Kathryn McGurk: h-index, Total Citations, and Citation Map
Kathryn McGurk's h-index is 19 (27 i10-index, 1,189+ total citations across 3+ publications) according to Google Scholar as of May 2026. Kathryn McGurk is affiliated with Cardiovascular Geneticist, Imperial College London.
Kathryn McGurk is a researcher affiliated with Cardiovascular Geneticist, Imperial College London, specializing in Genomics, Bioinformatics, Genetics. Their work has been cited 1,189 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Kathryn McGurk's Citation Metrics
Bibliometric impact based on 3 indexed publications.
- H-Index
- 19
- i10-Index
- 27
- Total Citations
- 1,189
- Citing Countries
- 17
As of May 2026.
Kathryn McGurk has an h-index of 19 and 1,189 total citations across 3 publications, with research cited by institutions in 17 countries.
Download Exports (PNG, CSV, Poster)
Free Viewing Kathryn McGurk's citation map is always free. Pay once to download poster, PNG, and CSV files for offline use or your visa packet.
Global Impact Map
Visualizing the geographic distribution of institutions that have cited your work.
Starting…
Pins will appear here as institutions are resolved — no need to refresh.
Top Cited Works
Tip: clickto hide a row from the map
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy
2021124
Top Citing Countries
Top Citing Institutions
Visa Evidence Package
Views and exports tuned for EB-1A, O-1A, and EB-2 NIW petitions. Sustained acclaim, geographic reach, and independent-citation filtering are the strongest evidence categories immigration adjudicators look for.
Significant Contributions
Auto-detected research lines — a seminal paper and the follow-up work building on it. Review and edit before using in a petition. Each Free PDF opens in a new tab — EB-1A organises this into the structure USCIS applies to Criterion 5 of 8 CFR § 204.5(h)(3)(v); EB-1B re-frames it under § 204.5(i)(3) (outstanding researcher); NIW presents it under prong 2 of Matter of Dhanasar.
The researcher advanced the clinical understanding of hypertrophic cardiomyopathy by characterizing phenotypic expression and outcomes associated with rare genetic variants, establishing a foundational reference in the field.
The researcher conducted a systematic large-scale assessment of the genetic architecture of left ventricular noncompaction, revealing diverse etiologies and establishing a foundational framework for understanding this cardiac condition.
The researcher identified novel genetic loci and mechanisms in hypertrophic cardiomyopathy through large-scale genome-wide association analyses published in Nature Genetics.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
Related Guides
Learn how to use citation maps for your research and visa applications.
