Institut for Biomedicin

Ditte Demontis

  1. 2019
  2. Udgivet

    Genome-wide association study implicates CHRNA2 in cannabis use disorder. / Demontis, Ditte; Rajagopal, Veera Manikandan; Thorgeirsson, Thorgeir E.; Als, Thomas D.; Grove, Jakob; Leppälä, Kalle; Gudbjartsson, Daniel F.; Pallesen, Jonatan; Hjorthøj, Carsten; Reginsson, Gunnar W.; Tyrfingsson, Thorarinn; Runarsdottir, Valgerdur; Qvist, Per; Christensen, Jane Hvarregaard; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Huckins, Laura M.; Stahl, Eli A.; Timmermann, Allan; Agerbo, Esben; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Nordentoft, Merete; Daly, Mark J.; Stefansson, Hreinn; Stefansson, Kari; Nyegaard, Mette; Børglum, Anders D.

    I: Nature Neuroscience, Bind 22, 06.2019, s. 1066-1074.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  3. Udgivet

    Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls. / Pettersson, E.; Lichtenstein, P.; Larsson, H.; Song, J.; Attention Deficit/Hyperactivity Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Autism Spectrum Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Bipolar Disorder Working Group of the PGC, Eating Disorder Working Group of the PGC, Major Depressive Disorder Working Group of the PGC, Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC, Schizophrenia CLOZUK, Substance Use Disorder Working Group of the PGC ; Agrawal, A.; Borglum, A. D.; Bulik, C. M.; Daly, M. J.; Davis, L. K.; Demontis, D.; Edenberg, H. J.; Grove, J.; Gelernter, J.; Neale, B. M.; Pardiñas, A. F.; Stahl, E.; Walters, J. T.R.; Walters, R.; Sullivan, P. F.; Posthuma, D.; Polderman, T. J.C.

    I: Psychological Medicine, Bind 49, Nr. 7, 05.2019, s. 1166-1173.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  4. Udgivet

    Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. / Huckins, Laura M; Dobbyn, Amanda; Ruderfer, Douglas M; Hoffman, Gabriel; Wang, Weiqing; Pardiñas, Antonio F; Rajagopal, Veera M; Als, Thomas D; T Nguyen, Hoang; Girdhar, Kiran; Boocock, James; Roussos, Panos; Fromer, Menachem; Kramer, Robin; Domenici, Enrico; Gamazon, Eric R; Purcell, Shaun; Demontis, Ditte; Børglum, Anders D; Walters, James T R; O'Donovan, Michael C; Sullivan, Patrick; Owen, Michael J; Devlin, Bernie; Sieberts, Solveig K; Cox, Nancy J; Im, Hae Kyung; Sklar, Pamela; Stahl, Eli A; CommonMind Consortium; The Schizophrenia Working Group of the Psychiatric Genomics Consortium; iPSYCH-GEMS Schizophrenia Working Group.

    I: Nature Genetics, Bind 51, Nr. 4, 04.2019, s. 659-674.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  5. Udgivet

    Identification of common genetic risk variants for autism spectrum disorder. / Grove, Jakob; Ripke, Stephan; Als, Thomas D; Mattheisen, Manuel; Walters, Raymond K; Won, Hyejung; Pallesen, Jonatan; Agerbo, Esben; Andreassen, Ole A; Anney, Richard; Awashti, Swapnil; Belliveau, Rich; Bettella, Francesco; Buxbaum, Joseph D; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Christensen, Jane H; Churchhouse, Claire; Dellenvall, Karin; Demontis, Ditte; De Rubeis, Silvia; Devlin, Bernie; Djurovic, Srdjan; Dumont, Ashley L; Goldstein, Jacqueline I; Hansen, Christine S; Hauberg, Mads Engel; Hollegaard, Mads V; Hope, Sigrun; Howrigan, Daniel P; Huang, Hailiang; Hultman, Christina M; Klei, Lambertus; Maller, Julian; Martin, Joanna; Martin, Alicia R; Moran, Jennifer L; Nyegaard, Mette; Nærland, Terje; Palmer, Duncan S; Palotie, Aarno; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; dPoterba, Timothy; Poulsen, Jesper Buchhave; Pourcain, Beate St; Qvist, Per; Rehnström, Karola ; Reichenberg, Abraham; Reichert, Jennifer ; Robinson, Elise B.; Roeder, Kathryn; Roussos, Panos; Saemundsen, Evald; Sandin, Sven; Satterstrom, F. Kyle; Smith, George Davey; Stefansson, Hreinn; Steinberg, Stacy; Stevens, Christine; Sullivan, Patrick F; Turley, Patrick; Walters, G. Bragi; Xu, Xinyi ; Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium; BUPGEN; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; 23andMe Research Team; Stefansson, Kari; Geschwind, Daniel H; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Neale, Benjamin M; Daly, Mark J; Børglum, Anders D.

    I: Nature Genetics, Bind 51, Nr. 3, 02.2019, s. 431-444.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  6. Udgivet

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. / Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gísli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Olafur O.; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads V.; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian B.; Martin, Alicia R.; Martin, Nicholas G.; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team ; Dalsgaard, Søren; Mors, Ole; Mortensen, Preben Bo; Børglum, Anders D.

    I: Nature Genetics, Bind 51, 2019, s. 63–75.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  7. Udgivet

    Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language. / Verhoef, Ellen; Demontis, Ditte; Burgess, Stephen; Shapland, Chin Yang; Dale, Philip S; Okbay, Aysu; Neale, Benjamin M; Faraone, Stephen V; iPSYCH-Broad-PGC ADHD Consortium ; Dalsgaard, Søren (Medlem af forfattersamarbejde).

    I: Translational Psychiatry, Bind 9, Nr. 1, 35, 2019.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  8. Udgivet

    Genetic markers of ADHD-related variations in intracranial volume. / Klein, Marieke; Walters, Raymond K.; Demontis, Ditte; Stein, Jason L.; Hibar, Derrek P.; Adams, Hieab H.; Bralten, Janita; Mota, Nina Roth; Schachar, Russell; Sonuga-Barke, Edmund; Mattheisen, Manuel; Neale, Benjamin M.; Thompson, Paul M.; Medland, Sarah E.; Børglum, Anders D.; Faraone, Stephen V.; Arias-Vasquez, Alejandro; Franke, Barbara.

    I: American Journal of Psychiatry, Bind 176, Nr. 3, 2019, s. 228-238.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  9. Udgivet

    Genetic risk factors for cancer-related cognitive impairment : a systematic review. / Buskbjerg, Cecilie D R; Amidi, Ali; Demontis, Ditte; Nissen, Eva R; Zachariae, Robert.

    I: Acta Oncologica, Bind 58, Nr. 5, 2019, s. 537-547.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisReviewForskningpeer review

  10. 2018
  11. Udgivet

    A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. / 23andMe Research Team; Psychiatric Genomics Consortium: ADHD Subgroup; iPSYCH–Broad ADHD Workgroup.

    I: Biological Psychiatry, Bind 83, Nr. 12, 2018, s. 1044-1053.

    Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  12. 2017
  13. Udgivet

    Sortilin gene SNP variant rs12037569 predicts chronic pain 12-14 years after whiplash injury. / Rasmussen, Martin Kaag; Demontis, D.; Kasch, H.

    2017. 669-669 Poster session præsenteret ved 3rd Congress of the European-Academy-of-Neurology, Amsterdam, Holland.

    Publikation: KonferencebidragPosterForskningpeer review

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