Maiken Elvestad Gabrielsen
+4773597579
Øya helsehus, 2 etg, Øya, Håkon Jarls gt 11
Publications
2024
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Austin, Thomas R.;
Nethander, Maria;
Fink, Howard A.;
Törnqvist, Anna E.;
Jalal, Diana I.;
Buzkova, Petra.
(2024)
A plasma protein-based risk score to predict hip fractures.
Nature Aging
Letter to the editor
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Austin, Thomas R.;
Nethander, Maria;
Fink, Howard A.;
Törnqvist, Anna E.;
Jalal, Diana I.;
Buzkova, Petra.
(2024)
Correction to: A plasma protein-based risk score to predict hip fractures (Nature Aging, (2024), 4, 8, (1064-1075), 10.1038/s43587-024-00639-7).
Nature Aging
Errata
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Austin, Thomas R.;
Fink, Howard A.;
Jalal, Diana I.;
Törnqvist, Anna E.;
Buzkova, Petra;
Barzilay, Joshua I..
(2024)
Large-scale circulating proteome association study (CPAS) meta-analysis identifies circulating proteins and pathways predicting incident hip fractures.
Journal of Bone and Mineral Research
Academic article
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Arnesen, Carl-Arne;
Evensen, Line Holtet;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Hansen, John Bjarne;
Brækkan, Sigrid Kufaas.
(2024)
Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women.
Research and Practice in Thrombosis and Haemostasis (RPTH)
Academic article
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de Vries, Paul S.;
Reventun, Paula;
Brown, Michael R.;
Heath, Adam S.;
Huffman, Jennifer E.;
Le, Ngoc-Quynh.
(2024)
A genetic-association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
Academic article
2023
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Solé-Navais, Pol;
Flatley, Christopher;
Steinthorsdottir, Valgerdur;
Vaudel, Marc;
Juodakis, Julius;
Chen, Jing.
(2023)
Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight (Nature Genetics, (2023), 55, 4, (559-567), 10.1038/s41588-023-01343-9).
Nature Genetics
Errata
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Grahnemo, Louise;
Nethander, Maria;
Coward, Eivind;
Gabrielsen, Maiken Elvestad;
Sree, Satya;
Billod, Jean-Marc.
(2023)
Identification of three bacterial species associated with increased appendicular lean mass: the HUNT study.
Nature Communications
Academic article
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Surakka, Ida;
Wu, Kuan-Han;
Hornsby, Whitney;
Wolford, Brooke N.;
Shen, Fred;
Zhou, Wei.
(2023)
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.
Cell Genomics
Academic article
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Solé-Navais, Pol;
Flatley, Christopher;
Steinthorsdottir, Valgerdur;
Vaudel, Marc;
Juodakis, Julius;
Chen, Jing.
(2023)
Genetic effects on the timing of parturition and links to fetal birth weight.
Nature Genetics
Academic article
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Zajac, Gregory J. M.;
Gagliano Taliun, Sarah A.;
Sidore, Carlo;
Graham, Sarah E.;
Åsvold, Bjørn Olav;
Brumpton, Ben Michael.
(2023)
A fast linkage method for population GWAS cohorts with related individuals.
Genetic Epidemiology
Academic article
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Winsvold, Bendik Kristoffer Slagsvold;
Harder, Aster V. E.;
Ran, Caroline;
Chalmer, Mona A.;
Dalmasso, Maria Carolina;
Ferkingstad, Egil.
(2023)
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.
Annals of Neurology
Academic article
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Surakka, Ida;
Wolford, Brooke Nichole;
Ritchie, Scott C.;
Hornsby, Whitney E.;
Sutton, Nadia R.;
Gabrielsen, Maiken Elvestad.
(2023)
Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction.
Circulation: Genomic and precision medicine
Academic article
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Jacobsen, Kaya Kvarme;
Børte, Sigrid;
Laborie, Lene Bjerke;
Kristiansen, Hege;
Schäfer, Annette;
Martinsen, Amy.
(2023)
COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study.
Osteoarthritis and Cartilage Open
Academic article
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Nethander, Maria;
Movérare-Skrtic, Sofia;
Kämpe, Anders;
Coward, Eivind;
Reimann, Ene;
Grahnemo, Louise.
(2023)
An atlas of genetic determinants of forearm fracture.
Nature Genetics
Academic article
2022
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Holtet Evensen, Line;
Arnesen, Carl-Arne;
Rosendaal, Frits Richard;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hveem, Kristian.
(2022)
The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.
Thrombosis and Haemostasis
Academic article
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Bahrami, Shahram;
Hindley, Guy Frederick Lanyon;
Winsvold, Bendik K S;
O'Connell, Kevin Sean;
Frei, Oleksandr;
Shadrin, Alexey.
(2022)
Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.
Brain
Academic article
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Nethander, Maria;
Coward, Eivind;
Reimann, Ene;
Grahnemo, Louise;
Gabrielsen, Maiken Elvestad;
Wibom, Carl.
(2022)
Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study.
Cell Reports Medicine
Academic article
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Hartley, April;
Sanderson, Eleanor;
Granell, Raquel;
Paternoster, Lavinia;
Zheng, Jie;
Smith, George Davey.
(2022)
Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index.
International Journal of Epidemiology
Academic article
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Damoah, Christabel Esi;
Snir, Omri;
Hindberg, Kristian Dalsbø;
Garred, Peter;
Ludviksen, Judith K;
Brækkan, Sigrid Kufaas.
(2022)
High Levels of Complement Activating Enzyme MASP-2 Are Associated With the Risk of Future Incident Venous Thromboembolism.
Arteriosclerosis, Thrombosis and Vascular Biology
Academic article
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Mishra, Aniket;
Malik, Rainer;
Hachiya, Tsuyoshi;
Jürgenson, Tuuli;
Namba, Shinichi;
Posner, Daniel C..
