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Items: 1 to 20 of 86

1.

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.

Meder B, Rühle F, Weis T, Homuth G, Keller A, Franke J, Peil B, Lorenzo Bermejo J, Frese K, Huge A, Witten A, Vogel B, Haas J, Völker U, Ernst F, Teumer A, Ehlermann P, Zugck C, Friedrichs F, Kroemer H, Dörr M, Hoffmann W, Maisch B, Pankuweit S, Ruppert V, Scheffold T, Kühl U, Schultheiss HP, Kreutz R, Ertl G, Angermann C, Charron P, Villard E, Gary F, Isnard R, Komajda M, Lutz M, Meitinger T, Sinner MF, Wichmann HE, Krawczak M, Ivandic B, Weichenhan D, Gelbrich G, El-Mokhtari NE, Schreiber S, Felix SB, Hasenfuß G, Pfeufer A, Hübner N, Kääb S, Arbustini E, Rottbauer W, Frey N, Stoll M, Katus HA.

Eur Heart J. 2014 Apr;35(16):1069-77. doi: 10.1093/eurheartj/eht251. Epub 2013 Jul 12.

PMID:
23853074
2.

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.

Villard E, Perret C, Gary F, Proust C, Dilanian G, Hengstenberg C, Ruppert V, Arbustini E, Wichter T, Germain M, Dubourg O, Tavazzi L, Aumont MC, DeGroote P, Fauchier L, Trochu JN, Gibelin P, Aupetit JF, Stark K, Erdmann J, Hetzer R, Roberts AM, Barton PJ, Regitz-Zagrosek V; Cardiogenics Consortium., Aslam U, Duboscq-Bidot L, Meyborg M, Maisch B, Madeira H, Waldenström A, Galve E, Cleland JG, Dorent R, Roizes G, Zeller T, Blankenberg S, Goodall AH, Cook S, Tregouet DA, Tiret L, Isnard R, Komajda M, Charron P, Cambien F.

Eur Heart J. 2011 May;32(9):1065-76. doi: 10.1093/eurheartj/ehr105. Epub 2011 Apr 1.

3.
4.

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy.

Stark K, Esslinger UB, Reinhard W, Petrov G, Winkler T, Komajda M, Isnard R, Charron P, Villard E, Cambien F, Tiret L, Aumont MC, Dubourg O, Trochu JN, Fauchier L, Degroote P, Richter A, Maisch B, Wichter T, Zollbrecht C, Grassl M, Schunkert H, Linsel-Nitschke P, Erdmann J, Baumert J, Illig T, Klopp N, Wichmann HE, Meisinger C, Koenig W, Lichtner P, Meitinger T, Schillert A, König IR, Hetzer R, Heid IM, Regitz-Zagrosek V, Hengstenberg C.

PLoS Genet. 2010 Oct 21;6(10):e1001167. doi: 10.1371/journal.pgen.1001167.

5.

The HLA class II allele DQB1 0309 is associated with dilated cardiomyopathy.

Pankuweit S, Ruppert V, Jónsdóttir T, Müller HH, Meyer T; German Competence Network of Heart Failure..

Gene. 2013 Dec 1;531(2):180-3. doi: 10.1016/j.gene.2013.09.022. Epub 2013 Sep 16.

PMID:
24050898
6.

Multiple Loci are associated with dilated cardiomyopathy in Irish wolfhounds.

Philipp U, Vollmar A, Häggström J, Thomas A, Distl O.

PLoS One. 2012;7(6):e36691. doi: 10.1371/journal.pone.0036691. Epub 2012 Jun 25.

7.

Inflammatory dilated cardiomyopathy (DCMI).

Maisch B, Richter A, Sandmöller A, Portig I, Pankuweit S; BMBF-Heart Failure Network..

Herz. 2005 Sep;30(6):535-44. Review.

PMID:
16170686
8.

Polymorphisms of presenilin-1 gene associate with dilated cardiomyopathy susceptibility.

Li H, Chen Y, Zhou B, Peng Y, Sheng Y, Rao L.

