Bertelsen B - Search Results

1

Sequence analysis of SLITRK1 for var321 in Danish patients with Tourette syndrome and review of the literature.

Yasmeen S, Melchior L, Bertelsen B, Skov L, Mol Debes N, Tümer Z. Yasmeen S, et al. Among authors: bertelsen b. Psychiatr Genet. 2013 Jun;23(3):130-3. doi: 10.1097/YPG.0b013e328360c880. Psychiatr Genet. 2013. PMID: 23528612 Review.

2

Three new loci for determining x chromosome inactivation patterns.

Bertelsen B, Tümer Z, Ravn K. Bertelsen B, et al. J Mol Diagn. 2011 Sep;13(5):537-40. doi: 10.1016/j.jmoldx.2011.05.003. Epub 2011 Jul 2. J Mol Diagn. 2011. PMID: 21726665 Free PMC article.

3

Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.

Tümer Z, Bertelsen B, Gredal O, Magyari M, Nielsen KC, Lucamp, Grønskov K, Brøndum-Nielsen K. Tümer Z, et al. Among authors: bertelsen b. Neurobiol Aging. 2012 Jan;33(1):208.e1-5. doi: 10.1016/j.neurobiolaging.2011.07.001. Epub 2011 Aug 26. Neurobiol Aging. 2012. PMID: 21852022

4

[The genetics of Gilles de la Tourette syndrome].

Bertelsen B, Melchior L, Debes NM, Skov L, Brøndum-Nielsen K, Tümer Z. Bertelsen B, et al. Ugeskr Laeger. 2012 Feb 20;174(8):484-7. Ugeskr Laeger. 2012. PMID: 22348669 Danish.

5

Microduplication of 15q13.3 and Xq21.31 in a family with Tourette syndrome and comorbidities.

Melchior L, Bertelsen B, Debes NM, Groth C, Skov L, Mikkelsen JD, Brøndum-Nielsen K, Tümer Z. Melchior L, et al. Among authors: bertelsen b. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec;162B(8):825-31. doi: 10.1002/ajmg.b.32186. Epub 2013 Jul 27. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23894120

6

Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literature.

Bertelsen B, Debes NM, Hjermind LE, Skov L, Brøndum-Nielsen K, Tümer Z. Bertelsen B, et al. Neurogenetics. 2013 Nov;14(3-4):197-203. doi: 10.1007/s10048-013-0372-y. Epub 2013 Aug 29. Neurogenetics. 2013. PMID: 23989977

7

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

Bertelsen B, Melchior L, Jensen LR, Groth C, Glenthøj B, Rizzo R, Debes NM, Skov L, Brøndum-Nielsen K, Paschou P, Silahtaroglu A, Tümer Z. Bertelsen B, et al. Eur J Hum Genet. 2014 Nov;22(11):1283-9. doi: 10.1038/ejhg.2014.24. Epub 2014 Feb 19. Eur J Hum Genet. 2014. PMID: 24549057 Free PMC article.

8

Association of the CHRNA7 promoter variant -86T with Tourette syndrome and comorbid obsessive-compulsive disorder.

Bertelsen B, Melchior L, Groth C, Mol Debes N, Skov L, Holst KK, Fagerlund B, Mikkelsen JD, Tümer Z. Bertelsen B, et al. Psychiatry Res. 2014 Nov 30;219(3):710-1. doi: 10.1016/j.psychres.2014.06.032. Epub 2014 Jun 28. Psychiatry Res. 2014. PMID: 25024057 No abstract available.

9

A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD.

Bertelsen B, Melchior L, Jensen LR, Groth C, Nazaryan L, Debes NM, Skov L, Xie G, Sun W, Brøndum-Nielsen K, Kuss AW, Chen W, Tümer Z. Bertelsen B, et al. Psychiatry Res. 2015 Feb 28;225(3):268-75. doi: 10.1016/j.psychres.2014.12.028. Epub 2014 Dec 30. Psychiatry Res. 2015. PMID: 25595337

10

A mosaic small supernumerary marker chromosome 17 in a patient with Tourette syndrome, ADHD and intellectual disability: A case story and review of the literature.

Cornelius N, Bertelsen B, Melchior L, Nazaryan L, Debes NM, Groth C, Skov L, Tümer Z. Cornelius N, et al. Among authors: bertelsen b. Psychiatry Res. 2015 Jul 30;228(1):179-81. doi: 10.1016/j.psychres.2015.03.022. Epub 2015 Mar 31. Psychiatry Res. 2015. PMID: 25935373 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

82 results

Search Page