Megan Marie Martin: h-index, Total Citations, and Citation Map
Megan Marie Martin's h-index is 12 (13 i10-index, 426+ total citations across 5+ publications) according to Google Scholar as of May 2026. Megan Marie Martin is affiliated with Unknown affiliation.
Megan Marie Martin is a researcher affiliated with Unknown affiliation, specializing in various fields. Their work has been cited 426 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Megan Marie Martin's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 12
- i10-Index
- 13
- Total Citations
- 426
- Citing Countries
- 15
As of May 2026.
Megan Marie Martin has an h-index of 12 and 426 total citations across 5 publications, with research cited by institutions in 15 countries.
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Top Cited Works
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Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders using an ultra-high resolution chromosomal microarray optimized for neurodevelopmental …
201693
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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 autism spectrum disorder diagnostics by applying ultra-high resolution chromosomal microarray analysis to consecutive clinical cohorts, establishing a methodological benchmark for detecting neurodevelopmental genetic variants.
The researcher identified a familial KANK1 deletion deviating from expected imprinting patterns, providing critical evidence for atypical genetic mechanisms in this locus.
The researcher advanced clinical genetics by documenting parental perspectives on variants of unknown significance in chromosomal microarray analysis, establishing a foundational reference for patient-centered interpretation.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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