Works matching Heart disease and genetics

Results: 1701

Large next-generation sequencing gene panels in genetic heart disease: challenges in clinical practice.

Published in:

Netherlands Heart Journal, 2019, v. 27, n. 6, p. 299, doi. 10.1007/s12471-019-1251-4

By:

Christiaans, I.;
Mook, O. R. F.;
Alders, M.;
Bikker, H.;
Lekanne dit Deprez, R. H.

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

Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance.

Published in:

Netherlands Heart Journal, 2019, v. 27, n. 6, p. 304, doi. 10.1007/s12471-019-1250-5

By:

van Lint, F. H. M.;
Mook, O. R. F.;
Alders, M.;
Bikker, H.;
Lekanne dit Deprez, R. H.;
Christiaans, I.

Publication type:

Article

Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease.

Published in:

JAMA: Journal of the American Medical Association, 2009, v. 302, n. 1, p. 37, doi. 10.1001/jama.2009.954

By:

Elliott, Paul;
Chambers, John C.;
Weihua Zhang;
Clarke, Robert;
Hopewell, Jemma C.;
Peden, John F.;
Erdmann, Jeanette;
Braund, Peter;
Engert, James C.;
Bennett, Derrick;
Coin, Lachlan;
Ashby, Deborah;
Tzoulaki, Ioanna;
Brown, Ian J.;
Mt-Isa, Shahrul;
McCarthy, Mark I.;
Peltonen, Leena;
Freimer, Nelson B.;
Farrall, Martin;
Ruokonen, Aimo

Publication type:

Article

Association study of genetic variants at newly identified lipid gene TRIB1 with coronary heart disease in Chinese Han population.

Published in:

Lipids in Health & Disease, 2015, v. 14, n. 1, p. 1, doi. 10.1186/s12944-015-0043-0

By:

Long Wang;
Jinjin Jing;
Qianxi Fu;
Xiaojun Tang;
Li Su;
Shishi Wu;
Ge Li;
Li Zhou

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

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

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

Post-mortem genetic investigation of cardiac disease–associated genes in sudden infant death syndrome (SIDS) cases.

Published in:

International Journal of Legal Medicine, 2021, v. 135, n. 1, p. 207, doi. 10.1007/s00414-020-02394-x

By:

Köffer, Jasmin;
Scheiper-Welling, Stefanie;
Verhoff, Marcel A.;
Bajanowski, Thomas;
Kauferstein, Silke

Publication type:

Article

Genetic investigations of 100 inherited cardiac disease-related genes in deceased individuals with schizophrenia.

Published in:

International Journal of Legal Medicine, 2021, v. 135, n. 4, p. 1395, doi. 10.1007/s00414-021-02595-y

By:

Christiansen, Sofie Lindgren;
Andersen, Jeppe Dyrberg;
Themudo, Gonçalo Espregueira;
Hertz, Christin Løth;
Busch, Johannes Rødbro;
Christensen, Martin Roest;
Olsen, Kristine Boisen;
Banner, Jytte;
Morling, Niels

Publication type:

Article

Rare Diseases and Congenital Heart Diseases: A Call for Genetic Insight.

Published in:

Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2025, v. 29, n. 5, p. 269, doi. 10.14744/AnatolJCardiol.2025.5297

By:

Çelebiler, Hande Kaymakçalan

Publication type:

Article

Molecular aspects of ischemic heart disease: ischemia/reperfusion-induced genetic changes and potential applications of gene and RNA interference therapy.

Published in:

2006

By:

Nordlie, Margaret A;
Wold, Loren E;
Simkhovich, Boris Z;
Sesti, Casilde;
Kloner, Robert A

Publication type:

journal article

Gene editing and cardiac disease modelling for the interpretation of genetic variants of uncertain significance in congenital heart disease.

Published in:

Stem Cell Research & Therapy, 2023, v. 14, n. 1, p. 1, doi. 10.1186/s13287-023-03592-1

By:

Fear, Vanessa S.;
Forbes, Catherine A.;
Shaw, Nicole C.;
Farley, Kathryn O.;
Mantegna, Jessica L.;
Htun, Jasmin P.;
Syn, Genevieve;
Viola, Helena;
Cserne Szappanos, Henrietta;
Hool, Livia;
Ward, Michelle;
Baynam, Gareth;
Lassmann, Timo

Publication type:

Article

Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease.

Published in:

PLoS ONE, 2010, v. 5, n. 5, p. 1, doi. 10.1371/journal.pone.0010855

By:

Stevens, Kristen N.;
Hakonarson, Hakon;
Kim, Cecilia E.;
Doevendans, Pieter A.;
Koeleman, Bobby P. C.;
Mital, Seema;
Raue, Jennifer;
Glessner, Joseph T.;
Coles, John G.;
Moreno, Victor;
Granger, Anne;
Gruber, Stephen B.;
Gruber, Peter J.

