2025

• Hatzikotoulas, Konstantinos; Southam, Lorraine; Stefansdottir, Lilja; Boer, Cindy G.; McDonald, Merry-Lynn; Pett, J. Patrick; Park, Young-Chan; Tuerlings, Margo; Mulders, Rick; Barysenka, Andrei. (2025) Translational genomics of osteoarthritis in 1,962,069 individuals. Nature
  Vitenskapelig artikkel
• Arnesen, Carl-Arne; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Hansen, John Bjarne; Brækkan, Sigrid Kufaas. (2025) Body height and risk of venous thromboembolism in men vs women. Journal of Thrombosis and Haemostasis
  Vitenskapelig artikkel

2024

• Austin, Thomas R.; Nethander, Maria; Fink, Howard A.; Törnqvist, Anna E.; Jalal, Diana I.; Buzkova, Petra; Barzilay, Joshua I.; Carbone, Laura; Gabrielsen, Maiken Elvestad; Grahnemo, Louise. (2024) A plasma protein-based risk score to predict hip fractures. Nature Aging
  Kommentar
• 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)
  Vitenskapelig artikkel
• Fongang, Bernard; Sargurupremraj, Muralidharan; Jian, Xueqiu; Mishra, Aniket; Damotte, Vincent; Rojas, Itziar De; Skrobot, Olivia; Bis, Joshua C; Fan, Kang-Hsien; Jacobsen, Erin. (2024) A genome-wide association meta-analysis of all-cause and vascular dementia. Alzheimer's & Dementia
  Vitenskapelig artikkel
• Austin, Thomas R.; Fink, Howard A.; Jalal, Diana I.; Törnqvist, Anna E.; Buzkova, Petra; Barzilay, Joshua I.; Lu, Tianyuan; Carbone, Laura; Gabrielsen, Maiken Elvestad; Grahnemo, Louise. (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
  Vitenskapelig artikkel
• Austin, Thomas R.; Nethander, Maria; Fink, Howard A.; Törnqvist, Anna E.; Jalal, Diana I.; Buzkova, Petra; Barzilay, Joshua I.; Carbone, Laura; Gabrielsen, Maiken Elvestad; Grahnemo, Louise. (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
  Korrigendum

2023

• Solé-Navais, Pol; Flatley, Christopher; Steinthorsdottir, Valgerdur; Vaudel, Marc; Juodakis, Julius; Chen, Jing; Laisk, Triin; LaBella, Abigail L.; Westergaard, David; Bacelis, Jonas. (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
  Korrigendum
• Zajac, Gregory J. M.; Taliun, Sarah A. Gagliano; Sidore, Carlo; Graham, Sarah E.; Åsvold, Bjørn Olav; Brumpton, Ben Michael; Nielsen, Jonas Bille; Zhou, Wei; Gabrielsen, Maiken Elvestad; Skogholt, Anne Heidi. (2023) A fast linkage method for population GWAS cohorts with related individuals. Genetic Epidemiology
  Vitenskapelig artikkel
• Nethander, Maria; Movérare-Skrtic, Sofia; Kämpe, Anders; Coward, Eivind; Reimann, Ene; Grahnemo, Louise; Borbély, Éva; Helyes, Zsuzsanna; Funck-Brentano, Thomas; Cohen-Solal, Martine. (2023) An atlas of genetic determinants of forearm fracture. Nature Genetics
  Vitenskapelig artikkel
• Winsvold, Bendik Kristoffer Slagsvold; Harder, Aster V. E.; Ran, Caroline; Chalmer, Mona A.; Dalmasso, Maria Carolina; Ferkingstad, Egil; Tripathi, Kumar Parijat; Bacchelli, Elena; Børte, Sigrid; Fourier, Carmen. (2023) Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. Annals of Neurology
  Vitenskapelig artikkel
• Solé-Navais, Pol; Flatley, Christopher; Steinthorsdottir, Valgerdur; Vaudel, Marc; Juodakis, Julius; Chen, Jing; Laisk, Triin; LaBella, Abigail L.; Westergaard, David; Bacelis, Jonas. (2023) Genetic effects on the timing of parturition and links to fetal birth weight. Nature Genetics
  Vitenskapelig artikkel
• Surakka, Ida; Wolford, Brooke Nichole; Ritchie, Scott C.; Hornsby, Whitney E.; Sutton, Nadia R.; Gabrielsen, Maiken Elvestad; Skogholt, Anne Heidi; Thomas, Laurent Francois; Inouye, Michael; Hveem, Kristian. (2023) Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction. Circulation: Genomic and precision medicine
  Vitenskapelig artikkel
• Grahnemo, Louise; Nethander, Maria; Coward, Eivind; Gabrielsen, Maiken Elvestad; Sree, Satya; Billod, Jean-Marc; Sjögren, Klara; Engstrand, Lars; Dekkers, Koen F.; Fall, Tove. (2023) Identification of three bacterial species associated with increased appendicular lean mass: the HUNT study. Nature Communications
  Vitenskapelig artikkel
• Surakka, Ida; Wu, Kuan-Han; Hornsby, Whitney; Wolford, Brooke N.; Shen, Fred; Zhou, Wei; Huffman, Jennifer E.; Pandit, Anita; Hu, Yao; Brumpton, Ben Michael. (2023) Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. Cell Genomics
  Vitenskapelig artikkel
• Jacobsen, Kaya Kvarme; Børte, Sigrid; Laborie, Lene Bjerke; Kristiansen, Hege; Schäfer, Annette; Martinsen, Amy; Skogholt, Anne Heidi; Brumpton, Ben Michael; Willer, Cristen J; Fors, Egil Andreas. (2023) COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study. Osteoarthritis and Cartilage Open
  Vitenskapelig artikkel