(2022)
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
Academic article
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Brumpton, Ben Michael;
Graham, Sarah;
Surakka, Ida;
Skogholt, Anne Heidi;
Løset, Mari;
Fritsche, Lars G..
(2022)
The HUNT study: A population-based cohort for genetic research.
Cell Genomics
Academic article
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Allarai, Elias;
Lee, Wei-Hsuan;
Burgess, Stephen;
Larsson, Susanna C.;
Lindstrom, Sara;
Wang, Lu.
(2022)
Genetically predicted cortisol levels and risk of venous thromboembolism.
PLOS ONE
Academic article
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Mars, Nina;
Kerminen, Sini;
Feng, Yen-Chen A.;
Kanai, Masahiro;
Läll, Kristi;
Thomas, Laurent Francois.
(2022)
Genome-wide risk prediction of common diseases across ancestries in one million people.
Cell Genomics
Academic article
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Saunders, Gretchen R. B.;
Wang, Xingyan;
Chen, Fang;
Jang, Seon-Kyeong;
Liu, Mengzhen;
Wang, Chen.
(2022)
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
Academic article
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Hautakangas, Heidi;
Winsvold, Bendik K S;
Ruotsalainen, Sanni;
Bjornsdottir, Gyda;
Harder, Aster V. E.;
Kogelman, Lisette J. A..
(2022)
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles .
Nature Genetics
Academic article
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Løset, Mari;
Thomas, Laurent Francois;
Brumpton, Ben Michael;
Modalsli, Ellen Heilmann;
Gabrielsen, Maiken Elvestad;
Solvin, Åshild Øksnevad.
(2022)
Discovering novel genes and causal relationships for psoriasis: The HUNT study.
Acta Dermato-Venereologica
Abstract
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Wightman, Douglas P.;
Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey;
Bahrami, Shahram;
Holland, Dominic.
(2022)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (Nature Genetics, (2021), 53, 9, (1276-1282), 10.1038/s41588-021-00921-z).
Nature Genetics
Errata
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Mishra, Aniket;
Malik, Rainer;
Hachiya, Tsuyoshi;
Jürgenson, Tuuli;
Namba, Shinichi;
Posner, Daniel C..
(2022)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
Errata
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Grahnemo, Louise;
Nethander, Maria;
Coward, Eivind;
Gabrielsen, Maiken Elvestad;
Sree, Satya;
Billod, Jean-Marc.
(2022)
Cross-sectional associations between the gut microbe Ruminococcus gnavus and features of the metabolic syndrome.
The Lancet Diabetes and Endocrinology
Letter to the editor
2021
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Rahman, Shafiqur;
Winsvold, Bendik K S;
Chavez, Sergio;
Børte, Sigrid;
Tsepilov, Vakov;
Sharapov, Sodbo Zh.
(2021)
Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain.
Annals of the Rheumatic Diseases
Academic article
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Khoury, Samar;
Parisien, Marc;
Thompson, Scott J.;
Vachon-Presseau, Etienne;
Roy, Mathieu;
Mitchell, Amy.
(2021)
Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions.
Brain
Academic article
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Freidin, Maxim B.;
Tsepilov, Yakov A.;
Stanaway, Ian B.;
Meng, Weihua;
Hayward, Caroline;
Smith, Blair H..
(2021)
Sex- and age-specific genetic analysis of chronic back pain.
Pain
Academic article
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Frischmuth, Tobias;
Hindberg, Kristian;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hveem, Kristian;
Brækkan, Sigrid Kufaas.
(2021)
Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism.
Thrombosis and Haemostasis
Academic article
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Skille, Hanne;
Paulsen, Benedikte;
Hveem, Kristian;
Severinsen, Marianne T.;
Gabrielsen, Maiken Elvestad;
Kristensen, Søren R..
(2021)
Prothrombotic genotypes and risk of venous thromboembolism in occult cancer.
Thrombosis Research
Academic article
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Zhou, Wei;
Brumpton, Ben Michael;
Kabil, Omer;
Gudmundsson, Julius;
Thorleifsson, Gudmar;
Weinstock, Joshua.
(2021)
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer (Nature Communications, (2020), 11, 1, (3981), 10.1038/s41467-020-17718-z).
Nature Communications
Errata
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McGuire, Daniel;
Jiang, Yu;
Liu, Mengzhen;
Weissenkampen, J. Dylan;
Eckert, Scott;
Yang, Lina.
(2021)
Model-based assessment of replicability for genome-wide association meta-analysis.
Nature Communications
Academic article
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Wightman, Douglas P.;
Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey A.;
Bahrami, Shahram;
Holland, Dominic.
(2021)
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (Nature Genetics, (2021), 53, 9, (1276-1282), 10.1038/s41588-021-00921-z).
Nature Genetics
Errata
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Zheng, Thenghao;
Ellinghaus, David;
Juzenas, Simonas;
Cossais, François;
Burmeister, Greta;
Mayr, Gabriele.
(2021)
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.
Gut
Academic article
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Rasheed, Humaira;
Zheng, Jie;
Rees, Jessica;
Sanderson, Eleanor;
Thomas, Laurent;
Richardson, Tom G..
(2021)
The causal effects of serum lipids and apolipoproteins on kidney function: Multivariable and bidirectional Mendelian-randomization analyses.
International Journal of Epidemiology
Academic article
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Wightman, Douglas P.;
Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey;
Bahrami, Shahram;
Holland, Dominic.
(2021)
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.
Nature Genetics
Academic article
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Boer, Cindy G.;
Hatzikotoulas, Konstantinos;
Southam, Lorraine;
Stefánsdóttir, Lilja;
Almeida, Rodrigo Coutinho de;
Zhang, Yanfei.
