Henrik Berg Rasmussen

Research output

Research output per year 2009 2010 2011 2015 2016 2017

• 20 Journal article
• 2 Comment/debate
• 1 Review

Research output per year

Research output per year

Search results

• 2017

  Nomenclature for alleles of the human carboxylesterase 1 gene

  INDICES Consortium, 1 Jan 2017, In: Pharmacogenetics and Genomics. 27, 2, p. 78-80 3 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review

  4 Citations (Scopus)
• 2016

  Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders

  Hoeffding, L. K. E., Duong, L. T. T., Ingason, A., Rosengren, A., Sorbanski, E., Witt, S. H., Djurovic, S., Andreassen, O. A., Hansen, T., Werge, T. & Rasmussen, H. B., 18 May 2016, In: Nordic Journal of Psychiatry. 70, 4, p. 276-279 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Dopamine Plasma Membrane Transport Proteins 100%
  • Mental Disorders 65%
  • Schizophrenia 49%
  • Mood Disorders 39%
  • Genes 32%
  2 Citations (Scopus)

• Investigating the impact of missense mutations in hCES1 by in silico structure-based approaches

  Nzabonimpa, G. S., Rasmussen, H. B., Brunak, S., Taboureau, O. & INDICES Consortium, 1 Jun 2016, In: Drug Metabolism and Personalized Therapy. 31, 2, p. 97-106 10 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • human CES1 protein 100%
  • Missense Mutation 54%
  • Computer Simulation 49%
  • Single Nucleotide Polymorphism 43%
  • Carboxylic Ester Hydrolases 34%
  3 Citations (Scopus)

• No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

  Johnson, E. C., Bjelland, D. W., Howrigan, D. P., Abdellaoui, A., Breen, G., Borglum, A. D., Cichon, S., Degenhardt, F., Forstner, A. J., Frank, J., Genovese, G., Heilmann-Heimbach, S., Herms, S., Hoffman, P., Maier, W., Mattheisen, M., Morris, D. W., Mowry, B. J., Müller-Mhysok, B., Neale, B. M., & 297 othersNenadic, I., Nöthen, M. M., O’Dushlaine, C., Rietschel, M., Ruderfer, D. M., Rujescu, D., Schulze, T. G., Simonson, M. A., Stahl, E. A., Strohmaier, J., Witt, S. H., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K-H., Holmans, P. A., Lee, P. H., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S-A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W. F., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chen, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Robert Cloninger, C., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Del-Favero, J., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Georgieva, L., Giegling, I., Giusti-Rodríguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., de Haan, L., Hammer, C., Hamshere, M. L., Hansen, M., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julià, A., Kahn, R. S., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kähler, A. K., Laurent, C., Chee Keong, J. L., Hong Lee, S., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K-Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lönnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Mallet, J., Marsal, S., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S. M., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Müller-Myhsok, B., Nelis, M., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C. T., Anthony O'Neill, F., Oh, S. Y., Olincy, A., Olsen, L., van Os, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietiläinen, O., Pimm, J., Pocklington, A. J., Powell, J., Price, A. L., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stahl, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Scott Stroup, T., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Watts-Williams, S. J., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gill, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jönsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarroll, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Nöthen, M. M., Ophoff, R. A., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Riley, B. P., Sham, P-C., Sklar, P., St Clair, D., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., O'Donovan, M. C., Sullivan, P. F. & Keller, M. C., 1 Oct 2016, In: PLOS Genetics. 12, 10, 20 p., e1006343.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • schizophrenia 100%
  • inbreeding 97%
  • homozygosity 77%
  • genome 67%
  • Schizophrenia 58%
  9 Citations (Scopus)

  82 Downloads (Pure)
• 2015

  Angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers in patients with abdominal aortic aneurysms: nation-wide cohort study