2022

• Brumpton, Ben Michael; Graham, Sarah; Surakka, Ida; Skogholt, Anne Heidi; Løset, Mari; Fritsche, Lars G.; Wolford, Brooke; Zhou, Wei; Nielsen, Jonas Bille; Holmen, Oddgeir Lingaas. (2022) The HUNT study: A population-based cohort for genetic research. Cell Genomics
  Vitenskapelig artikkel
• Mars, Nina; Kerminen, Sini; Feng, Yen-Chen A.; Kanai, Masahiro; Läll, Kristi; Thomas, Laurent Francois; Skogholt, Anne Heidi; Parolo, Pietro della Briotta; Neale, Benjamin M.; Smoller, Jordan W.. (2022) Genome-wide risk prediction of common diseases across ancestries in one million people. Cell Genomics
  Vitenskapelig artikkel
• Hartley, April; Sanderson, Eleanor; Granell, Raquel; Paternoster, Lavinia; Zheng, Jie; Smith, George Davey; Southam, Lorraine; Hatzikotoulas, Konstantinos; Boer, Cindy G.; Meurs, Joyce Van. (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
  Vitenskapelig artikkel
• Bahrami, Shahram; Hindley, Guy Frederick Lanyon; Winsvold, Bendik K S; O'Connell, Kevin Sean; Frei, Oleksandr; Shadrin, Alexey; Cheng, Weiqiu; Bettella, Francesco; Rødevand, Linn; Ødegaard, Ketil Joachim. (2022) Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools. Brain
  Vitenskapelig artikkel
• Nethander, Maria; Coward, Eivind; Reimann, Ene; Grahnemo, Louise; Gabrielsen, Maiken Elvestad; Wibom, Carl; Nelis, Mari; Milani, Lili; Esko, Tõnu; Metspalu, Andres. (2022) Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. Cell Reports Medicine
  Vitenskapelig artikkel
• Damoah, Christabel Esi; Snir, Omri; Hindberg, Kristian Dalsbø; Garred, Peter; Ludviksen, Judith K; Brækkan, Sigrid Kufaas; Morelli, Vania Maris; Mollnes, Tom Eirik; Hansen, John Bjarne; Smith, Erin N.. (2022) High Levels of Complement Activating Enzyme MASP-2 Are Associated With the Risk of Future Incident Venous Thromboembolism. Arteriosclerosis, Thrombosis and Vascular Biology
  Vitenskapelig artikkel
• Allarai, Elias; Lee, Wei-Hsuan; Burgess, Stephen; Larsson, Susanna C.; Lindstrom, Sara; Wang, Lu; Smith, Erin N.; Gordon, William; Vlieg, Astrid Van Hylckama; Andrade, Mariza De. (2022) Genetically predicted cortisol levels and risk of venous thromboembolism. PLOS ONE
  Vitenskapelig artikkel
• Saunders, Gretchen R. B.; Wang, Xingyan; Chen, Fang; Jang, Seon-Kyeong; Liu, Mengzhen; Wang, Chen; Gao, Shuang; Jiang, Yu; Khunsriraksakul, Chachrit; Otto, Jacqueline M.. (2022) Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature
  Vitenskapelig artikkel
• Hautakangas, Heidi; Winsvold, Bendik K S; Ruotsalainen, Sanni; Bjornsdottir, Gyda; Harder, Aster V. E.; Kogelman, Lisette J. A.; Thomas, Laurent; Noordam, Raymond; Benner, Christian; Gormley, Padhraig. (2022) Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Nature Genetics
  Vitenskapelig artikkel
• Evensen, Line Holtet; Arnesen, Carl-Arne; Rosendaal, Frits Richard; Gabrielsen, Maiken Elvestad; Brumpton, Ben Michael; Hveem, Kristian; Hansen, John Bjarne; Brækkan, Sigrid Kufaas. (2022) The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes. Thrombosis and Haemostasis
  Vitenskapelig artikkel
• Grahnemo, Louise; Nethander, Maria; Coward, Eivind; Gabrielsen, Maiken Elvestad; Sree, Satya; Billod, Jean-Marc; Engstrand, Lars; Abrahamsson, Sanna; Langhammer, Arnulf; Hveem, Kristian. (2022) Cross-sectional associations between the gut microbe Ruminococcus gnavus and features of the metabolic syndrome. The Lancet Diabetes and Endocrinology
  Kommentar
• Mishra, Aniket; Malik, Rainer; Hachiya, Tsuyoshi; Jürgenson, Tuuli; Namba, Shinichi; Posner, Daniel C.; Kamanu, Frederick K.; Koido, Masaru; Grand, Quentin Le; Shi, Mingyang. (2022) Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries. Nature
  Korrigendum
• Mishra, Aniket; Malik, Rainer; Hachiya, Tsuyoshi; Jürgenson, Tuuli; Namba, Shinichi; Posner, Daniel C.; Kamanu, Frederick K.; Koido, Masaru; Grand, Quentin Le; Shi, Mingyang. (2022) Stroke genetics informs drug discovery and risk prediction across ancestries. Nature
  Vitenskapelig artikkel
• Wightman, Douglas P.; Jansen, Iris E.; Savage, Jeanne E.; Shadrin, Alexey; Bahrami, Shahram; Holland, Dominic; Rongve, Arvid; Børte, Sigrid; Winsvold, Bendik K S; Drange, Ole Kristian. (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
  Korrigendum
• Løset, Mari; Thomas, Laurent Francois; Brumpton, Ben Michael; Modalsli, Ellen Heilmann; Gabrielsen, Maiken Elvestad; Solvin, Åshild Øksnevad; Saunes, Marit; Willer, Cristen; Åsvold, Bjørn Olav; Hveem, Kristian. (2022) Discovering novel genes and causal relationships for psoriasis: The HUNT study. Acta Dermato-Venereologica
  Konferanseabstract