Publication type:

Article

A systematic review of the factors associated with interest in predictive genetic testing for obesity, type II diabetes and heart disease.

Published in:

Journal of Human Nutrition & Dietetics, 2014, v. 27, n. 5, p. 479, doi. 10.1111/jhn.12179

By:

Collins, J.;
Ryan, L.;
Truby, H.

Publication type:

Article

Association Between a Genetic Variant Related to Glutamic Acid Metabolism and Coronary Heart Disease in Individuals With Type 2 Diabetes.

Published in:

JAMA: Journal of the American Medical Association, 2013, v. 310, n. 8, p. 821, doi. 10.1001/jama.2013.276305

By:

Lu Qi;
Qibin Qi;
Prudente, Sabrina;
Mendonca, Christine;
Andreozzi, Francesco;
di Pietro, Natalia;
Sturma, Mariella;
Novelli, Valeria;
Mannino, Gala Chiara;
Formoso, Gloria;
Gervino, Ernest V.;
Hauser, Thomas H.;
Muehlschlegel, Jochen D.;
Niewczas, Monika A.;
Krolewski, Andrzej S.;
Biolo, Gianni;
Pandolfi, Assunta;
Rimm, Eric;
Sesti, Giorgio;
Trischitta, Vincenzo

Publication type:

Article

Genetic testing for heart disease susceptibility: potential impact on motivation to quit smoking.

Published in:

Clinical Genetics, 2007, v. 71, n. 6, p. 501, doi. 10.1111/j.1399-0004.2007.00810.x

By:

Sanderson, S. C.;
Michie, S.

Publication type:

Article

Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-0050-1

By:

Suluba, Emmanuel;
Shuwei, Liu;
Xia, Qing;
Mwanga, Ally

Publication type:

Article

Association of the genetic and traditional risk factors of ischaemic heart disease with STEMI and NSTEMI development.

Published in:

2017

By:

Žaliaduonytė-Pekšienė, Diana;
Lesauskaitė, Vaiva;
Liutkevičienė, Rasa;
Tamakauskas, Vytenis;
Kviesulaitis, Vilius;
Šinkūnaitė-Maršalkienė, Giedrė;
Šimonytė, Sandrita;
Mačiulskytė, Simonita;
Tamulevičiūtė-Prascienė, Eglė;
Gustienė, Olivija;
Tamošiūnas, Abdonas;
Žaliūnas, Remigijus

Publication type:

journal article

Development and Evaluation of a Comprehensive Prediction Model for Incident Coronary Heart Disease Using Genetic, Social, and Lifestyle–Psychological Factors: A Prospective Analysis of the UK Biobank.

Published in:

Annals of Internal Medicine, 2025, v. 178, n. 1, p. 1, doi. 10.7326/ANNALS-24-00716

By:

Naderian, Mohammadreza;
Norland, Kristjan;
Schaid, Daniel J.;
Kullo, Iftikhar J.

Publication type:

Article

New KIF6 Genotyping Assay launched for the detection of those at increased risk of coronary heart disease.

Published in:: Expert Review of Cardiovascular Therapy, 2011, v. 9, n. 4, p. 417
Publication type:: Article

Utility of genetic and non-genetic risk factors in predicting coronary heart disease in Singaporean Chinese.

Published in:

European Journal of Preventive Cardiology, 2017, v. 24, n. 1, p. 153, doi. 10.1177/2047487316676609

By:

Chang, Xuling;
Salim, Agus;
Dorajoo, Rajkumar;
Han, Yi;
Khor, Chiea-Chuen;
van Dam, Rob M;
Yuan, Jian-Min;
Koh, Woon-Puay;
Liu, Jianjun;
Goh, Daniel YT;
Wang, Xu;
Teo, Yik-Ying;
Friedlander, Yechiel;
Heng, Chew-Kiat

Publication type:

Article

Discovering Novel Biochemical and Genetic Markers for Coronary Heart Disease in Qatari Individuals: The Initiative Qatar Cardiovascular Biorepository.

Published in:

Heart Views, 2020, v. 21, n. 1, p. 6, doi. 10.4103/HEARTVIEWS.HEARTVIEWS_98_19

By:

El-Menyar, Ayman;
Al Suwaidi, Jassim;
Badii, Ramin;
Mir, Fayaz;
Dalenberg, Angela K.;
Kullo, Iftikhar J.

Publication type:

Article

Genetic and genomics in congenital heart disease: a clinical review.

