BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Dainis AM, Ashley EA. Cardiovascular Precision Medicine in the Genomics Era. JACC Basic Transl Sci 2018;3:313-26. [PMID: 30062216 DOI: 10.1016/j.jacbts.2018.01.003] [Cited by in Crossref: 26] [Cited by in F6Publishing: 21] [Article Influence: 6.5] [Reference Citation Analysis]
Number Citing Articles
1 Ahmad F, Mcnally EM, Ackerman MJ, Baty LC, Day SM, Kullo IJ, Madueme PC, Maron MS, Martinez MW, Salberg L, Taylor MR, Wilcox JE; On behalf of the American Heart Association Council on Genomic and Precision Medicine; Council on Arteriosclerosis, Thrombosis and Vascular Biology; Council on Basic Cardiovascular Sciences; Council on Cardiovascular and Stroke Nursing; Council on Clinical Cardiology; and Stroke Council. Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association. Circ: Genomic and Precision Medicine 2019;12. [DOI: 10.1161/hcg.0000000000000054] [Cited by in Crossref: 23] [Cited by in F6Publishing: 10] [Article Influence: 7.7] [Reference Citation Analysis]
2 Hannon BA, Khan NA, Teran-Garcia M. Nutrigenetic Contributions to Dyslipidemia: A Focus on Physiologically Relevant Pathways of Lipid and Lipoprotein Metabolism. Nutrients 2018;10:E1404. [PMID: 30279335 DOI: 10.3390/nu10101404] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
3 Zhang H, Viveiros A, Nikhanj A, Nguyen Q, Wang K, Wang W, Freed DH, Mullen JC, MacArthur R, Kim DH, Tymchak W, Sergi CM, Kassiri Z, Wang S, Oudit GY. The Human Explanted Heart Program: A translational bridge for cardiovascular medicine. Biochim Biophys Acta Mol Basis Dis 2021;1867:165995. [PMID: 33141063 DOI: 10.1016/j.bbadis.2020.165995] [Reference Citation Analysis]
4 Tadros HJ, Life CS, Garcia G, Pirozzi E, Jones EG, Datta S, Parvatiyar MS, Chase PB, Allen HD, Kim JJ, Pinto JR, Landstrom AP. Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes. J Mol Cell Cardiol 2020;142:118-25. [PMID: 32278834 DOI: 10.1016/j.yjmcc.2020.04.005] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
5 Alvarez-Collazo J, López-Requena A, Alvarez JL, Talavera K. The Citrus Flavonoid Hesperetin Has an Inadequate Anti-Arrhythmic Profile in the ΔKPQ NaV1.5 Mutant of the Long QT Type 3 Syndrome. Biomolecules 2020;10:E952. [PMID: 32599724 DOI: 10.3390/biom10060952] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Mesleh AG, Abdulla SA, El-Agnaf O. Paving the Way toward Personalized Medicine: Current Advances and Challenges in Multi-OMICS Approach in Autism Spectrum Disorder for Biomarkers Discovery and Patient Stratification. J Pers Med 2021;11:41. [PMID: 33450950 DOI: 10.3390/jpm11010041] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
7 Liu JTC, Glaser AK, Bera K, True LD, Reder NP, Eliceiri KW, Madabhushi A. Harnessing non-destructive 3D pathology. Nat Biomed Eng 2021;5:203-18. [PMID: 33589781 DOI: 10.1038/s41551-020-00681-x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Cheung NYC, Fung JLF, Ng YNC, Wong WHS, Chung CCY, Mak CCY, Chung BHY. Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong. Hum Genomics 2021;15:54. [PMID: 34407885 DOI: 10.1186/s40246-021-00353-0] [Reference Citation Analysis]
9 Serra-Majem L, Román-Viñas B, Sanchez-Villegas A, Guasch-Ferré M, Corella D, La Vecchia C. Benefits of the Mediterranean diet: Epidemiological and molecular aspects. Mol Aspects Med 2019;67:1-55. [PMID: 31254553 DOI: 10.1016/j.mam.2019.06.001] [Cited by in Crossref: 56] [Cited by in F6Publishing: 43] [Article Influence: 18.7] [Reference Citation Analysis]
10 Hubáček JA, Šedová L, Olišarová V, Adámková V, Tóthová V. Increased prevalence of the CVD-associated ANRIL allele in the Roma/Gypsy population in comparison with the majority Czech population. Genet Mol Biol 2021;44:e20200405. [PMID: 33949622 DOI: 10.1590/1678-4685-GMB-2020-0405] [Reference Citation Analysis]
