Author details

Full Name

Bengt Sennblad

Affiliation

ORCID

Career Start Year

1998

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37004177	Stratified genetic analysis reveals sex differences in MPO-ANCA-associated vasculitis.	Rheumatology (Oxford)	2023
34888651	Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA.	Rheumatology (Oxford)	2022
33436761	The overlap of genetic susceptibility to schizophrenia and cardiometabolic disease can be used to identify metabolically different groups of individuals.	Scientific Reports	2021
33517400	Genome-wide association study of circulating interleukin 6 levels identifies novel loci.	Hum Mol Genet	2021
30935387	Conbase: a software for unsupervised discovery of clonal somatic mutations in single cells through read phasing.	Genome Biol	2019
31089183	Genetic variation in CADM2 as a link between psychological traits and obesity.	Scientific Reports	2019
30962452	Breast cancer quantitative proteome and proteogenomic landscape.	Nat Commun	2019
29669788	H19 Induces Abdominal Aortic Aneurysm Development and Progression.	Circulation	2018
30510157	GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.	Nat Commun	2018
30390057	Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.	Nat Genet	2018
28053049	Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels.	Hum Mol Genet	2017
28734077	Integrative studies implicate matrix metalloproteinase-12 as a culprit gene for large-artery atherosclerotic stroke.	Journal of Internal Medicine	2017
28898252	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.	PLoS Med	2017
28586362	Fast and general tests of genetic interaction for genome-wide association studies.	PLoS Computational Biology	2017
28369058	Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease.	PLoS Genet	2017
28443625	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Nat Commun	2017
28566273	An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.	Diabetes	2017
29040868	Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation.	Atherosclerosis	2017
27668658	Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.	Nat Genet	2016
26821299	Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.	Cytokine	2016
27355579	Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2016
27466198	Analysis with the exome array identifies multiple new independent variants in lipid loci.	Hum Mol Genet	2016
26561523	A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.	Hum Mol Genet	2016
27659228	Soluble CD93 Is Involved in Metabolic Dysregulation but Does Not Influence Carotid Intima-Media Thickness.		2016
26105150	Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.	Blood	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25631608	Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.	Nat Commun	2015
25587992	Plasma IL-5 concentration and subclinical carotid atherosclerosis.	Atherosclerosis	2015
25262344	HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials.	Lancet	2015
26276317	Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease.	J Am Heart Assoc	2015
26402789	Discovering Genetic Interactions in Large-Scale Association Studies by Stage-wise Likelihood Ratio Tests.	PLoS Genetics	2015
26131930	Directional dominance on stature and cognition inÂ diverse human populations.	Nature	2015
26130236	Integrating Sequence Evolution into Probabilistic Orthology Analysis.	Systematic Biology	2015
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
26426971	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2015
26449131	Gene-pseudogene evolution: a probabilistic approach.	BMC Genomics	2015
25150937	Low levels of IgM antibodies against phosphorylcholine are associated with fast carotid intima media thickness progression and cardiovascular risk in men.	Atherosclerosis	2014
25551457	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
24401246	Plasma autoantibodies against apolipoprotein B-100 peptide 210 in subclinical atherosclerosis.	Atherosclerosis	2014
24562812	A Bayesian method for analyzing lateral gene transfer.	Systematic Biology	2014
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
24564421	Genome-wide probabilistic reconciliation analysis across vertebrates.	BMC Bioinformatics	2013
24072691	Serum 25-hydroxyvitamin D concentration in subclinical carotid atherosclerosis.	Arterioscler Thromb Vasc Biol	2013
23803001	GenPhyloData: realistic simulation of gene family evolution.	BMC Bioinformatics	2013
23969696	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
23275344	Causal relevance of blood lipid fractions in the development of carotid atherosclerosis: Mendelian randomization analysis.	Circ Cardiovasc Genet	2013
23246012	A gene-centric study of common carotid artery remodelling.	Atherosclerosis	2013
23152477	Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk.	Circ Cardiovasc Genet	2012
22885924	Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.	Nat Genet	2012
22885922	Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.	Nat Genet	2012