Author details

Full Name

Maiken E Gabrielsen

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36739617	A fast linkage method for population GWAS cohorts with related individuals.	Genet Epidemiol	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
37080991	Identification of three bacterial species associated with increased appendicular lean mass: the HUNT study.	Nat Commun	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
33940655	Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism.	Thrombosis and Haemostasis	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
35662399	Cross-sectional associations between the gut microbe Ruminococcus gnavus and features of the metabolic syndrome.	Lancet Diabetes Endocrinol	2022
35591975	Genome-wide risk prediction of common diseases across ancestries in one million people.	Cell Genom	2022
34784644	The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.	Thrombosis and Haemostasis	2022
36777998	The HUNT study: A population-based cohort for genetic research.	Cell Genom	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	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
34746691	Type 2 diabetes sex-specific effects associated with E167K coding variant in .	iScience	2021
34237679	Prothrombotic genotypes and risk of venous thromboembolism in occult cancer.	Thrombosis Research	2021
34151951	The causal effects of serum lipids and apolipoproteins on kidney function: multivariable and bidirectional Mendelian-randomization analyses.	Int J Epidemiol	2021
31582554	Fibrinogen gamma gene <i>rs2066865</i> and risk of cancer-related venous thromboembolism.	Haematologica	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
32671915	Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event.	Journal of Thrombosis and Haemostasis	2020
32603359	Age-of-onset information helps identify 76 genetic variants associated with allergic disease.	PLoS Genet	2020
32424355	Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts.	Nat Genet	2020
30116028	Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.	Mol Psychiatry	2020
32360252	Development and validation of a prediction model for incident hand osteoarthritis in the HUNT study.	Osteoarthritis and Cartilage	2020
32056457	Mitochondrial genome-wide association study of migraine - the HUNT Study.	Cephalalgia	2020
31699788	Genetic variation of platelet glycoprotein VI and the risk of venous thromboembolism.	Haematologica	2020
31420334	Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.	Blood	2019
31124268	Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism.	Journal of Thrombosis and Haemostasis	2019
31074779	The effect of smoking intensity on all-cause and cause-specific mortality-a Mendelian randomization analysis.	Int J Epidemiol	2019
31015462	Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.	Nat Commun	2019
30645169	Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition.	Circ Genom Precis Med	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
30104761	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.	Nat Genet	2018
30061737	Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.	Nat Genet	2018
29509885	Is smoking heaviness causally associated with alcohol use? A Mendelian randomization study in four European cohorts.	International Journal of Epidemiology	2018
29025033	Heavier smoking increases coffee consumption: findings from a Mendelian randomization analysis.	Int J Epidemiol	2017
28861891	Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.	Genet Epidemiol	2017
28533558	Investigating the causal effect of smoking on hay fever and asthma: a Mendelian randomization meta-analysis in the CARTA consortium.	Sci Rep	2017
28358128	Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.	Nat Genet	2017
28049019	The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT study.	Osteoarthritis and Cartilage	2017
29083406	Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.	Nat Genet	2017
27754487	Exome chip analyses in adult attention deficit hyperactivity disorder.	Transl Psychiatry	2016
26264275	Heavier smoking may lead to a relative increase in waist circumference: evidence for a causal relationship from a Mendelian randomisation meta-analysis. The CARTA consortium.	BMJ Open	2015
26538566	Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium.	Circ Cardiovasc Genet	2015
26363033	Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.	Carcinogenesis	2015