Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
19951.7k citationsMark Curran, Igor Splawski et al.Cellprofile →
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
19961.3k citationsMark Curran, Igor Splawski et al.Nature Geneticsprofile →
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
19951.2k citationsQing Wang, Jiaxiang Shen et al.Cellprofile →
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism
20041.1k citationsIgor Splawski, Katherine W. Timothy et al.Cellprofile →
MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia
19991.0k citationsGeoffrey W. Abbott, Federico Sesti et al.Cellprofile →
Spectrum of Mutations in Long-QT Syndrome Genes
2000957 citationsIgor Splawski, Jiaxiang Shen et al.Circulationprofile →
Mutations in the hminK gene cause long QT syndrome and suppress lKs function
1997581 citationsIgor Splawski, Martin Tristani‐Firouzi et al.Nature Geneticsprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
hero ref
This map shows the geographic impact of Igor Splawski's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Igor Splawski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Igor Splawski more than expected).
This network shows the impact of papers produced by Igor Splawski. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Igor Splawski. The network helps show where Igor Splawski may publish in the future.
Co-authorship network of co-authors of Igor Splawski
This figure shows the co-authorship network connecting the top 25 collaborators of Igor Splawski.
A scholar is included among the top collaborators of Igor Splawski based on the total number of
citations received by their joint publications. Widths of edges
represent the number of papers authors have co-authored together.
Node borders
signify the number of papers an author published with Igor Splawski. Igor Splawski is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Bloise, Raffaella, Carlo Napolitano, Katherine W. Timothy, et al.. (2006). Abstract 2439: Clinical Profile and Risk of Sudden Death in Children with Timothy Syndrome. Circulation. 114.1 indexed citations
3.
Splawski, Igor, Dana Yoo, Stephanie C. Stotz, et al.. (2006). CACNA1H Mutations in Autism Spectrum Disorders. Journal of Biological Chemistry. 281(31). 22085–22091.183 indexed citations
Splawski, Igor, Katherine W. Timothy, Niels Decher, et al.. (2004). CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism. Cell. 119(1). 19–31.1112 indexed citations breakdown →
6.
Zhang, Li, G. Michael Vincent, Marco Baralle, et al.. (2004). An intronic mutation causes long QT syndrome. Journal of the American College of Cardiology. 44(6). 1283–1291.47 indexed citations
7.
Westenskow, Peter D., Igor Splawski, Katherine W. Timothy, Mark T. Keating, & Michael C. Sanguinetti. (2004). Compound Mutations. Circulation. 109(15). 1834–1841.232 indexed citations
Abbott, Geoffrey W., Federico Sesti, Igor Splawski, et al.. (1999). MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia. Cell. 97(2). 175–187.1006 indexed citations breakdown →
Splawski, Igor, Martin Tristani‐Firouzi, Michael H. Lehmann, Michael C. Sanguinetti, & Mark T. Keating. (1997). Mutations in the hminK gene cause long QT syndrome and suppress lKs function. Nature Genetics. 17(3). 338–340.581 indexed citations breakdown →
Curran, Mark, Igor Splawski, Timothy C. Burn, et al.. (1996). Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genetics. 12(1). 17–23.1321 indexed citations breakdown →
18.
Curran, Mark, et al.. (1995). A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell. 80(5). 795–803.1746 indexed citations breakdown →
19.
Wang, Qing, Jiaxiang Shen, Igor Splawski, et al.. (1995). SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 80(5). 805–811.1249 indexed citations breakdown →
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive
bibliographic database. While OpenAlex provides broad and valuable coverage of the global
research landscape, it—like all bibliographic datasets—has inherent limitations. These include
incomplete records, variations in author disambiguation, differences in journal indexing, and
delays in data updates. As a result, some metrics and network relationships displayed in
Rankless may not fully capture the entirety of a scholar's output or impact.