2025

• Løchen 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
  Academic article

2024

• 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
• 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
• 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
• Fongang, Bernard; Sargurupremraj, Muralidharan; Jian, Xueqiu; Mishra, Aniket; Damotte, Vincent; De Rojas, Itziar. (2024) A genome-wide association meta-analysis of all-cause and vascular dementia. Alzheimer's & Dementia
  Academic article
• 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

2023

• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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

2022

• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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

2021

• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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

2020

• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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

2019

• 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
• 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
• 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
• 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
• 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
• 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
• 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

• 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
• 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

• 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

• 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

• 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
• 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
• 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

2014

• 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
• 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

2013

• 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
• 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

2012

• 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
• 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
• 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

2010

• 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

2008

• 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
• 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