  Kristensen, K. E., Torp-Pedersen, C., Gislason, G. H., Egfjord, M., Rasmussen, H. B. & Hansen, P. R., 1 Mar 2015, In: Arteriosclerosis, Thrombosis, and Vascular Biology. 35, 3, p. 733-40 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Angiotensin II Type 1 Receptor Blockers 100%
  • Angiotensin Receptor Antagonists 83%
  • Abdominal Aortic Aneurysm 81%
  • Angiotensin-Converting Enzyme Inhibitors 73%
  • Cohort Studies 50%
  26 Citations (Scopus)

• Comment on Xie et al. The effects of CES1A2 A(-816)C and CYP2C19 loss-of-function polymorphisms on clopidogrel response variability among Chinese patients with coronary heart disease

  Bjerre, D., Ferrero, L., Madsen, M., Hansen, P. R., Rasmussen, H. B. & INDICES Consortium, 13 Mar 2015, In: Pharmacogenetics and Genomics. 25, 3, p. 147 1 p.

  Research output: Contribution to journal › Comment/debate › Research

  2 Citations (Scopus)

• Individualization of treatments with drugs metabolized by CES1: combining genetics and metabolomics

  Rasmussen, H. B., Bjerre, D., Linnet, K., Jürgens, G., Dalhoff, K., Stefansson, H., Hankemeier, T., Kaddurah-Daouk, R., Taboureau, O., Brunak, S., Houmann, T., Jeppesen, P., Pagsberg, A. K., Plessen, K., Dyrborg, J., Hansen, P. R., Hansen, P. E., Hughes, T., Werge, T. & INDICES Consortium, 1 Apr 2015, In: Pharmacogenomics. 16, 6, p. 649-65

  Research output: Contribution to journal › Review › peer-review

  • Metabolomics 100%
  • Pharmaceutical Preparations 37%
  • Metabolic Side Effects of Drugs and Substances 16%
  • Therapeutics 14%
  • Xenobiotics 11%
  20 Citations (Scopus)

• Linkage and whole genome sequencing identify a locus on 6q25-26 for formal thought disorder and implicate MEF2A regulation

  Thygesen, J. H., Zambach, S. K., Ingason, A., Lundin, P., Hansen, T., Bertalan, M., Rosengren, A., Bjerre, D., Ferrero-Miliani, L., Rasmussen, H. B., Parnas, J. & Werge, T., 1 Dec 2015, In: Schizophrenia Research. 169, 1-3, p. 441-6 6 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Whole Genome Sequencing 100%
  • Thinking 84%
  • Haplotypes 46%
  • Schizophrenia 40%
  • Pedigree 26%
  8 Citations (Scopus)

• Pharmacogenetic Risk Stratification in Angiotensin-Converting Enzyme Inhibitor-Treated Patients with Congestive Heart Failure: A Retrospective Cohort Study

  Nelveg-Kristensen, K. E., Busk Madsen, M., Torp-Pedersen, C., Køber, L., Egfjord, M., Berg Rasmussen, H. & Riis Hansen, P., 1 Dec 2015, In: PloS one. 10, 12, p. 1-16 16 p., e0144195.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Angiotensin 100%
  • Pharmacogenetics 91%
  • Congestive Heart Failure 89%
  • pharmacogenomics 81%
  • angiotensin-converting enzyme inhibitors 75%
  7 Citations (Scopus)

• Risk factors and mortality among patients with severe muco-cutaneous drug reactions

  Crüger, A-M. T., Kaur-Knudsen, D., Zachariae, C., Rasmussen, H. B. & Thomsen, S. F., 1 Aug 2015, In: Danish Medical Journal. 62, 8, p. 1-5 5 p., A5122.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Erythema Multiforme 100%
  • Stevens-Johnson Syndrome 81%
  • Skin 38%
  • Mortality 35%
  • Pharmaceutical Preparations 28%
  4 Citations (Scopus)
• 2013

  Neuropeptide Y genes and suicidal behaviour among schizophrenic patients

  Wang, A. G., Koefoed, P., Jacoby, A. S., Woldbye, D., Rasmussen, H. B., Timm, S., Dam, H., Jakobsen, K. D., Nordentoft, M., Jürgens, G., Sorensen, H. J., Garsdal, O., Hvid, M. & Werge, T., Jun 2013, In: Psychiatric Genetics. 23, 3, p. 139-40 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  1 Citation (Scopus)
• 2011

