Genetics of common forms of heart failure: challenges and potential solutions

scientific article published on May 2015

Genetics of common forms of heart failure: challenges and potential solutions is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1097/HCO.0000000000000160
P932PMC publication ID4406340
P698PubMed publication ID25768955

P50authorYibin WangQ40664206
Aldons Jake LusisQ60642067
P2093author name stringChristoph D Rau
P2860cites workHeart Disease and Stroke Statistics--2013 Update: A Report From the American Heart AssociationQ22306356
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyQ24601469
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataQ24612121
Biological, clinical and population relevance of 95 loci for blood lipidsQ24622541
Tnni3k modifies disease progression in murine models of cardiomyopathyQ27349094
Heart failure and mouse modelsQ27686849
Mapping genetic variants associated with beta-adrenergic responses in inbred miceQ28481719
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Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortiumQ28943463
Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortalityQ29416992
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Predictors of readmission among elderly survivors of admission with heart failureQ33807660
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) studyQ33836293
Common variants in HSPB7 and FRMD4B associated with advanced heart failureQ34096292
Progress and promise of genome-wide association studies for human complex trait geneticsQ34537519
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortiumQ34552350
A novel locus for dilated cardiomyopathy maps to canine chromosome 8Q34591160
Animal models of cardiovascular diseasesQ34591282
Mapping genetic contributions to cardiac pathology induced by Beta-adrenergic stimulation in miceQ35102230
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial functionQ35294331
Efficient control of population structure in model organism association mappingQ36515832
Genome-wide approach to identify novel candidate genes for beta blocker response in heart failure using an experimental model.Q37051265
Small animal models of heart failure: development of novel therapies, past and presentQ37609676
Proportion of the decline in cardiovascular mortality disease due to prevention versus treatment: public health versus clinical careQ37854652
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyQ43882133
A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscherQ44863885
FaST linear mixed models for genome-wide association studiesQ46661213
Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy.Q47594204
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The genetic determination of left ventricular mass in healthy adultsQ61713043
Hospitalization for congestive heart failure: United States, 2000-2010Q64128250
A genetic linkage map of the Syrian hamster and localization of cardiomyopathy locus on chromosome 9qa2.1-b1 using RLGS spot-mappingQ71167659
Genetic modifier loci affecting survival and cardiac function in murine dilated cardiomyopathyQ77948650
Evaluation of tafazzin as candidate for dilated cardiomyopathy in Irish wolfhoundsQ80591072
QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survivalQ80988562
Heart failure: advances through genomicsQ83667474
Direct detection of myocardial fibrosis by MRIQ84938192
P433issue3
P304page(s)222-227
P577publication date2015-05-01
P1433published inCurrent Opinion in CardiologyQ4626801
P1476titleGenetics of common forms of heart failure: challenges and potential solutions
P478volume30

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cites work (P2860)
Q90267583Atrial Fibrillation Genetics Update: Toward Clinical Implementation
Q28267272Deletion of MLIP (muscle-enriched A-type lamin-interacting protein) leads to cardiac hyperactivation of Akt/mammalian target of rapamycin (mTOR) and impaired cardiac adaptation
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