Olson TM - Search Results

1

Genetic Association Between Hypoplastic Left Heart Syndrome and Cardiomyopathies.

Theis JL, Hu JJ, Sundsbak RS, Evans JM, Bamlet WR, Qureshi MY, O'Leary PW, Olson TM. Theis JL, et al. Among authors: olson tm. Circ Genom Precis Med. 2021 Feb;14(1):e003126. doi: 10.1161/CIRCGEN.120.003126. Epub 2020 Dec 16. Circ Genom Precis Med. 2021. PMID: 33325730

2

Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology.

Olson TM, Karst ML, Whitby FG, Driscoll DJ. Olson TM, et al. Circulation. 2002 May 21;105(20):2337-40. doi: 10.1161/01.cir.0000018444.47798.94. Circulation. 2002. PMID: 12021217

3

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy.

Theis JL, Sharpe KM, Matsumoto ME, Chai HS, Nair AA, Theis JD, de Andrade M, Wieben ED, Michels VV, Olson TM. Theis JL, et al. Among authors: olson tm. Circ Cardiovasc Genet. 2011 Dec;4(6):585-94. doi: 10.1161/CIRCGENETICS.111.961052. Epub 2011 Sep 30. Circ Cardiovasc Genet. 2011. PMID: 21965549 Free PMC article.

4

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

Theis JL, Zimmermann MT, Larsen BT, Rybakova IN, Long PA, Evans JM, Middha S, de Andrade M, Moss RL, Wieben ED, Michels VV, Olson TM. Theis JL, et al. Among authors: olson tm. Hum Mol Genet. 2014 Nov 1;23(21):5793-804. doi: 10.1093/hmg/ddu297. Epub 2014 Jun 11. Hum Mol Genet. 2014. PMID: 24925317 Free PMC article.

5

Characterizing genetic variation of adrenergic signalling pathways in Takotsubo (stress) cardiomyopathy exomes.

Goodloe AH, Evans JM, Middha S, Prasad A, Olson TM. Goodloe AH, et al. Among authors: olson tm. Eur J Heart Fail. 2014 Sep;16(9):942-9. doi: 10.1002/ejhf.145. Epub 2014 Aug 8. Eur J Heart Fail. 2014. PMID: 25132214 Free article.

6

Regenerative therapy for hypoplastic left heart syndrome: first report of intraoperative intramyocardial injection of autologous umbilical-cord blood-derived cells.

Burkhart HM, Qureshi MY, Peral SC, O'Leary PW, Olson TM, Cetta F, Nelson TJ; Wanek Program Clinical Pipeline Group. Burkhart HM, et al. Among authors: olson tm. J Thorac Cardiovasc Surg. 2015 Mar;149(3):e35-7. doi: 10.1016/j.jtcvs.2014.10.093. Epub 2014 Oct 24. J Thorac Cardiovasc Surg. 2015. PMID: 25466856 Free article. No abstract available.

7

Exome sequencing establishes diagnosis of Alström syndrome in an infant presenting with non-syndromic dilated cardiomyopathy.

Long PA, Evans JM, Olson TM. Long PA, et al. Among authors: olson tm. Am J Med Genet A. 2015 Apr;167A(4):886-90. doi: 10.1002/ajmg.a.36994. Epub 2015 Feb 23. Am J Med Genet A. 2015. PMID: 25706677 Free PMC article.

8

Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.

Theis JL, Zimmermann MT, Evans JM, Eckloff BW, Wieben ED, Qureshi MY, O'Leary PW, Olson TM. Theis JL, et al. Among authors: olson tm. Circ Cardiovasc Genet. 2015 Aug;8(4):564-71. doi: 10.1161/CIRCGENETICS.115.001070. Epub 2015 Jun 17. Circ Cardiovasc Genet. 2015. PMID: 26085007

9

Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.

Theis JL, Hrstka SC, Evans JM, O'Byrne MM, de Andrade M, O'Leary PW, Nelson TJ, Olson TM. Theis JL, et al. Among authors: olson tm. Hum Genet. 2015 Sep;134(9):1003-11. doi: 10.1007/s00439-015-1582-1. Epub 2015 Jul 12. Hum Genet. 2015. PMID: 26164125

10

Familial Incidence of Cardiovascular Malformations in Hypoplastic Left Heart Syndrome.

Kelle AM, Qureshi MY, Olson TM, Eidem BW, O'Leary PW. Kelle AM, et al. Among authors: olson tm. Am J Cardiol. 2015 Dec 1;116(11):1762-6. doi: 10.1016/j.amjcard.2015.08.045. Epub 2015 Sep 10. Am J Cardiol. 2015. PMID: 26433269

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