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Items: 1 to 50 of 95

1.

Model system identification of novel congenital heart disease gene candidates: focus on RPL13.

Schroeder AM, Allahyari M, Vogler G, Missinato MA, Nielsen T, Yu MS, Theis JL, Larsen LA, Goyal P, Rosenfeld JA, Nelson TJ, Olson TM, Colas AR, Grossfeld P, Bodmer R.

Hum Mol Genet. 2019 Dec 1;28(23):3954-3969. doi: 10.1093/hmg/ddz213.

PMID:
31625562
2.

Hypoplastic Left Heart Syndrome: An Overview for Primary Care Providers.

Javed R, Cetta F, Said SM, Olson TM, O'Leary PW, Qureshi MY.

Pediatr Rev. 2019 Jul;40(7):344-353. doi: 10.1542/pir.2018-0005. Review.

PMID:
31263042
3.

Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.

Turley TN, Theis JL, Sundsbak RS, Evans JM, O'Byrne MM, Gulati R, Tweet MS, Hayes SN, Olson TM.

Circ Genom Precis Med. 2019 Apr;12(4):e002437. doi: 10.1161/CIRCGEN.118.002437. Epub 2019 Mar 19.

PMID:
30888838
4.

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.

Adlam D, Olson TM, Combaret N, Kovacic JC, Iismaa SE, Al-Hussaini A, O'Byrne MM, Bouajila S, Georges A, Mishra K, Braund PS, d'Escamard V, Huang S, Margaritis M, Nelson CP, de Andrade M, Kadian-Dodov D, Welch CA, Mazurkiewicz S, Jeunemaitre X; DISCO Consortium, Wong CMY, Giannoulatou E, Sweeting M, Muller D, Wood A, McGrath-Cadell L, Fatkin D, Dunwoodie SL, Harvey R, Holloway C, Empana JP, Jouven X; CARDIoGRAMPlusC4D Study Group, Olin JW, Gulati R, Tweet MS, Hayes SN, Samani NJ, Graham RM, Motreff P, Bouatia-Naji N.

J Am Coll Cardiol. 2019 Jan 8;73(1):58-66. doi: 10.1016/j.jacc.2018.09.085.

5.

Cell-Based Therapy for Myocardial Dysfunction After Fontan Operation in Hypoplastic Left Heart Syndrome.

Qureshi MY, Cabalka AK, Khan SP, Hagler DJ, Haile DT, Cannon BC, Olson TM, Cantero-Peral S, Dietz AB, Radel DJ, Taggart NW, Kelle AM, Rodriguez V, Dearani JA, O'Leary PW; Wanek Program Regenerative Medicine Pipeline.

Mayo Clin Proc Innov Qual Outcomes. 2017 Aug 2;1(2):185-191. doi: 10.1016/j.mayocpiqo.2017.07.002. eCollection 2017 Sep.

6.

Idiopathic Restrictive Cardiomyopathy in Children and Young Adults.

Anderson HN, Cetta F, Driscoll DJ, Olson TM, Ackerman MJ, Johnson JN.

Am J Cardiol. 2018 May 15;121(10):1266-1270. doi: 10.1016/j.amjcard.2018.01.045. Epub 2018 Feb 12.

PMID:
29526277
7.

Pediatric Dilated Cardiomyopathy-Associated LRRC10 (Leucine-Rich Repeat-Containing 10) Variant Reveals LRRC10 as an Auxiliary Subunit of Cardiac L-Type Ca2+ Channels.

Woon MT, Long PA, Reilly L, Evans JM, Keefe AM, Lea MR, Beglinger CJ, Balijepalli RC, Lee Y, Olson TM, Kamp TJ.

J Am Heart Assoc. 2018 Feb 3;7(3). pii: e006428. doi: 10.1161/JAHA.117.006428.

8.

Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy.

Long PA, Evans JM, Olson TM.

J Cardiovasc Dev Dis. 2017 Aug 8;4(3). pii: E11. doi: 10.3390/jcdd4030011.

9.

Biofilms in Full-Scale Drinking Water Ozone Contactors Contribute Viable Bacteria to Ozonated Water.

Kotlarz N, Rockey N, Olson TM, Haig SJ, Sanford L, LiPuma JJ, Raskin L.

Environ Sci Technol. 2018 Mar 6;52(5):2618-2628. doi: 10.1021/acs.est.7b04212. Epub 2018 Feb 13.

PMID:
29299927
10.

Characteristic Morphologies of the Bicuspid Aortic Valve in Patients with Genetic Syndromes.

Niaz T, Poterucha JT, Olson TM, Johnson JN, Craviari C, Nienaber T, Palfreeman J, Cetta F, Hagler DJ.

J Am Soc Echocardiogr. 2018 Feb;31(2):194-200. doi: 10.1016/j.echo.2017.10.008. Epub 2017 Nov 28.

