Oddgeir L. Holmen - Concepedia

Author

Oddgeir L. Holmen

Norwegian University of Science and Technology

Also Known As

Andrew D Morris, Caroline Hayward, Francesco Cucca, Hirschhorn, Joel N, Holmen, OL, Holmen, Oddgeir, Holmen, Oddgeir L, Hu, Youna, Kauko Heikkilä, Kristian Hveem

Publications

23.9K

Citations

H-Index

Concepts

All Affiliations

Norwegian University of Science and Technology University of Michigan Levanger Hospital St Olav's University Hospital University of Oslo

About

Oddgeir L. Holmen is an author at Norwegian University of Science and Technology specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	2.7K
2	Public Health	10	10	786
3	Health Sciences	3	3	527
4	Engineering	2	2	1.1K
5	Allergy	1	1	54

Oddgeir L. Holmen

Publications

5.6K

Citations

H-Index

Page 1

	Year	Citations
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology Jonas B. Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche, Nature Genetics CardiomyopathyFunctional GenomicsEngineeringTranslational BioinformaticsGenetics	2018	900
Rare and low-frequency coding variants alter human adult height Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez, Nature Allelic VariantGeneticsStatistical GeneticsVariant InterpretationHuman Adult Height	2017	647
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci Kyle J. Gaulton, Teresa Ferreira, Yeji Lee, Nature Genetics Genome-wide Association StudyGenetic DeterminantGenotype-phenotype AssociationGenetic Fine MappingGenetics	2015	420
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Valérie Turcot, Yingchang Lu, Heather M. Highland, Nature Genetics ObesityMetabolic SyndromeNutritionEnergy HomeostasisMetabolic Disorder	2017	420
Cohort Profile Update: The HUNT Study, Norway Bjørn Olav Åsvold, Arnulf Langhammer, Tommy Aune Rehn, International Journal of Epidemiology	2022	318
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk Oddgeir L. Holmen, He Zhang, Yanbo Fan, Nature Genetics EpidemiologyCardiovascular DiseaseMyocardial Infarction RiskGenetic EpidemiologyCandidate Causal Variant	2014	307
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease Tom R. Webb, Jeanette Erdmann, Kathleen Stirrups, Journal of the American College of Cardiology	2017	261
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol Leslie A. Lange, Youna Hu, He Zhang, The American Journal of Human Genetics Genome-wide Association StudyAllelic VariantEngineeringMedicineGenetics	2014	214
Rare and low-frequency coding variants alter human adult height Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez, Carolina Digital Repository (University of North Carolina at Chapel Hill)	2017	154
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes Viktoria Gusarova, Colm O’Dushlaine, Tanya M. Teslovich, Nature Communications	2018	149

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