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  1. Ansatte

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English

Laurent Thomas

Last ned pressefoto
Last ned pressefoto
Foto:

Laurent Thomas

Forsker
Institutt for klinisk og molekylær medisin
Fakultet for medisin og helsevitenskap

laurent.thomas@ntnu.no
73598416 Laboratoriesenteret, 231.05.058, Øya
Om Publikasjoner Formidling

Om

Forsker ved Instituttgruppe for Molekylærbiologi, i gruppen for Bioinformatikk og genregulering, og i K.G. Jebsen-senter for genetisk epidemiologi.

Tok en doktorgrad i bioinformatikk og en postdoktor stilling ved NTNU. Sine forskningsinteresser fokuserer på genregulering, spesielt på enkeltnukleotidpolymorfi, alternative polyadenylering og ikke-kodende RNA som microRNA og sirkulære RNA, men også genetiske varianter som Single Nucleotide Polymorphisms (SNP), spesielt SNP funksjonele effekter, helgenom-assosiasjonsstudier (GWAS) og genotyp kvalitetskontroll (QC).

Publikasjoner

  • Kronologisk
  • Etter kategori
  • Alle publikasjoner i Nasjonalt vitenarkiv (NVA)

2025

  • Hatzikotoulas, Konstantinos; Southam, Lorraine; Stefansdottir, Lilja; Boer, Cindy G.; McDonald, Merry-Lynn; Pett, J. Patrick. (2025) Translational genomics of osteoarthritis in 1,962,069 individuals. Nature
    Vitenskapelig artikkel
  • Jenssen, Marita; Arora, Nikhil; Løset, Mari; Åsvold, Bjørn Olav; Thomas, Laurent Francois; VAssmyr, Ole-Jørgen Bekkevold. (2025) Exploring Interaction between Genetically Predicted Body Mass Index and Serum 25-Hydroxyvitamin D Levels on the Odds for Psoriasis in UK Biobank and the HUNT Study: A Factorial Mendelian Randomization Study. JID Innovations
    Vitenskapelig artikkel
  • Ramessur, Ravi; Saklatvala, Jake; Løset, Mari; Thomas, Laurent Francois; Budu-Aggrey, Ashley; Mahil, Satveer K.. (2025) Investigating the Genetic Basis of the Influence of Adiposity on Psoriasis: A Cross-Sectional Study in a Large United Kingdom Population–Based Biobank. Journal of Investigative Dermatology
    Vitenskapelig artikkel
  • Alam, Mohammad Sayeef; Thomas, Laurent Francois; Brumpton, Ben Michael; Hveem, Kristian; Lundin, Knut; Withoff, Sebo. (2025) Population screening of adults identifies novel genetic variants associated with celiac disease. Scientific Reports
    Vitenskapelig artikkel
  • Standl, Marie; Budu-Aggrey, Ashley; Johnston, Luke J.; Elias, Martina S.; Arshad, S. Hasan; Bager, Peter. (2025) Gene–Environment Interaction Affects Risk of Atopic Eczema: Population and In Vitro Studies. Allergy. European Journal of Allergy and Clinical Immunology
    Vitenskapelig artikkel
  • Strom, Nora I.; Gerring, Zachary F.; Galimberti, Marco; Yu, Dongmei; Halvorsen, Matthew W.; Abdellaoui, Abdel. (2025) Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder. Nature Genetics
    Vitenskapelig artikkel
  • Liu, Hongbo; Abedini, Amin; Ha, Eunji; Ma, Ziyuan; Sheng, Xin; Dumoulin, Bernhard. (2025) Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants. Science
    Vitenskapelig artikkel
  • Dand, Nick; Stuart, Philip E.; Bowes, John; Ellinghaus, David; Nititham, Joanne; Saklatvala, Jake R.. (2025) GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets. Nature Communications
    Vitenskapelig artikkel

