Andrés Ingason

Research output

Research output per year 2009 2009 2010 2011 2018

• 13 Journal article
• 1 Ph.D. thesis

Research output per year

Research output per year

Search results

• 2018

  Molecular genetic overlap between migraine and major depressive disorder

  Yang, Y., Zhao, H., Boomsma, D. I., Ligthart, L., Belin, A. C., Smith, G. D., Esko, T., Freilinger, T. M., Hansen, T. F., Ikram, M. A., Kallela, M., Kubisch, C., Paraskevi, C., Strachan, D. P., Wessman, M., Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., & 30 othersPers, T. H., Farh, K. H., Cuenca-Leon, E., Muona, M., Furlotte, N. A., Kurth, T., Ingason, A., McMahon, G., Ligthart, L., Terwindt, G. M., Kallela, M., Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H., Steinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimäki, T., Sarin, A. P., Wedenoja, J., Hinds, D. A., Buring, J. E., Schürks, M., Christensen, A. F., Hansen, T. F., Werge, T. & Olesen, J., 2018, In: European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

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

  • Major Depressive Disorder 100%
  • Migraine Disorders 96%
  • Molecular Biology 77%
  • Single Nucleotide Polymorphism 40%
  • Genome-Wide Association Study 30%
  20 Citations (Scopus)
• 2014

  Sequence analysis of 17 NRXN1 deletions

  Hoeffding, L. K. E., Hansen, T., Ingason, A., Doung, L., Thygesen, J. H., Møller, R. S., Tommerup, N., Kirov, G., Rujescu, D., Larsen, L. A. & Werge, T., Jan 2014, In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 165, 1, p. 52-61 10 p.

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

  • Neurodevelopmental Disorders 100%
  • Sequence Analysis 79%
  • Nucleotides 68%
  • Chromosomes, Human, Pair 2 55%
  • Congenital, Hereditary, and Neonatal Diseases and Abnormalities 53%
  11 Citations (Scopus)
• 2012

  Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders

  Duong, L., Klitten, L. L., Møller, R. S., Ingason, A., Jakobsen, K. D., Skjødt, C., Didriksen, M., Hjalgrim, H., Werge, T. & Tommerup, N., Apr 2012, In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 159B, 3, p. 354-8 5 p.

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

  • Brain Diseases 100%
  • Point Mutation 76%
  • Mutation 58%
  • Autistic Disorder 52%
  • Intellectual Disability 49%
  47 Citations (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)

• GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

  Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, M. J., Craddock, N. J., O'Donovan, M. C., Blackman, J., Lewis, D., Kirov, G. K., & 42 othersQin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D., Bronstein, M., Darvasi, A., Lencz, T., Malhotra, A. K., Rujescu, D., Giegling, I., Werge, T., Hansen, T. F., Ingason, A., Nöethen, M. M., Rietschel, M., Cichon, S., Djurovic, S., Andreassen, O. A., Cantor, R. M., Ophoff, R., Corvin, A., Morris, D. W., Gill, M., Pato, C. N., Pato, M. T., Macedo, A., Gurling, H. M. D., McQuillin, A., Pimm, J., Hultman, C., Lichtenstein, P., Sklar, P., Purcell, S. M., Scolnick, E., St Clair, D., Blackwood, D. H. R. & Kendler, K. S., 1 Nov 2011, In: Molecular Psychiatry. 16, 11, p. 1117-29 13 p.

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

  • Data Mining 100%
  • Genome-Wide Association Study 86%
  • Cardiomyopathies 80%
  • Schizophrenia 67%
  • Antipsychotic Agents 45%
  54 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)
• 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)

• Genomic copy number variation in schizophrenia: rare structural variants as an important source of schizophrenia susceptibility: indications of aetiological overlap with other neurodevelopmental disorders

  Ingason, A., 2010, København. 45 p.

  Research output: Book/Report › Ph.D. thesis

• Neuregulin-1 genotypes and eye movements in schizophrenia

  Haraldsson, H. M., Ettinger, U., Magnusdottir, B. B., Ingason, A., Hutton, S. B., Sigmundsson, T., Sigurdsson, E. & Petursson, H., Feb 2010, In: European Archives of Psychiatry and Clinical Neuroscience. 260, 1, p. 77-85 9 p.

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

  • Neuregulin-1 100%
  • Smooth Pursuit 84%
  • Eye Movements 73%
  • Schizophrenia 57%
  • Genotype 50%
  7 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)

• COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia

  Haraldsson, H. M., Ettinger, U., Magnusdottir, B. B., Sigmundsson, T., Sigurdsson, E., Ingason, A. & Petursson, H., 2009, In: Psychiatry Research. 169, 2, p. 173-5 2 p.

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

  • Smooth Pursuit 100%
  • Catechol O-Methyltransferase 98%
  • Eye Movements 74%
  • Schizophrenia 58%
  • Genotype 51%
  13 Citations (Scopus)

• Neurexin 1 (NRXN1) deletions in schizophrenia

  Kirov, G., Rujescu, D., Ingason, A., Collier, D. A., O'Donovan, M. C. & Owen, M. J., 2009, In: Schizophrenia Bulletin. 35, 5, p. 851-4 3 p.

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

  176 Citations (Scopus)