2021

• Rasheed, Humaira; Zheng, Jie; Rees, Jessica; Sanderson, Eleanor; Thomas, Laurent; Richardson, Tom G.; Fang, Si; Bekkevold, Ole-Jørgen; Stovner, Endre Bakken; Gabrielsen, Maiken Elvestad. (2021) The causal effects of serum lipids and apolipoproteins on kidney function: Multivariable and bidirectional Mendelian-randomization analyses. International Journal of Epidemiology
  Vitenskapelig artikkel
• Fan, Yanbo; Wolford, Brooke N.; Lu, Haocheng; Liang, Wenying; Sun, Jinjian; Zhou, Wei; Rom, Oren; Mahajan, Anubha; Surakka, Ida; Graham, Sarah E.. (2021) Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2. iScience
  Vitenskapelig artikkel
• Wightman, Douglas P.; Jansen, Iris E.; Savage, Jeanne E.; Shadrin, Alexey A.; Bahrami, Shahram; Holland, Dominic; Rongve, Arvid; Børte, Sigrid; Winsvold, Bendik S.; Drange, Ole Kristian. (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
  Korrigendum
• Rahman, Shafiqur; Winsvold, Bendik K S; Chavez, Sergio; Børte, Sigrid; Tsepilov, Vakov; Sharapov, Sodbo Zh; Martinsen, Amy; Skogholt, Anne Heidi; Brumpton, Ben Michael; Willer, Cristen. (2021) Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain. Annals of the Rheumatic Diseases
  Vitenskapelig artikkel
• Johnsen, Marianne Bakke; Magnusson, Karin; Børte, Sigrid; Gabrielsen, Maiken Elvestad; Winsvold, Bendik K S; Skogholt, Anne Heidi; Thomas, Laurent; Storheim, Kjersti; Hveem, Kristian; Zwart, John-Anker. (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
  Kommentar
• Freidin, Maxim B.; Tsepilov, Yakov A.; Stanaway, Ian B.; Meng, Weihua; Hayward, Caroline; Smith, Blair H.; Khoury, Samar; Parisien, Marc; Bortsov, Andrey; Diatchenko, Luda. (2021) Sex- and age-specific genetic analysis of chronic back pain. Pain
  Vitenskapelig artikkel
• Khoury, Samar; Parisien, Marc; Thompson, Scott J.; Vachon-Presseau, Etienne; Roy, Mathieu; Mitchell, Amy; Winsvold, Bendik K S; Skogholt, Anne Heidi; Brumpton, Ben Michael; Willer, Cristen J.. (2021) Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions. Brain
  Vitenskapelig artikkel
• Frischmuth, Tobias; Hindberg, Kristian; Gabrielsen, Maiken Elvestad; Brumpton, Ben Michael; Hveem, Kristian; Brækkan, Sigrid Kufaas; Hansen, John-Bjarne; Morelli, Vania Maris. (2021) Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism. Thrombosis and Haemostasis
  Vitenskapelig artikkel
• Skille, Hanne; Paulsen, Benedikte; Hveem, Kristian; Severinsen, Marianne T.; Gabrielsen, Maiken Elvestad; Kristensen, Søren R.; Næss, Inger Anne; Hindberg, Kristian; Tjønneland, Anne; Brækkan, Sigrid Kufaas. (2021) Prothrombotic genotypes and risk of venous thromboembolism in occult cancer. Thrombosis Research
  Vitenskapelig artikkel
• Wightman, Douglas P.; Jansen, Iris E.; Savage, Jeanne E.; Shadrin, Alexey; Bahrami, Shahram; Holland, Dominic; Rongve, Arvid; Børte, Sigrid; Winsvold, Bendik K S; Drange, Ole Kristian. (2021) A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. Nature Genetics
  Vitenskapelig artikkel
• Zheng, Thenghao; Ellinghaus, David; Juzenas, Simonas; Cossais, François; Burmeister, Greta; Mayr, Gabriele; Jørgensen, Isabella Friis; Teder-Laving, Maris; Skogholt, Anne Heidi; Chen, Sisi. (2021) Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease. Gut
  Vitenskapelig artikkel
• McGuire, Daniel; Jiang, Yu; Liu, Mengzhen; Weissenkampen, J. Dylan; Eckert, Scott; Yang, Lina; Chen, Fang; Liu, MengZhen; Wedow, Robbee; Li, Yue. (2021) Model-based assessment of replicability for genome-wide association meta-analysis. Nature Communications
  Vitenskapelig artikkel
• Zhou, Wei; Brumpton, Ben Michael; Kabil, Omer; Gudmundsson, Julius; Thorleifsson, Gudmar; Weinstock, Joshua; Zawistowski, Matthew; Nielsen, Jonas B.; Chaker, Layal; Medici, Marco. (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
  Korrigendum
• Winsvold, Bendik K S; Kitsos, Ioannis; Thomas, Laurent; Skogholt, Anne Heidi; Gabrielsen, Maiken Elvestad; Zwart, John Anker Henrik; Nilsen, Kristian Bernhard. (2021) Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci. Frontiers in Neurology
  Vitenskapelig artikkel
• Boer, Cindy G.; Hatzikotoulas, Konstantinos; Southam, Lorraine; Stefánsdóttir, Lilja; Almeida, Rodrigo Coutinho de; Zhang, Yanfei; Wu, Tian T.; Zheng, Jie; Hartley, April; Teder-Laving, Maris. (2021) Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Cell
  Vitenskapelig artikkel

