article
-
Mark
Using Human Genetics to Understand Mechanisms in Ischemic Stroke Outcome : From Early Brain Injury to Long-Term Recovery
(
- Contribution to journal › Scientific review
-
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
-
Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
-
Mark
The trans-ancestral genomic architecture of glycemic traits
(
- 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
Association of thyroid function with blood pressure and cardiovascular disease : A mendelian randomization
(
- Contribution to journal › Article
- 2020
-
Mark
Mortality risks associated with sibling heart failure
(
- Contribution to journal › Article
-
Mark
Heritability of Caries Scores, Trajectories, and Disease Subtypes
(
- Contribution to journal › Article
-
Mark
Profiling of lincRNAs in human pluripotent stem cell derived forebrain neural progenitor cells
(
- Contribution to journal › Article
-
Mark
Familial Risks of Heart Failure in Sweden
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Calcitonin gene-related peptide (CGRP) and cluster headache
(
- Contribution to journal › Scientific review
-
Mark
Risk of Stroke in Patients With Atrial Fibrillation Is Associated With Stroke in Siblings : A Nationwide Study
(
- Contribution to journal › Article
-
Mark
Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk
(
- Contribution to journal › Article
-
Mark
Biological and environmental predictors of heterogeneity in neurocognitive ageing : Evidence from Betula and other longitudinal studies
(
- Contribution to journal › Scientific review
-
Mark
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
(
- Contribution to journal › Article
-
Mark
High genetic contribution to anterior cruciate ligament rupture : Heritability ∼69%
2020) In British journal of sports medicine(
- Contribution to journal › Article
-
Mark
Next-generation epidemiology : the role of high-resolution molecular phenotyping in diabetes research
(
- Contribution to journal › Scientific review
-
Mark
Association of Established Blood Pressure Loci With 10-Year Change in Blood Pressure and Their Ability to Predict Incident Hypertension
(
- Contribution to journal › Article
-
Mark
Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
-
Mark
New generation genetic testing entering the clinic
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
- 2019
-
Mark
International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology : Report of the Dubai, Copenhagen and Toronto meetings
(
- Contribution to journal › Article
-
Mark
The Applicability of Mouse Models to the Study of Human Disease
(
- Contribution to journal › Article
-
Mark
Models and Nomenclature for Cytoplasmic Incompatibility : Caution over Premature Conclusions – A Response to Beckmann et al.
(
- Contribution to journal › Letter
-
Mark
The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysis
(
- Contribution to journal › Article
-
Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
(
- Contribution to journal › Article
-
Mark
Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
(
- Contribution to journal › Article
-
Mark
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
(
- Contribution to journal › Article
-
Mark
Nature vs nurture in knee osteoarthritis – the importance of age, sex and body mass index
(
- Contribution to journal › Article
-
Mark
Nomenclature of Genetically Determined Myoclonus Syndromes : Recommendations of the International Parkinson and Movement Disorder Society Task Force
(
- Contribution to journal › Scientific review
-
Mark
Advancing research toward faster diagnosis, better treatment, and end of stigma in epilepsy
2019) In Epilepsia(
- Contribution to journal › Article
-
Mark
Subsequent Event Risk in Individuals With Established Coronary Heart Disease
(
- Contribution to journal › Article
-
Mark
Heritability of glomerulonephritis : A Swedish adoption study
(
- Contribution to journal › Article
-
Mark
Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
(
- Contribution to journal › Article
- 2018
-
Mark
Gestational diabetes and maternal obesity are associated with epigenome-wide methylation changes in children
(
- Contribution to journal › Article
-
Mark
Genetic and environmental factors affecting birth size variation : A pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts
(
- Contribution to journal › Article
-
Mark
17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
(
- Contribution to journal › Article
-
Mark
The lived experience of Huntington’s disease : A phenomenological perspective on genes, the body and the lived experience of a genetic disease
(
- Contribution to journal › Article
-
Mark
Predictors of responses to clinic-based childhood obesity care
(
- Contribution to journal › Article
-
Mark
Sources of Parent-Child Transmission of Drug Abuse : Path Analyses of Not-Lived-With Parental, Stepparental, Triparental, and Adoptive Families
(
- Contribution to journal › Article
-
Mark
Ordet och djuren : En dubbel blick på det mänskliga
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Genetic variation of acquired structural chromosomal aberrations
