Anders Mälarstig

The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.

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How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.

Assessed papers (1)

• Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
  2023 L1 93/100

1 assessed by us (1 reproduced) · 186 not yet assessed — every PubMed paper on record, linked below.

• Retrospective evaluation of human genetic evidence for clinical trial success using Mendelian randomization and machine learning ↗

  medRxiv · 2026
  not yet assessed
• FOXC1 Controls Smooth Muscle Cell Differentiation and Plasticity in Vascular Disease ↗

  JACC Basic to Translational Science · 2026 · PMID 42127570
  not yet assessed
• Proteogenomics in human populations ↗

  Nature Reviews Genetics · 2026 · PMID 42625025
  not yet assessed
• Protein Biomarkers in Risk and Prognosis of Amyotrophic Lateral Sclerosis ↗

  European Journal of Neurology · 2026 · PMID 42698373
  not yet assessed
• Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes ↗

  Nature Genetics · 2025 · PMID 40038546
  not yet assessed
• Data- and knowledge-derived functional landscape of human solute carriers ↗

  Molecular Systems Biology · 2025 · PMID 40355757
  not yet assessed
• Blood Pressure Lowering and Risk of Cancer ↗

  JACC CardioOncology · 2025 · PMID 40366326
  not yet assessed
• Human genetic variants in SLC39A8 impact uptake and steady-state metal levels within the cell ↗

  Life Science Alliance · 2025 · PMID 39884836
  not yet assessed
• A Method for Comparing Proteins Measured in Serum and Plasma by Olink Proximity Extension Assay ↗

  Molecular & Cellular Proteomics · 2025 · PMID 40441439
  not yet assessed
• Genetically Determined Inflammation‐Related Proteins in Asthma and Type‐2 Signatures ↗

  Allergy · 2025 · PMID 40464643
  not yet assessed
• Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty ↗

  Nature Aging · 2025 · PMID 40764432
  not yet assessed
• PCSK6 ablation in blood circulating cells increases atherosclerotic burden, but improves plaque stability by activating Th17-smooth muscle cell modulatory axis ↗

  Vascular Pharmacology · 2025 · PMID 40097084
  not yet assessed
• KDM5 demethylases suppress R-loop-mediated ‘viral mimicry’ and DNA damage in breast cancer cells ↗

  eLife · 2025 · PMID 41081756
  not yet assessed
• KDM5 demethylases suppress R-loop-mediated “viral mimicry” and DNA damage in breast cancer cells ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2025
  not yet assessed
• KDM5 demethylases suppress R-loop-mediated “viral mimicry” and DNA damage in breast cancer cells ↗

  eLife · 2025
  not yet assessed
• Proteomic Profiling of Glucose Metabolism Disturbances Yields Novel Plasma Proteins that May Be Associated With Development or Early Complications of Diabetes ↗

  Research Square · 2025
  not yet assessed
• Proteomic screening using NGS-based method identifies cardiovascular diseases biomarkers in patients without cardiovascular disease but with glucose metabolism disturbances ↗

  European Journal of Preventive Cardiology · 2025
  not yet assessed
• GENOME-WIDE ASSOCIATION STUDY OF AORTIC STIFFNESS DERIVED FROM DEEP LEARNING IN CMR IMAGES OF 45 789 INDIVIDUALS IDENTIFIES LOCI LINKED WITH CELL-MATRIX STRUCTURE ↗

  Postgraduate Medical Journal · 2025
  not yet assessed
• KDM5 demethylases suppress R-loop-mediated “viral mimicry” and DNA damage in breast cancer cells ↗

  eLife · 2025
  not yet assessed
• Author response: KDM5 demethylases suppress R-loop-mediated “viral mimicry” and DNA damage in breast cancer cells ↗

  2025
  not yet assessed
• KDM5 demethylases suppress R-loop-mediated ‘viral mimicry’ and DNA damage in breast cancer cells ↗

  eLife · 2025
  not yet assessed
• Genetic Landscape of the ACE2 Coronavirus Receptor ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2025
  not yet assessed
• Plasma Protein Profile Associated With a Family History of Early-Onset Coronary Heart Disease ↗