2020

• Zhou, Wei; Brumpton, Ben Michael; Kabil, Omer; Gudmundsson, Julius; Thorleifsson, Gudmar; Weinstock, Joshua; Zawistowski, Matthew; Nielsen, Jonas Bille; Chaker, Layal; Medici, Marco. (2020) GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. Nature Communications
  Vitenskapelig artikkel
• Surakka, Ida; Fritsche, Lars; Zhou, Wei; Backman, Joshua; Kosmicki, Jack A.; Lu, Haocheng; Brumpton, Ben Michael; Nielsen, Jonas B.; Gabrielsen, Maiken Elvestad; Skogholt, Anne Heidi. (2020) MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk. Nature Communications
  Vitenskapelig artikkel
• Nielsen, Jonas Bille; Rom, Oren; Surakka, Ida; Graham, Sarah E.; Zhou, Wei; Roychowdhury, Tanmoy; Fritsche, Lars; Taliun, Sarah Gagliano; Sidore, Carlo; Liu, Yuhao. (2020) Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Nature Communications
  Vitenskapelig artikkel
• Johnsen, Marianne Bakke; Magnusson, Karin; Børte, Sigrid; Gabrielsen, Maiken Elvestad; Winsvold, Bendik K S; Skogholt, Anne Heidi; Thomas, Laurent; Storheim, Kjersti; Hveem, Kristian; Zwart, John-Anker. (2020) Development and validation of a prediction model for incident hand osteoarthritis in the HUNT study. Osteoarthritis and Cartilage
  Vitenskapelig artikkel
• Ferreira, Manuel A R; Vonk, Judith M.; Baurecht, Hansjörg; Marenholz, Ingo; Tian, Chao; Hoffman, Joshua D.; Helmer, Quinta; Tillander, Annika; Ullemar, Vilhelmina; Lu, Yi. (2020) Age-of-onset information helps identify 76 genetic variants associated with allergic disease. PLoS Genetics
  Vitenskapelig artikkel
• Skille, Hanne; Paulsen, Benedikte; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Brumpton, Ben Michael; Hindberg, Kristian; Gran, Olga Vikhammer; Rosendaal, Frits Richard; Brækkan, Sigrid Kufaas; Hansen, John-Bjarne. (2020) Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event. Journal of Thrombosis and Haemostasis
  Vitenskapelig artikkel
• Børte, Sigrid; Zwart, John-Anker; Skogholt, Anne Heidi; Gabrielsen, Maiken Elvestad; Thomas, Laurent; Fritsche, Lars; Surakke, Ida; Nielsen, Jonas B.; Zhou, Wei; Wolford, Brooke. (2020) Mitochondrial genome-wide association study of migraine – the HUNT Study. Cephalalgia
  Vitenskapelig artikkel
• Klarin, Derek; Verma, Shefali Setia; Judy, Renae; Dikilitas, Ozan; Wolford, Brooke N.; Paranjpe, Ishan; Levin, Michael G.; Pan, Cuiping; Tcheandjieu, Catherine; Spin, Joshua M.. (2020) Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation
  Vitenskapelig artikkel
• Zhou, Wei; Zhao, Zhangchen; Nielsen, Jonas B.; Fritsche, Lars; LeFaive, Jonathon; Taliun, Sarah A. Gagliano; Bi, Wenjian; Gabrielsen, Maiken Elvestad; Daly, Mark J.; Neale, Benjamin M.. (2020) Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts. Nature Genetics
  Vitenskapelig artikkel