(
- Contribution to journal › Article
-
Mark
Heritability of End-Stage Renal Disease : A Swedish Adoption Study
(
- Contribution to journal › Article
-
Mark
Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway : a meta-analysis
(
- Contribution to journal › Article
-
Mark
Examining the Association Between Autistic Traits and Atypical Sensory Reactivity : A Twin Study
(
- Contribution to journal › Article
-
Mark
Fifth Åland Island conference on von Willebrand disease
(
- Contribution to journal › Article
-
Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
-
Mark
Immunogenetics of Parkinson's disease
2018) p.27-44(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2017
-
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
The importance of genetic factors for the development of arthropathy : A longitudinal study of children and adolescents with haemophilia A
(
- Contribution to journal › Article
-
Mark
The second Team Haemophilia Education Meeting, 2016, Frankfurt, Germany
(
- 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
Causal inference in obesity research
(
- Contribution to journal › Scientific review
-
Mark
Naumovozyma castellii: an alternative model for budding yeast molecular biology
(
- Contribution to journal › Article
-
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
Molecular Epidemiology of Heart Failure : Translational Challenges and Opportunities
(
- Contribution to journal › Scientific review
-
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
(
- Contribution to journal › Article
-
Mark
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
(
- 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
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
(
- Contribution to journal › Article
-
Mark
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke
(
- Contribution to journal › Article
-
Mark
DNA methylation links genetics, fetal environment, and an unhealthy lifestyle to the development of type 2 diabetes
(
- Contribution to journal › Scientific review
-
Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
-
Mark
Allelic difference in Mhc2ta confers altered microglial activation and susceptibility to α-synuclein-induced dopaminergic neurodegeneration
(
- Contribution to journal › Article
-
Mark
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
(
- Contribution to journal › Article
-
Mark
Cerebellar mutism syndrome in children with brain tumours of the posterior fossa
(
- Contribution to journal › Article
-
Mark
Genetics of complex disease
2017)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Parental responsibility in the context of neuroscience and genetics
Hens, Kristien ; Cutas, Daniela LU and Horstkötter, Dorothee (2017)
- Book/Report › Anthology (editor)
-
Mark
Parental responsibility : a moving target
(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2016
-
Mark
The genetic and environmental structure jof the character sub-skales of the temperament and character inventory in adolescence
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Epidemiology of Familial Aggregation of Venous Thromboembolism
(
- Contribution to journal › Scientific review
-
Mark
Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program
(
- Contribution to journal › Article
-
Mark
Diet quality and change in blood lipids during 16 years of follow-up and their interaction with genetic risk for dyslipidemia
(
- Contribution to journal › Article
-
Mark
Third European stroke science workshop
2016) p.178-186(
- Contribution to conference › Paper, not in proceeding
-
Mark
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden
(
- Contribution to journal › Article
-
Mark
Sibling risk of hospitalization for heart failure – A nationwide study
(
- Contribution to journal › Article
-
Mark
Do Genetic Factors Modify the Relationship Between Obesity and Hypertriglyceridemia? : Findings From the GLACIER and the MDC Studies
(
- Contribution to journal › Article
-
Mark
Thrombin Cleavage of Osteopontin Modulates Its Activities in Human Cells In Vitro and Mouse Experimental Autoimmune Encephalomyelitis In Vivo
(
- 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
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- 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
Rural avenues as dispersal corridors for the vulnerable saproxylic beetle Elater ferrugineus in a fragmented agricultural landscape
(
- Contribution to journal › Article
-
Mark
Genetics of complications in patients with type 2 diabetes
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic Variations in Type 2 Diabetes and Cardiovascular Disease: A Focus on Gene-Lifestyle Interactions and Mendelian Randomization
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Strategies for reducing inhibitor formation in severe haemophilia
(
- Contribution to journal › Scientific review
-
Mark
Autism spectrum disorders and coexisting disorders in a nationwide Swedish twin study
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for inhibitors in haemophilia A
(
- Contribution to journal › Scientific review
-
Mark