Mol Cell Biochem. 2011 Dec;358(1-2):31-6. doi: 10.1007/s11010-011-0916-0. Epub 2011 Jun 8.

PMID:
21656036
9.

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers.

Mausberg TB, Wess G, Simak J, Keller L, Drögemüller M, Drögemüller C, Webster MT, Stephenson H, Dukes-McEwan J, Leeb T.

PLoS One. 2011;6(5):e20042. doi: 10.1371/journal.pone.0020042. Epub 2011 May 20.

10.

Polymorphisms in genes encoding nonsarcomeric proteins and their role in the pathogenesis of dilated cardiomyopathy.

Staab J, Ruppert V, Pankuweit S, Meyer T.

Herz. 2012 Dec;37(8):836-41. doi: 10.1007/s00059-012-3698-6. Review.

PMID:
23188159
11.

Association of the LMNA gene single nucleotide polymorphism rs4641 with bdilated cardiomyopathy.

Yin J, Yang J, Ren FX, Sun CM, Li LD, Han LY, Cai SL, Zhang CH, Zhang ZQ, Zhang ZT, Wang H.

Genet Mol Res. 2015 Nov 30;14(4):15427-34. doi: 10.4238/2015.November.30.20.

12.

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.

Slager SL, Rabe KG, Achenbach SJ, Vachon CM, Goldin LR, Strom SS, Lanasa MC, Spector LG, Rassenti LZ, Leis JF, Camp NJ, Glenn M, Kay NE, Cunningham JM, Hanson CA, Marti GE, Weinberg JB, Morrison VA, Link BK, Call TG, Caporaso NE, Cerhan JR.

Blood. 2011 Feb 10;117(6):1911-6. doi: 10.1182/blood-2010-09-308205. Epub 2010 Dec 3.

13.

TNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han Chinese.

Li YD, Ji YT, Zhou XH, Li HL, Zhang HT, Xing Q, Hong YF, Tang BP.

Med Sci Monit. 2015 Nov 3;21:3343-7.

14.

Analysis of IL-17 gene polymorphisms in Chinese patients with dilated cardiomyopathy.

Peng Y, Zhou B, Wang YY, Shi S, Zhang K, Zhang L, Rao L.

Hum Immunol. 2013 May;74(5):635-9. doi: 10.1016/j.humimm.2013.01.019. Epub 2013 Jan 31.

PMID:
23376081
15.

Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population.

Li X, Luo R, Mo X, Jiang R, Kong H, Hua W, Wu X.

Eur J Med Res. 2013 Apr 9;18:10. doi: 10.1186/2047-783X-18-10.

16.

Genome-environment interactions in the molecular pathogenesis of dilated cardiomyopathy.

Poller W, Kühl U, Tschoepe C, Pauschinger M, Fechner H, Schultheiss HP.

J Mol Med (Berl). 2005 Aug;83(8):579-86. Epub 2005 Jun 2. Review.

PMID:
15931504
17.

Relationship between dilated cardiomyopathy and the E23K and I337V polymorphisms in the Kir6.2 subunit of the KATP channel.

Xi HL, Liu JF, Li L, Wan J.

Genet Mol Res. 2013 Oct 10;12(4):4383-92. doi: 10.4238/2013.October.10.4.

18.

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

Schönberger J, Levy H, Grünig E, Sangwatanaroj S, Fatkin D, MacRae C, Stäcker H, Halpin C, Eavey R, Philbin EF, Katus H, Seidman JG, Seidman CE.

Circulation. 2000 Apr 18;101(15):1812-8.

19.

[Familial dilated cardiomyopathy].

Osterziel KJ, Hassfeld S, Geier C, Perrot A.

Herz. 2005 Sep;30(6):529-34. Review. German.

PMID:
16170685
20.

Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy.

Ruppert V, Meyer T, Struwe C, Petersen J, Perrot A, Posch MG, Ozcelik C, Richter A, Maisch B, Pankuweit S; German Heart Failure Network..

Eur J Hum Genet. 2010 Jun;18(6):694-9. doi: 10.1038/ejhg.2010.3. Epub 2010 Feb 10.

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