Works matching DE "HEART disease genetics"

Results: 211

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for ...

Published in:

Nature, 1992, v. 359, n. 6396, p. 641, doi. 10.1038/359641a0

By:

Cambien, Francois;
Poirier, Odette

Publication type:

Article

The ACE of hearts.

Published in:

Nature, 1992, v. 359, n. 6396, p. 588, doi. 10.1038/359588a0

By:

Kurt, Theodore W.

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

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

Published in:

Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 5, p. 592, doi. 10.1002/mgg3.305

By:

Bdier, Amnah Y.;
Al ‐ Ghamdi, Saleh;
Verma, Prashant K.;
Dagriri, Khalid;
Alshehri, Bandar;
Jiman, Omamah A.;
Ahmed, Sherif E.;
Wilde, Arthur A. M.;
Bhuiyan, Zahurul A.;
Al ‐ Aama, Jumana Y.

Publication type:

Article

The genetics of hypertrophic cardiomyopathy.

Published in:

Global Cardiology Science & Practice, 2018, v. 2018, n. 3, p. 1, doi. 10.21542/gcsp.2018.36

By:

Akhtar, Mohammed;
Elliott, Perry

Publication type:

Article

Genetics of channelopathies associated with sudden cardiac death.

Published in:

Global Cardiology Science & Practice, 2015, v. 2015, n. 3, p. 1, doi. 10.5339/gcsp.2015.39

By:

Campuzano, Oscar;
Sarquella-Brugada, Georgia;
Brugada, Ramon;
Brugada, Josep

Publication type:

Article

Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.

Published in:

Ultrasound in Obstetrics & Gynecology, 2013, v. 41, n. 3, p. 336, doi. 10.1002/uog.12279

By:

Hoedemaekers, Y. M.;
Cohen‐Overbeek, T. E.;
Frohn‐Mulder, I. M. E.;
Dooijes, D.;
Majoor‐Krakauer, D. F.

Publication type:

Article

NIH Data Sharing.

Published in:

JAMA: Journal of the American Medical Association, 2007, v. 298, n. 20, p. 2361, doi. 10.1001/jama.298.20.2361-a

By:

Kuehn, Bridget M.

Publication type:

Article

Validity of Reported Genetic Risk Factors for Acute Coronary Syndrome.

Published in:

2007

By:

McCarthy, Jeanette J.;
Topol, Eric J.

Publication type:

Letter

Validity of Reported Genetic Risk Factors for Acute Coronary Syndrome.

Published in:

2007

By:

Morgan, Thomas M.;
Krumholz, Harlan M.;
Lifton, Richard P.;
Spertus, John A.

Publication type:

Letter

Validity of Reported Genetic Risk Factors for Acute Coronary Syndrome.

Published in:

2007

By:

Wang, William Y.S.

Publication type:

Letter

Validity of Reported Genetic Risk Factors for Acute Coronary Syndrome.

Published in:

2007

By:

Bochud, Murielle;
Chiolero, Arnaud;
Paccaud, Fred

Publication type:

Letter

Validity of Reported Genetic Risk Factors for Acute Coronary Syndrome.

Published in:

2007

By:

Ferro, W. Gregory;
Manolio, Teri A.;
Guttmacher, Alan E.;
Collins, Francis S.

Publication type:

Letter

Nonvalidation of Reported Genetic Risk Factors for Acute Coronary Syndrome in a Large-Scale Replication Study.

Published in:

JAMA: Journal of the American Medical Association, 2007, v. 297, n. 14, p. 1551, doi. 10.1001/jama.297.14.1551

By:

Morgan, Thomas M.;
Krumholz, Harlan M.;
Lifton, Richard P.;
Spertus, John A.

Publication type:

Article

Mitochondrial defects may play role in the metabolic syndrome.

Published in:

2004

By:

Hampton, Tracy

Publication type:

journal article

Parental Cardiovascular Disease as a Risk Factor for Cardiovascular Disease in Middle-aged Adults: A Prospective Study of Parents and Offspring.

Published in:

JAMA: Journal of the American Medical Association, 2004, v. 291, n. 18, p. 2204, doi. 10.1001/jama.291.18.2204

By:

Lloyd-Jones, Donald M.;
Nam, Byung-Ho;
D'Agostino, Sr, Ralph B.;
Levy, Daniel;
Murabito, Joanne M.;
Wang, Thomas J.;
Wilson, Peter W. F.;
O'Donnell, Christopher J.