(2021)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Cell
Academic article
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Fan, Yanbo;
Wolford, Brooke N.;
Lu, Haocheng;
Liang, Wenying;
Sun, Jinjian;
Zhou, Wei.
(2021)
Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2.
iScience
Academic article
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Winsvold, Bendik K S;
Kitsos, Ioannis;
Thomas, Laurent;
Skogholt, Anne Heidi;
Gabrielsen, Maiken Elvestad;
Zwart, John Anker Henrik.
(2021)
Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci.
Frontiers in Neurology
Academic article
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Johnsen, Marianne Bakke;
Magnusson, Karin;
Børte, Sigrid;
Gabrielsen, Maiken Elvestad;
Winsvold, Bendik K S;
Skogholt, Anne Heidi.
(2021)
Response to Letter to the Editor: ‘Comments on the paper presenting prediction models for incident hand OA in the HUNT study’.
Osteoarthritis and Cartilage
Letter to the editor
2020
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Zhou, Wei;
Brumpton, Ben Michael;
Kabil, Omer;
Gudmundsson, Julius;
Thorleifsson, Gudmar;
Weinstock, Joshua.
(2020)
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.
Nature Communications
Academic article
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Johnsen, Marianne Bakke;
Magnusson, Karin;
Børte, Sigrid;
Gabrielsen, Maiken Elvestad;
Winsvold, Bendik K S;
Skogholt, Anne Heidi.
(2020)
Development and validation of a prediction model for incident hand
osteoarthritis in the HUNT study.
Osteoarthritis and Cartilage
Academic article
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Klarin, Derek;
Verma, Shefali Setia;
Judy, Renae;
Dikilitas, Ozan;
Wolford, Brooke N.;
Paranjpe, Ishan.
(2020)
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Circulation
Academic article
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Surakka, Ida;
Fritsche, Lars;
Zhou, Wei;
Backman, Joshua;
Kosmicki, Jack A.;
Lu, Haocheng.
(2020)
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.
Nature Communications
Academic article
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Børte, Sigrid;
Zwart, John-Anker;
Skogholt, Anne Heidi;
Gabrielsen, Maiken Elvestad;
Thomas, Laurent;
Fritsche, Lars.
(2020)
Mitochondrial genome-wide association study of migraine – the HUNT Study .
Cephalalgia
Academic article
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Ferreira, Manuel A R;
Vonk, Judith M.;
Baurecht, Hansjörg;
Marenholz, Ingo;
Tian, Chao;
Hoffman, Joshua D..
(2020)
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genetics
Academic article
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Nielsen, Jonas Bille;
Rom, Oren;
Surakka, Ida;
Graham, Sarah E.;
Zhou, Wei;
Roychowdhury, Tanmoy.
(2020)
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.
Nature Communications
Academic article
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Skille, Hanne;
Paulsen, Benedikte;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hindberg, Kristian.
(2020)
Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event.
Journal of Thrombosis and Haemostasis
Academic article
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Zhou, Wei;
Zhao, Zhangchen;
Nielsen, Jonas B.;
Fritsche, Lars;
LeFaive, Jonathon;
Gagliano Taliun, Sarah A..
(2020)
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts.
Nature Genetics
Academic article
2019
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Liu, Mengzhen;
Jiang, Yu;
Wedow, Robbee;
Li, Yue;
Brazel, David M.;
Chen, Fang.
(2019)
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Nature Genetics
Academic article
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Småbrekke, Birgit;
Balteskard Rinde, Ludvig;
Evensen, Line Holtet;
Morelli, Vania Maris;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad.
(2019)
Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism.
Journal of Thrombosis and Haemostasis
Academic article
-
Brumpton, Ben Michael;
Fritsche, Lars;
Zheng, Jie;
Nielsen, Jonas Bille;
Mannila, Maria Nastase;
Surakka, Ida.
(2019)
Variation in serum PCSK9 (proprotein convertase subtilisin/kexin type 9), cardiovascular disease risk, and an investigation of potential unanticipated effects of PCSK9 inhibition.
Circulation: Genomic and precision medicine
Academic article
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Lane, Jacqueline M.;
Jones, Samuel E.;
Dashti, Hassan S.;
Wood, Andrew R.;
Aragam, Krishna G;
van Hees, Vincent T..
(2019)
Biological and clinical insights from genetics of insomnia symptoms.
Nature Genetics
Academic article
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Løset, Mari;
Thomas, Laurent;
Brumpton, Ben Michael;
Wolford, Brooke N.;
Holmen, Oddgeir;
Luetge, Almut.
(2019)
Genome-wide association study of psoriasis suggests a new risk locus on chromosome 10: The HUNT Study.
Forum for Nordic Dermato-Venereology
Abstract
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Graham, Sarah E.;
Nielsen, Jonas B.;
Zawistowski, Matthew;
Zhou, Wei;
Fritsche, Lars G.;
Gabrielsen, Maiken Elvestad.
(2019)
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Nature Communications
Academic article
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Vie, Gunnhild Åberge;
Wootton, Robyn E;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Taylor, AE;
Gabrielsen, Maiken Elvestad.
(2019)
The effect of smoking intensity on all-cause and cause-specific mortality-a Mendelian randomization analysis.
International Journal of Epidemiology
Academic article
-
Lindström, Sara;
Wang, Lu;
Smith, Erin N.;
Gordon, William;
van Hylckama Vlieg, Astrid;
de Andrade, Mariza.
(2019)
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood
Academic article
-
Paulsen, Benedikte;
Skille, Hanne;
Smith, Erin N.;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Brækkan, Sigrid Kufaas.
(2019)
Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism.
Haematologica
Academic article
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Skille, Hanne;
Paulsen, Benedikte;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hindberg, Kristian.
(2019)
Genetic Variation Of Platelet Glycoprotein VI And The Risk Of Venous Thromboembolism.