2019

• Småbrekke, Birgit; Rinde, Ludvig Balteskard; Evensen, Line Holtet; Morelli, Vania Maris; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Njølstad, Inger; Mathiesen, Ellisiv B.; Rosendaal, Frits Richard; Brækkan, Sigrid Kufaas. (2019) Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism. Journal of Thrombosis and Haemostasis
  Vitenskapelig artikkel
• Graham, Sarah E.; Nielsen, Jonas B.; Zawistowski, Matthew; Zhou, Wei; Fritsche, Lars G.; Gabrielsen, Maiken Elvestad; Skogholt, Anne Heidi; Surakka, Ida; Hornsby, Whitney E.; Fermin, Damian. (2019) Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Nature Communications
  Vitenskapelig artikkel
• Liu, Mengzhen; Jiang, Yu; Wedow, Robbee; Li, Yue; Brazel, David M.; Chen, Fang; Datta, Gargi; Davila-Velderrain, Jose; Mitchell, Amy; Skogholt, Anne Heidi. (2019) Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nature Genetics
  Vitenskapelig artikkel
• Skille, Hanne; Paulsen, Benedikte; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Brumpton, Ben Michael; Hindberg, Kristian; Gran, Olga Vikhammer; Rosendaal, Frits Richard; Brækkan, Sigrid Kufaas; Hansen, John-Bjarne. (2019) Genetic Variation Of Platelet Glycoprotein VI And The Risk Of Venous Thromboembolism. Haematologica
  Kommentar
• Lindström, Sara; Wang, Lu; Smith, Erin N.; Gordon, William; Vlieg, Astrid van Hylckama; Andrade, Mariza de; Brody, Jennifer A.; Pattee, Jack W.; Haessler, Jeffrey; Brumpton, Ben Michael. (2019) Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. Blood
  Vitenskapelig artikkel
• Vie, Gunnhild Åberge; Wootton, Robyn E; Bjørngaard, Johan Håkon; Åsvold, Bjørn Olav; Taylor, AE; Gabrielsen, Maiken Elvestad; Davey, George Smith; Romundstad, Pål Richard; Munafo, Marcus R. (2019) The effect of smoking intensity on all-cause and cause-specific mortality-a Mendelian randomization analysis. International Journal of Epidemiology
  Vitenskapelig artikkel
• Lane, Jacqueline M.; Jones, Samuel E.; Dashti, Hassan S.; Wood, Andrew R.; Aragam, Krishna G; Hees, Vincent T. van; Strand, Linn B; Winsvold, Bendik K S; Wang, Heming; Bowden, Jack. (2019) Biological and clinical insights from genetics of insomnia symptoms. Nature Genetics
  Vitenskapelig artikkel
• Løset, Mari; Thomas, Laurent; Brumpton, Ben Michael; Wolford, Brooke N.; Holmen, Oddgeir; Luetge, Almut; Skogholt, Anne Heidi; Modalsli, Ellen Heilmann; Solvin, Åshild Øksnevad; Fritsche, Lars. (2019) Genome-wide association study of psoriasis suggests a new risk locus on chromosome 10: The HUNT Study. Forum for Nordic Dermato-Venereology
