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  1. Article

    Open Access

    Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

    **g Hua Zhao, David Stacey, Niclas Eriksson, Erin Macdonald-Dunlop in Nature Immunology (2023)

  2. Article

    Open Access

    Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

    Circulating proteins have important functions in inflammation and a broad range of diseases. To identify genetic influences on inflammation-related proteins, we conducted a genome-wide protein quantitative tra...

    **g Hua Zhao, David Stacey, Niclas Eriksson, Erin Macdonald-Dunlop in Nature Immunology (2023)

  3. Article

    Open Access

    Peripheral blood cellular dynamics of rheumatoid arthritis treatment informs about efficacy of response to disease modifying drugs

    Rheumatoid arthritis (RA) is an autoimmune disease characterized by systemic inflammation and is mediated by multiple immune cell types. In this work, we aimed to determine the relevance of changes in cell pro...

    Åsa K. Hedman, Eitan Winter, Niyaz Yoosuf, Yair Benita, Louise Berg in Scientific Reports (2023)

  4. Article

    Open Access

    Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

    A promise of genomics in precision medicine is to provide individualized genetic risk predictions. Polygenic risk scores (PRS), computed by aggregating effects from many genomic variants, have been developed a...

    Jiangming Sun, Yunpeng Wang, Lasse Folkersen, Yan Borné in Nature Communications (2021)

  5. Article

    Open Access

    Author Correction: Expression of CARD8 in human atherosclerosis and its regulation of inflammatory proteins in human endothelial cells

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    Geena V. Paramel, Glykeria Karadimou, Anna Göthlin Eremo in Scientific Reports (2021)

  6. Article

    Open Access

    Expression of CARD8 in human atherosclerosis and its regulation of inflammatory proteins in human endothelial cells

    The Caspase activation and recruitment domain 8 (CARD8) protein is a component of innate immunity and overexpression of CARD8 mRNA was previously identified in atherosclerosis. However, very little is known ab...

    Geena V. Paramel, Glykeria Karadimou, Anna Göthlin Eremo in Scientific Reports (2020)

  7. No Access

    Article

    Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

    Circulating proteins are vital in human health and disease and are frequently used as biomarkers for clinical decision-making or as targets for pharmacological intervention. Here, we map and replicate protein ...

    Lasse Folkersen, Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen in Nature Metabolism (2020)

  8. Article

    Open Access

    Genetic stratification of depression in UK Biobank

    Depression is a common and clinically heterogeneous mental health disorder that is frequently comorbid with other diseases and conditions. Stratification of depression may align sub-diagnoses more closely with...

    David M. Howard, Lasse Folkersen, Jonathan R. I. Coleman in Translational Psychiatry (2020)

  9. Article

    Open Access

    Genome-wide analysis yields new loci associating with aortic valve stenosis

    Aortic valve stenosis (AS) is the most common valvular heart disease, and valve replacement is the only definitive treatment. Here we report a large genome-wide association (GWA) study of 2,457 Icelandic AS ca...

    Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir in Nature Communications (2018)

  10. Article

    Open Access

    Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

    Bicuspid aortic valve (BAV) is a heritable congenital heart defect and an important risk factor for valvulopathy and aortopathy. Here we report a genome-wide association scan of 466 BAV cases and 4,660 age, se...

    Bo Yang, Wei Zhou, Jiao Jiao, Jonas B. Nielsen, Michael R. Mathis in Nature Communications (2017)

  11. Article

    Open Access

    Discovery of new candidate genes for rheumatoid arthritis through integration of genetic association data with expression pathway analysis

    Here we integrate verified signals from previous genetic association studies with gene expression and pathway analysis for discovery of new candidate genes and signaling networks, relevant for rheumatoid arthr...

    Klementy Shchetynsky, Lina-Marcella Diaz-Gallo in Arthritis Research & Therapy (2017)

  12. No Access

    Article

    The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

    Patricia Munroe, Christopher Newton-Cheh, Andrew Morris and colleagues perform association studies in over 340,000 individuals of European ancestry and identify 66 loci, of which 17 are novel, involved in bloo...

    Georg B Ehret, Teresa Ferreira, Daniel I Chasman, Anne U Jackson in Nature Genetics (2016)

  13. Article

    Open Access

    Neil3-dependent base excision repair regulates lipid metabolism and prevents atherosclerosis in Apoe-deficient mice

    Increasing evidence suggests that oxidative DNA damage accumulates in atherosclerosis. Recently, we showed that a genetic variant in the human DNA repair enzyme NEIL3 was associated with increased risk of myocard...

    Tonje Skarpengland, Sverre Holm, Katja Scheffler, Ida Gregersen in Scientific Reports (2016)

  14. Article

    Open Access

    Integration of Known DNA, RNA and Protein Biomarkers Provides Prediction of Anti-TNF Response in Rheumatoid Arthritis: Results from the COMBINE Study

    OBJECTIVE: In rheumatoid arthritis (RA) several recent efforts have sought to discover means of predicting which patients would benefit from treatment. However, results have been discrepant with few successful...

    Lasse Folkersen, Boel Brynedal, Lina Marcela Diaz-Gallo in Molecular Medicine (2016)

  15. Article

    Open Access

    AllelicImbalance: an R/ bioconductor package for detecting, managing, and visualizing allele expression imbalance data from RNA sequencing

    One aspect in which RNA sequencing is more valuable than microarray-based methods is the ability to examine the allelic imbalance of the expression of a gene. This process is often a complex task that entails ...

    Jesper R. Gådin, Ferdinand M. van’t Hooft, Per Eriksson in BMC Bioinformatics (2015)

  16. Article

    SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes

    The genetic determinants of diabetic nephropathy remain poorly understood. We aimed to identify novel susceptibility genes for diabetic nephropathy.

    Marine Germain, Marcus G. Pezzolesi, Niina Sandholm, Amy J. McKnight in Diabetologia (2015)

  17. No Access

    Article

    New genetic loci link adipose and insulin biology to body fat distribution

    Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our understanding of the genetic basis of body fat distr...

    Dmitry Shungin, Thomas W. Winkler, Damien C. Croteau-Chonka, Teresa Ferreira in Nature (2015)

  18. No Access

    Article

    Genetic studies of body mass index yield new insights for obesity biology

    Obesity is heritable and predisposes to many diseases. To understand the genetic basis of obesity better, here we conduct a genome-wide association study and Metabochip meta-analysis of body mass index (BMI), ...

    Adam E. Locke, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers in Nature (2015)

  19. No Access

    Article

    Defining the role of common variation in the genomic and biological architecture of adult human height

    Timothy Frayling, Joel Hirschhorn, Peter Visscher and colleagues report a meta-analysis of genome-wide association studies for adult height in 253,288 individuals. They identify 697 variants in 423 loci signif...

    Andrew R Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H Pers in Nature Genetics (2014)

  20. No Access

    Article

    A serum 25-hydroxyvitamin D concentration-associated genetic variant in DHCR7 interacts with type 2 diabetes status to influence subclinical atherosclerosis (measured by carotid intima–media thickness)

    The findings of studies investigating whether or not low serum 25-hydroxyvitamin D [25(OH)D] concentration promotes development of atherosclerosis have been contradictory. The present study employed a Mendelia...

    Rona J. Strawbridge, Anna Deleskog, Olga McLeod, Lasse Folkersen in Diabetologia (2014)

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