Standout Papers
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome (1995)
- Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias (1996)
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome (1995)
- CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism (2004)
- MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia (1999)
- Spectrum of Mutations in Long-QT Syndrome Genes (2000)
- Mutations in the hminK gene cause long QT syndrome and suppress lKs function (1997)
Immediate Impact
15 by Nobel laureates 65 from Science/Nature 133 standout
Citing Papers
Antisense oligonucleotide therapeutic approach for Timothy syndrome
2024 StandoutNature
Cryo-EM Structure of the Open Human Ether-à-go-go -Related K + Channel hERG
2017 StandoutNobel
Works of Igor Splawski being referenced
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1995 Standout
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
1994
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Igor Splawski | 9088 | 8755 | 2253 | 24 | 10.7k | |
| Katherine W. Timothy | 8702 | 9456 | 1642 | 44 | 10.9k | |
| Mark Curran | 7641 | 7129 | 2245 | 50 | 9.8k | |
| Donald L. Atkinson | 5045 | 4560 | 1408 | 23 | 7.0k | |
| Morten Grunnet | 4723 | 3497 | 1678 | 146 | 6.4k | |
| Glenn E. Kirsch | 5339 | 4162 | 2495 | 80 | 6.4k | |
| James Maylie | 6055 | 2716 | 4508 | 88 | 8.0k | |
| Leanne L. Cribbs | 5331 | 2406 | 3246 | 71 | 6.5k | |
| Michel Fink | 4721 | 2393 | 2478 | 27 | 5.5k | |
| Stephan Grissmer | 4788 | 1851 | 2256 | 85 | 5.8k | |
| W. Jonathan Lederer | 8131 | 6529 | 3721 | 74 | 10.2k |
All Works
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