Works about HEART disease genetics

Results: 211

Cost-effectiveness of genetic studies in inherited heart diseases.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 28, doi. 10.4081/cardiogenetics.2013.e5

By:

Sabater-Molina, María;
García-Molina, Esperanza;
Tovar, Isabel;
Ruiz-Espejo, Francisco;
Gimeno, Juan Ramón;
Valdés, Mariano

Publication type:

Article

Cardiovascular disease risk factor knowledge assessment among medical students.

Published in:

National Journal of Physiology, Pharmacy & Pharmacology, 2016, v. 6, n. 3, p. 251, doi. 10.5455/njppp.2016.6.20022016129

By:

Sadasivam, Kanimozhi;
Nagarajan, Poornima K.;
Ramraj, Balaji;
Chinnasami, Balaji;
Nedunchezhian, Karthick;
Aiyyavoo, Saravanan

Publication type:

Article

Leveraging gene co-expression networks to pinpoint the regulation of complex traits and disease, with a focus on cardiovascular traits.

Published in:

Briefings in Functional Genomics, 2014, v. 13, n. 1, p. 66, doi. 10.1093/bfgp/elt030

By:

Rotival, Maxime;
Petretto, Enrico

Publication type:

Article

Heart genetics in a small package, exploiting the condensed genome of Ciona intestinalis.

Published in:

Briefings in Functional Genomics, 2014, v. 13, n. 1, p. 3, doi. 10.1093/bfgp/elt034

By:

Cota, Christina D.;
Segade, Fernando;
Davidson, Brad

Publication type:

Article

CARDIOVASCULAR DRUGS AND THE GENETIC RESPONSE.

Published in:

Methodist DeBakey Cardiovascular Journal, 2014, v. 10, n. 1, p. 13, doi. 10.14797/mdcj-10-1-13

By:

Dandona, Sonny

Publication type:

Article

GENETICS OF CORONARY ARTERY DISEASE: AN UPDATE.

Published in:

Methodist DeBakey Cardiovascular Journal, 2014, v. 10, n. 1, p. 7, doi. 10.14797/mdcj-10-1-7

By:

Roberts, Robert

Publication type:

Article

The World in Medicine.

Published in:

JAMA: Journal of the American Medical Association, 1999, v. 282, n. 18, p. 1713

By:

Voelker, Rebecca

Publication type:

Article

Attacking Heart Disease at Its Genetic Base.

Published in:

Agricultural Research, 1999, v. 47, n. 7, p. 20

By:

McBride, Judy

Publication type:

Article

CASE STUDY ON SUDDEN CARDIAC DEATH.

Published in:

2010

By:

Bulzan, Ovidiu;
Pribac, George Ciprian

Publication type:

Case Study

TNF alpha—Still a Therapeutic Target.

Published in:

CTS: Clinical & Translational Science, 2008, v. 1, n. 2, p. 145, doi. 10.1111/j.1752-8062.2008.00012.x

By:

Feldman, Arthur M.

Publication type:

Article

Effects of peri-operative glucose levels on adverse outcomes in infants receiving open-heart surgery for congenital heart disease with cardiopulmonary bypass.

Published in:

Perfusion, 2011, v. 26, n. 2, p. 133, doi. 10.1177/0267659110389843

By:

Song Lou;
Fan Ding;
Cun Long;
Jinping Liu;
Ju Zhao;
Zhengyi Feng

Publication type:

Article

Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease.

Published in:

Molecular & Cellular Biochemistry, 2011, v. 355, n. 1/2, p. 289, doi. 10.1007/s11010-011-0866-6

By:

Masud, Rizwan;
Qureshi, Irfan

Publication type:

Article

Cell type-specific expression of endogenous cardiac Troponin I antisense RNA in the neonatal rat heart.

Published in:

Molecular & Cellular Biochemistry, 2009, v. 324, n. 1/2, p. 1

By:

Stefanie Voigtsberger;
Holger Bartsch;
Gert Baumann;
Hans Luther

Publication type:

Article

MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts.

