Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
|
Cell
|
1995
|
10.18
|
2
|
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
|
Circulation
|
2000
|
7.50
|
3
|
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
|
Circulation
|
2001
|
7.47
|
4
|
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
|
Nat Genet
|
1996
|
7.35
|
5
|
Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.
|
Circulation
|
2000
|
5.09
|
6
|
Diagnostic criteria for the long QT syndrome. An update.
|
Circulation
|
1993
|
4.48
|
7
|
The long QT syndrome. Prospective longitudinal study of 328 families.
|
Circulation
|
1991
|
3.99
|
8
|
ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
|
Circulation
|
1995
|
3.79
|
9
|
Influence of genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.
|
N Engl J Med
|
1998
|
3.41
|
10
|
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.
|
Science
|
1991
|
3.38
|
11
|
Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.
|
Circulation
|
2000
|
2.95
|
12
|
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
|
Circulation
|
1996
|
2.70
|
13
|
Molecular basis of the long-QT syndrome associated with deafness.
|
N Engl J Med
|
1997
|
2.57
|
14
|
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.
|
Circulation
|
1998
|
2.53
|
15
|
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
|
Hum Mol Genet
|
1995
|
2.30
|
16
|
Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease.
|
Arterioscler Thromb Vasc Biol
|
1996
|
1.94
|
17
|
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
|
Genomics
|
1998
|
1.93
|
18
|
Coronary spasm producing coronary thrombosis and myocardial infarction.
|
N Engl J Med
|
1983
|
1.91
|
19
|
Q-T interval syndromes.
|
Prog Cardiovasc Dis
|
1974
|
1.69
|
20
|
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.
|
Nat Genet
|
1994
|
1.55
|
21
|
Hypothesis for the molecular physiology of the Romano-Ward long QT syndrome.
|
J Am Coll Cardiol
|
1992
|
1.55
|
22
|
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
|
Circulation
|
1998
|
1.53
|
23
|
Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.
|
Am J Cardiol
|
1999
|
1.25
|
24
|
Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease.
|
Clin Chem
|
1994
|
1.24
|
25
|
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
|
Clin Genet
|
2003
|
1.16
|
26
|
Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.
|
Am J Hum Genet
|
1991
|
1.15
|
27
|
Lipoprotein(a) interactions with lipid and nonlipid risk factors in early familial coronary artery disease.
|
Arterioscler Thromb Vasc Biol
|
1997
|
1.05
|
28
|
Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.
|
J Am Coll Cardiol
|
1997
|
1.01
|
29
|
Role of DNA testing for diagnosis, management, and genetic screening in long QT syndrome, hypertrophic cardiomyopathy, and Marfan syndrome.
|
Heart
|
2001
|
0.99
|
30
|
Clinically practical lead systems for improved electrocardiography: comparison with precordial grids and conventional lead systems.
|
Circulation
|
1979
|
0.92
|
31
|
Clinical implications for affected parents and siblings of probands with long-QT syndrome.
|
Circulation
|
2001
|
0.92
|
32
|
Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome.
|
Am J Cardiol
|
2000
|
0.92
|
33
|
The financial impact of Medicare diagnosis-related groups. Effect upon hospitals receiving cardiac patients referred for tertiary care.
|
Chest
|
1987
|
0.87
|
34
|
Higher plasma homocyst(e)ine and increased susceptibility to adverse effects of low folate in early familial coronary artery disease.
|
Arterioscler Thromb Vasc Biol
|
1995
|
0.85
|
35
|
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.
|
Am J Hum Genet
|
1994
|
0.84
|
36
|
Locus heterogeneity of autosomal dominant long QT syndrome.
|
J Clin Invest
|
1993
|
0.84
|
37
|
Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
|
J Med Screen
|
2001
|
0.83
|
38
|
Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases:hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association.
|
Circulation
|
1998
|
0.82
|
39
|
Reversible segmental myocardial dysfunction in septic shock.
|
Crit Care Med
|
1986
|
0.82
|
40
|
Mechanisms of ischemic ST-segment displacement. Evaluation by direct current recordings.
|
Circulation
|
1977
|
0.81
|
41
|
George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
|
Proc Assoc Am Physicians
|
1997
|
0.77
|
42
|
The heart rate of Romano-Ward syndrome patients.
|
Am Heart J
|
1986
|
0.76
|
43
|
Prevention of drug-induced long QT syndrome: gender, chemistry, and education.
|
J Cardiovasc Electrophysiol
|
2001
|
0.75
|
44
|
QRS-wave detector evaluation.
|
Am Heart J
|
1972
|
0.75
|
45
|
Long QT syndrome in children: the value of the rate corrected QT interval in children who present with fainting.
|
J Med Screen
|
2001
|
0.75
|
46
|
In vivo canine coronary artery laser irradiation: photodynamic therapy using dihematoporphyrin ether and 632 nm laser. A safety and dose-response relationship study.
|
Lasers Surg Med
|
1991
|
0.75
|
47
|
Diagnosis of old inferior myocardial infarction by body surface isopotential mapping.
|
Am J Cardiol
|
1977
|
0.75
|
48
|
The expression of normal ventricular repolarization in the body surface distribution of T potentials.
|
Circulation
|
1976
|
0.75
|
49
|
An evaluation of potential prognostic indicators in cardiac patients.
|
J Air Med Transp
|
1991
|
0.75
|
50
|
Optothermal mathematical model and experimental studies for laser irradiation of arteries in the presence of blood flow.
|
Appl Opt
|
1989
|
0.75
|
51
|
Multifiber gradient-index lens laser angioplasty probe.
|
Lasers Surg Med
|
1990
|
0.75
|
52
|
Application of body surface mapping to exercise testing: S-T80 isoarea maps in patients with coronary artery disease.
|
Am J Cardiol
|
1982
|
0.75
|