Jabbari J - Search Results

1

Rare variants in GJA5 are associated with early-onset lone atrial fibrillation.

Christophersen IE, Holmegard HN, Jabbari J, Sajadieh A, Haunsø S, Tveit A, Svendsen JH, Olesen MS. Christophersen IE, et al. Among authors: jabbari j. Can J Cardiol. 2013 Jan;29(1):111-6. doi: 10.1016/j.cjca.2012.08.002. Epub 2012 Oct 2. Can J Cardiol. 2013. PMID: 23040431

2

Screening of KCNN3 in patients with early-onset lone atrial fibrillation.

Olesen MS, Jabbari J, Holst AG, Nielsen JB, Steinbrüchel DA, Jespersen T, Haunsø S, Svendsen JH. Olesen MS, et al. Among authors: jabbari j. Europace. 2011 Jul;13(7):963-7. doi: 10.1093/europace/eur007. Epub 2011 Mar 11. Europace. 2011. PMID: 21398315

3

Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.

Jabbari J, Olesen MS, Holst AG, Nielsen JB, Haunso S, Svendsen JH. Jabbari J, et al. Cardiology. 2011;118(2):116-20. doi: 10.1159/000323840. Epub 2011 May 9. Cardiology. 2011. PMID: 21555883

4

Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.

Olesen MS, Holst AG, Jabbari J, Nielsen JB, Christophersen IE, Sajadieh A, Haunsø S, Svendsen JH. Olesen MS, et al. Among authors: jabbari j. Can J Cardiol. 2012 Mar-Apr;28(2):191-5. doi: 10.1016/j.cjca.2011.11.016. Epub 2012 Feb 14. Can J Cardiol. 2012. PMID: 22336519

5

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.

Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N. Olesen MS, et al. Among authors: jabbari j. BMC Med Genet. 2012 Apr 3;13:24. doi: 10.1186/1471-2350-13-24. BMC Med Genet. 2012. PMID: 22471742 Free PMC article.

6

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.

Olesen MS, Andreasen L, Jabbari J, Refsgaard L, Haunsø S, Olesen SP, Nielsen JB, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: jabbari j. Heart Rhythm. 2014 Feb;11(2):246-51. doi: 10.1016/j.hrthm.2013.10.034. Epub 2013 Oct 18. Heart Rhythm. 2014. PMID: 24144883

7

Brugada syndrome risk loci seem protective against atrial fibrillation.

Andreasen L, Nielsen JB, Darkner S, Christophersen IE, Jabbari J, Refsgaard L, Thiis JJ, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS. Andreasen L, et al. Among authors: jabbari j. Eur J Hum Genet. 2014 Dec;22(12):1357-61. doi: 10.1038/ejhg.2014.46. Epub 2014 Mar 26. Eur J Hum Genet. 2014. PMID: 24667784 Free PMC article.

8

Common and rare variants in SCN10A modulate the risk of atrial fibrillation.

Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Jabbari J, et al. Circ Cardiovasc Genet. 2015 Feb;8(1):64-73. doi: 10.1161/HCG.0000000000000022. Circ Cardiovasc Genet. 2015. PMID: 25691686 Free PMC article. Clinical Trial.

9

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

Gregers E, Ahlberg G, Christensen T, Jabbari J, Larsen KO, Herfelt CB, Henningsen KM, Andreasen L, Thiis JJ, Lund J, Holme S, Haunsø S, Bentzen BH, Schmitt N, Svendsen JH, Olesen MS. Gregers E, et al. Among authors: jabbari j. Heart Rhythm. 2017 Oct;14(10):1531-1538. doi: 10.1016/j.hrthm.2017.05.027. Epub 2017 May 24. Heart Rhythm. 2017. PMID: 28549997

10

New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia.

Jabbari J, Jabbari R, Nielsen MW, Holst AG, Nielsen JB, Haunsø S, Tfelt-Hansen J, Svendsen JH, Olesen MS. Jabbari J, et al. Among authors: jabbari r. Circ Cardiovasc Genet. 2013 Oct;6(5):481-9. doi: 10.1161/CIRCGENETICS.113.000118. Epub 2013 Sep 11. Circ Cardiovasc Genet. 2013. PMID: 24025405

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