Haematologica
Letter to the editor
2018
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Corominas, Jordi;
Klein, Marieke;
Zayats, Tetyana;
Rivero, Olga;
Ziegler, Georg C.;
Pauper, Marc.
(2018)
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Molecular Psychiatry
Academic article
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Taylor, Michelle;
Rode, Line;
Bjørngaard, Johan Håkon;
Taylor, Amy E.;
Bojesen, Stig E.;
Åsvold, Bjørn Olav.
(2018)
Is smoking heaviness causally associated with alcohol use? A Mendelian randomization study in four European cohorts.
International Journal of Epidemiology
Academic article
-
Nielsen, Jonas B.;
Thorolfsdottir, Rosa B.;
Fritsche, Lars;
Zhou, Wei;
Skov, Morten W.;
Graham, Sarah E..
(2018)
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature Genetics
Academic article
-
Zhou, Wei;
Nielsen, Jonas B.;
Fritsche, Lars;
Dey, Rounak;
Gabrielsen, Maiken Elvestad;
Wolford, Brooke N..
(2018)
Efficiently controlling for
case-control imbalance and sample relatedness in large-scale genetic association
studies.
Nature Genetics
Academic article
-
Nielsen, Jonas B.;
Fritsche, Lars;
Zhou, Wei;
Teslovich, Tanya M.;
Holmen, Oddgeir Lingaas;
Gustafsson, Stefan.
(2018)
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
American Journal of Human Genetics
Academic article
-
Løset, Mari;
Modalsli, Ellen Heilmann;
Snekvik, Ingrid;
Solvin, Åshild Øksnevad;
Holmen, Oddgeir Lingaas;
Gabrielsen, Maiken Elvestad.
(2018)
743 HUNTing for genes that affect inflammatory skin disease in 4,071 cases and 40,430 controls.
Journal of Investigative Dermatology
Abstract
2017
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Wang, Yufei;
McKay, James D.;
Rafnar, Thorunn;
Wang, Zhaoming;
Timofeeva, Maria N.;
Broderick, Peter.
(2017)
Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (Nature Genetics (2014) 46 (736-741)).
Nature Genetics
Errata
-
Ferreira, Manuel A.;
Vonk, Judith M;
Baurecht, Hansjörg;
Marenholz, Ingo;
Tian, Chao;
Hoffman, Joshua D.
(2017)
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Nature Genetics
Academic article
-
Skaaby, Tea;
Taylor, Amy E;
Jacobsen, Rikke K.;
Paternoster, Lavinia;
Thuesen, Betina H.;
Ahluwalia, Tarunveer S..
(2017)
Investigating the causal effect of smoking on hay fever and asthma: A Mendelian randomization meta-analysis in the CARTA consortium.
Scientific Reports
Academic article
-
Johnsen, Marianne Bakke;
Vie, Gunnhild Åberge;
Winsvold, Bendik K S;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Gabrielsen, Maiken Elvestad.
(2017)
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
Academic article
-
Bjørngaard, Johan Håkon;
Nordestgaard, AT;
Taylor, Amy E;
Treur, Jorien L;
Gabrielsen, Maiken Elvestad;
Munafo, Marcus R.
(2017)
Heavier smoking increases coffee consumption: findings from a Mendelian randomization analysis.
International Journal of Epidemiology
Academic article
-
Zhou, Wei;
Fritsche, Lars;
Das, Sayantan;
Zhang, He;
Nielsen, Jonas B.;
Holmen, Oddgeir Lingaas.
(2017)
Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.
Genetic Epidemiology
Academic article
2016
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Zayats, Tetyana;
Jacobsen, Kaya Kvarme;
Kleppe, Rune;
Jacob, CP;
Kittel-Schneider, Sarah;
Ribases, Marta.
(2016)
Exome chip analyses in adult attention deficit hyperactivity disorder.
Translational Psychiatry
Academic article
-
Løset, Mari;
Modalsli, Ellen Heilmann;
Snekvik, Ingrid;
Zhou, Wei;
Chu, Yunhan;
Gabrielsen, Maiken Elvestad.
(2016)
HUNTing for Genes that Affect Psoriasis in ~2,900 Cases and ~48,000 Controls.
Forum for Nordic Dermato-Venereology
Abstract
2015
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Morris, Richard W.;
Taylor, Amy E.;
Fluharty, Meg E.;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Gabrielsen, Maiken Elvestad.
(2015)
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
Academic article
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Linneberg, Allan;
Jacobseb, Rikke;
Skaaby, Tea;
Taylor, Amy E.;
Fluharty, Meg E.;
Jeppesen, Jørgen L..
(2015)
Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium.
Circulation: Cardiovascular Genetics
Academic article
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Brenner, Darren. R.;
Amos, Christopher I.;
Brhane, Yonathan;
Timofeeva, Maria N.;
Caporaso, Neil;
Wang, Yufei.
(2015)
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Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers.
PLoS Genetics
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Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium.
BMJ Open
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Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Nature Genetics
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Causal associations of tobacco smoking with cardiovascular risk factors: a Mendelian randomization analysis of the HUNT Study in Norway.
International Journal of Epidemiology
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Davey Smith, George;
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The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study.
Psychological Medicine
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Association between a 15q25 gene variant, nicotine-related habits, lung cancer and COPD among 56 307 individuals from the HUNT study in Norway.
European Journal of Human Genetics
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Timofeeva, MN;
Hung, RJ;
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Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Human Molecular Genetics
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Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium.
Carcinogenesis
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Iversen, Ann-Charlotte;
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Genome-wide association scans identify novel maternal susceptibility loci for preeclampsia.
Pregnancy Hypertension
Abstract
2010
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Lips, EH;
Gaborieau, V;
Mckay, JD;
Chabrier, A;
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International Journal of Epidemiology
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Heath, SC;
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Investigation of the fine structure of European populations with applications to disease association studies.