Published in:

2008

By:

Thum, Thomas;
Gross, Carina;
Fiedler, Jan;
Fischer, Thomas;
Kissler, Stephan;
Bussen, Markus;
Galuppo, Paolo;
Just, Steffen;
Rottbauer, Wolfgang;
Frantz, Stefan;
Castoldi, Mirco;
Soutschek, Jürgen;
Koteliansky, Victor;
Rosenwald, Andreas;
Basson, M. Albert;
Licht, Jonathan D.;
Pena, John T. R.;
Rouhanifard, Sara H.;
Muckenthaler, Martina U.;
Tuschl, Thomas

Publication type:

Letter

A genetic framework for improving arrhythmia therapy.

Published in:

Nature, 2008, v. 451, n. 7181, p. 929, doi. 10.1038/nature06799

By:

Knollmann, Bj&;#x00F6;rn C.;
Roden, Dan M.

Publication type:

Article

Heart Failure in Women.

Published in:

Indian Journal of Cardiovascular Disease in Women - WINCARS, 2022, v. 7, n. 3, p. 162, doi. 10.25259/mm_ijcdw_482

By:

Maddury, Jyotsna

Publication type:

Article

The Missing "lnc" between Genetics and Cardiac Disease.

Published in:

Non-Coding RNA, 2020, v. 6, n. 1, p. 1, doi. 10.3390/ncrna6010003

By:

Azodi, Maral;
Kamps, Rick;
Heymans, Stephane;
Robinson, Emma Louise

Publication type:

Article

Genetic Testing in Cardiovascular Medicine.

Published in:

Texas Heart Institute Journal, 2018, v. 45, n. 04, p. 231, doi. 10.14503/THIJ-18-6674

By:

Marian, Ali J.

Publication type:

Article

Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.

Published in:

2007

By:

Kaski, Juan Pablo;
Burch, Michael;
Elliott, Perry M.

Publication type:

Case Study

Clinical investigations over 13 years to establish the nature of the cardiac defects in patients having abnormalities of lateralization.

Published in:

2007

By:

Yildirim, Selman Vefa;
Tokel, Kürsad;
Varan, Birgül;
Aslamaci, Sait;
Ekici, Enver;
Tokel, Kürsad;
Varan, Birgül

Publication type:

journal article

Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.

Published in:

Cardiology in the Young, 2007, v. 17, n. 3, p. 268, doi. 10.1017/S1047951107000455

By:

Tierney, Elif Seda Selamet;
Marans, Zvi;
Rutkin, Melissa B.;
Chung, Wendy K.

Publication type:

Article

Searching for order among disorders of laterality.

Published in:

2007

By:

McElhinney, Doff B.

Publication type:

commentary

Psychological symptoms in patients after surgery for congenital cardiac disease.

Published in:

Cardiology in the Young, 2006, v. 16, n. 6, p. 540, doi. 10.1017/S1047951106001442

By:

Geyer, Siegfried;
Norozi, Kambiz;
Zoege, Monika;
Kempa, Almut;
Buchhorn, Reiner;
Wessel, Armin

Publication type:

Article

Distinguishing pathogenic mutations from background genetic noise in cardiology: The use of large genome databases for genetic interpretation.

Published in:

Clinical Genetics, 2018, v. 93, n. 3, p. 459, doi. 10.1111/cge.13066

By:

Ghouse, J.;
Skov, M. W.;
Bigseth, R. S.;
Ahlberg, G.;
Kanters, J. K.;
Olesen, M. S.

Publication type:

Article

A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1462, doi. 10.1038/ejhg.2015.10

By:

Otten, Ellen;
Birnie, Erwin;
Ranchor, Adelita V;
van Tintelen, J Peter;
van Langen, Irene M

Publication type:

Article

Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 1, p. 88, doi. 10.1038/ejhg.2013.81

By:

Ormondroyd, Elizabeth;
Oates, Stephanie;
Parker, Michael;
Blair, Edward;
Watkins, Hugh

Publication type:

Article

Genome-wide association analysis of Framingham Heart Study data for the Genetics Analysis Workshop 16: effects due to medication use.

Published in:

BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S52

By:

Rice, Treva K.;
Yun Ju Sung;
Gang Shi;
Gu, C. Charles;
Rao, D. C.

Publication type:

Article

Transmission-ratio distortion in the Framingham Heart Study.