  Konferanseabstract
• Paulsen, Benedikte; Skille, Hanne; Smith, Erin N.; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Brækkan, Sigrid Kufaas; Rosendaal, Frits Richard; Frazer, Kelly A.; Gran, Olga Vikhammer; Hansen, John-Bjarne. (2019) Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism. Haematologica
  Vitenskapelig artikkel
• Brumpton, Ben Michael; Fritsche, Lars; Zheng, Jie; Nielsen, Jonas Bille; Mannila, Maria Nastase; Surakka, Ida; Rasheed, Humaira; Vie, Gunnhild Åberge; Graham, Sarah E.; Gabrielsen, Maiken Elvestad. (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
  Vitenskapelig artikkel

2018

• Løset, Mari; Modalsli, Ellen Heilmann; Snekvik, Ingrid; Solvin, Åshild Øksnevad; Holmen, Oddgeir Lingaas; Gabrielsen, Maiken Elvestad; Fritsche, Lars; Zhou, Wei; Nielsen, Jonas Bille; Brumpton, Ben Michael. (2018) 743 HUNTing for genes that affect inflammatory skin disease in 4,071 cases and 40,430 controls. Journal of Investigative Dermatology
  Konferanseabstract
• Taylor, Michelle; Rode, Line; Bjørngaard, Johan Håkon; Taylor, Amy E.; Bojesen, Stig E.; Åsvold, Bjørn Olav; Gabrielsen, Maiken Elvestad; Lewis, Glyn; Nordestgaard, Børge G.; Romundstad, Pål Richard. (2018) Is smoking heaviness causally associated with alcohol use? A Mendelian randomization study in four European cohorts. International Journal of Epidemiology
  Vitenskapelig artikkel
• Corominas, Jordi; Klein, Marieke; Zayats, Tetyana; Rivero, Olga; Ziegler, Georg C.; Pauper, Marc; Neveling, Kornelia; Poelmans, Geert; Jansch, Charline; Svirin, Evgeniy. (2018) Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Molecular Psychiatry
  Vitenskapelig artikkel
• Zhou, Wei; Nielsen, Jonas B.; Fritsche, Lars; Dey, Rounak; Gabrielsen, Maiken Elvestad; Wolford, Brooke N.; LeFaive, Jonathon; VandeHaar, Peter; Gagliano, Sarah A; Gifford, Aliya. (2018) Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Nature Genetics
  Vitenskapelig artikkel
• Nielsen, Jonas B.; Fritsche, Lars; Zhou, Wei; Teslovich, Tanya M.; Holmen, Oddgeir Lingaas; Gustafsson, Stefan; Gabrielsen, Maiken Elvestad; Schmidt, Ellen M.; Beaumont, Robin; Wolford, Brooke N.. (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
  Vitenskapelig artikkel
• Nielsen, Jonas B.; Thorolfsdottir, Rosa B.; Fritsche, Lars; Zhou, Wei; Skov, Morten W.; Graham, Sarah E.; Herron, Todd J.; McCarthy, Shane; Schmidt, Ellen M.; Sveinbjornsson, Gardar. (2018) Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. Nature Genetics
  Vitenskapelig artikkel