European Journal of Human Genetics
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Lung cancer susceptibility locus at 5p15.33.
Nature Genetics
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A plasma protein-based risk score to predict hip fractures.
Nature Aging
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Austin, Thomas R.;
Nethander, Maria;
Fink, Howard A.;
Törnqvist, Anna E.;
Jalal, Diana I.;
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(2024)
Correction to: A plasma protein-based risk score to predict hip fractures (Nature Aging, (2024), 4, 8, (1064-1075), 10.1038/s43587-024-00639-7).
Nature Aging
Errata
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Austin, Thomas R.;
Fink, Howard A.;
Jalal, Diana I.;
Törnqvist, Anna E.;
Buzkova, Petra;
Barzilay, Joshua I..
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Large-scale circulating proteome association study (CPAS) meta-analysis identifies circulating proteins and pathways predicting incident hip fractures.
Journal of Bone and Mineral Research
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Arnesen, Carl-Arne;
Evensen, Line Holtet;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Hansen, John Bjarne;
Brækkan, Sigrid Kufaas.
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Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women.
Research and Practice in Thrombosis and Haemostasis (RPTH)
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de Vries, Paul S.;
Reventun, Paula;
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A genetic-association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
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Solé-Navais, Pol;
Flatley, Christopher;
Steinthorsdottir, Valgerdur;
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Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight (Nature Genetics, (2023), 55, 4, (559-567), 10.1038/s41588-023-01343-9).
Nature Genetics
Errata
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Grahnemo, Louise;
Nethander, Maria;
Coward, Eivind;
Gabrielsen, Maiken Elvestad;
Sree, Satya;
Billod, Jean-Marc.
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Identification of three bacterial species associated with increased appendicular lean mass: the HUNT study.
Nature Communications
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Wu, Kuan-Han;
Hornsby, Whitney;
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Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.
Cell Genomics
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Flatley, Christopher;
Steinthorsdottir, Valgerdur;
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Genetic effects on the timing of parturition and links to fetal birth weight.
Nature Genetics
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Gagliano Taliun, Sarah A.;
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A fast linkage method for population GWAS cohorts with related individuals.
Genetic Epidemiology
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Winsvold, Bendik Kristoffer Slagsvold;
Harder, Aster V. E.;
Ran, Caroline;
Chalmer, Mona A.;
Dalmasso, Maria Carolina;
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Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.
Annals of Neurology
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Surakka, Ida;
Wolford, Brooke Nichole;
Ritchie, Scott C.;
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Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction.
Circulation: Genomic and precision medicine
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Jacobsen, Kaya Kvarme;
Børte, Sigrid;
Laborie, Lene Bjerke;
Kristiansen, Hege;
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COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study.
Osteoarthritis and Cartilage Open
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Nethander, Maria;
Movérare-Skrtic, Sofia;
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An atlas of genetic determinants of forearm fracture.
Nature Genetics
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Holtet Evensen, Line;
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The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.
Thrombosis and Haemostasis
Academic article
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Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.
Brain
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Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study.
Cell Reports Medicine
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Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index.
International Journal of Epidemiology
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Snir, Omri;
Hindberg, Kristian Dalsbø;
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High Levels of Complement Activating Enzyme MASP-2 Are Associated With the Risk of Future Incident Venous Thromboembolism.
Arteriosclerosis, Thrombosis and Vascular Biology
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Malik, Rainer;
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Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
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The HUNT study: A population-based cohort for genetic research.
Cell Genomics
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Genetically predicted cortisol levels and risk of venous thromboembolism.
PLOS ONE
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Genome-wide risk prediction of common diseases across ancestries in one million people.
Cell Genomics
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Nature
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Hautakangas, Heidi;
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Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles .
Nature Genetics
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Løset, Mari;
Thomas, Laurent Francois;
Brumpton, Ben Michael;
Modalsli, Ellen Heilmann;
Gabrielsen, Maiken Elvestad;
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Discovering novel genes and causal relationships for psoriasis: The HUNT study.
Acta Dermato-Venereologica
Abstract
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Wightman, Douglas P.;
Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey;
Bahrami, Shahram;
Holland, Dominic.
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Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (Nature Genetics, (2021), 53, 9, (1276-1282), 10.1038/s41588-021-00921-z).
Nature Genetics
Errata
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Mishra, Aniket;
Malik, Rainer;
Hachiya, Tsuyoshi;
Jürgenson, Tuuli;
Namba, Shinichi;
Posner, Daniel C..
(2022)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
Errata
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Grahnemo, Louise;
Nethander, Maria;
Coward, Eivind;
Gabrielsen, Maiken Elvestad;
Sree, Satya;
Billod, Jean-Marc.
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Cross-sectional associations between the gut microbe Ruminococcus gnavus and features of the metabolic syndrome.
The Lancet Diabetes and Endocrinology
Letter to the editor
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Rahman, Shafiqur;
Winsvold, Bendik K S;
Chavez, Sergio;
Børte, Sigrid;
Tsepilov, Vakov;
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Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain.
Annals of the Rheumatic Diseases
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Khoury, Samar;
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Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions.
Brain
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Sex- and age-specific genetic analysis of chronic back pain.
Pain
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Frischmuth, Tobias;
Hindberg, Kristian;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hveem, Kristian;
Brækkan, Sigrid Kufaas.
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Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism.
Thrombosis and Haemostasis
Academic article
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Skille, Hanne;
Paulsen, Benedikte;
Hveem, Kristian;
Severinsen, Marianne T.;
Gabrielsen, Maiken Elvestad;
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Prothrombotic genotypes and risk of venous thromboembolism in occult cancer.