Published in:

BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S51

By:

Paterson, Andrew D.;
Waggott, Daryl;
Schillert, Arne;
Infante-Rivard, Claire;
Bull, Shelley B.;
Yun Joo Yoo;
Pinnaduwage, Dushanthi

Publication type:

Article

Using a latent growth curve model for an integrative assessment of the effects of genetic and environmental factors on multiple phenotypes.

Published in:

BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S44

By:

Hamid, Jemila S.;
Roslin, Nicole M.;
Paterson, Andrew D.;
Beyene, Joseph

Publication type:

Article

The effect of minor allele frequency on the likelihood of obtaining false positives.

Published in:

BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S41

By:

Tabangin, Meredith E.;
Woo, Jessica G.;
Martin, Lisa J.

Publication type:

Article

Genetics Analysis Workshop 16 Problem 2: the Framingham Heart Study data.

Published in:

BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S3

By:

Cupples, L. Adrienne;
Heard-Costa, Nancy;
Lee, Monica;
Atwood, Larry D.

Publication type:

Article

Cardiac Emergency Prevention Through Personal and Environmental Factors.

Published in:

Medico-Legal Update, 2020, v. 20, n. 1, p. 1312, doi. 10.37506/v20/i1/2020/mlu/194484

By:

Bambang Guruh Irianto;
Loetfia Dwi Rahariyani

Publication type:

Article

Enhanced SMAD1 Signaling Contributes to Impairments of Early Development in CFC-i PSCs.

Published in:

Stem Cells, 2015, v. 33, n. 5, p. 1447, doi. 10.1002/stem.1963

By:

Han, Kyu-Min;
Kim, Seung-Kyoon;
Kim, Dongkyu;
Choi, Jung-Yun;
Im, Ilkyun;
Hwang, Kyu-Seok;
Kim, Cheol-Hee;
Lee, Beom Hee;
Yoo, Han-Wook;
Han, Yong-Mahn

Publication type:

Article

Large-scale discovery of enhancers from human heart tissue.

Published in:

Nature Genetics, 2012, v. 44, n. 1, p. 89, doi. 10.1038/ng.1006

By:

May, Dalit;
Blow, Matthew J;
Kaplan, Tommy;
McCulley, David J;
Jensen, Brian C;
Akiyama, Jennifer A;
Holt, Amy;
Plajzer-Frick, Ingrid;
Shoukry, Malak;
Wright, Crystal;
Afzal, Veena;
Simpson, Paul C;
Rubin, Edward M;
Black, Brian L;
Bristow, James;
Pennacchio, Len A;
Visel, Axel

Publication type:

Article

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.

Published in:

Nature Genetics, 2011, v. 43, n. 6, p. 531, doi. 10.1038/ng.834

By:

Kato, Norihiro;
Takeuchi, Fumihiko;
Tabara, Yasuharu;
Kelly, Tanika N.;
Min Jin Go;
Xueling Sim;
Wan Ting Tay;
Chien-Hsiun Chen;
Yi Zhang;
Yamamoto, Ken;
Katsuya, Tomohiro;
Yokota, Mitsuhiro;
Young Jin Kim;
Ong, Rick Twee Hee;
Nabika, Toru;
Dongfeng Gu;
Li-ching Chang;
Kokubo, Yoshihiro;
Wei Huang;
Ohnaka, Keizo

Publication type:

Article

Research highlights.

Published in:

Nature Genetics, 2007, v. 39, n. 6, p. 713, doi. 10.1038/ng0607-713

By:

Niemitz, Emily;
Packer, Alan;
Vogan, Kyle

Publication type:

Article

A Rare Rs139365823 Polymorphism in Pre-miR-138 Is Associated with Risk of Congenital Heart Disease in a Chinese Population.

Published in:

DNA & Cell Biology, 2018, v. 37, n. 2, p. 109, doi. 10.1089/dna.2017.4013

By:

Gao, Xiaobo;
Yang, Liping;
Luo, Haiyan;
Tan, Fengwei;
Ma, Xu;
Lu, Cailing

Publication type:

Article

Dissecting the genetics of cardiomyopathy in India: A tale of ten steps.

