Resultats de la cerca - Anders Mälarstig
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Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants per Lasse Folkersen, Theodosios Kyriakou, Anuj Goel, John F. Peden, Anders Mälarstig, Gabrielle Paulsson‐Berne, Anders Hamsten, Anders Franco‐Cereceda, Anders Gabrielsen, Per Eriksson
Publicat 2009Artigo -
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Circulating Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Predicts Future Risk of Cardiovascular Events Independently of Established Risk Factors per Karin Leander, Anders Mälarstig, Ferdinand M. van’t Hooft, Craig Hyde, Mai-Lis Hellénius, Jason S. Troutt, Robert J. Konrad, John Öhrvik, Anders Hamsten, Ulf dé Fairé
Publicat 2016Artigo -
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Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population per Guillaume Paré, Daniel I. Chasman, Alexander N. Parker, Robert R.Y. Zee, Anders Mälarstig, Udo Seedorf, Rory Collins, Hugh Watkins, Anders Hamsten, Joseph P. Miletich, Paul M. Ridker
Publicat 2009Artigo -
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Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimer’s disease per Christopher D. Whelan, Niklas Mattsson, Michael W. Nagle, Swetha Vijayaraghavan, Craig Hyde, Shorena Janelidze, Erik Stomrud, Julie Lee, Lori Fitz, Tarek A. Samad, Gayathri Ramaswamy, Richard Margolin, Anders Mälarstig, Oskar Hansson
Publicat 2019Artigo -
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Therapeutic Targets for Heart Failure Identified Using Proteomics and Mendelian Randomization per Albert Henry, María Gordillo‐Marañón, Chris Finan, Amand F. Schmidt, João Pedro Ferreira, Ravi Karra, Johan Sundström, Lars Lind, Johan Ärnlöv, Faı̈ez Zannad, Anders Mälarstig, Aroon D. Hingorani, R. Thomas Lumbers
Publicat 2022Revisão -
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The genetic regulation of protein expression in cerebrospinal fluid per Oskar Hansson, Atul Kumar, Shorena Janelidze, Erik Stomrud, Philip S. Insel, Kaj Blennow, Henrik Zetterberg, Eric B. Fauman, Åsa K. Hedman, Michael W. Nagle, Christopher D. Whelan, Denis Baird, Anders Mälarstig, Niklas Mattsson
Publicat 2022Artigo -
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Identification of novel pheno-groups in heart failure with preserved ejection fraction using machine learning per Åsa K. Hedman, Camilla Hage, Anil Kumar Sharma, M. Julia Brosnan, Leonard Buckbinder, Li‐Ming Gan, Sanjiv J. Shah, Cecilia Linde, Erwan Donal, Jean‐Claude Daubert, Anders Mälarstig, Daniel Ziemek, Lars H. Lund
Publicat 2020Artigo -
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Mapping the serum proteome to neurological diseases using whole genome sequencing per Grace Png, Andrei Barysenka, L. Repetto, Pau Navarro, Xia Shen, Maik Pietzner, Eleanor Wheeler, Nicholas J. Wareham, Claudia Langenberg, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Anders Mälarstig, James F. Wilson, Arthur Gilly, Eleftheria Zeggini
Publicat 2021Artigo -
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Common and Low-Frequency Genetic Variants in the <i>PCSK9</i> Locus Influence Circulating <i>PCSK9</i> Levels per Ekaterina Chernogubova, Rona J. Strawbridge, Hovsep Mahdessian, Anders Mälarstig, Sergey Krapivner, Bruna Gigante, Mai-Lis Hellénius, Ulf dé Fairé, Anders Franco‐Cereceda, Ann‐Christine Syvänen, Jason S. Troutt, Robert J. Konrad, Per Eriksson, Anders Hamsten, Christian Dina