Thrombosis Research
Academic article
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Zhou, Wei;
Brumpton, Ben Michael;
Kabil, Omer;
Gudmundsson, Julius;
Thorleifsson, Gudmar;
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Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer (Nature Communications, (2020), 11, 1, (3981), 10.1038/s41467-020-17718-z).
Nature Communications
Errata
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McGuire, Daniel;
Jiang, Yu;
Liu, Mengzhen;
Weissenkampen, J. Dylan;
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Model-based assessment of replicability for genome-wide association meta-analysis.
Nature Communications
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Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey A.;
Bahrami, Shahram;
Holland, Dominic.
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Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (Nature Genetics, (2021), 53, 9, (1276-1282), 10.1038/s41588-021-00921-z).
Nature Genetics
Errata
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Zheng, Thenghao;
Ellinghaus, David;
Juzenas, Simonas;
Cossais, François;
Burmeister, Greta;
Mayr, Gabriele.
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Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.
Gut
Academic article
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Rasheed, Humaira;
Zheng, Jie;
Rees, Jessica;
Sanderson, Eleanor;
Thomas, Laurent;
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The causal effects of serum lipids and apolipoproteins on kidney function: Multivariable and bidirectional Mendelian-randomization analyses.
International Journal of Epidemiology
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Jansen, Iris E.;
Savage, Jeanne E.;
Shadrin, Alexey;
Bahrami, Shahram;
Holland, Dominic.
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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.
Nature Genetics
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Boer, Cindy G.;
Hatzikotoulas, Konstantinos;
Southam, Lorraine;
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Almeida, Rodrigo Coutinho de;
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Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Cell
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Fan, Yanbo;
Wolford, Brooke N.;
Lu, Haocheng;
Liang, Wenying;
Sun, Jinjian;
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Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2.
iScience
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Kitsos, Ioannis;
Thomas, Laurent;
Skogholt, Anne Heidi;
Gabrielsen, Maiken Elvestad;
Zwart, John Anker Henrik.
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Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci.
Frontiers in Neurology
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Johnsen, Marianne Bakke;
Magnusson, Karin;
Børte, Sigrid;
Gabrielsen, Maiken Elvestad;
Winsvold, Bendik K S;
Skogholt, Anne Heidi.
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Response to Letter to the Editor: ‘Comments on the paper presenting prediction models for incident hand OA in the HUNT study’.
Osteoarthritis and Cartilage
Letter to the editor
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Zhou, Wei;
Brumpton, Ben Michael;
Kabil, Omer;
Gudmundsson, Julius;
Thorleifsson, Gudmar;
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GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.
Nature Communications
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Johnsen, Marianne Bakke;
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Børte, Sigrid;
Gabrielsen, Maiken Elvestad;
Winsvold, Bendik K S;
Skogholt, Anne Heidi.
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Development and validation of a prediction model for incident hand
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Osteoarthritis and Cartilage
Academic article
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Klarin, Derek;
Verma, Shefali Setia;
Judy, Renae;
Dikilitas, Ozan;
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Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Circulation
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Surakka, Ida;
Fritsche, Lars;
Zhou, Wei;
Backman, Joshua;
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Lu, Haocheng.
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MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.
Nature Communications
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Børte, Sigrid;
Zwart, John-Anker;
Skogholt, Anne Heidi;
Gabrielsen, Maiken Elvestad;
Thomas, Laurent;
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Mitochondrial genome-wide association study of migraine – the HUNT Study .
Cephalalgia
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Ferreira, Manuel A R;
Vonk, Judith M.;
Baurecht, Hansjörg;
Marenholz, Ingo;
Tian, Chao;
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Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genetics
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Nielsen, Jonas Bille;
Rom, Oren;
Surakka, Ida;
Graham, Sarah E.;
Zhou, Wei;
Roychowdhury, Tanmoy.
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Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.
Nature Communications
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Skille, Hanne;
Paulsen, Benedikte;
Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
Brumpton, Ben Michael;
Hindberg, Kristian.
(2020)
Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event.
Journal of Thrombosis and Haemostasis
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Zhou, Wei;
Zhao, Zhangchen;
Nielsen, Jonas B.;
Fritsche, Lars;
LeFaive, Jonathon;
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Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts.
Nature Genetics
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Liu, Mengzhen;
Jiang, Yu;
Wedow, Robbee;
Li, Yue;
Brazel, David M.;
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Nature Genetics
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Småbrekke, Birgit;
Balteskard Rinde, Ludvig;
Evensen, Line Holtet;
Morelli, Vania Maris;
Hveem, Kristian;
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Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism.
Journal of Thrombosis and Haemostasis
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Brumpton, Ben Michael;
Fritsche, Lars;
Zheng, Jie;
Nielsen, Jonas Bille;
Mannila, Maria Nastase;
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Variation in serum PCSK9 (proprotein convertase subtilisin/kexin type 9), cardiovascular disease risk, and an investigation of potential unanticipated effects of PCSK9 inhibition.
Circulation: Genomic and precision medicine
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Lane, Jacqueline M.;
Jones, Samuel E.;
Dashti, Hassan S.;
Wood, Andrew R.;
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Biological and clinical insights from genetics of insomnia symptoms.
Nature Genetics
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Løset, Mari;
Thomas, Laurent;
Brumpton, Ben Michael;
Wolford, Brooke N.;
Holmen, Oddgeir;
Luetge, Almut.
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Genome-wide association study of psoriasis suggests a new risk locus on chromosome 10: The HUNT Study.
Forum for Nordic Dermato-Venereology
Abstract
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Graham, Sarah E.;
Nielsen, Jonas B.;
Zawistowski, Matthew;
Zhou, Wei;
Fritsche, Lars G.;
Gabrielsen, Maiken Elvestad.
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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Nature Communications
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Vie, Gunnhild Åberge;
Wootton, Robyn E;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
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The effect of smoking intensity on all-cause and cause-specific mortality-a Mendelian randomization analysis.
