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- 2020
-
Mark
New generation genetic testing entering the clinic
(
- 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
Heritability of Caries Scores, Trajectories, and Disease Subtypes
(
- 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
Profiling of lincRNAs in human pluripotent stem cell derived forebrain neural progenitor cells
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
-
Mark
Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk
(
- Contribution to journal › Article
- 2019
-
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
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
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
Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
(
- 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 Applicability of Mouse Models to the Study of Human Disease
(
- Contribution to journal › Article
-
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
Heritability of glomerulonephritis : A Swedish adoption study
(
- Contribution to journal › Article
- 2018
-
Mark
17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage
(
- 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
Predictors of responses to clinic-based childhood obesity care
(
- Contribution to journal › Article
-
Mark
Examining the Association Between Autistic Traits and Atypical Sensory Reactivity : A Twin Study
(
- Contribution to journal › Article
-
Mark
Ordet och djuren : En dubbel blick på det mänskliga
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
(
- 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
Genetic variation of acquired structural chromosomal aberrations
(
- 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
Fifth Åland Island conference on von Willebrand disease
(
- 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
Heritability of End-Stage Renal Disease : A Swedish Adoption Study
(
- Contribution to journal › Article
-
Mark
Immunogenetics of Parkinson's disease
2018) p.27-44(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Gestational diabetes and maternal obesity are associated with epigenome-wide methylation changes in children
(
- Contribution to journal › Article
-
Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
- 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
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
Molecular Epidemiology of Heart Failure : Translational Challenges and Opportunities
(
- Contribution to journal › Scientific review
-
Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
-
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
Naumovozyma castellii: an alternative model for budding yeast molecular biology
(
- 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
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke
(
- 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
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
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
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
(
- Contribution to journal › Article
-
Mark
Causal inference in obesity research
(
- Contribution to journal › Scientific review
-
Mark
Family history of venous thromboembolism and mortality after venous thromboembolism : a Swedish population-based cohort study
(
- Contribution to journal › Article
-
Mark
Cerebellar mutism syndrome in children with brain tumours of the posterior fossa
(
- 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
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
Epidemiology of Familial Aggregation of Venous Thromboembolism
(
- Contribution to journal › Scientific review
-
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
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
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
Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program
(
- Contribution to journal › Article
-
Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- 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
- 2015
-
Mark
Rural avenues as dispersal corridors for the vulnerable saproxylic beetle Elater ferrugineus in a fragmented agricultural landscape
(
- Contribution to journal › Article
-
Mark
Genetic Variations in Type 2 Diabetes and Cardiovascular Disease: A Focus on Gene-Lifestyle Interactions and Mendelian Randomization
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetics of complications in patients with type 2 diabetes
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Autism spectrum disorders and coexisting disorders in a nationwide Swedish twin study
(
- Contribution to journal › Article
-
Mark
Strategies for reducing inhibitor formation in severe haemophilia
(
- Contribution to journal › Scientific review
-
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
Frontotemporal dementia - symptoms and brain pathology
(
- Thesis › Doctoral thesis (compilation)
-
Mark
The relationship between reduced renal function and cardiovascular disease
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Hereditary myopathy with early respiratory failure: occurrence in various populations
(
- Contribution to journal › Article
-
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
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
A Common SCN5A Variant Is Associated with PR Interval and Atrial Fibrillation Among African Americans
(
- 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
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
A Swedish national adoption study of criminality
(
- Contribution to journal › Article
-
Mark
Socioekonomisk status har enbart en svag koppling till kriminalitet
2014) 111.(
- Other contribution › Miscellaneous
-
Mark
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
(
- Contribution to journal › Article
- 2013
-
Mark
The Social Defeat Hypothesis of Schizophrenia: An Update
(
- Contribution to journal › Article
-
Mark
High Familial Risk of Atrial Fibrillation/Atrial Flutter in Multiplex Families: A Nationwide Family Study in Sweden
(
- Contribution to journal › Article
-
Mark
Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage
(
- 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
-
Mark
Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
(
- 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