Author details

Full Name

Anne Heidi Skogholt

Affiliation

ORCID

Career Start Year

2016

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36337027	Increased levels of microRNA-320 in blood serum and plasma is associated with imminent and advanced lung cancer.	Mol Oncol	2023
38007577	Increased expression of individual genes in whole blood is associated with late-stage lung cancer at and close to diagnosis.		2023
37601974	Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.	Cell Genom	2023
37486023	Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.	Ann Neurol	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
36739617	A fast linkage method for population GWAS cohorts with related individuals.	Genet Epidemiol	2023
36580301	Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction.		2023
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
35726068	Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.	Nat Genet	2022
35591975	Genome-wide risk prediction of common diseases across ancestries in one million people.	Cell Genom	2022
36777998	The HUNT study: A population-based cohort for genetic research.	Cell Genom	2022
33888516	Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.	Gut	2021
33279719	Response to Letter to the Editor: 'Comments on the paper presenting prediction models for incident hand OA in the HUNT study'.	Osteoarthritis and Cartilage	2021
34975738	Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci.	Frontiers in Neurology	2021
34916535	Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.	Nat Commun	2021
34773122	Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.	Nat Genet	2021
34265237	Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.	Am J Hum Genet	2021
34151951	The causal effects of serum lipids and apolipoproteins on kidney function: multivariable and bidirectional Mendelian-randomization analyses.	Int J Epidemiol	2021
32056457	Mitochondrial genome-wide association study of migraine - the HUNT Study.	Cephalalgia	2020
33339817	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Nat Commun	2020
32981348	Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.	Circulation	2020
32769997	GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.	Nat Commun	2020
32360252	Development and validation of a prediction model for incident hand osteoarthritis in the HUNT study.	Osteoarthritis and Cartilage	2020
31015462	Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.	Nat Commun	2019
29290336	Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.	Am J Hum Genet	2018
30061737	Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.	Nat Genet	2018
29992351	The accuracy of the clinical diagnosis of Parkinson disease. The HUNT study.	Journal of Neurology	2018
28335817	Gene expression differences between PAXgene and Tempus blood RNA tubes are highly reproducible between independent samples and biobanks.	BMC Res Notes	2017
27113810	The rare Arg181Cys mutation in the Î¼ opioid receptor can abolish opioid responses.	Acta Anaesthesiologica Scandinavica	2016