International Journal of Epidemiology
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van Hylckama Vlieg, Astrid;
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Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood
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Hveem, Kristian;
Gabrielsen, Maiken Elvestad;
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Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism.
Haematologica
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Genetic Variation Of Platelet Glycoprotein VI And The Risk Of Venous Thromboembolism.
Haematologica
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Corominas, Jordi;
Klein, Marieke;
Zayats, Tetyana;
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Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Molecular Psychiatry
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Rode, Line;
Bjørngaard, Johan Håkon;
Taylor, Amy E.;
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Åsvold, Bjørn Olav.
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Is smoking heaviness causally associated with alcohol use? A Mendelian randomization study in four European cohorts.
International Journal of Epidemiology
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Thorolfsdottir, Rosa B.;
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Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature Genetics
Academic article
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Zhou, Wei;
Nielsen, Jonas B.;
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Efficiently controlling for
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Nature Genetics
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Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
American Journal of Human Genetics
Academic article
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Løset, Mari;
Modalsli, Ellen Heilmann;
Snekvik, Ingrid;
Solvin, Åshild Øksnevad;
Holmen, Oddgeir Lingaas;
Gabrielsen, Maiken Elvestad.
(2018)
743 HUNTing for genes that affect inflammatory skin disease in 4,071 cases and 40,430 controls.
Journal of Investigative Dermatology
Abstract
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Wang, Yufei;
McKay, James D.;
Rafnar, Thorunn;
Wang, Zhaoming;
Timofeeva, Maria N.;
Broderick, Peter.
(2017)
Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (Nature Genetics (2014) 46 (736-741)).
Nature Genetics
Errata
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Ferreira, Manuel A.;
Vonk, Judith M;
Baurecht, Hansjörg;
Marenholz, Ingo;
Tian, Chao;
Hoffman, Joshua D.
(2017)
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Nature Genetics
Academic article
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Skaaby, Tea;
Taylor, Amy E;
Jacobsen, Rikke K.;
Paternoster, Lavinia;
Thuesen, Betina H.;
Ahluwalia, Tarunveer S..
(2017)
Investigating the causal effect of smoking on hay fever and asthma: A Mendelian randomization meta-analysis in the CARTA consortium.
Scientific Reports
Academic article
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Johnsen, Marianne Bakke;
Vie, Gunnhild Åberge;
Winsvold, Bendik K S;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Gabrielsen, Maiken Elvestad.
(2017)
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
Academic article
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Bjørngaard, Johan Håkon;
Nordestgaard, AT;
Taylor, Amy E;
Treur, Jorien L;
Gabrielsen, Maiken Elvestad;
Munafo, Marcus R.
(2017)
Heavier smoking increases coffee consumption: findings from a Mendelian randomization analysis.
International Journal of Epidemiology
Academic article
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Zhou, Wei;
Fritsche, Lars;
Das, Sayantan;
Zhang, He;
Nielsen, Jonas B.;
Holmen, Oddgeir Lingaas.
(2017)
Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.
Genetic Epidemiology
Academic article
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Zayats, Tetyana;
Jacobsen, Kaya Kvarme;
Kleppe, Rune;
Jacob, CP;
Kittel-Schneider, Sarah;
Ribases, Marta.
(2016)
Exome chip analyses in adult attention deficit hyperactivity disorder.
Translational Psychiatry
Academic article
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Løset, Mari;
Modalsli, Ellen Heilmann;
Snekvik, Ingrid;
Zhou, Wei;
Chu, Yunhan;
Gabrielsen, Maiken Elvestad.
(2016)
HUNTing for Genes that Affect Psoriasis in ~2,900 Cases and ~48,000 Controls.
Forum for Nordic Dermato-Venereology
Abstract
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Morris, Richard W.;
Taylor, Amy E.;
Fluharty, Meg E.;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Gabrielsen, Maiken Elvestad.
(2015)
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
Academic article
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Linneberg, Allan;
Jacobseb, Rikke;
Skaaby, Tea;
Taylor, Amy E.;
Fluharty, Meg E.;
Jeppesen, Jørgen L..
(2015)
Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium.
Circulation: Cardiovascular Genetics
Academic article
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Brenner, Darren. R.;
Amos, Christopher I.;
Brhane, Yonathan;
Timofeeva, Maria N.;
Caporaso, Neil;
Wang, Yufei.
(2015)
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.
Carcinogenesis
Academic article
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Taylor, Amy E;
Morris, Richard W;
Fluharty, Meg;
Bjørngaard, Johan Håkon;
Åsvold, Bjørn Olav;
Gabrielsen, Maiken Elvestad.
(2014)
Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers.
PLoS Genetics
Academic article
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Taylor, Amy E;
Fluharty, Meg;
Bjørngaard, Johan Håkon;
Gabrielsen, Maiken Elvestad;
Skorpen, Frank;
Marioni, Riccardo R..
(2014)
Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium.
BMJ Open
Academic article
-
Wang, Yufei;
McKay, JD;
Rafnar, T;
Wang, Z;
Timofeeva, MN;
Broderick, P.
(2014)
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Nature Genetics
Academic article
-
Åsvold, Bjørn Olav;
Bjørngaard, Johan Håkon;
Carslake, D;
Gabrielsen, Maiken Elvestad;
Skorpen, Frank;
Smith, GD.
(2014)
Causal associations of tobacco smoking with cardiovascular risk factors: a Mendelian randomization analysis of the HUNT Study in Norway.
International Journal of Epidemiology
Academic article
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Bjørngaard, Johan Håkon;
Gunnell, David;
Gabrielsen, Maiken Elvestad;
Davey Smith, George;
Skorpen, Frank;
Krokan, Hans Einar.
(2013)
The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study.
Psychological Medicine
Academic article
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Gabrielsen, Maiken Elvestad;
Romundstad, Pål Richard;
Langhammer, Arnulf;
Krokan, Hans Einar;
Skorpen, Frank.