2024

  • Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Thomas, Laurent Francois; Steinsland, Ingelin. (2024) Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study. Journal of the American Heart Association (JAHA)
    Vitenskapelig artikkel
  • Potenza, Maria Letizia; Blankvoort, Stefan Matthias Adriaan; Carvalho, Miguel; Grimstvedt, Joachim Schweder; Maria, Valentina Di; Moan, Kristian Magnus. (2024) Generation of an enhancer-driven gene expression viral tool specific to dentate granule cell-types through direct hippocampal injection. Frontiers in Neuroscience
    Vitenskapelig artikkel
  • Scholz, Markus; Horn, Katrin; Pott, Janne; Wuttke, Matthias; Kühnapfel, Andreas; Nasr, M. Kamal. (2024) X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Nature Communications
    Vitenskapelig artikkel
  • Fongang, Bernard; Sargurupremraj, Muralidharan; Jian, Xueqiu; Mishra, Aniket; Damotte, Vincent; Rojas, Itziar De. (2024) A genome-wide association meta-analysis of all-cause and vascular dementia. Alzheimer's & Dementia
    Vitenskapelig artikkel
  • Moksnes, Marta R.; Hansen, Ailin F.; Wolford, Brooke N.; Thomas, Laurent F.; Rasheed, Humaira; Simic, Anica. (2024) A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. Communications Biology
    Vitenskapelig artikkel
  • Ramessur, Ravi; Saklatvala, Jake; Løset, Mari; Thomas, Laurent Francois; Budu-Aggrey, Ashley; Mahil, Satveer K.. (2024) The impact of central adiposity and genetic factors on psoriasis risk: insights from the UK Biobank. British Journal of Dermatology
    Sammendrag/Abstract
  • Hernandez-Cordero, Ariana; Thomas, Laurent Francois; Smail, Alice; Lim, Zhao Qin; Saklatvala, Jake R.; Chung, Raymond. (2024) A genome-wide meta-analysis of palmoplantar pustulosis implicates TH2 responses and cigarette smoking in disease pathogenesis. Journal of Allergy and Clinical Immunology
    Vitenskapelig artikkel

2023

  • 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)
    Vitenskapelig artikkel
  • Williams, Alexander T.; Shrine, Nick; Gijzel, Hardeep Naghra-van; Betts, Joanna C.; Chen, Jing; Hessel, Edith M.. (2023) Genome-wide association study of susceptibility to hospitalised respiratory infections. Wellcome Open Research
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel

2022

  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
  • 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
    Vitenskapelig artikkel
  • 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
    Sammendrag/Abstract
  • 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
    Vitenskapelig artikkel
  • 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
  • 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
    Sammendrag/Abstract

2021

  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Leserinnlegg
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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)
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel

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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel

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
    Sammendrag/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
    Vitenskapelig artikkel

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
    Vitenskapelig artikkel
  • Thomas, Laurent; Sætrom, Pål. (2014) Circular RNAs are depleted of polymorphisms at microRNA binding sites. Bioinformatics
    Vitenskapelig artikkel

2012

  • Thomas, Laurent. (2012) Effects of Single-nucleotide Polymorphisms on microRNA-Based Gene Regulation and Their Association With Disease. Norges teknisk-naturvitenskapelige universitet Doktoravhandlinger ved NTNU, 1503-8181; 2012:307 (Dissertations at the Faculty of Medicine, 0805-7680; 578)
    Doktorgradsavhandling
  • 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
    Vitenskapelig artikkel

