Marit Nyholm Nielsen

  1. 2018
  2. Published

    Exploring the sortilin related receptor, SorLA, in depression. / Buttenschøn, Henriette N; Elfving, Betina; Nielsen, Marit; Skeldal, Sune; Kaas, Mathias; Mors, Ole; Glerup, Simon.

    In: Journal of Affective Disorders, Vol. 232, 05.2018, p. 260-267.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  3. Published

    Investigation of serum levels of sortilin in response to antidepressant treatment. / Buttenschøn, Henriette Nørmølle; Nielsen, Marit; Glerup, Simon; Mors, Ole.

    In: Acta Neuropsychiatrica, Vol. 30, No. 2, 04.2018, p. 111-116.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  4. 2017
  5. Published

    Progranulin gene variation affects serum progranulin levels differently in Danish bipolar individuals compared with healthy controls. / Buttenschøn, Henriette N; Nielsen, Marit N; Thotakura, Gangadaar; Lee, Chris W; Nykjær, Anders; Mors, Ole; Glerup, Simon.

    In: Psychiatric Genetics, Vol. 27, No. 3, 06.2017, p. 89-95.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  6. Published

    Association analyses of depression and genes in the hypothalamus-pituitary-adrenal axis. / Buttenschøn, Henriette Nørmølle; Krogh, Jesper; Nielsen, Marit Nyholm; Nordentoft, Merete; Mors, Ole.

    In: Acta Neuropsychiatrica, Vol. 29, No. 1, 02.2017, p. 59-64.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  7. 2016
  8. Published

    Association between genes on chromosome 19p13.2 and panic disorder. / Gregersen, Noomi; Buttenschøn, Henriette Nørmølle; Hedemand, Anne; Nielsen, Marit Nyholm; Dahl, Hans; Kristensen, Ann Suhl; Johansen, Oddbjørg; Woldbye, David; Erhardt, Angelika; Kruse, Torben A; Wang, August G.; Børglum, Anders; Mors, Ole.

    In: Psychiatric Genetics, Vol. 26, No. 6, 2016, p. 287-292.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  9. 2012
  10. Published

    Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allele. / Bross, Peter; Frederiksen, Jane B; Bie, Anne S; Hansen, Jakob; Palmfeldt, Johan; Nielsen, Marit N; Duno, Morten; Lund, Allan Meldgaard; Christensen, Ernst.

    In: Journal of Inherited Metabolic Disease, Vol. 35, No. 5, 08.2012, p. 787-796.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  11. 2010
  12. Published

    Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice. / Christensen, Jane H; Nielsen, Marit N; Hansen, Jakob; Füchtbauer, Annette; Füchtbauer, Ernst-Martin; West, Mark; Corydon, Thomas J; Gregersen, Niels; Bross, Peter.

    In: Cell Stress & Chaperones, Vol. 15, No. 6, 2010, p. 851-863.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  13. 2006
  14. Published

    Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential. / Bross, Peter; Li, Zhijie; Hansen, Jakob; Hansen, Jens Jacob; Nielsen, Marit Nyholm; Corydon, Thomas Juhl; Georgopoulos, Costa; Ang, Debbie; Lundemose, Jytte Banner; Niezen-Koning, Klary; Eiberg, Hans; Yang, Huanming; Kølvraa, Steen; Bolund, Lars; Gregersen, Niels.

    In: Journal of Human Genetics, Vol. 52, No. 1, 2006, p. 56-65.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  15. 2003
  16. Published

    Erratum : Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter (Human Genetics (2003) 112 (71-77)). / Hansen, Jens J.; Bross, Peter; Westergaard, Majken; Nielsen, Marit Nyholm; Eiberg, Hans; Børglum, Anders D.; Mogensen, Jens; Kristiansen, Karsten; Bolund, Lars; Gregersen, Niels.

    In: Human Genetics, Vol. 112, No. 4, 01.04.2003.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperComment/debateResearchpeer-review

  17. 2002
  18. Published

    Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter. / Hansen, Jens J; Bross, Peter; Westergaard, Majken; Nielsen, Marit Nyholm; Eiberg, Hans; Børglum, Anders; Mogensen, Jens; Kristiansen, Karsten; Bolund, Lars; Gregersen, Niels.

    In: Human Genetics, Vol. 112, No. 1, 2002, p. 71-7.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review