Published in:

Journal of Biosciences, 2009, v. 34, n. 1, p. 1, doi. 10.1007/s12038-009-0002-x

By:

MAJUMDER, PARTHA P.

Publication type:

Article

Researchers find gene responsible for heart damage caused by chemotherapy.

Published in:: British Columbia Medical Journal, 2015, v. 57, n. 9, p. 1
Publication type:: Article

Coronary Heart Disease-Associated Variation in <i>TCF21</i> Disrupts a miR-224 Binding Site and miRNA-Mediated Regulation.

Published in:

PLoS Genetics, 2014, v. 10, n. 3, p. 1, doi. 10.1371/journal.pgen.1004263

By:

Miller, Clint L.;
Haas, Ulrike;
Diaz, Roxanne;
Leeper, Nicholas J.;
Kundu, Ramendra K.;
Patlolla, Bhagat;
Assimes, Themistocles L.;
Kaiser, Frank J.;
Perisic, Ljubica;
Hedin, Ulf;
Maegdefessel, Lars;
Schunkert, Heribert;
Erdmann, Jeanette;
Quertermous, Thomas;
Sczakiel, Georg

Publication type:

Article

Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy.

Published in:: PLoS Genetics, 2010, v. 6, n. 10, p. 1, doi. 10.1371/journal.pgen.1001167
Publication type:: Article

Landmark genetics study to improve prediction of heart disease recruits 20,000th participant.

Published in:: Operating Theatre Journal, 2016, n. 314, p. 10
Publication type:: Article

A conversation with Christine Seidman.

Published in:

2013

By:

Neill, Ushma S.

Publication type:

Interview

Response to Thum et al.

Published in:

2011

By:

Patrick, David M.;
Kauppinen, Sakari;
van Rooij, Eva;
Olson, Eric N.

Publication type:

Letter

Comparison of different miR-21 inhibitor chemistries in a cardiac disease model.

Published in:

2011

By:

Thum, Thomas;
Chau, Nelson;
Bhat, Balkrishen;
Gupta, Shashi Kumar;
Linsley, Peter S.;
Bauersachs, Johann;
Engelhardt, Stefan

Publication type:

commentary

Stress-dependent cardiac remodeling occurs in the absence of microRNA-21 in mice.

Published in:

2010

By:

Patrick, David M.;
Montgomery, Rusty L.;
Xiaoxia Qi;
Obad, Susanna;
Kauppinen, Sakari;
Hill, Joseph A.;
van Rooij, Eva;
Olson, Eric N.;
Qi, Xiaoxia

Publication type:

journal article

"FISHed" out the diagnosis: A case of DiGeorge syndrome.

Published in:

2016

By:

Bajaj, S.;
Thombare, T. S.;
Tullu, M. S.;
Agrawal, M.

Publication type:

Case Study

Assessment of arterial stiffness in women with gestational diabetes.

Published in:

Diabetic Medicine, 2012, v. 29, n. 2, p. 227, doi. 10.1111/j.1464-5491.2011.03471.x

By:

Bulzico, D. A.;
Zajdenverg, L.;
Cabizuca, C. A.;
de Oliveira, J. E. P.;
Salles, G. F.

Publication type:

Article

Association of Increased Levels of lncRNA H19 in PBMCs with Risk of Coronary Artery Disease.

Published in:

Cell Journal (Yakhteh), 2019, v. 20, n. 4, p. 564, doi. 10.22074/cellj.2019.5544

By:

Bitarafan, Sara;
Yari, Mohsen;
Broumand, Mohammad Ali;
Hossein Ghaderian, Sayyed Mohammad;
Rahimi, Mahnoosh;
Mirfakhraie, Reza;
Azizi, Faezeh;
Omrani, Mir Davood

Publication type:

Article

Major congenital coronary artery anomalies in a paediatric and adult population: a prospective echocardiographic study.

Published in:

European Heart Journal - Cardiovascular Imaging, 2014, v. 15, n. 7, p. 761, doi. 10.1093/ehjci/jet287

By:

Labombarda, Fabien;
Coutance, Guillaume;
Pellissier, Arnaud;
Mery-Alexandre, Claire;
Roule, Vincent;
Maragnes, Pascale;
Milliez, Paul;
Saloux, Eric

Publication type:

Article