2011

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

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
    Vitenskapelig artikkel

Tidsskriftspublikasjoner

  • Hatzikotoulas, Konstantinos; Southam, Lorraine; Stefansdottir, Lilja; Boer, Cindy G.; McDonald, Merry-Lynn; Pett, J. Patrick. (2025) Translational genomics of osteoarthritis in 1,962,069 individuals. Nature
    Vitenskapelig artikkel
  • Jenssen, Marita; Arora, Nikhil; Løset, Mari; Åsvold, Bjørn Olav; Thomas, Laurent Francois; VAssmyr, Ole-Jørgen Bekkevold. (2025) Exploring Interaction between Genetically Predicted Body Mass Index and Serum 25-Hydroxyvitamin D Levels on the Odds for Psoriasis in UK Biobank and the HUNT Study: A Factorial Mendelian Randomization Study. JID Innovations
    Vitenskapelig artikkel
  • Ramessur, Ravi; Saklatvala, Jake; Løset, Mari; Thomas, Laurent Francois; Budu-Aggrey, Ashley; Mahil, Satveer K.. (2025) Investigating the Genetic Basis of the Influence of Adiposity on Psoriasis: A Cross-Sectional Study in a Large United Kingdom Population–Based Biobank. Journal of Investigative Dermatology
    Vitenskapelig artikkel
  • Alam, Mohammad Sayeef; Thomas, Laurent Francois; Brumpton, Ben Michael; Hveem, Kristian; Lundin, Knut; Withoff, Sebo. (2025) Population screening of adults identifies novel genetic variants associated with celiac disease. Scientific Reports
    Vitenskapelig artikkel
  • Standl, Marie; Budu-Aggrey, Ashley; Johnston, Luke J.; Elias, Martina S.; Arshad, S. Hasan; Bager, Peter. (2025) Gene–Environment Interaction Affects Risk of Atopic Eczema: Population and In Vitro Studies. Allergy. European Journal of Allergy and Clinical Immunology
    Vitenskapelig artikkel
  • Strom, Nora I.; Gerring, Zachary F.; Galimberti, Marco; Yu, Dongmei; Halvorsen, Matthew W.; Abdellaoui, Abdel. (2025) Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder. Nature Genetics
    Vitenskapelig artikkel
  • Liu, Hongbo; Abedini, Amin; Ha, Eunji; Ma, Ziyuan; Sheng, Xin; Dumoulin, Bernhard. (2025) Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants. Science
    Vitenskapelig artikkel
  • Dand, Nick; Stuart, Philip E.; Bowes, John; Ellinghaus, David; Nititham, Joanne; Saklatvala, Jake R.. (2025) GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets. Nature Communications
    Vitenskapelig artikkel
  • Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Thomas, Laurent Francois; Steinsland, Ingelin. (2024) Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study. Journal of the American Heart Association (JAHA)
    Vitenskapelig artikkel
  • Potenza, Maria Letizia; Blankvoort, Stefan Matthias Adriaan; Carvalho, Miguel; Grimstvedt, Joachim Schweder; Maria, Valentina Di; Moan, Kristian Magnus. (2024) Generation of an enhancer-driven gene expression viral tool specific to dentate granule cell-types through direct hippocampal injection. Frontiers in Neuroscience
    Vitenskapelig artikkel
  • Scholz, Markus; Horn, Katrin; Pott, Janne; Wuttke, Matthias; Kühnapfel, Andreas; Nasr, M. Kamal. (2024) X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Nature Communications
    Vitenskapelig artikkel
  • Fongang, Bernard; Sargurupremraj, Muralidharan; Jian, Xueqiu; Mishra, Aniket; Damotte, Vincent; Rojas, Itziar De. (2024) A genome-wide association meta-analysis of all-cause and vascular dementia. Alzheimer's & Dementia
    Vitenskapelig artikkel
  • Moksnes, Marta R.; Hansen, Ailin F.; Wolford, Brooke N.; Thomas, Laurent F.; Rasheed, Humaira; Simic, Anica. (2024) A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. Communications Biology
    Vitenskapelig artikkel
  • Ramessur, Ravi; Saklatvala, Jake; Løset, Mari; Thomas, Laurent Francois; Budu-Aggrey, Ashley; Mahil, Satveer K.. (2024) The impact of central adiposity and genetic factors on psoriasis risk: insights from the UK Biobank. British Journal of Dermatology
    Sammendrag/Abstract
  • Hernandez-Cordero, Ariana; Thomas, Laurent Francois; Smail, Alice; Lim, Zhao Qin; Saklatvala, Jake R.; Chung, Raymond. (2024) A genome-wide meta-analysis of palmoplantar pustulosis implicates TH2 responses and cigarette smoking in disease pathogenesis. Journal of Allergy and Clinical Immunology
    Vitenskapelig artikkel
  • 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)
    Vitenskapelig artikkel
  • Williams, Alexander T.; Shrine, Nick; Gijzel, Hardeep Naghra-van; Betts, Joanna C.; Chen, Jing; Hessel, Edith M.. (2023) Genome-wide association study of susceptibility to hospitalised respiratory infections. Wellcome Open Research
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
  • 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
    Vitenskapelig artikkel
  • 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
    Sammendrag/Abstract
  • 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
    Vitenskapelig artikkel
  • 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
  • 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
    Sammendrag/Abstract
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Leserinnlegg
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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)
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • 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
    Sammendrag/Abstract
  • 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
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • Thomas, Laurent; Sætrom, Pål. (2014) Circular RNAs are depleted of polymorphisms at microRNA binding sites. Bioinformatics
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel
  • Thomas, Laurent; Saito, Takaya; Sætrom, Pål. (2011) Inferring causative variants in microRNA target sites. Nucleic Acids Research (NAR)
    Vitenskapelig artikkel
  • 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
    Vitenskapelig artikkel

