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Author Details

Mattias Frånberg
2015
16
13
PMIDPaper TitleJournal TitlePublished Year
30642921A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.Blood2019
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30390057Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Nat Genet2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30388399Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.Am J Hum Genet2018
28107422Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.PLoS One2017
28586362Fast and general tests of genetic interaction for genome-wide association studies.PLoS Computational Biology2017
28369058Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease.PLoS Genet2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
27681236Structural Variation Detection with Read Pair Information: An Improved Null Hypothesis Reduces Bias.Journal of Computational Biology2017
27668658Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Nat Genet2016
27742707PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study.Blood2016
26551672Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Nat Genet2015
26402789Discovering Genetic Interactions in Large-Scale Association Studies by Stage-wise Likelihood Ratio Tests.PLoS Genetics2015
25631608Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.Nat Commun2015
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Anders Hamsten
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Robert A Scott
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Claudia Langenberg
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Andr?? G Uitterlinden
Erasmus University Medical Center
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Rona J Strawbridge
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Jian'an Luan
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Cecilia M Lindgren
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Oscar H Franco
Institute of Social and Preventive Medicine (I.S.P.M.), University of Bern
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Erik Ingelsson
Stanford University School of Medicine
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Cornelia M van Duijn
University of Oxford
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Albert Hofman
Harvard T.H. Chan School of Public Health
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Eleftheria Zeggini
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Bengt Sennblad
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Bruce M Psaty
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Michael Boehnke
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Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
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Lars Lind
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Eric Boerwinkle
Baylor College of Medicine
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Andrew P Morris
The University of Manchester
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Hugh Watkins
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Nicholas J Wareham
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Ruth J F Loos
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Alanna C Morrison
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Kent D Taylor
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Najaf Amin
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Abbas Dehghan
School of Public Health, Imperial College London
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Jaspal S Kooner
London NorthWest Healthcare NHS Trust
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Weihua Zhang
Imperial College London
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Veikko Salomaa
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Paul M Ridker
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