Nielsen MN - Search Results

1

Association between genes on chromosome 19p13.2 and panic disorder.

Gregersen NO, Buttenschøn HN, Hedemand A, Nielsen MN, Dahl HA, Kristensen AS, Johansen O, Woldbye DP, Erhardt A, Kruse TA, Wang AG, Børglum AD, Mors O. Gregersen NO, et al. Among authors: nielsen mn. Psychiatr Genet. 2016 Dec;26(6):287-292. doi: 10.1097/YPG.0000000000000147. Psychiatr Genet. 2016. PMID: 27610895

2

Progranulin gene variation affects serum progranulin levels differently in Danish bipolar individuals compared with healthy controls.

Buttenschøn HN, Nielsen MN, Thotakura G, Lee CW, Nykjær A, Mors O, Glerup S. Buttenschøn HN, et al. Among authors: nielsen mn. Psychiatr Genet. 2017 Jun;27(3):89-95. doi: 10.1097/YPG.0000000000000168. Psychiatr Genet. 2017. PMID: 28225367

3

Exploring the sortilin related receptor, SorLA, in depression.

Buttenschøn HN, Elfving B, Nielsen M, Skeldal S, Kaas M, Mors O, Glerup S. Buttenschøn HN, et al. J Affect Disord. 2018 May;232:260-267. doi: 10.1016/j.jad.2018.02.050. Epub 2018 Feb 21. J Affect Disord. 2018. PMID: 29499509

4

Association analyses of depression and genes in the hypothalamus-pituitary-adrenal axis.

Buttenschøn HN, Krogh J, Nielsen MN, Kaerlev L, Nordentoft M, Mors O. Buttenschøn HN, et al. Among authors: nielsen mn. Acta Neuropsychiatr. 2017 Feb;29(1):59-64. doi: 10.1017/neu.2016.26. Epub 2016 Jun 6. Acta Neuropsychiatr. 2017. PMID: 27264499

5

Investigation of serum levels of sortilin in response to antidepressant treatment.

Buttenschøn HN, Nielsen M, Glerup S, Mors O. Buttenschøn HN, et al. Acta Neuropsychiatr. 2018 Apr;30(2):111-116. doi: 10.1017/neu.2017.13. Epub 2017 May 8. Acta Neuropsychiatr. 2018. PMID: 28478778

6

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 JJ, Bross P, Westergaard M, Nielsen MN, Eiberg H, Børglum AD, Mogensen J, Kristiansen K, Bolund L, Gregersen N. Hansen JJ, et al. Among authors: nielsen mn. Hum Genet. 2003 Jan;112(1):71-7. doi: 10.1007/s00439-002-0837-9. Epub 2002 Oct 16. Hum Genet. 2003. PMID: 12483302

7

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 JJ, Bross P, Westergaard M, Nielsen M, Eiberg H, Børglum AD, Mogensen J, Kristiansen K, Bolund L, Gregersen N. Hansen JJ, et al. Hum Genet. 2003 Apr;112(4):436. doi: 10.1007/s00439-003-0927-3. Hum Genet. 2003. PMID: 27519232 No abstract available.

8

Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13).

Hansen J, Corydon TJ, Palmfeldt J, Dürr A, Fontaine B, Nielsen MN, Christensen JH, Gregersen N, Bross P. Hansen J, et al. Among authors: nielsen mn. Neuroscience. 2008 May 2;153(2):474-82. doi: 10.1016/j.neuroscience.2008.01.070. Epub 2008 Feb 19. Neuroscience. 2008. PMID: 18378094

9

Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.

Bross P, Li Z, Hansen J, Hansen JJ, Nielsen MN, Corydon TJ, Georgopoulos C, Ang D, Lundemose JB, Niezen-Koning K, Eiberg H, Yang H, Kølvraa S, Bolund L, Gregersen N. Bross P, et al. Among authors: nielsen mn. J Hum Genet. 2007;52(1):56-65. doi: 10.1007/s10038-006-0080-7. Epub 2006 Oct 27. J Hum Genet. 2007. PMID: 17072495

10

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.

Hansen JJ, Dürr A, Cournu-Rebeix I, Georgopoulos C, Ang D, Nielsen MN, Davoine CS, Brice A, Fontaine B, Gregersen N, Bross P. Hansen JJ, et al. Among authors: nielsen mn. Am J Hum Genet. 2002 May;70(5):1328-32. doi: 10.1086/339935. Epub 2002 Mar 15. Am J Hum Genet. 2002. PMID: 11898127 Free PMC article.

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