Elysa Marco

604 citations
2 papers · 32 · h-index 2

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Prenatal Screening and Diagnostics
    • Fetal and Pediatric Neurological Disorders

Papers in

    • Genetics and Neurodevelopmental Disorders 1
    • Genomics and Rare Diseases 1
    • Genomic variations and chromosomal abnormalities 1
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
    • RNA and protein synthesis mechanisms 1

Elysa Marco

2 papers receiving 20 citations

Peers

Elysa Marco
Comparison fields: 5 of 14
  • Genetics 25
  • Pediatrics, Perinatology and Child Health 10
  • Reproductive Medicine 3
  • Plant Science 7
  • Molecular Biology 13
Replace Una Maye with:
Una Maye United Kingdom
Arveen Kamath United Kingdom
Karol Rubin United States
Stefania Rassu Italy
H Fujimaki Japan
Naomi Yachelevich United States
Katherine Yates United Kingdom
Randa Bassiouni Saudi Arabia
Shlomit Barzilai Israel
Jonathon Waters United Kingdom
Elysa Marco relative to Una Maye United Kingdom Una Maye's profile →
Citations per field
00.5×
Una Maye · 1×
Citations per year

Countries citing papers authored by Elysa Marco

Since Specialization
Citations

This map shows the geographic impact of Elysa Marco'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 Elysa Marco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elysa Marco more than expected).

Fields of papers citing papers by Elysa Marco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elysa Marco. 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 Elysa Marco. The network helps show where Elysa Marco may publish in the future.

Co-authors

The 16 scholars most cited alongside Elysa Marco, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elysa Marco Line = papers co-authored together Elysa Marco links everyone, so they are left out of the graph.

All Works

2 of 2 papers shown

About Elysa Marco

Elysa Marco is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Infectious Diseases and Organic Chemistry, having authored 2 papers that have together received 32 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Genomics and Rare Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Genetics (25 citations), Pediatrics, Perinatology and Child Health (10 citations), Reproductive Medicine (3 citations), Plant Science (7 citations) and Molecular Biology (13 citations). Elysa Marco has collaborated with scholars based in United States and Canada. Frequent co-authors include Elliott H. Sherr, Ophir D. Klein, Philip D. Cotter, Anne Slavotinek, Kendall H. Backstrand, Monica Konstantino, Stanley F. Nelson, Julián A. Martínez-Agosto, Rebecca Signer and Saquib A. Lakhani. Their work appears in journals such as American Journal of Medical Genetics Part A and Clinical Dysmorphology.

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.

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