2017

• Bjørngaard, Johan Håkon; Nordestgaard, AT; Taylor, Amy E; Treur, Jorien L; Gabrielsen, Maiken Elvestad; Munafo, Marcus R; Nordestgaard, BG; Åsvold, Bjørn Olav; Romundstad, Pål Richard; Smith, George Davey. (2017) Heavier smoking increases coffee consumption: findings from a Mendelian randomization analysis. International Journal of Epidemiology
  Vitenskapelig artikkel
• Wang, Yufei; McKay, James D.; Rafnar, Thorunn; Wang, Zhaoming; Timofeeva, Maria N.; Broderick, Peter; Zong, Xuchen; Laplana, Marina; Wei, Yongyue; Han, Younghun. (2017) Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (Nature Genetics (2014) 46 (736-741)). Nature Genetics
  Korrigendum
• Ferreira, Manuel A.; Vonk, Judith M; Baurecht, Hansjörg; Marenholz, Ingo; Tian, Chao; Hoffman, Joshua D; Helmer, Quinta; Tillander, Annika; Ullemar, Vilhelmina; Dongen, Jenny Van. (2017) Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nature Genetics
  Vitenskapelig artikkel
• Johnsen, Marianne Bakke; Vie, Gunnhild Åberge; Winsvold, Bendik K S; Bjørngaard, Johan Håkon; Åsvold, Bjørn Olav; Gabrielsen, Maiken Elvestad; Pedersen, Linda Margareth; Hellevik, Alf Inge; Langhammer, Arnulf; Furnes, Ove. (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
  Vitenskapelig artikkel
• Zhou, Wei; Fritsche, Lars; Das, Sayantan; Zhang, He; Nielsen, Jonas B.; Holmen, Oddgeir Lingaas; Chen, Jin; Lin, Maoxuan; Gabrielsen, Maiken Elvestad; Hveem, Kristian. (2017) Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. Genetic Epidemiology
  Vitenskapelig artikkel
• Skaaby, Tea; Taylor, Amy E; Jacobsen, Rikke K.; Paternoster, Lavinia; Thuesen, Betina H.; Ahluwalia, Tarunveer S.; Larsen, Sofus C.; Zhou, Ang; Wong, Andrew; Gabrielsen, Maiken Elvestad. (2017) Investigating the causal effect of smoking on hay fever and asthma: A Mendelian randomization meta-analysis in the CARTA consortium. Scientific Reports
  Vitenskapelig artikkel

2016

• Løset, Mari; Modalsli, Ellen Heilmann; Snekvik, Ingrid; Zhou, Wei; Chu, Yunhan; Gabrielsen, Maiken Elvestad; Holmen, Oddgeir Lingaas; Romundstad, Pål Richard; Abecasis, Goncalo; Willer, Cristen. (2016) HUNTing for Genes that Affect Psoriasis in ~2,900 Cases and ~48,000 Controls. Forum for Nordic Dermato-Venereology
  Konferanseabstract
• Zayats, Tetyana; Jacobsen, Kaya Kvarme; Kleppe, Rune; Jacob, CP; Kittel-Schneider, Sarah; Ribases, Marta; Ramos-Quiroga, JA; Richarte, Vanesa; Casas, M; Mota, NR. (2016) Exome chip analyses in adult attention deficit hyperactivity disorder. Translational Psychiatry
  Vitenskapelig artikkel

2015

• Linneberg, Allan; Jacobseb, Rikke; Skaaby, Tea; Taylor, Amy E.; Fluharty, Meg E.; Jeppesen, Jørgen L.; Bjørngaard, Johan Håkon; Åsvold, Bjørn Olav; Gabrielsen, Maiken Elvestad; Campbell, Archie. (2015) Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium. Circulation: Cardiovascular Genetics
  Vitenskapelig artikkel
• Morris, Richard W.; Taylor, Amy E.; Fluharty, Meg E.; Bjørngaard, Johan Håkon; Åsvold, Bjørn Olav; Gabrielsen, Maiken Elvestad; Campbell, Archie; Marioni, Riccardo; Kumari, Meena; Korhonen, Tellervo. (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
  Vitenskapelig artikkel
• Brenner, Darren. R.; Amos, Christopher I.; Brhane, Yonathan; Timofeeva, Maria N.; Caporaso, Neil; Wang, Yufei; Christiani, David C.; Bickeböller, Heike; Yang, Ping; Albanes, Demetrius. (2015) Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. Carcinogenesis
  Vitenskapelig artikkel