  At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia

  Hansen, T., Ingason, A., Djurovic, S., Melle, I., Fenger, M., Gustafsson, O., Jakobsen, K. D., Rasmussen, H. B., Tosato, S., Rietschel, M., Frank, J., Owen, M., Bonetto, C., Suvisaari, J., Thygesen, J. H., Pétursson, H., Lönnqvist, J., Sigurdsson, E., Giegling, I., Craddock, N., & 12 othersO'Donovan, M. C., Ruggeri, M., Cichon, S., Ophoff, R. A., Pietiläinen, O., Peltonen, L., Nöthen, M. M., Rujescu, D., St Clair, D., Collier, D. A., Andreassen, O. A. & Werge, T., 1 Jul 2011, In: Biological Psychiatry. 70, 1, p. 59-63 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Schizophrenia 100%
  • Type 2 Diabetes Mellitus 92%
  • Comorbidity 57%
  • Antipsychotic Agents 22%
  • Life Style 20%
  99 Citations (Scopus)

• Copy number variations of chromosome 16p13.1 region associated with schizophrenia

  Ingason, A., Rujescu, D., Cichon, S., Sigurdsson, E., Sigmundsson, T., Pietiläinen, O. P. H., Buizer-Voskamp, J. E., Strengman, E., Francks, C., Muglia, P., Gylfason, A., Gustafsson, O., Olason, P. I., Steinberg, S., Hansen, T. F., Jakobsen, K. D., Rasmussen, H. B., Giegling, I., Möller, H-J., Hartmann, A., & 29 othersCrombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Bramon, E., Kiemeney, L. A., Franke, B., Murray, R., Vassos, E., Toulopoulou, T., Mühleisen, T. W., Tosato, S., Ruggeri, M., Djurovic, S., Andreassen, O. A., Zhang, Z., Werge, T., Ophoff, R. A., Rietschel, M., Nöthen, M. M., Petursson, H., Stefansson, H., Peltonen, L., Collier, D., Stefansson, K., St Clair, D. M. & GROUP Investigators, 1 Jan 2011, In: Molecular Psychiatry. 16, 1, p. 17-25 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Schizophrenia 100%
  • Chromosomes 97%
  • Autistic Disorder 40%
  • Intellectual Disability 38%
  • Genomic Segmental Duplications 31%
  172 Citations (Scopus)

• Expanding the range of ZNF804A variants conferring risk of psychosis

  Steinberg, S., Mors, O., Børglum, A., Gustafsson, O., Werge, T., Mortensen, P. B., Andreassen, O. A., Sigurdsson, E., Thorgeirsson, T. E., Böttcher, Y., Olason, P., Ophoff, R. A., Cichon, S., Gudjonsdottir, I. H., Pietiläinen, O. P. H., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T. F., Athanasiu, L., & 31 othersSuvisaari, J., Lonnqvist, J., Paunio, T., Hartmann, A., Jürgens, G., Nordentoft, M., Hougaard, D., Norgaard-Pedersen, B., Breuer, R., Möller, H-J., Giegling, I., Glenthøj, B., Rasmussen, H. B., Mattheisen, M., Bitter, I., Réthelyi, J. M., Sigmundsson, T., Fossdal, R., Thorsteinsdottir, U., Ruggeri, M., Tosato, S., Strengman, E., Genetic Risk and Outcome in Psychosis, Kiemeney, L. A., Melle, I., Djurovic, S., Abramova, L., Kaleda, V., Walshe, M., Bramon, E. & Vassos, E., 1 Jan 2011, In: Molecular Psychiatry. 16, 1, p. 59-66 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Psychotic Disorders 100%
  • Schizophrenia 87%
  • Bipolar Disorder 34%
  • Mental Disorders 28%
  • Genome-Wide Association Study 18%
  122 Citations (Scopus)

• Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

  Ingason, A., Kirov, G., Giegling, I., Hansen, T., Isles, A. R., Jakobsen, K. D., Kristinsson, K. T., le Roux, L., Gustafsson, O., Craddock, N., Möller, H-J., McQuillin, A., Muglia, P., Cichon, S., Rietschel, M., Ophoff, R. A., Djurovic, S., Andreassen, O. A., Pietiläinen, O. P. H., Peltonen, L., & 22 othersDempster, E., Collier, D. A., St Clair, D., Rasmussen, H. B., Glenthøj, B. Y., Kiemeney, L. A., Franke, B., Tosato, S., Bonetto, C., Saemundsen, E., Hreidarsson, S. J., Nöthen, M. M., Gurling, H., O'Donovan, M. C., Owen, M. J., Sigurdsson, E., Petursson, H., Stefansson, H., Rujescu, D., Stefansson, K., Werge, T. & GROUP Investigators, 1 Apr 2011, In: American Journal of Psychiatry. 168, 4, p. 408-417 10 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Prader-Willi Syndrome 100%
  • Psychotic Disorders 91%
  • Angelman Syndrome 72%
  • Schizophrenia 59%
  • Genes 59%
  81 Citations (Scopus)

• The etiology of multiple sclerosis: genetic evidence for the involvement of the human endogenous retrovirus HERV-Fc1

  Nexø, B. A., Christensen, T., Frederiksen, J., Møller-Larsen, A., Oturai, A. B., Fredsted, P. V., Hansen, B., Nissen, K. K., Laska, M. J., Petersen, T. S., Bonnesen, S., Hedemand, A., Wu, T., Wang, X., Zhang, X., Brudek, T., Maric, R., Søndergaard, H. B., Sellebjerg, F., Brusgaard, K., & 7 othersKjeldbjerg, A. L., Rasmussen, H. B., Nielsen, A. L., Nyegaard, M., Petersen, T., Børglum, A. & Pedersen, F. S., 1 Feb 2011, In: P L o S One. 6, 2, p. e16652 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Multiple Sclerosis 100%
  • Endogenous Retroviruses 87%
  • sclerosis 87%
  • etiology 78%
  • Retroviridae 76%
  52 Citations (Scopus)
• 2010

  A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

  Ingason, A., Giegling, I., Cichon, S., Hansen, T., Rasmussen, H. B., Nielsen, J., Jürgens, G., Muglia, P., Hartmann, A. M., Strengman, E., Vasilescu, C., Mühleisen, T. W., Djurovic, S., Melle, I., Lerer, B., Möller, H-J., Francks, C., Pietiläinen, O. P. H., Lonnqvist, J., Suvisaari, J., & 21 othersTuulio-Henriksson, A., Walshe, M., Vassos, E., Di Forti, M., Murray, R., Bonetto, C., Tosato, S., Cantor, R. M., Rietschel, M., Craddock, N., Owen, M. J., Peltonen, L., Andreassen, O. A., Nöthen, M. M., St Clair, D., Ophoff, R. A., O'Donovan, M. C., Collier, D. A., Werge, T., Rujescu, D. & GROUP Investigators, 12 Jan 2010, In: Human Molecular Genetics. 19, 7, p. 1379-86 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Schizophrenia 100%
  • Meta-Analysis 91%
  • Chromosome Mapping 50%
  • Genes 49%
  • Phosphoric Diester Hydrolases 47%
  38 Citations (Scopus)

• Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia

  Vares, M., Saetre, P., Deng, H., Cai, G., Liu, X., Hansen, T., Rasmussen, H. B., Werge, T., Melle, I., Djurovic, S., Andreassen, O. A., Agartz, I., Hall, H., Terenius, L. & Jönsson, E. G., 5 Mar 2010, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 153B, 2, p. 610-8 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Methylenetetrahydrofolate Reductase (NADPH2) 100%
  • Age of Onset 73%
  • Schizophrenia 63%
  • Single Nucleotide Polymorphism 21%
  • Alleles 18%
  27 Citations (Scopus)

