Literature DB >> 28057368

Genomic translational research: Paving the way to individualized cardiac functional analyses and personalized cardiology.

Ares Pasipoularides1.   

Abstract

For most of Medicine's past, the best that physicians could do to cope with disease prevention and treatment was based on the expected response of an average patient. Currently, however, a more personalized/precise approach to cardiology and medicine in general is becoming possible, as the cost of sequencing a human genome has declined substantially. As a result, we are witnessing an era of precipitous advances in biomedicine and bourgeoning understanding of the genetic basis of cardiovascular and other diseases, reminiscent of the resurgence of innovations in physico-mathematical sciences and biology-anatomy-cardiology in the Renaissance, a parallel time of radical change and reformation of medical knowledge, education and practice. Now on the horizon is an individualized, diverse patient-centered, approach to medical practice that encompasses the development of new, gene-based diagnostics and preventive medicine tactics, and offers the broadest range of personalized therapies based on pharmacogenetics. Over time, translation of genomic and high-tech approaches unquestionably will transform clinical practice in cardiology and medicine as a whole, with the adoption of new personalized medicine approaches and procedures. Clearly, future prospects far outweigh present accomplishments, which are best viewed as a promising start. It is now essential for pluridisciplinary health care providers to examine the drivers and barriers to the clinical adoption of this emerging revolutionary paradigm, in order to expedite the realization of its potential. So, we are not there yet, but we are definitely on our way.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  CRISPR-Cas9 genetic–phenotypic screen; DNA microarrays; Genome-wide association studies (GWAS); Molecular genetic biomarkers; Molecular genomic decoding of phenotypic diversity; Next-generation genome sequencing (NGS); Omics-based tests; Personalized/precise medicine; Pharmacogenomics and pharmacogenetics

Mesh:

Year:  2016        PMID: 28057368      PMCID: PMC5332127          DOI: 10.1016/j.ijcard.2016.12.097

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  131 in total

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Authors:  Ares Pasipoularides
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4.  Homophila: human disease gene cognates in Drosophila.

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5.  Noninvasive assessment of intrinsic ventricular load dynamics in dilated cardiomyopathy.

Authors:  K Isaaz; A Pasipoularides
Journal:  J Am Coll Cardiol       Date:  1991-01       Impact factor: 24.094

Review 6.  Genetics of cardiovascular diseases: from single mutations to the whole genome.

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Journal:  Circulation       Date:  2007-10-09       Impact factor: 29.690

7.  CRISPR germline engineering--the community speaks.

Authors:  Katrine S Bosley; Michael Botchan; Annelien L Bredenoord; Dana Carroll; R Alta Charo; Emmanuelle Charpentier; Ron Cohen; Jacob Corn; Jennifer Doudna; Guoping Feng; Henry T Greely; Rosario Isasi; Weihzi Ji; Jin-Soo Kim; Bartha Knoppers; Edward Lanphier; Jinsong Li; Robin Lovell-Badge; G Steven Martin; Jonathan Moreno; Luigi Naldini; Martin Pera; Anthony C F Perry; J Craig Venter; Feng Zhang; Qi Zhou
Journal:  Nat Biotechnol       Date:  2015-05       Impact factor: 54.908

Review 8.  Molecular genetics of prostate cancer: new prospects for old challenges.

Authors:  Michael M Shen; Cory Abate-Shen
Journal:  Genes Dev       Date:  2010-09-15       Impact factor: 11.361

Review 9.  Evaluation of right and left ventricular diastolic filling.

Authors:  Ares Pasipoularides
Journal:  J Cardiovasc Transl Res       Date:  2013-04-13       Impact factor: 4.132

Review 10.  RNA-Seq: a revolutionary tool for transcriptomics.

Authors:  Zhong Wang; Mark Gerstein; Michael Snyder
Journal:  Nat Rev Genet       Date:  2009-01       Impact factor: 53.242

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  11 in total

Review 1.  Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 2: Pluridisciplinary perspective on their genetic and molecular origins.

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Journal:  J Mol Cell Cardiol       Date:  2019-06-06       Impact factor: 5.000

2.  Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 1: Pluridisciplinary perspective on their hemodynamics and morphomechanics.

Authors:  Ares Pasipoularides
Journal:  J Mol Cell Cardiol       Date:  2019-05-28       Impact factor: 5.000

3.  Challenges and Controversies in Hypertrophic Cardiomyopathy: Clinical, Genomic and Basic Science Perspectives.

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4.  The new era of whole-exome sequencing in congenital heart disease: brand-new insights into rare pathogenic variants.

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Journal:  J Thorac Dis       Date:  2018-06       Impact factor: 2.895

Review 5.  Morphomechanic phenotypic variability of sarcomeric cardiomyopathies: A multifactorial polygenic perspective.

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Journal:  J Mol Cell Cardiol       Date:  2018-11-10       Impact factor: 5.000

6.  Know Me! Unraveling the Riddle of Calcific Aortic Valve Disease by Bioinformatics.

Authors:  Ares Pasipoularides
Journal:  Tohoku J Exp Med       Date:  2017-12       Impact factor: 1.848

Review 7.  Implementing genome-driven personalized cardiology in clinical practice.

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Journal:  J Mol Cell Cardiol       Date:  2018-01-16       Impact factor: 5.000

8.  Exploring Genetic Numeracy Skills in a Sample of U.S. University Students.

Authors:  Margo W Bergman; Patricia Goodson; Heather Honoré Goltz
Journal:  Front Public Health       Date:  2017-08-29

9.  Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in TNNI3 and TNNT2 That Are Common in Chinese Patients.

Authors:  Chee Jian Pua; Nevin Tham; Calvin W L Chin; Roddy Walsh; Chiea Chuen Khor; Christopher N Toepfer; Giuliana G Repetti; Amanda C Garfinkel; Jourdan F Ewoldt; Paige Cloonan; Christopher S Chen; Shi Qi Lim; Jiashen Cai; Li Yang Loo; Siew Ching Kong; Charleston W K Chiang; Nicola Whiffin; Antonio de Marvao; Pei Min Lio; An An Hii; Cheng Xi Yang; Thu Thao Le; Yasmin Bylstra; Weng Khong Lim; Jing Xian Teo; Kallyandra Padilha; Gabriela V Silva; Bangfen Pan; Risha Govind; Rachel J Buchan; Paul J R Barton; Patrick Tan; Roger Foo; James W L Yip; Raymond C C Wong; Wan Xian Chan; Alexandre C Pereira; Hak Chiaw Tang; Saumya Shekhar Jamuar; James S Ware; Jonathan G Seidman; Christine E Seidman; Stuart A Cook
Journal:  Circ Genom Precis Med       Date:  2020-08-20

10.  Clinical utility of brain-derived neurotrophic factor as a biomarker with left ventricular echocardiographic indices for potential diagnosis of coronary artery disease.

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