Self-fertilization and inbreeding limit the scope for sexually antagonistic polymorphism
(
- Contribution to journal › Article
-
Mark
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation
(
- Contribution to journal › Article
-
Mark
Non-motor symptoms in genetically defined dystonia : Homogenous groups require systematic assessment
(
- Contribution to journal › Scientific review
- 2014
-
Mark
The relationship between reduced renal function and cardiovascular disease
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Frontotemporal dementia - symptoms and brain pathology
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Variations in apolipoprotein D and sigma non-opioid intracellular receptor 1 genes with relation to risk, severity and outcome of ischemic stroke
(
- Contribution to journal › Article
-
Mark
Genetic predisposition to salt sensitivity and cardiovascular disease
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes
(
- Contribution to journal › Article
-
Mark
A Common SCN5A Variant Is Associated with PR Interval and Atrial Fibrillation Among African Americans
(
- Contribution to journal › Article
-
Mark
Loss-of-Function of the Voltage-Gated Sodium Channel Na(V)1.5 (Channelopathies) in Patients With Irritable Bowel Syndrome
(
- Contribution to journal › Article
-
Mark
Environmental influences on familial resemblance for drug abuse in first-cousin pairs: a Swedish national study
(
- Contribution to journal › Article
-
Mark
A Swedish national adoption study of criminality
(
- Contribution to journal › Article
-
Mark
Factor VIII therapy for hemophilia A: current and future issues
(
- Contribution to journal › Scientific review
-
Mark
Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes
(
- Contribution to journal › Article
-
Mark
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
(
- Contribution to journal › Article
-
Mark
Socioekonomisk status har enbart en svag koppling till kriminalitet
2014) 111.(
- Other contribution › Miscellaneous
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Mark
Hereditary myopathy with early respiratory failure: occurrence in various populations
(
- Contribution to journal › Article
- 2013
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Mark
The Social Defeat Hypothesis of Schizophrenia: An Update
(
- Contribution to journal › Article
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Mark
High Familial Risk of Atrial Fibrillation/Atrial Flutter in Multiplex Families: A Nationwide Family Study in Sweden
(
- Contribution to journal › Article
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Mark
Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage
(
- Contribution to journal › Article
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Mark
Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
(
- Contribution to journal › Article
-
Mark
Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women
(
- Contribution to journal › Article
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Mark
Familial Risk of Small Intestinal Carcinoid and Adenocarcinoma
(
- Contribution to journal › Article
-
Mark
Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
(
- Contribution to journal › Article
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Mark
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
(
- Contribution to journal › Article
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Mark
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
(
- Contribution to journal › Article
-
Mark
Modern Genes : Body, Rationality and Ambivalence
(
- Thesis › Doctoral thesis (compilation)
- 2012
-
Mark
Learning to eat strawberries in a disciplined way: Normalization practices following organ transplantation
(
- Contribution to journal › Article
-
Mark
Genetic and epigenetic influence on oxidative phosphorylation, islet function and type 2 diabetes in humans
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Burden of Risk Alleles for Hypertension Increases Risk of Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Population-based prediction of atrial fibrillation
(
- Thesis › Doctoral thesis (compilation)
-
Mark
MyelomA Genetics International Consortium
(
- Contribution to journal › Scientific review
-
Mark
Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
(
- Contribution to journal › Article
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Mark
A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels.
(
- Contribution to journal › Article
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Mark
SNP in the genome-wide association study hotspot on chromosome 9p21 confers susceptibility to diabetic nephropathy in type 1 diabetes
(
- Contribution to journal › Article
-
Mark
Editorial: Genetics and Democracy
(
- Contribution to journal › Letter
-
Mark
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk
(
- Contribution to journal › Article
-
Mark
Participation in evolution and sustainability
(
- Contribution to journal › Article
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Mark
Friedreich ataxia in patients with FXN p.R165P point mutation.