  Circulation Genomic and Precision Medicine · 2025 · PMID 41200820
  not yet assessed
• Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women ↗

  Journal of Clinical Oncology · 2024 · PMID 38422475
  not yet assessed
• Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers ↗

  Nature Communications · 2024 · PMID 38684708
  not yet assessed
• Identifying proteomic risk factors for overall, aggressive, and early onset prostate cancer using Mendelian Randomisation and tumour spatial transcriptomics ↗

  EBioMedicine · 2024 · PMID 38878676
  not yet assessed
• The genetic landscape of neuro-related proteins in human plasma ↗

  Nature Human Behaviour · 2024 · PMID 39210026
  not yet assessed
• Genetic Susceptibility to Acute Viral Bronchiolitis ↗

  The Journal of Infectious Diseases · 2024 · PMID 39299705
  not yet assessed
• ProteoMutaMetrics: machine learning approaches for solute carrier family 6 mutation pathogenicity prediction ↗

  RSC Advances · 2024 · PMID 38655474
  not yet assessed
• Plasma Protein Profile of Carotid Artery Atherosclerosis and Atherosclerotic Outcomes: Meta-Analyses and Mendelian Randomization Analyses ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2024
  not yet assessed
• Proteogenomic analysis in population biobanks identifies new therapeutic targets across heart failure subtypes ↗

  European Heart Journal · 2024
  not yet assessed
• Data- and knowledge-derived functional landscape of human solute carriers ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2024
  not yet assessed
• Abstract 4141107: Genome-wide association study of aortic stiffness derived from deep learning in CMR images of 45,789 individuals identifies loci linked with cell-matrix structure ↗

  Circulation · 2024
  not yet assessed
• Exploration of the circulating human secretome through protein quantitative trait analysis identifies an association between circulating levels of apolipoprotein L1 and risk of giant cell arteritis ↗

  medRxiv · 2024
  not yet assessed
• Abstract 7330: Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using mendelian randomization and tumor spatial transcriptomics ↗

  Cancer Research · 2024
  not yet assessed
• Author response for "ProteoMutaMetrics: machine learning approaches for solute carrier family 6 mutation pathogenicity prediction" ↗

  2024
  not yet assessed
• Technological readiness and implementation of genomic-driven precision medicine for complex diseases ↗

  UTUPub (University of Turku) · 2024
  not yet assessed
• Genome-wide association study of CMR image-based aortic stiffness in 45,789 individuals identifies loci linked with cardiovascular diseases ↗

  European Heart Journal · 2024
  not yet assessed
• FinnGen provides genetic insights from a well-phenotyped isolated population ↗

  Nature · 2023 · PMID 36653562
  not yet assessed
• Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

  Nature Immunology · 2023 · PMID 37563310
  L1 93/100
• An atlas of genetic scores to predict multi-omic traits ↗

  Nature · 2023 · PMID 36991119
  not yet assessed
• Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy ↗

  JAMA Cardiology · 2023 · PMID 37285119
  not yet assessed
• Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy ↗

  Nature Communications · 2023 · PMID 37188663
  not yet assessed
• Evaluation of circulating plasma proteins in breast cancer using Mendelian randomisation ↗

  Nature Communications · 2023 · PMID 37996402
  not yet assessed
• Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry) ↗

  International Journal of Epidemiology · 2023 · PMID 37365732
  not yet assessed
• Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study ↗

  Stroke · 2023 · PMID 37212139
  not yet assessed
• Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata ↗

  Nature Communications · 2023 · PMID 36726022
  not yet assessed
• Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals ↗

  Molecular Biology and Evolution · 2023 · PMID 37315093
  not yet assessed
• Experimental and Computational Analysis of Newly Identified Pathogenic Mutations in the Creatine Transporter SLC6A8 ↗

