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Items: 1 to 20 of 837

1.

Are Double Mutations Double Trouble?

Fatkin D, Johnson R.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001749. doi: 10.1161/CIRCGENETICS.117.001749. No abstract available.

PMID:
28420667
2.

Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.

Fourey D, Care M, Siminovitch KA, Weissler-Snir A, Hindieh W, Chan RH, Gollob MH, Rakowski H, Adler A.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001685. doi: 10.1161/CIRCGENETICS.116.001685.

PMID:
28420666
3.

Correction.

[No authors listed]

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e000036. doi: 10.1161/HCG.0000000000000036. No abstract available.

PMID:
28420665
4.

Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.

Mosley JD, Shoemaker MB, Wells QS, Darbar D, Shaffer CM, Edwards TL, Bastarache L, McCarty CA, Thompson W, Chute CG, Jarvik GP, Crosslin DR, Larson EB, Kullo IJ, Pacheco JA, Peissig PL, Brilliant MH, Linneman JG, Witte JS, Denny JC, Roden DM.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001482. doi: 10.1161/CIRCGENETICS.116.001482.

PMID:
28416512
5.

Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle).

Schmidt B, Frölich S, Dragano N, Frank M, Eisele L, Pechlivanis S, Forstner AJ, Nöthen MM, Mahabadi AA, Erbel R, Moebus S, Jöckel KH.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001441. doi: 10.1161/CIRCGENETICS.116.001441.

PMID:
28411192
6.

Delivering Clinical Grade Sequencing and Genetic Test Interpretation for Cardiovascular Medicine.

Harper AR, Parikh VN, Goldfeder RL, Caleshu C, Ashley EA.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001221. doi: 10.1161/CIRCGENETICS.116.001221. No abstract available.

PMID:
28411191
7.

Local Ancestry Association, Admixture Mapping, and Ongoing Challenges.

Mani A.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001747. doi: 10.1161/CIRCGENETICS.117.001747. No abstract available.

PMID:
28408710
8.

Heritability of the Severity of the Metabolic Syndrome in Whites and Blacks in 3 Large Cohorts.

Musani SK, Martin LJ, Woo JG, Olivier M, Gurka MJ, DeBoer MD.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001621. doi: 10.1161/CIRCGENETICS.116.001621.

PMID:
28408709
9.

Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.

Ingles J, Burns C, Bagnall RD, Lam L, Yeates L, Sarina T, Puranik R, Briffa T, Atherton JJ, Driscoll T, Semsarian C.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001620. doi: 10.1161/CIRCGENETICS.116.001620.

PMID:
28408708
10.

Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies.

Shendre A, Wiener H, Irvin MR, Zhi D, Limdi NA, Overton ET, Wassel CL, Divers J, Rotter JI, Post WS, Shrestha S.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001569. doi: 10.1161/CIRCGENETICS.116.001569.

PMID:
28408707
11.

Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.

Klarin D, Emdin CA, Natarajan P, Conrad MF; INVENT Consortium., Kathiresan S.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001643. doi: 10.1161/CIRCGENETICS.116.001643.

PMID:
28373160
12.

Potential Impact and Study Considerations of Metabolomics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association.

Cheng S, Shah SH, Corwin EJ, Fiehn O, Fitzgerald RL, Gerszten RE, Illig T, Rhee EP, Srinivas PR, Wang TJ, Jain M; American Heart Association Council on Functional Genomics and Translational Biology; Council on Cardiovascular and Stroke Nursing; Council on Clinical Cardiology; and Stroke Council..

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e000032. doi: 10.1161/HCG.0000000000000032. Review.

PMID:
28360086
13.

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients.

Gómez J, Lorca R, Reguero JR, Morís C, Martín M, Tranche S, Alonso B, Iglesias S, Alvarez V, Díaz-Molina B, Avanzas P, Coto E.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001584. doi: 10.1161/CIRCGENETICS.116.001584.

PMID:
28356264
14.

Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

Li C, Kim YK, Dorajoo R, Li H, Lee IT, Cheng CY, He M, Sheu WH, Guo X, Ganesh SK, He J, Lee J, Liu J, Hu Y, Rao DC, Tsai FJ, Koh JY, Hu H, Liang KW, Palmas W, Hixson JE, Han S, Teo YY, Wang Y, Chen J, Lu CH, Zheng Y, Gui L, Lee WJ, Yao J, Gu D, Han BG, Sim X, Sun L, Zhao J, Chen CH, Kumari N, He Y, Taylor KD, Raffel LJ, Moon S, Rotter JI, Ida Chen YD, Wu T, Wong TY, Wu JY, Lin X, Tai ES, Kim BJ, Kelly TN.

Circ Cardiovasc Genet. 2017 Apr;10(2):e001527. doi: 10.1161/CIRCGENETICS.116.001527.

PMID:
28348047
15.

Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization.

Haitjema S, Meddens CA, van der Laan SW, Kofink D, Harakalova M, Tragante V, Foroughi Asl H, van Setten J, Brandt MM, Bis JC, O'Donnell C, Cheng C, Hoefer IE, Waltenberger J, Biessen E, Jukema JW, Doevendans PA, Nieuwenhuis EE, Erdmann J, Björkegren JL, Pasterkamp G, Asselbergs FW, den Ruijter HM, Mokry M.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001664. doi: 10.1161/CIRCGENETICS.116.001664.

PMID:
28320757
16.

Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.

Mayosi BM, Fish M, Shaboodien G, Mastantuono E, Kraus S, Wieland T, Kotta MC, Chin A, Laing N, Ntusi NB, Chong M, Horsfall C, Pimstone SN, Gentilini D, Parati G, Strom TM, Meitinger T, Pare G, Schwartz PJ, Crotti L.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001605. doi: 10.1161/CIRCGENETICS.116.001605.

PMID:
28280076
17.

Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies.

Hedman ÅK, Mendelson MM, Marioni RE, Gustafsson S, Joehanes R, Irvin MR, Zhi D, Sandling JK, Yao C, Liu C, Liang L, Huan T, McRae AF, Demissie S, Shah S, Starr JM, Cupples LA, Deloukas P, Spector TD, Sundström J, Krauss RM, Arnett DK, Deary IJ, Lind L, Levy D, Ingelsson E.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001487. doi: 10.1161/CIRCGENETICS.116.001487.

18.

Ankyrin-B Defects: Serendipity and Inquisitiveness are the Mothers of Invention.

Duff H, Sheldon RS.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001698. doi: 10.1161/CIRCGENETICS.117.001698. No abstract available.

PMID:
28196903
19.

Hyaluronidase 2 Deficiency Causes Increased Mesenchymal Cells, Congenital Heart Defects, and Heart Failure.

Chowdhury B, Xiang B, Liu M, Hemming R, Dolinsky VW, Triggs-Raine B.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001598. doi: 10.1161/CIRCGENETICS.116.001598.

20.

Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome.

Swayne LA, Murphy NP, Asuri S, Chen L, Xu X, McIntosh S, Wang C, Lancione PJ, Roberts JD, Kerr C, Sanatani S, Sherwin E, Kline CF, Zhang M, Mohler PJ, Arbour LT.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001537. doi: 10.1161/CIRCGENETICS.116.001537.

PMID:
28196901

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