PMID:
29191731
11.

Degradation of Extracellular Antibiotic Resistance Genes with UV254 Treatment.

Chang PH, Juhrend B, Olson TM, Marrs CF, Wigginton KR.

Environ Sci Technol. 2017 Jun 6;51(11):6185-6192. doi: 10.1021/acs.est.7b01120. Epub 2017 May 15.

PMID:
28475324
12.

Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy.

Long PA, Theis JL, Shih YH, Maleszewski JJ, Abell Aleff PC, Evans JM, Xu X, Olson TM.

Hum Mol Genet. 2017 Aug 1;26(15):2874-2881. doi: 10.1093/hmg/ddx169.

13.

A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene.

Ding Y, Long PA, Bos JM, Shih YH, Ma X, Sundsbak RS, Chen J, Jiang Y, Zhao L, Hu X, Wang J, Shi Y, Ackerman MJ, Lin X, Ekker SC, Redfield MM, Olson TM, Xu X.

JCI Insight. 2017 Apr 20;2(8). pii: 94086. doi: 10.1172/jci.insight.94086. eCollection 2017 Apr 20. No abstract available.

14.

gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.

Larson NB, McDonnell S, Cannon Albright L, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson JE, Cussenot O, Cancel-Tassin G, Giles GG, MacInnis RJ, Maier C, Whittemore AS, Hsieh CL, Wiklund F, Catalona WJ, Foulkes W, Mandal D, Eeles R, Kote-Jarai Z, Ackerman MJ, Olson TM, Klein CJ, Thibodeau SN, Schaid DJ.

Genet Epidemiol. 2017 May;41(4):297-308. doi: 10.1002/gepi.22036. Epub 2017 Feb 16. Erratum in: Genet Epidemiol. 2017 Nov;41(7):710.

15.

A breakthrough in spontaneous coronary artery dissection pathogenesis: is it an inherited condition?

Kanwar SS, Hayes SN, Olson TM, Gulati R.

Expert Rev Cardiovasc Ther. 2017 Jan;15(1):1-2. Epub 2016 Dec 14. No abstract available.

PMID:
27960566
16.

A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene.

Ding Y, Long PA, Bos JM, Shih YH, Ma X, Sundsbak RS, Chen J, Jiang Y, Zhao L, Hu X, Wang J, Shi Y, Ackerman MJ, Lin X, Ekker SC, Redfield MM, Olson TM, Xu X.

JCI Insight. 2016 Sep 8;1(14). pii: e88797. Erratum in: JCI Insight. 2017 Apr 20;2(8):.

17.

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.

Larson NB, McDonnell S, Albright LC, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson J, Cussenot O, Cancel-Tassin G, Giles G, MacInnis R, Maier C, Whittemore AS, Hsieh CL, Wiklund F, Catalona WJ, Foulkes W, Mandal D, Eeles R, Kote-Jarai Z, Ackerman MJ, Olson TM, Klein CJ, Thibodeau SN, Schaid DJ.

Genet Epidemiol. 2016 Sep;40(6):461-9. doi: 10.1002/gepi.21983. Epub 2016 Jun 17. Erratum in: Genet Epidemiol. 2017 Nov;41(7):710.

18.

De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.

Long PA, Zimmermann MT, Kim M, Evans JM, Xu X, Olson TM.

Hum Genet. 2016 Aug;135(8):909-917. doi: 10.1007/s00439-016-1685-3. Epub 2016 May 27.

19.

Ebstein anomaly, left ventricular non-compaction, and early onset heart failure associated with a de novo α-tropomyosin gene mutation.

Kelle AM, Bentley SJ, Rohena LO, Cabalka AK, Olson TM.

Am J Med Genet A. 2016 Aug;170(8):2186-90. doi: 10.1002/ajmg.a.37745. Epub 2016 May 13.

PMID:
27177193
20.

Pharmacological Modulation of Calcium Homeostasis in Familial Dilated Cardiomyopathy: An In Vitro Analysis From an RBM20 Patient-Derived iPSC Model.

Wyles SP, Hrstka SC, Reyes S, Terzic A, Olson TM, Nelson TJ.

Clin Transl Sci. 2016 Jun;9(3):158-67. doi: 10.1111/cts.12393. Epub 2016 Apr 22.

21.

Modeling GATAD1-Associated Dilated Cardiomyopathy in Adult Zebrafish.

Yang J, Shah S, Olson TM, Xu X.

J Cardiovasc Dev Dis. 2016 Mar;3(1). pii: 6. doi: 10.3390/jcdd3010006. Epub 2016 Jan 26.

22.

Spontaneous coronary artery dissection and its association with heritable connective tissue disorders.