  Journal of Molecular Biology · 2023 · PMID 38070861
  not yet assessed
• The impact of circulating protein levels identified by affinity proteomics on short-term, overall breast cancer risk ↗

  British Journal of Cancer · 2023 · PMID 38135714
  not yet assessed
• NTHL1 is a recessive cancer susceptibility gene ↗

  Scientific Reports · 2023 · PMID 38036545
  not yet assessed
• A FinnGen pilot clinical recall study for Alzheimer’s disease ↗

  Scientific Reports · 2023 · PMID 37537264
  not yet assessed
• Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases ↗

  Clinical Proteomics · 2023 · PMID 37550624
  not yet assessed
• Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population ↗

  Nature · 2023 · PMID 36829046
  not yet assessed
• Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets ↗

  Nature Immunology · 2023 · PMID 37679551
  not yet assessed
• Mapping the aetiological foundations of the heart failure spectrum using human genetics ↗

  medRxiv · 2023
  not yet assessed
• Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using Mendelian randomization and tumor spatial transcriptomics ↗

  medRxiv · 2023 · PMID 37790472
  not yet assessed
• Identifying therapeutic targets for cancer: 2,094 circulating proteins and risk of nine cancers ↗

  medRxiv · 2023
  not yet assessed
• Genetic mechanisms of 184 neuro-related proteins in human plasma ↗

  medRxiv · 2023 · PMID 36824751
  not yet assessed
• Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases ↗

  Research Square · 2023
  not yet assessed
• Mapping pQTLs of circulating inflammatory proteins identifies drivers of immune-related disease risk and novel therapeutic targets ↗

  medRxiv · 2023
  not yet assessed
• Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders ↗

  Research Square · 2023 · PMID 37034613
  not yet assessed
• Evaluation of Circulating Plasma Proteins in Breast Cancer: A Mendelian Randomization Analysis ↗

  Research Square · 2023
  not yet assessed
• PCSK6 ablation increases atherosclerotic burden, but provides plaque stability by regulating TH17 and smooth muscle cell content ↗

  Atherosclerosis · 2023
  not yet assessed
• FOXC1 controls smooth muscle cell activation in vascular disease ↗

  Atherosclerosis · 2023
  not yet assessed
• Summary statistics of cis-pQTLs for plasma proteins measured using Olink Explore I and II technology in the KARMA cohort. ↗

  Zenodo (CERN European Organization for Nuclear Research) · 2023
  not yet assessed
• Summary statistics of cis-pQTLs for plasma proteins measured using Olink Explore I and II technology in the KARMA cohort. ↗

  Zenodo (CERN European Organization for Nuclear Research) · 2023
  not yet assessed
• New insights into the genetic etiology of Alzheimer’s disease and related dementias ↗

  Nature Genetics · 2022 · PMID 35379992
  not yet assessed
• Therapeutic Targets for Heart Failure Identified Using Proteomics and Mendelian Randomization

  UCL Discovery (University College London) · 2022
  not yet assessed
• The genetic regulation of protein expression in cerebrospinal fluid ↗

  EMBO Molecular Medicine · 2022 · PMID 36504281
  not yet assessed
• Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis ↗

  Communications Biology · 2022 · PMID 35978133
  not yet assessed
• Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases ↗

  Clinical Journal of the American Society of Nephrology · 2022 · PMID 36719157
  not yet assessed
• Causal analysis of plasma IL-8 on carotid intima media thickness, a measure of subclinical atherosclerosis ↗

  Current Research in Translational Medicine · 2022 · PMID 36493747
  not yet assessed
• Circulating proteins reveal prior use of menopausal hormonal therapy and increased risk of breast cancer ↗

  Translational Oncology · 2022 · PMID 35033985
  not yet assessed
• FinnGen: Unique genetic insights from combining isolated population and national health register data ↗

  medRxiv · 2022
  not yet assessed
• An atlas of genetic scores to predict multi-omic traits ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2022
  not yet assessed
• Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases: a Mendelian Randomisation study ↗

  medRxiv · 2022
  not yet assessed
• Hypothesis generation for variant effects using a KNIME workflow for automatic mapping of disease-related mutations onto 3D protein structures ↗

