Werge T - Search Results

1

Human Disease Variation in the Light of Population Genomics.

Prohaska A, Racimo F, Schork AJ, Sikora M, Stern AJ, Ilardo M, Allentoft ME, Folkersen L, Buil A, Moreno-Mayar JV, Korneliussen T, Geschwind D, Ingason A, Werge T, Nielsen R, Willerslev E. Prohaska A, et al. Among authors: werge t. Cell. 2019 Mar 21;177(1):115-131. doi: 10.1016/j.cell.2019.01.052. Cell. 2019. PMID: 30901534 Free article. Review.

2

No significant association of the 5' end of neuregulin 1 and schizophrenia in a large Danish sample.

Ingason A, Søeby K, Timm S, Wang AG, Jakobsen KD, Fink-Jensen A, Hemmingsen R, Berg Rasmussen H, Werge T. Ingason A, et al. Among authors: werge t. Schizophr Res. 2006 Mar;83(1):1-5. doi: 10.1016/j.schres.2005.12.850. Epub 2006 Feb 17. Schizophr Res. 2006. PMID: 16483744

3

[Submicroscopic chromosomal anomalies as a cause of schizophrenia].

Hansen T, Ingason A, Werge T. Hansen T, et al. Among authors: werge t. Ugeskr Laeger. 2008 Nov 10;170(46):3773-6. Ugeskr Laeger. 2008. PMID: 19014729 Danish.

4

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

Duong L, Klitten LL, Møller RS, Ingason A, Jakobsen KD, Skjødt C, Didriksen M, Hjalgrim H, Werge T, Tommerup N. Duong L, et al. Among authors: werge t. Am J Med Genet B Neuropsychiatr Genet. 2012 Apr;159B(3):354-8. doi: 10.1002/ajmg.b.32036. Epub 2012 Feb 15. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22337556

5

Redox dysregulation in the pathophysiology of schizophrenia and bipolar disorder: insights from animal models.

Kulak A, Steullet P, Cabungcal JH, Werge T, Ingason A, Cuenod M, Do KQ. Kulak A, et al. Among authors: werge t. Antioxid Redox Signal. 2013 Apr 20;18(12):1428-43. doi: 10.1089/ars.2012.4858. Epub 2012 Oct 12. Antioxid Redox Signal. 2013. PMID: 22938092 Review.

6

Sequence analysis of 17 NRXN1 deletions.

Enggaard Hoeffding LK, Hansen T, Ingason A, Doung L, Thygesen JH, Møller RS, Tommerup N, Kirov G, Rujescu D, Larsen LA, Werge T. Enggaard Hoeffding LK, et al. Among authors: werge t. Am J Med Genet B Neuropsychiatr Genet. 2014 Jan;165B(1):52-61. doi: 10.1002/ajmg.b.32204. Epub 2013 Sep 25. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24339137

7

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

Thygesen JH, Zambach SK, Ingason A, Lundin P, Hansen T, Bertalan M, Rosengren A, Bjerre D, Ferrero-Miliani L, Rasmussen HB, Parnas J, Werge T. Thygesen JH, et al. Among authors: werge t. Schizophr Res. 2015 Dec;169(1-3):441-446. doi: 10.1016/j.schres.2015.08.037. Epub 2015 Oct 1. Schizophr Res. 2015. PMID: 26421691

8

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort.

Bertelsen B, Stefánsson H, Riff Jensen L, Melchior L, Mol Debes N, Groth C, Skov L, Werge T, Karagiannidis I, Tarnok Z, Barta C, Nagy P, Farkas L, Brøndum-Nielsen K, Rizzo R, Gulisano M, Rujescu D, Kiemeney LA, Tosato S, Nawaz MS, Ingason A, Unnsteinsdottir U, Steinberg S, Ludvigsson P, Stefansson K, Kuss AW, Paschou P, Cath D, Hoekstra PJ, Müller-Vahl K, Stuhrmann M, Silahtaroglu A, Pfundt R, Tümer Z. Bertelsen B, et al. Among authors: werge t. Biol Psychiatry. 2016 Mar 1;79(5):383-391. doi: 10.1016/j.biopsych.2015.08.027. Epub 2015 Sep 3. Biol Psychiatry. 2016. PMID: 26444075

9

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

Hoeffding LK, Duong LT, Ingason A, Rosengren A, Sorbanski E, Witt SH, Djurovic S, Andreassen OA, Hansen T, Werge T, Rasmussen HB. Hoeffding LK, et al. Among authors: werge t. Nord J Psychiatry. 2016;70(4):276-9. doi: 10.3109/08039488.2015.1095944. Epub 2015 Nov 11. Nord J Psychiatry. 2016. PMID: 26559242

10

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family.

Duong LT, Hoeffding LK, Petersen KB, Knudsen CD, Thygesen JH, Klitten LL, Tommerup N, Ingason A, Werge T. Duong LT, et al. Among authors: werge t. Eur J Med Genet. 2015 Dec;58(12):650-3. doi: 10.1016/j.ejmg.2015.11.004. Epub 2015 Nov 10. Eur J Med Genet. 2015. PMID: 26563496

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