Published in:

Jornal de Pediatria, 2020, v. 96, n. 3, p. 279, doi. 10.1016/j.jped.2019.07.004

By:

Saliba, Aline;
Figueiredo, Ana Carolina Vaqueiro;
Baroneza, José Eduardo;
Afiune, Jorge Yuseff;
Pic-Taylor, Aline;
de Oliveira, Silviene Fabiana;
Mazzeu, Juliana Forte

Publication type:

Article

Genetik Durum Varlığı ile Konjenital Kalp Hastalıkları Birlikteliği: Cerrahi Sonuçlar Nasıl Etkilenir?

Published in:

Journal of Harran University Medical Faculty / Harran Üniversitesi Tıp Fakültesi Dergisi, 2019, v. 16, n. 1, p. 63

By:

Yıldız, Okan;
Öztürk, Erkut;
Şen, Onur;
Haydin, Sertaç

Publication type:

Article

The challenges of genetic risk scores for the prediction of coronary heart disease.

Published in:

2017

By:

Börnigen, Daniela;
Karakas, Mahir;
Zeller, Tanja

Publication type:

Editorial

Is Chronic Low Back Pain Associated with the Prevalence of Coronary Heart Disease when Genetic Susceptibility Is Considered? A Co-Twin Control Study of Spanish Twins.

Published in:

PLoS ONE, 2016, v. 11, n. 5, p. 1, doi. 10.1371/journal.pone.0155194

By:

Fernandez, Matt;
Ordoñana, Juan R.;
Hartvigsen, Jan;
Ferreira, Manuela L.;
Refshauge, Kathryn M.;
Sánchez-Romera, Juan F.;
Pinheiro, Marina B.;
Simpson, Stephen J.;
Hopper, John L.;
Ferreira, Paulo H.

Publication type:

Article

De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes.

Published in:

Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12582-y

By:

Watkins, W. Scott;
Hernandez, E. Javier;
Wesolowski, Sergiusz;
Bisgrove, Brent W.;
Sunderland, Ryan T.;
Lin, Edwin;
Lemmon, Gordon;
Demarest, Bradley L.;
Miller, Thomas A.;
Bernstein, Daniel;
Brueckner, Martina;
Chung, Wendy K.;
Gelb, Bruce D.;
Goldmuntz, Elizabeth;
Newburger, Jane W.;
Seidman, Christine E.;
Shen, Yufeng;
Yost, H. Joseph;
Yandell, Mark;
Tristani-Firouzi, Martin

Publication type:

Article

Clinical, demographic and genetic features of patients with congenital heart disease : A single center experience.

Published in:

Marmara Medical Journal, 2022, v. 35, n. 2, p. 159, doi. 10.5472/marumj.1120570

By:

KAYMAKCALAN, Hande;
YALCINKAYA, Leyla;
NIKEREL, Emrah;
YALCIN, Yalim;
Weilai DONG;
ERCAN SENCICEK, Adife Gulhan

Publication type:

Article

Genetics of Congenital Heart Disease: Past and Present.

Published in:

Biochemical Genetics, 2017, v. 55, n. 2, p. 105, doi. 10.1007/s10528-016-9780-7

By:

Muntean, Iolanda;
Togănel, Rodica;
Benedek, Theodora

Publication type:

Article

Common genetic variants do not predict recurrent events in coronary heart disease patients.

Published in:

2022

By:

Thompson, P. L.;
Hui, J.;
Beilby, J.;
Palmer, L. J.;
Watts, G. F.;
West, M. J.;
Kirby, A.;
Marschner, S.;
Simes, R. J.;
Sullivan, D. R.;
White, H. D.;
Stewart, R.;
Tonkin, A. M.

Publication type:

journal article

ACE Gene Polymorphism in Coronary Artery Disease in West Bank, Palestine.

Published in:

Hebron University Research Journal (Natural Sciences), 2020, v. 9, p. 1

By:

Saghir, Sabri;
Darwish, Alaa;
Rajabi, Raghad;
Huiseen, Ayman

Publication type:

Article

Yagel S, Silverman NH, Gembruch U (eds): Fetal cardiology: embryology, genetics, physiology, echocardiographic evaluation, diagnosis and perinatal management of cardiac diseases: Martin Dunitz, London, 2003, X 593 pp with illustrations and tables (ISBN 1-85317-905-1), £ 99.95

Published in:

2003

By:

Suter, Susanne

Publication type:

Book Review

Congenital Heart Disease and Genetic Changes in Folate/Methionine Cycles.

Published in:

Genes, 2024, v. 15, n. 7, p. 872, doi. 10.3390/genes15070872

By:

Karas Kuželički, Nataša;
Doljak, Bojan

Publication type:

Article

The Ratio of Second to Fourth Digit Length (2D:4D) and Heart Disease.