  2022
  not yet assessed
• Completion of data-mining workflow ↗

  Zenodo (CERN European Organization for Nuclear Research) · 2022
  not yet assessed
• Genetic assessment of all SLC family members ↗

  Zenodo (CERN European Organization for Nuclear Research) · 2022
  not yet assessed
• Abstract 420: Proprotein Convertase Subtilisin/Kexin 6 Is Involved In Lipid Metabolism In Liver ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2022
  not yet assessed
• Abstract 105: Proprotein Convertase Subtilisin/kexin Type 6 (Pcsk6) Plays A Role In Angiogenesis Regulation ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2022
  not yet assessed
• Abstract 217: PCSK6 Is A Key Regulator Of Immune Status In Mice And Its Ablation Increases Atherosclerotic Plaque Burden In A Bone Marrow Transplant Model ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2022
  not yet assessed
• Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries ↗

  Nature Communications · 2021 · PMID 33627673
  not yet assessed
• Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection ↗

  Nature Medicine · 2021 · PMID 34099924
  not yet assessed
• Accelerated inflammatory aging in Alzheimer’s disease and its relation to amyloid, tau, and cognition ↗

  Scientific Reports · 2021 · PMID 33479445
  not yet assessed
• Mapping the serum proteome to neurological diseases using whole genome sequencing ↗

  Nature Communications · 2021 · PMID 34857772
  not yet assessed
• Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices ↗

  Nature Communications · 2021 · PMID 33846329
  not yet assessed
• Plasma Protein Profile of Carotid Artery Atherosclerosis and Atherosclerotic Outcomes ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2021 · PMID 33657885
  not yet assessed
• Technological readiness and implementation of genomic‐driven precision medicine for complex diseases ↗

  Journal of Internal Medicine · 2021 · PMID 34213793
  not yet assessed
• Inflammation-related plasma protein levels and association with adiposity measurements in young adults ↗

  Scientific Reports · 2021 · PMID 34059769
  not yet assessed
• The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium ↗

  ESC Heart Failure · 2021 · PMID 34480422
  not yet assessed
• Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population ↗

  JAMA Ophthalmology · 2021 · PMID 34081096
  not yet assessed
• Proprotein convertase subtilisin/kexin 6 is involved in lipid metabolism in liver and adipose tissue ↗

  Atherosclerosis · 2021
  not yet assessed
• Mapping genetic determinants of 184 circulating proteins in 26,494 individuals to connect proteins and diseases ↗

  medRxiv · 2021
  not yet assessed
• Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19 ↗

  medRxiv · 2021 · PMID 33851187
  not yet assessed
• IL-18 and Lower Risk for Lung Cancer: Triangulated Evidence from Germline Predictions, Pre-Diagnostic Measurements, and Tumor Expression ↗

  medRxiv · 2021
  not yet assessed
• Circulating proteins reveal prior use of menopausal hormonal therapy and increased risk of breast cancer ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2021
  not yet assessed
• Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

  RePEc: Research Papers in Economics · 2021
  not yet assessed
• Abstract MP02: Proprotein Convertase Subtilisin/kexin Type 6 (PCSK6) Is Involved In Regulation Of Vasculogenesis ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2021
  not yet assessed
• Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure ↗

  Nature Communications · 2020 · PMID 31919418
  not yet assessed
• Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals ↗

  Nature Metabolism · 2020 · PMID 33067605
  not yet assessed
• The role of polygenic risk and susceptibility genes in breast cancer over the course of life ↗

  Nature Communications · 2020 · PMID 33318493
  not yet assessed
• Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells ↗

  Nature · 2020 · PMID 33057200
  not yet assessed
• Identification of novel pheno-groups in heart failure with preserved ejection fraction using machine learning ↗

