Author details

Full Name

Elisabeth Widen

Affiliation

ORCID

Career Start Year

1989

Papers

157

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37419095	Response to Li and Hopper.		2023
37848354	Novel Finnish-enriched variants causing severe hypercholesterolemia and their clinical impact on coronary artery disease.		2023
37743161	Effect of biological sex on human circulating lipidome: An overview of the literature.		2023
37907536	Genome-wide association analysis of plasma lipidome identifies 495 genetic associations.	Nat Commun	2023
37468507	Biobank-scale methods and projections for sparse polygenic prediction from machine learning.		2023
36503927	Scientific refutation of ESHG statement on embryo selection.		2023
36865330	Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes Mellitus.	medRxiv	2023
36611071	Sibling variation in polygenic traits and DNA recombination mapping with UK Biobank and IVF family data.		2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
35197564	Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes.	Communications Biology	2022
36307513	Polygenic Health Index, General Health, and Pleiotropy: Sibling Analysis and Disease Risk Reduction.	Scientific Reports	2022
35451785	From Genotype to Phenotype: Polygenic Prediction of Complex Human Traits.	Methods in Molecular Biology	2022
36347255	Systematic comparison of family history and polygenic risk across 24 common diseases.	American Journal of Human Genetics	2022
36193934	Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids.	J Am Heart Assoc	2022
35978133	Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.	Commun Biol	2022
36600884	Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study.		2022
34856119	Multiomics and digital monitoring during lifestyle changes reveal independent dimensions of human biology and health.	Cell Syst	2022
35130028	How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study.	Circulation. Genomic and precision medicine	2022
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
32064741	Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.	Addict Biol	2021
34209487	Machine Learning Prediction of Biomarkers from SNPs and of Disease Risk from Biomarkers in the UK Biobank.	Genes	2021
33045005	Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.	PLoS Genet	2020
32154731	Polygenic Hyperlipidemias and Coronary Artery Disease Risk.	Circ Genom Precis Med	2020
33315912	Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.	PLoS ONE	2020
31374203	Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.	Am J Hum Genet	2019
31792362	LIN28B affects gene expression at the hypothalamic-pituitary axis and serum testosterone levels.	Scientific Reports	2019
31840077	GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI.	Sci Adv	2019
30196135	Transient modification of lin28b expression - Permanent effects on zebrafish growth.	Molecular and Cellular Endocrinology	2019
29273806	Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.	Nat Genet	2018
29032884	The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?	International Journal of Cardiology	2018
30270054	Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC).	Atherosclerosis	2018
30001766	Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018).	Twin Res Hum Genet	2018
29942086	Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.	Nat Genet	2018
28093568	GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.	Mol Psychiatry	2017
28724990	Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.	Nat Commun	2017
28436984	Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.	Nat Genet	2017
29186694	Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.	Cell Rep	2017
29116125	Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.	Nat Commun	2017
29240343	Assessment of multifactorial coronary artery disease by utilizing genomic data.	Duodecim; laaketieteellinen aikakauskirja	2017
29068436	GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.	Mol Psychiatry	2017
27680694	Genome-wide associations for birth weight and correlations with adult disease.	Nature	2016
26833246	New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.	Nat Commun	2016
26965448	Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Nav 1.5 Sodium Channel.	Annals of Noninvasive Electrocardiology	2016
26833098	Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.	Nat Commun	2016
26997408	Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies.	Psychol Med	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
26362575	Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium.	Behav Genet	2016
26604143	Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.	Hum Mol Genet	2016
26574646	The genetics of pubertal timing in the general population: recent advances and evidence for sex-specificity.	Curr Opin Endocrinol Diabetes Obes	2016
27939304	Pooling and expanding registries of familial hypercholesterolaemia to assess gaps in care and improve disease management and outcomes: Rationale and design of the global EAS Familial Hypercholesterolaemia Studies Collaboration.	Atheroscler Suppl	2016