Rapport

  • Thomas, Laurent. (2012) Effects of Single-nucleotide Polymorphisms on microRNA-Based Gene Regulation and Their Association With Disease. Norges teknisk-naturvitenskapelige universitet Doktoravhandlinger ved NTNU, 1503-8181; 2012:307 (Dissertations at the Faculty of Medicine, 0805-7680; 578)
    Doktorgradsavhandling

Formidling

2024

  • Poster
    Alam, Mohammad Sayeef; Hjort, Rebecka Louise; Thomas, Laurent Francois; Brumpton, Ben Michael; Hveem, Kristian; Lundin, Knut. (2024) The IRX1 locus is associated with celiac disease: results from a screened population-based cohort, the HUNT study. Nordic Conference on Future Health (NCFH) 2024 , Trondheim 2024-09-10 - 2024-09-13
  • Vitenskapelig foredrag
    Alam, Mohammad Sayeef; Hjort, Rebecka Louise; Thomas, Laurent Francois; Brumpton, Ben Michael; Hveem, Kristian; Lundin, Knut. (2024) The IRX1 locus is associated with celiac disease: results from a screened population-based cohort, the HUNT study. International Coeliac Disease Symposium (ICDS) 2024 , Sheffield, UK 2024-09-05 - 2024-09-07

2023

  • Poster
    Lund-Hanssen, Charlotte; Olsen, Lene Christin; Thomas, Laurent Francois; O'Reilly, Kally; Witter, Menno Peter; Sætrom, Pål. (2023) The Conserved Expression of Long Non-Coding RNAs in the Entorhinal Cortex During Postnatal Development. Gene Regulatory Mechanisms in Neural Fate Decisions , Alicante, Spain 2023-09-07 - 2023-09-10
  • Poster
    Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Wade, Kaitlin Hazel; Thomas, Laurent Francois. (2023) Polygenic risk scores predict blood pressure traits across the lifespan. American Society of Human Genetics 2023 Annual Meeting 2023-11-03 -

2022

  • Poster
    Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Wade, Kaitlin Hazel; Thomas, Laurent Francois. (2022) Polygenic predictions and interactions in hypertension. K.G. Jebsen for Genetic Epidemiology Symposium 2022-11-29 - 2022-11-30
  • Vitenskapelig foredrag
    Øvretveit, Karsten; Ingeström, Emma Maria Lovisa; Spitieris, Michail; Tragante, Vinicius; Wade, Kaitlin Hazel; Thomas, Laurent Francois. (2022) Polygenic predictions and interactions in hypertension. Exercise in Medicine , Trondheim 2022-12-14 - 2022-12-15
  • Poster
    Lund-Hanssen, Charlotte; Olsen, Lene Christin; Thomas, Laurent Francois; Sætrom, Pål. (2022) The Conserved Expression of Long Non-Coding RNAs in the Entorhinal Cortex During Postnatal Development. 8th Annual NORBIS Conference , Rosendal, Norway 2022-10-24 - 2022-10-28
  • Poster
    Solvin, Åshild Øksnevad; Bjarkø, Vera Vik; Thomas, Laurent Francois; Berropsi, 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. 51st Annual ESDR meeting , Amsterdam 2022-09-28 - 2022-10-01
  • Vitenskapelig foredrag
    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. 35th Nordic Congres of Dermatology and Venereology , København 2022-04-19 - 2022-04-22