  Heart · 2020 · PMID 31911501
  not yet assessed
• CDH6 and HAGH protein levels in plasma associate with Alzheimer’s disease in APOE ε4 carriers ↗

  Scientific Reports · 2020 · PMID 32427856
  not yet assessed
• An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease ↗

  European Journal of Human Genetics · 2020 · PMID 33110245
  not yet assessed
• The plasma protein profile and cardiovascular risk differ between intima-media thickness of the common carotid artery and the bulb: A meta-analysis and a longitudinal evaluation ↗

  Atherosclerosis · 2020 · PMID 31981948
  not yet assessed
• Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study ↗

  Genes · 2020 · PMID 33105679
  not yet assessed
• Genomic evaluation of circulating proteins for drug target characterisation and precision medicine ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Genome‐wide polygenic risk scores for identification of gene therapeutic target ↗

  Alzheimer s & Dementia · 2020
  not yet assessed
• Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020
  not yet assessed
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗

  UNC Libraries · 2020
  not yet assessed
• Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimer’s disease ↗

  Acta Neuropathologica Communications · 2019 · PMID 31694701
  not yet assessed
• Genetic architecture of human plasma lipidome and its link to cardiovascular disease ↗

  Nature Communications · 2019 · PMID 31551469
  not yet assessed
• Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure ↗

  Apollo (University of Cambridge) · 2019
  not yet assessed
• Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Genetic architecture of human plasma lipidome and its link to cardiovascular disease

  UEF eRepo (University of Eastern Finland) · 2019
  not yet assessed
• Additional file 1: of Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimerâ s disease ↗

  Figshare · 2019
  not yet assessed
• A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes ↗

  Diabetes · 2018 · PMID 29703844
  not yet assessed
• Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ↗

  Biological Psychiatry · 2018 · PMID 30679032
  not yet assessed
• Application of Machine Learning Methods to Predict Non-Alcoholic Steatohepatitis (NASH) in Non-Alcoholic Fatty Liver (NAFL) Patients. ↗

  PubMed · 2018 · PMID 30815083
  not yet assessed
• Associations of Circulating Protein Levels With Lipid Fractions in the General Population ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2018 · PMID 30354202
  not yet assessed
• Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function ↗

  Wellcome Open Research · 2018 · PMID 29682616
  not yet assessed
• Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function ↗

  Wellcome Open Research · 2018
  not yet assessed
• P3645Interleukin 8 (IL-8), but not GRO-a, associates with carotid intima-media thickness. Results from the IMPROVE study ↗

  European Heart Journal · 2018
  not yet assessed
• Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Exome-wide association study of plasma lipids in >300,000 individuals ↗

  Nature Genetics · 2017 · PMID 29083408
  not yet assessed
• Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease ↗

  PLoS Genetics · 2017 · PMID 28369058
  not yet assessed
• Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms ↗

  Nature Genetics · 2017 · PMID 28530674
  not yet assessed
• Exome-wide association study of plasma lipids in > 300,000 individuals

  Figshare · 2017
  not yet assessed
• Integrative studies implicate matrix metalloproteinase‐12 as a culprit gene for large‐artery atherosclerotic stroke ↗

  Journal of Internal Medicine · 2017 · PMID 28734077
  not yet assessed
• Improving Assessment of Drug Safety Through Proteomics ↗

  Circulation · 2017 · PMID 28974520
  not yet assessed
• Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline ↗

  Thorax · 2017 · PMID 28174340
  not yet assessed
• EARLY DETECTION OF THE UNEXPECTED, HARMFUL, PHARMACOLOGIC EFFECTS OF TORCETRAPIB: A RETROSPECTIVE PROTEOMICS ANALYSIS OF PLASMA SAMPLES FROM THE ILLUMINATE TRIAL ↗

  Journal of the American College of Cardiology · 2017
  not yet assessed
• Webinar | Proteogenomic strategies to advance drug development and precision medicine ↗

