2023

• Surakka, Ida; Wolford, Brooke N.; 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
• Solvin, Åshild Øksnevad; Bjarkø, Vera Vik; Thomas, Laurent Francois; Berrospi, Patricia; Hveem, Kristian; Saunes, Marit. (2023) Body Composition, Cardiometabolic Risk Factors and Comorbidities in Psoriasis and the Effect of HLA-C*06:02 Status: The HUNT Study, Norway. Acta Dermato-Venereologica
  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
• Budu-Aggrey, Ashley; Kilanowski, Anna; Sobczyk, Maria K.; Shringarpure, Suyash S.; Mitchell, Ruth; Reis, Kadri. (2023) European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nature Communications
  Academic article
• McSweeney, Sheila Mary; Saklatvala, Jake; Rispoli, Rossella; Ganier, Clarisse; Woszczek, Grzegorz; Thomas, Laurent Francois. (2023) Genome-wide meta-analysis implicates variation affecting mast cell biology in urticaria. Journal of Allergy and Clinical Immunology
  Academic article
• Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Wade, Kaitlin Hazel; Thomas, Laurent Francois. (2023) Polygenic risk scores associate with blood pressure traits across the lifespan. European Journal of Preventive Cardiology (EJPC)
  Academic article

2022

• 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
• Solvin, Åshild Øksnevad; Bjarkø, Vera Vik; Thomas, Laurent Francois; Berrospi, Patricia; Hveem, Kristian; Saunes, Marit. (2022) Body composition, cardiometabolic risk factors and comorbidities in psoriasis and the effect of HLA-C*06:02 status in a general population. Journal of Investigative Dermatology
  Abstract
• 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
• 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
• 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
• 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
• Mitchell, Brittany L.; Saklatvala, Jake R.; Dand, Nick; Hagenbeek, Fiona A.; Li, Xin; Min, Josine L.. (2022) Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications
  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
• Winkler, Thomas W.; Rasheed, Humaira; Teumer, Alexander; Gorski, Mathias; Rowan, Bryce X.; Stanzick, Kira J.. (2022) Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. Communications Biology
  Academic article
• Gorski, Mathias; Rasheed, Humaira; Teumer, Alexander; Thomas, Laurent; Graham, Sarah E.; Sveinbjornsson, Gardar. (2022) Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies. Kidney International
  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
• 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
• 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

2021

• 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
• 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
• 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
• 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
• Harder, Aster V.E.; Winsvold, Bendik K S; Noordam, Raymond; Vijfhuizen, Lisanne S.; Børte, Sigrid; Kogelman, Lisette J.A.. (2021) Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache. Annals of Neurology
  Academic article
• Rogne, Tormod; Liyanarachi, Kristin Vardheim; Rasheed, Humaira; Thomas, Laurent; Flatby, Helene Marie; Stenvik, Jørgen. (2021) GWAS Identifies LINC01184/SLC12A2 as a Risk Locus for Skin and Soft Tissue Infections. Journal of Investigative Dermatology
  Academic article
• Stanzick, Kira J.; Li, Yong; Schlosser, Pascal; Gorski, Mathias; Wuttke, Matthias; Thomas, Laurent. (2021) Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Nature Communications
  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
• Moksnes, Marta Riise; Røsjø, Helge; Richmond, Anne; Lyngbakken, Magnus N; Graham, Sarah E; Hansen, Ailin Falkmo. (2021) Genome-wide association study of cardiac troponin i in the general population. Human Molecular Genetics
  Academic article
• Flatby, Helene Marie; Rasheed, Humaira; Ravi, Anuradha; Thomas, Laurent; Liyanarachi, Kristin Vardheim; Afset, Jan Egil. (2021) Risk of lower respiratory tract infections: a genome-wide association study with Mendelian randomization analysis in three independent European populations. Clinical Microbiology and Infection (CMI)
  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
• Zheng, Jie; Zhang, Yuemiao; Rasheed, Humaira; Walker, Venexia M.; Sugawara, Yuka; Li, Jiachen. (2021) Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease. International Journal of Epidemiology
  Academic article
• 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
• 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

2020

• 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
• 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

2019

• 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

2016

• Stracquadanio, Giovanni; Wang, Xuting; Wallace, Marsha D; Grawenda, Anna M.; Zhang, Ping; Hewitt, Juliet. (2016) The importance of p53 pathway genetics in inherited and somatic cancer genomes. Nature Reviews Cancer
  Academic article

2014

• Razick, Sabry; Mocnik, Rok; Thomas, Laurent; Ryeng, Einar; Drabløs, Finn; Sætrom, Pål. (2014) The eGenVar data management system--cataloguing and sharing sensitive data and metadata for the life sciences. Database: The Journal of Biological Databases and Curation
  Academic article
• Thomas, Laurent; Sætrom, Pål. (2014) Circular RNAs are depleted of polymorphisms at microRNA binding sites. Bioinformatics
  Academic article

2012

• Thomas, Laurent; Sætrom, Pål. (2012) Single Nucleotide Polymorphisms Can Create Alternative Polyadenylation Signals and Affect Gene Expression through Loss of MicroRNA-Regulation. PLoS Computational Biology
  Academic article
• Thomas, Laurent. (2012) Effects of single-nucleotide polymorphisms on microRNA-based gene regulation and their association with disease. Doktoravhandlinger ved NTNU (2012:307)
  Doctoral dissertation

2011

• Thomas, Laurent; Saito, Takaya; Sætrom, Pål. (2011) Inferring causative variants in microRNA target sites. Nucleic Acids Research (NAR)
  Academic article

2009

• Sætrom, Pål; Biesinger, Jacob; Li, Sierra M.; Smith, David; Thomas, Laurent Francois; Majzoub, Karim. (2009) A Risk Variant in an miR-125b Binding Site in BMPR1B Is Associated with Breast Cancer Pathogenesis. Cancer Research
  Academic article