11 Kalman JM, Lavandero S, Mahfoud F, Nahrendorf M, Yacoub MH, Zhao D. Looking back and thinking forwards - 15 years of cardiology and cardiovascular research. Nat Rev Cardiol 2019;16:651-60. [PMID: 31570832 DOI: 10.1038/s41569-019-0261-7] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
12 Correa Rojo A, Heylen D, Aerts J, Thas O, Hooyberghs J, Ertaylan G, Valkenborg D. Towards Building a Quantitative Proteomics Toolbox in Precision Medicine: A Mini-Review. Front Physiol 2021;12:723510. [PMID: 34512391 DOI: 10.3389/fphys.2021.723510] [Reference Citation Analysis]
13 Solomon T, Filipovska A, Hool L, Viola H. Preventative therapeutic approaches for hypertrophic cardiomyopathy. J Physiol 2021;599:3495-512. [PMID: 32822065 DOI: 10.1113/JP279410] [Reference Citation Analysis]
14 Angelidis G, Valotassiou V, Satra M, Psimadas D, Koutsikos J, Skoularigis J, Kollia P, Georgoulias P. Investigating the genetic characteristics of CAD: Is there a role for myocardial perfusion imaging techniques? J Nucl Cardiol 2020. [PMID: 33141407 DOI: 10.1007/s12350-020-02403-x] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Pan Z, Ebert A, Liang P. Human-induced pluripotent stem cells as models for rare cardiovascular diseases: from evidence-based medicine to precision medicine. Pflugers Arch - Eur J Physiol 2021;473:1151-65. [DOI: 10.1007/s00424-020-02486-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Vizirianakis IS, Chatzopoulou F, Papazoglou AS, Karagiannidis E, Sofidis G, Stalikas N, Stefopoulos C, Kyritsis KA, Mittas N, Theodoroula NF, Lampri A, Mezarli E, Kartas A, Chatzidimitriou D, Papa-Konidari A, Angelis E, Karvounis Η, Sianos G. The GEnetic Syntax Score: a genetic risk assessment implementation tool grading the complexity of coronary artery disease-rationale and design of the GESS study. BMC Cardiovasc Disord 2021;21:284. [PMID: 34103005 DOI: 10.1186/s12872-021-02092-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Fatunde OA, Brown SA. The Role of CYP450 Drug Metabolism in Precision Cardio-Oncology. Int J Mol Sci 2020;21:E604. [PMID: 31963461 DOI: 10.3390/ijms21020604] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
18 Baragetti A, Catapano AL, Magni P. Multifactorial Activation of NLRP3 Inflammasome: Relevance for a Precision Approach to Atherosclerotic Cardiovascular Risk and Disease. Int J Mol Sci 2020;21:E4459. [PMID: 32585928 DOI: 10.3390/ijms21124459] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
19 Al-Zahrani J, Shubair MM, Al-Ghamdi S, Alrasheed AA, Alduraywish AA, Alreshidi FS, Alshahrani SM, Alsalamah M, Al-Khateeb BF, Ashathri AI, El-Metwally A, Aldossari KK. The prevalence of hypercholesterolemia and associated risk factors in Al-Kharj population, Saudi Arabia: a cross-sectional survey. BMC Cardiovasc Disord 2021;21:22. [PMID: 33413091 DOI: 10.1186/s12872-020-01825-2] [Reference Citation Analysis]
20 Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams SG, Keavney BD, Thiruvahindrapuram B, Scherer SW, Bassett AS. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. Circ Genom Precis Med 2021;14:e003410. [PMID: 34328347 DOI: 10.1161/CIRCGEN.121.003410] [Reference Citation Analysis]
21 Zhao Z, Gong C, Gao Y, Liu X, Wu S, Zhao H, Wang X, Liu H, Xiao C, Liu J, Li J, He Y. Association between Single Nucleotide Polymorphisms in Cardiovascular Developmental Critical Genes and Hypertension: A Propensity Score Matching Analysis. Int J Hypertens 2020;2020:9185697. [PMID: 32257424 DOI: 10.1155/2020/9185697] [Reference Citation Analysis]
22 Dib I, Khalil A, Chouaib R, El-Makhour Y, Noureddine H. Apolipoprotein C-III and cardiovascular diseases: when genetics meet molecular pathologies. Mol Biol Rep 2021;48:875-86. [PMID: 33389539 DOI: 10.1007/s11033-020-06071-5] [Reference Citation Analysis]