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

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

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

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

Prevalence of cardiac channelopathies in a tertiary referral centre in Northern Ireland.

Published in:

Ulster Medical Journal, 2008, v. 77, n. 2, p. 135

By:

Bennett, J. R.;
McOsker, J.;
Jardine, T. C. L.;
Scott, P. J.;
McKeown, P. P.

Publication type:

Article

Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos.

Published in:

BMC Anesthesiology, 2016, p. 1, doi. 10.1186/s12871-016-0188-z

By:

Ran Guo;
Guangjian Liu;
Min Du;
Yu Shi;
Pu Jiang;
Xiaoli Liu;
Lan Liu;
Jianxia Liu;
Ying Xu

Publication type:

Article

Cascade Screening in Families with Inherited Cardiac Diseases Driven by Cardiologists: Feasibility and Nationwide Outcome in Long QT Syndrome.

Published in:

Cardiology, 2013, v. 126, n. 2, p. 131, doi. 10.1159/000350825

By:

Theilade, Juliane;
Kanters, Jørgen;
Henriksen, Finn Lund;
Gilså-Hansen, Michael;
Svendsen, Jesper Hastrup;
Eschen, Ole;
Toft, Egon;
Reimers, Jesper Irving;
Tybjærg-Hansen, anne;
Christiansen, Michael;
Jensen, Henrik Kjærulf;
Bundgaard, Henning

Publication type:

Article

Stress-Induced Cardiomyopathy in Sweden: Evidence for Different Ethnic Predisposition and Altered Cardio-Circulatory Status.

Published in:

Cardiology, 2012, v. 122, n. 3, p. 180, doi. 10.1159/000338814

By:

Schultz, Tomas;
Yangzhen Shao;
Redfors, Björn;
Sverrisdóttir, Yrsa Bergmann;
Råmunddal, Truls;
Albertsson, Per;
Matejka, Göran;
Omerovic, Elmir

Publication type:

Article

Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe[sup 110] →Ile Mutation in Cardiac Troponin T.

Published in:

Cardiology, 2000, v. 93, n. 3, p. 155, doi. 10.1159/000007020

By:

Tong-Lang Lin, Boris;
Ichihara, Sahoko;
Yamada, Yoshiji;
Nagasaka, Tetsuo;
Ishihara, Hitoshi;
Nakashima, Nobuo;
Yokota, Mitsuhiro

Publication type:

Article

What Is QT Interval Prolongation?

Published in:

Journal of Family Practice, 2005, v. 54, p. S4

By:

Vorchheimer, David A.

Publication type:

Article

A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-73048-6

By:

Park, Han Sung;
Kim, In Jai;
Kim, Eun Gyo;
Ryu, Chang Soo;
Lee, Jeong Yong;
Ko, Eun Ju;
Park, Hyeon Woo;
Sung, Jung Hoon;
Kim, Nam Keun

Publication type:

Article

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64525-z

By:

Mosley, Jonathan D.;
Levinson, Rebecca T.;
Farber-Eger, Eric;
Edwards, Todd L.;
Hellwege, Jacklyn N.;
Hung, Adriana M.;
Giri, Ayush;
Shuey, Megan M.;
Shaffer, Christian M.;
Shi, Mingjian;
Brittain, Evan L.;
Chung, Wendy K.;
Kullo, Iftikhar J.;
Arruda-Olson, Adelaide M.;
Jarvik, Gail P.;
Larson, Eric B.;
Crosslin, David R.;
Williams, Marc S.;
Borthwick, Ken M.;
Hakonarson, Hakon

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

Efficient generation of adipocytes in a dish.

Published in:

Nature Cell Biology, 2012, v. 14, n. 2, p. 126, doi. 10.1038/ncb2430

By:

Elefanty, Andrew G.;
Stanley, Edouard G.

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

Increasing sensitivity—a common-sense approach?

Published in:

Netherlands Heart Journal, 2019, v. 27, n. 6, p. 287, doi. 10.1007/s12471-019-1280-z

By:

Michels, M.;
Asselbergs, F. W.;
van der Velden, J.

