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Items: 1 to 20 of 81


Reproductive Decision Making and Genetic Predisposition to Sudden Cardiac Death.

Barlevy D, Wasserman D, Stolerman M, Erskine KE, Dolan SM.

AJOB Prim Res. 2012 Jul 1;3(3):30-39. Epub 2012 Jun 19.


Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.

Earle N, Yeo Han D, Pilbrow A, Crawford J, Smith W, Shelling AN, Cameron V, Love DR, Skinner JR.

Heart Rhythm. 2014 Jan;11(1):76-82. doi: 10.1016/j.hrthm.2013.10.005. Epub 2013 Oct 3.


Reproductive decision-making in young female carriers of a BRCA mutation.

Donnelly LS, Watson M, Moynihan C, Bancroft E, Evans DG, Eeles R, Lavery S, Ormondroyd E.

Hum Reprod. 2013 Apr;28(4):1006-12. doi: 10.1093/humrep/des441. Epub 2013 Jan 4.


Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.

Tester DJ, Ackerman MJ.

J Am Coll Cardiol. 2007 Jan 16;49(2):240-6. Epub 2006 Dec 29.


Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer.

Derks-Smeets IA, Gietel-Habets JJ, Tibben A, Tjan-Heijnen VC, Meijer-Hoogeveen M, Geraedts JP, van Golde R, Gomez-Garcia E, van den Bogaart E, van Hooijdonk M, de Die-Smulders CE, van Osch LA.

Hum Reprod. 2014 May;29(5):1103-12. doi: 10.1093/humrep/deu034. Epub 2014 Mar 6.


Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.

Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK.

Heart Rhythm. 2013 Nov;10(11):1653-60. doi: 10.1016/j.hrthm.2013.08.022. Epub 2013 Aug 22.


Attitudes to reproductive genetic testing in women who had a positive BRCA test before having children: a qualitative analysis.

Ormondroyd E, Donnelly L, Moynihan C, Savona C, Bancroft E, Evans DG, Eeles R, Lavery S, Watson M.

Eur J Hum Genet. 2012 Jan;20(1):4-10. doi: 10.1038/ejhg.2011.146. Epub 2011 Aug 3.


[Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age].

Akkerhuis JM, Baars HF, Marcelis CL, Akkerhuis KM, Wilde AA.

Ned Tijdschr Geneeskd. 2007 Oct 27;151(43):2357-64. Dutch.


Motivation to pursue genetic testing in individuals with a personal or family history of cardiac events or sudden cardiac death.

Erskine KE, Hidayatallah NZ, Walsh CA, McDonald TV, Cohen L, Marion RW, Dolan SM.

J Genet Couns. 2014 Oct;23(5):849-59. doi: 10.1007/s10897-014-9707-6. Epub 2014 Mar 25.


Genetic screening in sudden cardiac death in the young can save future lives.

Stattin EL, Westin IM, Cederquist K, Jonasson J, Jonsson BA, Mörner S, Norberg A, Krantz P, Wisten A.

Int J Legal Med. 2016 Jan;130(1):59-66. doi: 10.1007/s00414-015-1237-8. Epub 2015 Jul 31.


Association between pacifier use and breast-feeding, sudden infant death syndrome, infection and dental malocclusion.

Callaghan A, Kendall G, Lock C, Mahony A, Payne J, Verrier L.

JBI Libr Syst Rev. 2005;3(6):1-33.


Experiential knowledge of disability, impairment and illness: The reproductive decisions of families genetically at risk.

Boardman F.

Health (London). 2014 Sep;18(5):476-92. doi: 10.1177/1363459313507588. Epub 2013 Nov 6.


Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.

Hobbs JB, Peterson DR, Moss AJ, McNitt S, Zareba W, Goldenberg I, Qi M, Robinson JL, Sauer AJ, Ackerman MJ, Benhorin J, Kaufman ES, Locati EH, Napolitano C, Priori SG, Towbin JA, Vincent GM, Zhang L.

JAMA. 2006 Sep 13;296(10):1249-54.


The sudden infant death syndrome gene: does it exist?

Opdal SH, Rognum TO.

Pediatrics. 2004 Oct;114(4):e506-12.


Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.

Khositseth A, Tester DJ, Will ML, Bell CM, Ackerman MJ.

Heart Rhythm. 2004 May;1(1):60-4.


Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.

Tester DJ, Benton AJ, Train L, Deal B, Baudhuin LM, Ackerman MJ.

Am J Cardiol. 2010 Oct 15;106(8):1124-8. doi: 10.1016/j.amjcard.2010.06.022.


A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome.

Riuró H, Campuzano O, Arbelo E, Iglesias A, Batlle M, Pérez-Villa F, Brugada J, Pérez GJ, Scornik FS, Brugada R.

Heart Rhythm. 2014 Jul;11(7):1202-9. doi: 10.1016/j.hrthm.2014.03.044. Epub 2014 Mar 21.


Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.

Horigome H, Nagashima M, Sumitomo N, Yoshinaga M, Ushinohama H, Iwamoto M, Shiono J, Ichihashi K, Hasegawa S, Yoshikawa T, Matsunaga T, Goto H, Waki K, Arima M, Takasugi H, Tanaka Y, Tauchi N, Ikoma M, Inamura N, Takahashi H, Shimizu W, Horie M.

Circ Arrhythm Electrophysiol. 2010 Feb;3(1):10-7. doi: 10.1161/CIRCEP.109.882159. Epub 2009 Dec 8. Erratum in: Circ Arrhythm Electrophysiol. 2012 Dec;5(6):e120-2.


KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.

Chen S, Zhang L, Bryant RM, Vincent GM, Flippin M, Lee JC, Brown E, Zimmerman F, Rozich R, Szafranski P, Oberti C, Sterba R, Marangi D, Tchou PJ, Chung MK, Wang Q.

Clin Genet. 2003 Apr;63(4):273-82.

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