2014

• Taylor, Amy E; Morris, Richard W; Fluharty, Meg; Bjørngaard, Johan Håkon; Åsvold, Bjørn Olav; Gabrielsen, Maiken Elvestad; Campbell, A.; Marioni, Riccardo R.; Kumari, Meena; Hällfors, Jenni. (2014) Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers. PLoS Genetics
  Vitenskapelig artikkel
• Taylor, Amy E; Fluharty, Meg; Bjørngaard, Johan Håkon; Gabrielsen, Maiken Elvestad; Skorpen, Frank; Marioni, Riccardo R.; Campbell, A.; Engmann, J; Mirza, Saira Saeed; Loukola, A.. (2014) Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium. BMJ Open
  Vitenskapelig artikkel
• Wang, Yufei; McKay, JD; Rafnar, T; Wang, Z; Timofeeva, MN; Broderick, P; Zong, X; Laplana, M; Wei, Y; Han, Y. (2014) Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Nature Genetics
  Vitenskapelig artikkel
• Åsvold, Bjørn Olav; Bjørngaard, Johan Håkon; Carslake, D; Gabrielsen, Maiken Elvestad; Skorpen, Frank; Smith, GD; Romundstad, Pål Richard. (2014) Causal associations of tobacco smoking with cardiovascular risk factors: a Mendelian randomization analysis of the HUNT Study in Norway. International Journal of Epidemiology
  Vitenskapelig artikkel

2013

• 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
  Vitenskapelig artikkel
• Bjørngaard, Johan Håkon; Gunnell, David; Gabrielsen, Maiken Elvestad; Smith, George Davey; Skorpen, Frank; Krokan, Hans Einar; Vatten, Lars Johan; Romundstad, Pål Richard. (2013) The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study. Psychological Medicine
  Vitenskapelig artikkel

2012

• Kazma, R; Babron, MC; Gaborieau, Valerie; Génin, E; Brennan, P; Hung, Rayjean J.; McLaughlin, Jon; Krokan, Hans Einar; Gabrielsen, Maiken Elvestad; Skorpen, Frank. (2012) Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium. Carcinogenesis
  Vitenskapelig artikkel
• Johnson, Matthew P; Brennecke, Shaun P.; Iversen, Ann-Charlotte; East, Christine; Olsen, Guro Dalheim; Kent, Jack W; Dyer, Thomas D.; Said, Joanne M; Roten, Linda Tømmerdal; Abraham, Lawrence J. (2012) Genome-wide association scans identify novel maternal susceptibility loci for preeclampsia. Pregnancy Hypertension
  Konferanseabstract
• Timofeeva, MN; Hung, RJ; Rafnar, T; Christiani, DC; Field, JK; Bickeboller, H; Risch, A; McKay, JD; Wang, Y; Dai, J. (2012) Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Human Molecular Genetics
  Vitenskapelig artikkel

2009

• Lips, EH; Gaborieau, V; Mckay, JD; Chabrier, A; Hung, RJ; Boffetta, P; Hashibe, M; Zaridze, D; Szeszenia-Dabrowska, N; Lissowska, J. (2009) Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals. International Journal of Epidemiology
  Vitenskapelig artikkel

2008

• McKay, JD; Mckay, JD; Hung, RJ; Gaborieau, V; Boffetta, Paolo; Chabrier, Amelie; Byrnes, GB; Zaridze, D; Mukeria, A; Szeszenia-Dabrowska, N. (2008) Lung cancer susceptibility locus at 5p15.33. Nature Genetics
  Vitenskapelig artikkel
• Hung, RJ; Mckay, JD; Gaborieau, V; Boffetta, P; Hashibe, M; Zaridze, D; Mukeria, A; Szeszenia-Dabrowska, N; Lissowska, J; Rudnai, P. (2008) A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature
  Vitenskapelig artikkel
• Heath, SC; Gut, IG; Brennan, P; Mckay, JD; Bencko, V; Fabianova, E; Foretova, L; Georges, M; Janout, V; Kabesch, M. (2008) Investigation of the fine structure of European populations with applications to disease association studies. European Journal of Human Genetics
  Vitenskapelig artikkel