Publication type:

Article

Evaluation of gene panels for inherited cardiac disease—is less more?

Published in:

2019

By:

Dooijes, D.;
Siemelink, M.;
Baas, A. F.

Publication type:

Editorial

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

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

Variety of roles for molecular genetics in dealing with cardiovascular disease.

Published in:

JAMA: Journal of the American Medical Association, 1993, v. 270, n. 19, p. 2269, doi. 10.1001/jama.1993.03510190017004

By:

Cotton, Paul

Publication type:

Article

Arytmogenní kardiomyopatie.

Published in:

Medicina Sportiva Bohemica et Slovaca, 2013, v. 22, n. 3, p. 135

By:

Elbl, Lubomír;
Balcárková, Pavla;
Jedlička, František

Publication type:

Article

RETKA UROĐENA SRCANA MANA KAO UZROK AKTIVACIJE TUBERKULOZE.

Published in:

Medical Review / Medicinski Pregled, 2010, v. 63, n. 7/8, p. 565, doi. 10.2298/MPNS1008565R

By:

RADOVIĆ, Milan;
RISTIĆ, Lidija;
STANKOVIĆ, Ivana;
PETROVIĆ, Dejan

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

Changes in gene methylation patterns in neonatal murine hearts: Implications for the regenerative potential.

Published in:

BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-2545-1

By:

Górnikiewicz, Bartosz;
Ronowicz, Anna;
Krzemiński, Michał;
Sachadyn, Paweł

Publication type:

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

A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy.

Published in:

Journal of Interventional Cardiac Electrophysiology, 2012, v. 34, n. 1, p. 11, doi. 10.1007/s10840-011-9643-4

By:

Ostrowska Dahlgren, Bozena;
Allen, Marie;
Lindström, Anne-Cristine;
Bjerke, Mia;
Blomström-Lundqvist, Carina

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

Myocardial Fibrosis in the Pathogenesis, Diagnosis, and Treatment of Hypertrophic Cardiomyopathy.

Published in:

Cardiovascular Innovations & Applications (CVIA), 2021, v. 5, n. 4, p. 267, doi. 10.15212/CVIA.2021.0008

By:

Zeyi Cheng;
Miaomiao Qi;
Chengyuan Zhang;
Yanxia Mao

Publication type:

Article

Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study.

Published in:

Cardio-Oncology, 2024, v. 10, n. 1, p. 1, doi. 10.1186/s40959-024-00231-3

By:

Boen, Hanne M.;
Alaerts, Maaike;
Goovaerts, Inge;
Saenen, Johan B.;
Franssen, Constantijn;
Vorlat, Anne;
Vermeulen, Tom;
Heidbuchel, Hein;
Van Laer, Lut;
Loeys, Bart;
Van Craenenbroeck, Emeline M.

Publication type:

Article

Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1105, doi. 10.1007/s00439-014-1451-3

By:

Lusk, Christine;
Dyson, Greg;
Clark, Andrew;
Ballantyne, Christie;
Frikke-Schmidt, Ruth;
Tybjærg-Hansen, Anne;
Boerwinkle, Eric;
Sing, Charles

Publication type:

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

The Effect of Educational Programs on Hypertension Management.

Published in:

International Cardiovascular Research Journal, 2014, v. 8, n. 3, p. 94

By:

Babaee Beigi, Mohammad Ali;
Zibaeenezhad, Mohammad Javad;
Aghasadeghi, Kamran;
Jokar, Abutaleb;
Shekarforoush, Shahnaz;
Khazraei, Hajar

Publication type:

Article

A snapshot of genetic and epigenetic basis of arrhythmia and heart failure.

Published in:

2015

By:

Junjie Xiao;
Sluijter, Joost P. G.;
Das, Saumya;
Yiqing Yang;
Zhongming Shen

Publication type:

Editorial

IMPACT OF MULTIPLE GENE MUTATIONS IN DETERMINING THE SEVERITY OF CARDIOMYOPATHY AND HEART FAILURE.

Published in:

Clinical & Experimental Pharmacology & Physiology, 2008, v. 35, n. 11, p. 1349, doi. 10.1111/j.1440-1681.2008.05037.x

By:

Tsoutsman, Tatiana;
Bagnall, Richard D;
Semsarian, Christopher

Publication type:

Article