(2013)
Association between a 15q25 gene variant, nicotine-related habits, lung cancer and COPD among 56 307 individuals from the HUNT study in Norway.
European Journal of Human Genetics
Academic article
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Timofeeva, MN;
Hung, RJ;
Rafnar, T;
Christiani, DC;
Field, JK;
Bickeboller, H.
(2012)
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Human Molecular Genetics
Academic article
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Kazma, R;
Babron, MC;
Gaborieau, Valerie;
Génin, E;
Brennan, P;
Hung, Rayjean J..
(2012)
Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium.
Carcinogenesis
Academic article
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Johnson, Matthew P;
Brennecke, Shaun P.;
Iversen, Ann-Charlotte;
East, Christine;
Olsen, Guro Dalheim;
Kent, Jack W.
(2012)
Genome-wide association scans identify novel maternal susceptibility loci for preeclampsia.
Pregnancy Hypertension
Abstract
-
Lips, EH;
Gaborieau, V;
Mckay, JD;
Chabrier, A;
Hung, RJ;
Boffetta, P.
(2010)
Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals.
International Journal of Epidemiology
Academic article
-
Heath, SC;
Gut, IG;
Brennan, P;
Mckay, JD;
Bencko, V;
Fabianova, E.
(2008)
Investigation of the fine structure of European populations with applications to disease association studies.
European Journal of Human Genetics
Academic article
-
McKay, JD;
Mckay, JD;
Hung, RJ;
Gaborieau, V;
Boffetta, Paolo;
Chabrier, Amelie.
(2008)
Lung cancer susceptibility locus at 5p15.33.
Nature Genetics
Academic article
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Hung, RJ;
Mckay, JD;
Gaborieau, V;
Boffetta, P;
Hashibe, M;
Zaridze, D.
(2008)
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.
Nature
Academic article
Knowledge Transfer
2022
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Academic lectureLøset, Mari; Thomas, Laurent Francois; Brumpton, Ben Michael; Modalsli, Ellen Heilmann; Gabrielsen, Maiken Elvestad; Solvin, Åshild Øksnevad. (2022) Discovering novel genes and causal relationships for psoriasis: The HUNT study. Nordic Dermatology Association 35th Nordic Congres of Dermatology and Venereology , København 2022-04-19 - 2022-04-22
2019
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Academic lectureLøset, Mari; Thomas, Laurent; Brumpton, Ben Michael; Wolford, Brooke N.; Holmen, Oddgeir; Luetge, Almut. (2019) Genome-wide association study of psoriasis suggests a new risk locus on chromosome 10: The HUNT Study. The 34th Nordic Congress of Dermatology & Venereology , Gøteborg 2019-05-08 - 2019-05-10
2016
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Academic lectureLøset, Mari; Modalsli, Ellen Heilmann; Snekvik, Ingrid; Zhou, Wei; Chu, Yunhan; Gabrielsen, Maiken Elvestad. (2016) HUNTing for Genes that Affect Psoriasis in ~2,900 Cases and ~48,000 Controls. The 33rd Nordic Congress of Dermatology and Venereolgy 2016-04-27 - 2016-04-29
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Academic lectureSolvin, Åshild Øksnevad; Modalsli, Ellen Heilmann; Snekvik, Ingrid; Gabrielsen, Maiken Elvestad; Holmen, Oddgeir Lingaas; Saunes, Marit. (2016) Establishing a biobank for gene expression studies of psoriasis. Frampeik , Bergen 2016-10-21 - 2016-10-23
2012
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Programme participation
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Academic lectureJohnson, Matthew P; Brennecke, Shaun P.; Iversen, Ann-Charlotte; East, C; Olsen, Guro Dalheim; Kent, J. (2012) Genome-wide association scans identify novel maternal susceptibility loci for preeclampsia. ISSHP The XVIII ISSHP World Congress , Geneva 2012-07-09 - 2012-07-12
2011
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Programme participationElvestad, Maiken Bratt. (2011) Kunnskapskanalen, Forsker Grand Prix Trondheim 2010. NRK 2 NRK 2 [TV] 2011-04-09
2010
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Popular scientific lectureElvestad, Maiken Bratt. (2010) Forsker Grand Prix 2010, "A eller G, spille det nån rolle? Æ røyke jo bare Prince Mild!". NTNU Forsker Grand Prix 2010 , Studentersamfundet, Trondheim 2010-11-10 - 2010-11-10
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Programme participation
2009
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Programme participationElvestad, Maiken Bratt; Gjerde, Anne Heidi; Hanssen-Bauer, Audun; Fladvad, Torill; Gilljam, Karin Margaretha; Bergstrøm, Bjarte. (2009) Forskningsdagene 2009. Forskningstorget Forskningstorget [TV] 2009-09-25
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Programme participationElvestad, Maiken Bratt; Hagen, Lars; Hanssen-Bauer, Audun; Liabakk, Nina-Beate. (2009) Reportasje fra "Drømmedag". NRK P3 NRK P3 [Radio] 2009-06-18
2007
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InterviewElvestad, Maiken Bratt. (2007) Kvinner kupper doktorgraden. Adressavisen Adressavisen [Newspaper] 2007-10-27
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Academic lectureElvestad, Maiken Bratt. (2007) DNA polymorphisms associated with lung cancer. EMBO and University of Helsinki, The Finnish genome center EMBO Practical course, Genome-wide association studies , Helsinki 2007-08-27 - 2007-08-31
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Academic lectureElvestad, Maiken Bratt. (2007) SNP's associated with lung cancer. Wallenberg Consortium North, Uppsala University, Karolinska Kurs: Applied bioinformatics and methodologies in SNP genotyping , Uppsala 2007-03-10 - 2007-03-15