  Science · 2017
  not yet assessed
• P5282Differentiated health outcomes and potential protein markers based on unsupervised analysis of heart failure patients with preserved ejection fraction in the KaRen study ↗

  European Heart Journal · 2017
  not yet assessed
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗

  Nature Genetics · 2016 · PMID 27618447
  not yet assessed
• Circulating Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Predicts Future Risk of Cardiovascular Events Independently of Established Risk Factors ↗

  Circulation · 2016 · PMID 26896437
  not yet assessed
• Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis ↗

  Human Molecular Genetics · 2016 · PMID 26908601
  not yet assessed
• The Ser82 RAGE Variant Affects Lung Function and Serum RAGE in Smokers and sRAGE Production In Vitro ↗

  PLoS ONE · 2016 · PMID 27755550
  not yet assessed
• Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles ↗

  European Journal of Preventive Cardiology · 2016 · PMID 27940953
  not yet assessed
• Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity ↗

  BMC Genetics · 2016 · PMID 27514831
  not yet assessed
• Abstract 318: Matrix Metalloproteinase 12 is Causally Implicated in Cardiovascular Disease ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2016
  not yet assessed
• Abstract 13512: Chemokines and Carotid Intima-Media Thickness in a European Population at High Risk for Cardiovascular Events: Results From the IMPROVE Study ↗

  Circulation · 2016
  not yet assessed
• Abstract 18399: Higher Plasma Cxcl12 Levels Are Causally Associated With Increased Risk of Coronary Heart Disease

  Circulation · 2016
  not yet assessed
• Common Genetic Determinants of Lung Function, Subclinical Atherosclerosis and Risk of Coronary Artery Disease ↗

  PLoS ONE · 2014 · PMID 25093840
  not yet assessed
• Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction ↗

  PLoS Genetics · 2014 · PMID 24786987
  not yet assessed
• No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects ↗

  PLoS ONE · 2014 · PMID 25551457
  not yet assessed
• Functional IL6R 358Ala Allele Impairs Classical IL-6 Receptor Signaling and Influences Risk of Diverse Inflammatory Diseases ↗

  PLoS Genetics · 2013 · PMID 23593036
  not yet assessed
• Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease ↗

  American Journal of Clinical Nutrition · 2013 · PMID 23824729
  not yet assessed
• Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease ↗

  Circulation · 2013 · PMID 23969696
  not yet assessed
• The HLA locus contains novel foetal susceptibility alleles for congenital heart block with significant paternal influence ↗

  Journal of Internal Medicine · 2013 · PMID 24354957
  not yet assessed
• HTR4 gene structure and altered expression in the developing lung ↗

  Respiratory Research · 2013 · PMID 23890215
  not yet assessed
• Using Mendelian randomization to assess and develop clinical interventions: limitations and benefits ↗

  Journal of Comparative Effectiveness Research · 2013 · PMID 24236616
  not yet assessed
• A7.23 The HLA Locus Contains Novel Foetal Susceptibility Alleles for Congenital Heart Block with Significant Paternal Influence ↗

  Annals of the Rheumatic Diseases · 2013
  not yet assessed
• Use of Mendelian randomisation to assess potential benefit of clinical intervention ↗

  BMJ · 2012 · PMID 23131671
  not yet assessed
• Genes Contributing to Pain Sensitivity in the Normal Population: An Exome Sequencing Study ↗

  PLoS Genetics · 2012 · PMID 23284290
  not yet assessed
• Common and Low-Frequency Genetic Variants in the PCSK9 Locus Influence Circulating PCSK9 Levels ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2012 · PMID 22460556
  not yet assessed
• Combined Chromatin and Expression Analysis Reveals Specific Regulatory Mechanisms within Cytokine Genes in the Macrophage Early Immune Response ↗

  PLoS ONE · 2012 · PMID 22384210
  not yet assessed
• Correction: Combined Chromatin and Expression Analysis Reveals Specific Regulatory Mechanisms within Cytokine Genes in the Macrophage Early Immune Response ↗