Henkin S, Negrotto SM, Tweet MS, Kirmani S, Deyle DR, Gulati R, Olson TM, Hayes SN.

Heart. 2016 Jun 1;102(11):876-81. doi: 10.1136/heartjnl-2015-308645. Epub 2016 Feb 10.

PMID:
26864667
23.

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.

Long PA, Larsen BT, Evans JM, Olson TM.

J Am Heart Assoc. 2015 Dec 9;4(12). pii: e002443. doi: 10.1161/JAHA.115.002443.

24.

LRRC10 is required to maintain cardiac function in response to pressure overload.

Brody MJ, Feng L, Grimes AC, Hacker TA, Olson TM, Kamp TJ, Balijepalli RC, Lee Y.

Am J Physiol Heart Circ Physiol. 2016 Jan 15;310(2):H269-78. doi: 10.1152/ajpheart.00717.2014. Epub 2015 Nov 25.

25.

Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.

Wyles SP, Li X, Hrstka SC, Reyes S, Oommen S, Beraldi R, Edwards J, Terzic A, Olson TM, Nelson TJ.

Hum Mol Genet. 2016 Jan 15;25(2):254-65. doi: 10.1093/hmg/ddv468. Epub 2015 Nov 24.

26.

Familial Incidence of Cardiovascular Malformations in Hypoplastic Left Heart Syndrome.

Kelle AM, Qureshi MY, Olson TM, Eidem BW, O'Leary PW.

Am J Cardiol. 2015 Dec 1;116(11):1762-6. doi: 10.1016/j.amjcard.2015.08.045. Epub 2015 Sep 10.

PMID:
26433269
27.

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.

Hum Genet. 2015 Sep;134(9):1003-11. doi: 10.1007/s00439-015-1582-1. Epub 2015 Jul 12.

PMID:
26164125
28.

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.

Circ Cardiovasc Genet. 2015 Aug;8(4):564-71. doi: 10.1161/CIRCGENETICS.115.001070. Epub 2015 Jun 17.

PMID:
26085007
29.

Familial spontaneous coronary artery dissection: evidence for genetic susceptibility.

Goel K, Tweet M, Olson TM, Maleszewski JJ, Gulati R, Hayes SN.

JAMA Intern Med. 2015 May;175(5):821-6. doi: 10.1001/jamainternmed.2014.8307.

PMID:
25798899
30.

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

Long PA, Evans JM, Olson TM.

Am J Med Genet A. 2015 Apr;167A(4):886-90. doi: 10.1002/ajmg.a.36994. Epub 2015 Feb 23.

31.

Cardiac transcriptome and dilated cardiomyopathy genes in zebrafish.

Shih YH, Zhang Y, Ding Y, Ross CA, Li H, Olson TM, Xu X.

Circ Cardiovasc Genet. 2015 Apr;8(2):261-9. doi: 10.1161/CIRCGENETICS.114.000702. Epub 2015 Jan 11.

32.

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.

J Thorac Cardiovasc Surg. 2015 Mar;149(3):e35-7. doi: 10.1016/j.jtcvs.2014.10.093. Epub 2014 Oct 24. No abstract available.

33.

Circulating atrial natriuretic peptide genetic association study identifies a novel gene cluster associated with stroke in whites.

Pereira NL, Tosakulwong N, Scott CG, Jenkins GD, Prodduturi N, Chai Y, Olson TM, Rodeheffer RJ, Redfield MM, Weinshilboum RM, Burnett JC.

Circ Cardiovasc Genet. 2015 Feb;8(1):141-9. doi: 10.1161/CIRCGENETICS.114.000624. Epub 2014 Dec 1.

34.

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

Goodloe AH, Evans JM, Middha S, Prasad A, Olson TM.

Eur J Heart Fail. 2014 Sep;16(9):942-9. doi: 10.1002/ejhf.145. Epub 2014 Aug 8.

35.

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.

Hum Mol Genet. 2014 Nov 1;23(21):5793-804. doi: 10.1093/hmg/ddu297. Epub 2014 Jun 11.

36.

Transcriptional atlas of cardiogenesis maps congenital heart disease interactome.

Li X, Martinez-Fernandez A, Hartjes KA, Kocher JP, Olson TM, Terzic A, Nelson TJ.

Physiol Genomics. 2014 Jul 1;46(13):482-95. doi: 10.1152/physiolgenomics.00015.2014. Epub 2014 May 6.

37.

Rbm20-deficient cardiogenesis reveals early disruption of RNA processing and sarcomere remodeling establishing a developmental etiology for dilated cardiomyopathy.

Beraldi R, Li X, Martinez Fernandez A, Reyes S, Secreto F, Terzic A, Olson TM, Nelson TJ.

Hum Mol Genet. 2014 Jul 15;23(14):3779-91. doi: 10.1093/hmg/ddu091. Epub 2014 Feb 28.