• Genetic susceptibility factors for multiple chemical sensitivity revisited

  Berg, N. D., Rasmussen, H. B., Linneberg, A., Andersen, C. B., Fenger, M., Dirksen, A., Vesterhauge, S., Werge, T., Elberling, J. & Berg, N. D., 1 Mar 2010, In: International Journal of Hygiene and Environmental Health. 213, 2, p. 131-9 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Genetic Susceptibility 100%
  • Multiple Chemical Sensitivity 94%
  • Genetic Predisposition to Disease 60%
  • Arylamine N-Acetyltransferase 24%
  • Cholecystokinin B Receptor 21%
  26 Citations (Scopus)

• No influence of the polymorphisms CYP2C19 and CYP2D6 on the efficacy of cyclophosphamide, thalidomide, and bortezomib in patients with Multiple Myeloma

  Vangsted, A. J., Søeby, K., Klausen, T. W., Abildgaard, N., Andersen, N. F., Gimsing, P., Gregersen, H., Vogel, U., Werge, T. & Rasmussen, H. B., 4 Aug 2010, In: B M C Cancer. 10, p. 404 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Cytochrome P-450 CYP2C19 100%
  • Cytochrome P-450 CYP2D6 95%
  • Thalidomide 94%
  • Bortezomib 92%
  • Multiple Myeloma 74%
  20 Citations (Scopus)

• The tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: a multi-centre case-control study and meta-analysis

  Saetre, P., Lundmark, P., Wang, A., Hansen, T., Rasmussen, H. B., Djurovic, S., Melle, I., Andreassen, O. A., Werge, T., Agartz, I., Hall, H., Terenius, L. & Jönsson, E. G., 5 Mar 2010, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 153B, 2, p. 387-96 10 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Tryptophan Hydroxylase 100%
  • Schizophrenia 59%
  • Case-Control Studies 58%
  • Meta-Analysis 54%
  • Suicide 33%
  43 Citations (Scopus)
• 2009

  Common variants conferring risk of schizophrenia

  Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Cichon, S., Rujescu, D., Werge, T., Pietiläinen, O. P. H., Mors, O., Mortensen, P. B., Sigurdsson, E., Gustafsson, O., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T., Suvisaari, J., Lonnqvist, J., Paunio, T., Børglum, A. D., & 31 othersHartmann, A., Fink-Jensen, A., Nordentoft, M., Hougaard, D., Norgaard-Pedersen, B., Böttcher, Y., Olesen, J., Breuer, R., Möller, H-J., Giegling, I., Rasmussen, H. B., Timm, S., Mattheisen, M., Bitter, I., Réthelyi, J. M., Magnusdottir, B. B., Sigmundsson, T., Olason, P., Masson, G., Gulcher, J. R., Haraldsson, M., Fossdal, R., Thorgeirsson, T. E., Thorsteinsdottir, U., Ruggeri, M., Tosato, S., Franke, B., Strengman, E., Kiemeney, L. A., Melle, I. & Genetic Risk and Outcome in Psychosis (GROUP), 6 Aug 2009, In: Nature. 460, 7256, p. 744-7 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Schizophrenia 100%
  • Neurogranin 83%
  • Transcription Factor 4 73%
  • Genome-Wide Association Study 51%
  • Major Histocompatibility Complex 50%
  1260 Citations (Scopus)

• Suicidal Behavior and the Serotonin Transporter Gene Polymorphism (5-HTTLPR) with Novel Subtypes, in Danish Schizophrenic Patients

  Wang, A. G., Rasmussen, H. B., Sørensen, H. J., Hvid, M., Breddam, C. H., Hansen, B., Bille, V. H., Garsdal, O., Jacoby, A., Søbye, K., Dam, O. H., Krogsbøl, H., Timm, S. & Werge, T. M., 2009, In: Open Psychiatry Journal.

  Research output: Contribution to journal › Journal article › Research › peer-review