2019

  • Vitenskapelig foredrag
    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. The 34th Nordic Congress of Dermatology & Venereology , Gøteborg 2019-05-08 - 2019-05-10

2018

  • Poster
    Blankvoort, Stefan; Thomas, Laurent; Witter, Menno; Sætrom, Pål; cotney, Justin; Kentros, Clifford. (2018) The marked diversity of unique cortical enhancers enables neuron-specific tools by Enhancer-Driven Gene Expression (EDGE). FENS 2018 , Berlin 2018-07-07 - 2018-07-11

2017

  • Vitenskapelig foredrag
    Thomas, Laurent. (2017) SNPs affecting microRNA-based gene regulation. Jebsen center for genetic epidemiology meeting 2017-03-27 - 2017-03-27
  • Vitenskapelig foredrag
    Thomas, Laurent. (2017) SNPs affecting microRNA-based gene regulation. Mandagsmøte IKM 2017-04-03 - 2017-04-03

2015

  • Vitenskapelig foredrag
    Thomas, Laurent. (2015) Detection of circular RNAs in Rat. Mandagsmøte IKM 2015-11-02 - 2015-11-02

2014

  • Vitenskapelig foredrag
    Thomas, Laurent. (2014) Circular RNAs are depleted of polymorphisms at microRNA binding sites. Mandagsmøte IKM 2014-12-01 - 2014-12-01

2013

  • Vitenskapelig foredrag
    Thomas, Laurent. (2013) Single nucleotide polymorphisms in microRNA Binding Sites of circular RNAs. Systems Biology meetings at NTNU 2013-10-11 - 2013-10-11
  • Vitenskapelig foredrag
    Sætrom, Pål; Thomas, Laurent. (2013) Finding SNPs that affect microRNA regulation. 10th International RNAi, MicroRNAs & Single Cell Biology – 2013 Meeting 2013-05-01 - 2013-05-02

2012

  • Vitenskapelig foredrag
    Thomas, Laurent. (2012) Effects of single-nucleotide polymorphisms on microRNA-based gene regulation. Systems Biology meetings at NTNU 2012-10-05 - 2012-10-05

2011

  • Vitenskapelig foredrag
    Thomas, Laurent. (2011) SNPs can create alternative polyadenylation signals and affect gene expression through loss of microRNA-regulation. Systems Biology meetings at NTNU , Trondheim 2011-09-30 - 2011-09-30
  • Vitenskapelig foredrag
    Thomas, Laurent. (2011) Identifying disease-causative variants in microRNA target sites. Mandagsmøte IKM , Trondheim 2011-03-21 - 2011-03-21
  • Vitenskapelig foredrag
    Thomas, Laurent. (2011) Identifying disease-causative variants in microRNA target sites. eGenVar møte , Trondheim 2011-03-25 - 2011-03-25
  • Vitenskapelig foredrag
    Thomas, Laurent. (2011) Identifying disease-causative variants in microRNA target sites. Bioinformatics for Young Scientists 2011 , Ullensvang, Hardanger 2011-03-16 - 2011-03-18

2010

  • Vitenskapelig foredrag
    Thomas, Laurent Francois. (2010) Identifying disease-causative variants in microRNA target sites. Systems Biology meetings at NTNU , Trondheim 2010-10-22 - 2010-10-22
  • Poster
    Thomas, Laurent Francois; Saito, Takaya; Sætrom, Pål. (2010) Identifying causative variants in microRNA target sites. RECOMB Computational Cancer Biology , Oslo 2010-06-24 - 2010-06-25

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