Published in:

Bangladesh Journal of Medical Science, 2016, v. 15, n. 4, p. 529, doi. 10.3329/bjms.v15i4.23958

By:

Kumar, N.;
Sallehuddin, M. A. B.;
Syed, S. M. F. B.;
Idris, M. H. B.;
Jamba, T. A.;
Ravindra, S.;
patil, J.;
Aithal, A.

Publication type:

Article

Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility.

Published in:

Cardiology in the Young, 2021, v. 31, n. 6, p. 965, doi. 10.1017/S1047951120004874

By:

Borghini, Andrea;
Vecoli, Cecilia;
Mercuri, Antonella;
Turchi, Stefano;
Andreassi, Maria Grazia

Publication type:

Article

Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec.

Published in:

2011

By:

Dubé MP;
Bigras JL;
Thibeault M;
Bureau N;
Chetaille P;
Richter A;
Mercier J;
Bellavance M;
Rohlicek C;
Rozen R;
Nemer M;
Khairy P;
Gendron R;
Andelfinger G

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

Genetic evaluation of Congenital Heart Disease by gynealogical research in São Miguel Island, Azores (Portugal).

Published in:: Cardiology in the Young, 2005, v. 15, n. S2, p. 48
Publication type:: Article

Value of genetic testing in the prevention of coronary heart disease events.

Published in:

PLoS ONE, 2019, v. 14, n. 1, p. 1, doi. 10.1371/journal.pone.0210010

By:

Hynninen, Yrjänä;
Linna, Miika;
Vilkkumaa, Eeva

Publication type:

Article

PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.

Published in:

2018

By:

Adler, Angela;
Kirchmeier, Pia;
Reinhard, Julian;
Brauner, Barbara;
Dunger, Irmtraud;
Fobo, Gisela;
Frishman, Goar;
Montrone, Corinna;
Mewes, H.-Werner;
Arnold, Matthias;
Ruepp, Andreas

Publication type:

journal article

Rheumatic Fever and Rheumatic Heart Disease: Genetics and Pathogenesis.

Published in:

Scandinavian Journal of Immunology, 2007, v. 66, n. 2/3, p. 199, doi. 10.1111/j.1365-3083.2007.01974.x

By:

Guilherme, L.;
Ramasawmy, R.;
Kalil, J.

Publication type:

Article

Genetic Epidemiology of Coronary Heart Disease: Past, Present and Future.

Published in:

1985

By:

Poole-Wilson, P. A.

Publication type:

Book Review

PATHOGENIC MECHANISMS OF CONGENITAL HEART DISEASE.

Published in:

Fetal & Pediatric Pathology, 2010, v. 29, n. 5, p. 359, doi. 10.3109/15513811003789628

By:

Huang, Jing-Bin;
Liu, Ying-Long;
Lv, Xiao-Dong

Publication type:

Article

Do genetic determinates of ischaemic heart disease imply that prevention may become more difficult?

Published in:

1998

By:

Tonstad;
Tonstad, S

Publication type:

journal article

The Genetic Basis of Paediatric Heart Disease.

Published in:

Annals of Medicine, 1995, v. 27, n. 3, p. 289, doi. 10.3109/07853899509002580

By:

Johnson, Mark C.;
Payne, R. Mark;
Grant, James W.;
Strauss, Arnold W.

Publication type:

Article

Complex Genetic Architecture of Cardiac Disease in a Wild Type Inbred Strain of <i>Drosophila melanogaster</i>.

Published in:

PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062909

By:

Zhang, Zhi;
Hsieh, Benjamin;
Poe, Amy;
Anderson, Julie;
Ocorr, Karen;
Gibson, Greg;
Bodmer, Rolf

Publication type:

Article

Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease.

Published in:

PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046573

By:

Sobenin, Igor A.;
Sazonova, Margarita A.;
Ivanova, Maria M.;
Zhelankin, Andrey V.;
Myasoedova, Veronika A.;
Postnov, Anton Y.;
Nurbaev, Serik D.;
Bobryshev, Yuri V.;
Orekhov, Alexander N.;
Zeller, Tanja

Publication type:

Article

A Locus on Chromosome 5 Is Associated with Dilated Cardiomyopathy in Doberman Pinschers.

Published in:

PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0020042

By:

Mausberg, Theresa-Bernadette;
Wess, Gerhard;
Simak, Julia;
Keller, Lisa;
Drögemüller, Michaela;
Drögemüller1, Cord;
Webster, Matthew T.;
Stephenson^4, Hannah;
Dukes-McEwan, Joanna;
Leeb, Tosso

Publication type:

Article