  PLoS ONE · 2012
  not yet assessed
• Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes ↗

  Diabetes · 2011 · PMID 21873549
  not yet assessed
• Plasma CD93 concentration is a potential novel biomarker for coronary artery disease ↗

  Journal of Internal Medicine · 2011 · PMID 21332844
  not yet assessed
• Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

  Diabetes · 2011
  not yet assessed
• A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease ↗

  Surrey Research Insight Open Access (The University of Surrey) · 2011
  not yet assessed
• HLA-DRB1*04 is a novel fetal susceptibility allele in congenital heart block ↗

  Annals of the Rheumatic Diseases · 2011
  not yet assessed
• Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor ↗

  Circulation · 2010 · PMID 20231535
  not yet assessed
• Genetics of Atherothrombosis and Thrombophilia ↗

  Current Atherosclerosis Reports · 2010 · PMID 20425254
  not yet assessed
• W58 COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE ↗

  Atherosclerosis Supplements · 2010
  not yet assessed
• Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease ↗

  New England Journal of Medicine · 2009 · PMID 20032323
  not yet assessed
• Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis ↗

  PLoS Genetics · 2009 · PMID 19936222
  not yet assessed
• Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants ↗

  PLoS ONE · 2009 · PMID 19888323
  not yet assessed
• Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population ↗

  Circulation Cardiovascular Genetics · 2009 · PMID 20031578
  not yet assessed
• Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study ↗

  Blood · 2009 · PMID 19525478
  not yet assessed
• ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP ↗

  Atherosclerosis · 2009
  not yet assessed
• Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease

  Surrey Research Insight Open Access (The University of Surrey) · 2009
  not yet assessed
• IGF-I/IGFBP-3 ratio: a mechanistic insight into the metabolic syndrome ↗

  Clinical Science · 2008 · PMID 18816247
  not yet assessed
• Genetic Variants of Tumor Necrosis Factor Superfamily, Member 4 ( TNFSF4 ), and Risk of Incident Atherothrombosis and Venous Thromboembolism ↗

  Clinical Chemistry · 2008 · PMID 18356244
  not yet assessed
• Variants of the Interferon Regulatory Factor 5 Gene Regulate Expression of IRF5 mRNA in Atherosclerotic Tissue But Are Not Associated With Myocardial Infarction ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2008 · PMID 18323517
  not yet assessed
• Raised interleukin-10 is an indicator of poor outcome and enhanced systemic inflammation in patients with acute coronary syndrome ↗

  Heart · 2007 · PMID 17690160
  not yet assessed
• Genetic variation in the interleukin-6 gene in relation to risk and outcomes in acute coronary syndrome ↗

  Thrombosis Research · 2006 · PMID 16782174
  not yet assessed
• Soluble CD40L Levels Are Regulated by the −3459 A>G Polymorphism and Predict Myocardial Infarction and the Efficacy of Antithrombotic Treatment in Non-ST Elevation Acute Coronary Syndrome ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2006 · PMID 16627810
  not yet assessed
• The intersubject variability of tissue factor mRNA production in human monocytes—relation with the toll-like receptor 4 ↗

  Thrombosis Research · 2006 · PMID 17157899
  not yet assessed
• Tissue Factor and CD40 Ligand : Markers for the Interplay of Coagulation and Inflammation in the Acute Coronary Syndrome

  KTH Publication Database DiVA (KTH Royal Institute of Technology) · 2006
  not yet assessed
• Genetic Variations in the Tissue Factor Gene Are Associated With Clinical Outcome in Acute Coronary Syndrome and Expression Levels in Human Monocytes ↗

  Arteriosclerosis Thrombosis and Vascular Biology · 2005 · PMID 16239598
  not yet assessed
• A quantitative real-time PCR method for tissue factor mRNA ↗

  Thrombosis Research · 2003 · PMID 14967415
  not yet assessed
• Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles ↗

  Institutional Repositories DataBase (IRDB) ·
  not yet assessed