(
- Contribution to journal › Published meeting abstract
-
Mark
Experiences of living with increased risk of developing colorectal and gynaecological cancer in individuals with no identified gene mutation
(
- Contribution to journal › Article
- 2011
-
Mark
Autistic-like traits
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Anaesthesia and Genetics of the Ryanodine 1 Receptor
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Venous Thromboembolism Does Not Share Strong Familial Susceptibility with Ischemic Stroke: A Nationwide Family Study in Sweden.
(
- Contribution to journal › Article
-
Mark
Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium
(
- Contribution to journal › Article
-
Mark
Lack of association between genetic variations in the KALRN region and ischemic stroke
(
- Contribution to journal › Article
-
Mark
The Manifestation of Modernity in Genetic Science
2011) p.43-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
The Child and Adolescent Twin Study in Sweden (CATSS)
(
- Contribution to journal › Article
- 2010
-
Mark
Genetic and Metabolic Markers for the Development of Diabetes after Gestational Diabetes Mellitus
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Low plasma levels of monocyte chemoattractant protein-1 (MCP-1), tumor necrosis factor-alpha (TNF alpha), and vascular endothelial growth factor (VEGF) in patients with alpha1-antitrypsin deficiency-related fibromyalgia
(
- Contribution to journal › Article
-
Mark
Migratory behaviour and otolith chemistry suggest fine-scale sub-population structure within a genetically homogenous Atlantic Cod population
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Analysis of TBC1D4 in patients with severe insulin resistance
(
- Contribution to journal › Letter
-
Mark
Genetic association analysis of LARS2 with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The denial of a psychosis epidemic: A commentary on ‘The social determinants of psychosis in migrant and ethnic minority populations: a public health tragedy’ by Morgan & Hutchinson (2009)
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
What Can Human Genetics Teach Us About the Causes of Cardiovascular Disease?
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
LRRK2 variation and Parkinson's disease in African Americans
(
- Contribution to journal › Article
- 2009
-
Mark
Beta Cell Function: from Human Genetics to Animal Models
(
- Thesis › Doctoral thesis (compilation)
-
Mark
The T allele of rs7903146 TCF7L2 is associated with impaired insulinotropic action of incretin hormones, reduced 24 h profiles of plasma insulin and glucagon, and increased hepatic glucose production in young healthy men
(
- Contribution to journal › Article
-
Mark
Genetic Loci Contributing to Spontaneous Autoimmune Diabetes
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden
(
- Contribution to journal › Article
-
Mark
International Society of Blood Transfusion Committee on Terminology for Red Blood Cell Surface Antigens: Macao report
(
- Contribution to journal › Article
-
Mark
Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke A Large-Scale Genetic Association Study
(
- Contribution to journal › Article
-
Mark
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population
(
- Contribution to journal › Article
-
Mark
Functional Variant Disrupts Insulin Induction of USF1 Mechanism for USF1-Associated Dyslipidemias
(
- Contribution to journal › Article
-
Mark
A Genotype-Dependent Intermediate ECG Phenotype in Patients With Persistent Lone Atrial Fibrillation Genotype ECG-Phenotype Correlation in Atrial Fibrillation
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Genetic Variation in Sex Hormone Genes Influences Heel Ultrasound Parameters in Middle-Aged and Elderly Men: Results From the European Male Aging Study (EMAS)
(
- Contribution to journal › Article
-
Mark
Karl Pearson and the Scandinavian school of statistics
(
- Contribution to journal › Scientific review
-
Mark
Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
(
- Contribution to journal › Article
-
Mark
A genotype dependent intermediate ECG phenotype in patients with persistent lone atrial fibrillation
(
- Contribution to journal › Article
-
Mark
The Manifestation of Modernity in Genetic Science
2009) Biology, Anthropology and Cultural Criticism in the European Modern Age(
- Contribution to conference › Paper, not in proceeding
- 2008
-
Mark
Genetic characterization of families with von Willebrand disease
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
(
- Contribution to journal › Scientific review