Publicat 2012Artigo -
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Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis per Daniel I. Chasman, Guillaume Paré, Samia Mora, Jemma C. Hopewell, Gina M. Peloso, Robert Clarke, L. Adrienne Cupples, Anders Hamsten, Sekar Kathiresan, Anders Mälarstig, José M. Ordovás, Samuli Ripatti, Alex Parker, Joseph P. Miletich, Paul M. Ridker
Publicat 2009Artigo -
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Integrative studies implicate matrix metalloproteinase‐12 as a culprit gene for large‐artery atherosclerotic stroke per Hovsep Mahdessian, Ljubica Matic, Mariette Lengquist, Karl Gertow, Bengt Sennblad, Damiano Baldassarre, Fabrizio Veglia, Steve E. Humphries, Rainer Rauramaa, Ulf dé Fairé, Andries J. Smit, Philippe Giral, Sudhir Kurl, Elmo Mannarino, Elena Tremoli, Anders Hamsten, Per Eriksson, Ulf Hedin, Anders Mälarstig
Publicat 2017Artigo -
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Genome-wide association study of varenicline-aided smoking cessation per Kayesha Coley, Qingning Wang, Richard Packer, Catherine John, Erik Abner, Kadri Reis, Khaled Bedair, Sundararajan Srinivasan, Sara A. Paciga, Craig Hyde, Robert C. Free, Nicola Reeve, David Shepherd, Tõnu Esko, Colin N. A. Palmer, Ewan R. Pearson, Anders Mälarstig, Martin D. Tobin, Chiara Batini
Publicat 2025Artigo -
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Functional IL6R 358Ala Allele Impairs Classical IL-6 Receptor Signaling and Influences Risk of Diverse Inflammatory Diseases per Ricardo C. Ferreira, Daniel F. Freitag, Antony J. Cutler, Joanna M. M. Howson, Daniel B. Rainbow, Deborah J. Smyth, Stephen Kaptoge, Clarke Pamela, Charlotte Boreham, Richard Coulson, Marcin Ł. Pękalski, Wei‐Min Chen, Suna Önengüt-Gümüşcü, Stephen S. Rich, Adam S. Butterworth, Anders Mälarstig, John Danesh, John A. Todd
Publicat 2013Artigo -
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Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis per David A. Hinds, Alfonso Buil, Daniel Ziemek, Ángel Martínez-Pérez, Rainer Malik, Lasse Folkersen, Marine Germain, Anders Mälarstig, Andrew Brown, José Manuel Soria, Martin Dichgans, Nan Bing, Anders Franco‐Cereceda, Juan Carlos Souto, Emmanouil T. Dermitzakis, Anders Hamsten, Bradford B. Worrall, Joyce Y. Tung, Maria Sabater‐Lleal
Publicat 2016Artigo -
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Common Genetic Determinants of Lung Function, Subclinical Atherosclerosis and Risk of Coronary Artery Disease per Maria Sabater‐Lleal, Anders Mälarstig, Lasse Folkersen, María Soler Artigas, Damiano Baldassarre, Maryam Kavousi, Peter Almgren, Fabrizio Veglia, Guy Brusselle, Albert Hofman, Gunnar Engström, Oscar H. Franco, Olle Melander, Gabrielle Paulsson‐Berne, Hugh Watkins, Per Eriksson, Steve E. Humphries, Elena Tremoli, Ulf dé Fairé, Martin D. Tobin, Anders Hamsten
Publicat 2014Artigo
Eines de cerca:
Matèries relacionades
Medicine
Biology
Genetics
Internal medicine
Gene
Genotype
Bioinformatics
Single-nucleotide polymorphism
Genome-wide association study
Computational biology
Disease
Genetic association
Endocrinology
Population
Cardiology
Environmental health
Genetic variants
Mendelian randomization
Coronary artery disease
Immunology
Oncology
Allele
Computer science
Confidence interval
Genome
Inflammation
Biobank
Cancer
Cholesterol
Diabetes mellitus