38.

A functional genetic variant (N521D) in natriuretic peptide receptor 3 is associated with diastolic dysfunction: the prevalence of asymptomatic ventricular dysfunction study.

Pereira NL, Redfield MM, Scott C, Tosakulwong N, Olson TM, Bailey KR, Rodeheffer RJ, Burnett JC Jr.

PLoS One. 2014 Jan 22;9(1):e85708. doi: 10.1371/journal.pone.0085708. eCollection 2014.

39.

Atrial natriuretic peptide genetic variant rs5065 and risk for cardiovascular disease in the general community: a 9-year follow-up study.

Cannone V, Huntley BK, Olson TM, Heublein DM, Scott CG, Bailey KR, Redfield MM, Rodeheffer RJ, Burnett JC Jr.

Hypertension. 2013 Nov;62(5):860-5. doi: 10.1161/HYPERTENSIONAHA.113.01344. Epub 2013 Sep 16.

40.

Late outcomes for surgical repair of supravalvar aortic stenosis.

Deo SV, Burkhart HM, Schaff HV, Li Z, Stensrud PE, Olson TM, Connolly HM, Dearani JA.

Ann Thorac Surg. 2012 Sep;94(3):854-9. doi: 10.1016/j.athoracsur.2012.04.022. Epub 2012 Jun 22.

PMID:
22727249
41.

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.

Circ Cardiovasc Genet. 2011 Dec;4(6):585-94. doi: 10.1161/CIRCGENETICS.111.961052. Epub 2011 Sep 30.

42.

Advances in cardiac ATP-sensitive K+ channelopathies from molecules to populations.

Terzic A, Alekseev AE, Yamada S, Reyes S, Olson TM.

Circ Arrhythm Electrophysiol. 2011 Aug;4(4):577-85. doi: 10.1161/CIRCEP.110.957662. No abstract available.

43.

A genetic variant of the atrial natriuretic peptide gene is associated with cardiometabolic protection in the general community.

Cannone V, Boerrigter G, Cataliotti A, Costello-Boerrigter LC, Olson TM, McKie PM, Heublein DM, Lahr BD, Bailey KR, Averna M, Redfield MM, Rodeheffer RJ, Burnett JC Jr.

J Am Coll Cardiol. 2011 Aug 2;58(6):629-36. doi: 10.1016/j.jacc.2011.05.011.

44.

Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillation.

Goodloe AH, Herron KJ, Olson TM.

Am J Cardiol. 2011 Jun 15;107(12):1802-5. doi: 10.1016/j.amjcard.2011.02.326. Epub 2011 Apr 8.

PMID:
21481830
45.

The effect of the brain-type natriuretic peptide single-nucleotide polymorphism rs198389 on test characteristics of common assays.

Costello-Boerrigter LC, Boerrigter G, Ameenuddin S, Mahoney DW, Slusser JP, Heublein DM, Redfield MM, Rodeheffer RJ, Olson TM, Burnett JC Jr.

Mayo Clin Proc. 2011 Mar;86(3):210-8. doi: 10.4065/mcp.2010.0708. Erratum in: Mayo Clin Proc. 2011 May;86(5):469.

46.

Human K(ATP) channelopathies: diseases of metabolic homeostasis.

Olson TM, Terzic A.

Pflugers Arch. 2010 Jul;460(2):295-306. doi: 10.1007/s00424-009-0771-y. Epub 2009 Dec 24. Review.

47.

Life-cycle case study comparison of permeable reactive barrier versus pump-and-treat remediation.

Higgins MR, Olson TM.

Environ Sci Technol. 2009 Dec 15;43(24):9432-8. doi: 10.1021/es9015537.

PMID:
20000540
48.

Investigating genetic variation of adrenergic receptors in familial stress cardiomyopathy (apical ballooning syndrome).

Handy AD, Prasad A, Olson TM.

J Cardiol. 2009 Dec;54(3):516-7. doi: 10.1016/j.jjcc.2009.08.008. Epub 2009 Oct 12. No abstract available.

49.

A human atrial natriuretic peptide gene mutation reveals a novel peptide with enhanced blood pressure-lowering, renal-enhancing, and aldosterone-suppressing actions.

McKie PM, Cataliotti A, Huntley BK, Martin FL, Olson TM, Burnett JC Jr.

J Am Coll Cardiol. 2009 Sep 8;54(11):1024-32. doi: 10.1016/j.jacc.2009.04.080.

50.

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.

Brauch KM, Karst ML, Herron KJ, de Andrade M, Pellikka PA, Rodeheffer RJ, Michels VV, Olson TM.

J Am Coll Cardiol. 2009 Sep 1;54(10):930-41. doi: 10.1016/j.jacc.2009.05.038.

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