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Items: 18

1.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Z├╝chner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE.

Am J Hum Genet. 2011 Mar 11;88(3):273-82. doi: 10.1016/j.ajhg.2011.01.016. Epub 2011 Feb 25.

2.

Genetic evaluation of dilated cardiomyopathy.

Morales A, Hershberger RE.

Curr Cardiol Rep. 2013 Jul;15(7):375. doi: 10.1007/s11886-013-0375-1. Review.

PMID:
23686784
3.

[Genetics of dilated cardiomyopathy].

Osterziel KJ, Scheffold T, Perrot A, Dietz R; Netzwerk Myokardiale Erkrankungen..

Z Kardiol. 2001 Jul;90(7):461-9. Review. German.

PMID:
11515275
4.

BAG3: a new player in the heart failure paradigm.

Knezevic T, Myers VD, Gordon J, Tilley DG, Sharp TE 3rd, Wang J, Khalili K, Cheung JY, Feldman AM.

Heart Fail Rev. 2015 Jul;20(4):423-34. doi: 10.1007/s10741-015-9487-6. Review.

5.

Dilated cardiomyopathy: the complexity of a diverse genetic architecture.

Hershberger RE, Hedges DJ, Morales A.

Nat Rev Cardiol. 2013 Sep;10(9):531-47. doi: 10.1038/nrcardio.2013.105. Epub 2013 Jul 30. Review.

PMID:
23900355
6.

Where genome meets phenome: rationale for integrating genetic and protein biomarkers in the diagnosis and management of dilated cardiomyopathy and heart failure.

Piran S, Liu P, Morales A, Hershberger RE.

J Am Coll Cardiol. 2012 Jul 24;60(4):283-9. doi: 10.1016/j.jacc.2012.05.005. Review.

7.

Genetics and genomics of dilated cardiomyopathy and systolic heart failure.

Tayal U, Prasad S, Cook SA.

Genome Med. 2017 Feb 22;9(1):20. doi: 10.1186/s13073-017-0410-8. Review.

8.

Genomic approaches for the discovery of genes mutated in inherited retinal degeneration.

Siemiatkowska AM, Collin RW, den Hollander AI, Cremers FP.

Cold Spring Harb Perspect Med. 2014 Jun 17;4(8). pii: a017137. doi: 10.1101/cshperspect.a017137. Review.

9.

Exome sequencing: a transformative technology.

Singleton AB.

Lancet Neurol. 2011 Oct;10(10):942-6. doi: 10.1016/S1474-4422(11)70196-X. Review.

10.

[Genetic factors of the development of dilated cardiomyopathy].

Lushnikova EL, Nepomniashchikh LM.

Vestn Ross Akad Med Nauk. 2006;(7):43-52. Review. Russian.

PMID:
16924878
11.

Genetics and genetic testing of dilated cardiomyopathy: a new perspective.

Mestroni L, Taylor MR.

Discov Med. 2013 Jan;15(80):43-9. Review.

12.

Complex genetics and the etiology of human congenital heart disease.

Gelb BD, Chung WK.

Cold Spring Harb Perspect Med. 2014 Jul 1;4(7):a013953. doi: 10.1101/cshperspect.a013953. Review.

13.

Whole exome sequencing of intracranial aneurysm.

Foroud T; FIA Study Investigators..

Stroke. 2013 Jun;44(6 Suppl 1):S26-8. doi: 10.1161/STROKEAHA.113.001174. Review. No abstract available.

14.

Statistical analysis strategies for association studies involving rare variants.

Bansal V, Libiger O, Torkamani A, Schork NJ.

Nat Rev Genet. 2010 Nov;11(11):773-85. doi: 10.1038/nrg2867. Epub 2010 Oct 13. Review.

15.

Advancing epilepsy genetics in the genomic era.

Myers CT, Mefford HC.

Genome Med. 2015 Aug 25;7:91. doi: 10.1186/s13073-015-0214-7. Review.

16.

What can we learn about lipoprotein metabolism and coronary heart disease from studying rare variants?

Jeff JM, Peloso GM, Do R.

Curr Opin Lipidol. 2016 Apr;27(2):99-104. doi: 10.1097/MOL.0000000000000277. Review.

PMID:
26844526
17.

Context and Applications of Targeted Genetic Testing, with Emphasis on Copy Number Variants.

Ahn JW, Ogilvie C.

Adv Clin Chem. 2016;75:33-51. doi: 10.1016/bs.acc.2016.03.004. Epub 2016 Apr 20. Review.

PMID:
27346615
18.

Interpreting human genetic variation with in vivo zebrafish assays.

Davis EE, Frangakis S, Katsanis N.

Biochim Biophys Acta. 2014 Oct;1842(10):1960-1970. doi: 10.1016/j.bbadis.2014.05.024. Epub 2014 Jun 2. Review.

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