Glenda M. Espinal

547 citations
18 papers · 426 · h-index 10

Impact in

  • Genetics top 10%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Autism Spectrum Disorder Research

Papers in

Glenda M. Espinal

17 papers receiving 421 citations

Peers

Glenda M. Espinal
Comparison fields: 5 of 59
  • Genetics 303
  • Cognitive Neuroscience 148
  • Molecular Biology 226
  • Cellular and Molecular Neuroscience 54
  • Endocrine and Autonomic Systems 17
Replace Stephanie M. Kyle with:
Stephanie M. Kyle United States
Jussara Mendonça dos Santos Brazil
Vinh Tai Truong Canada
Gloria Zollo Italy
Marja‐Leena Väisänen Finland
Isabella Barbiero Italy
Mehrnoush Aghadavoud Jolfaei Netherlands
Carrie A. Sheeler United States
Karim Hyder United States
Glenda M. Espinal relative to Stephanie M. Kyle United States Stephanie M. Kyle's profile →
Citations per field
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Stephanie M. Kyle · 1×
Citations per year

Countries citing papers authored by Glenda M. Espinal

Since Specialization
Citations

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

Fields of papers citing papers by Glenda M. Espinal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Glenda M. Espinal. 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 Glenda M. Espinal. The network helps show where Glenda M. Espinal may publish in the future.

Co-authors

The 25 scholars most cited alongside Glenda M. Espinal, 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 Glenda M. Espinal Line = papers co-authored together Glenda M. Espinal links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 201487
2 201961
3 201957
4 201751
5 201749
6 200729
7 200920
8 200419
9 202115
10 201714
11 20007
12 20234
13 20244
14 20254
15 20093
16 20221
17 20221
18 20250

About Glenda M. Espinal

Glenda M. Espinal is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Endocrine and Autonomic Systems and Clinical Biochemistry, having authored 18 papers that have together received 426 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Autism Spectrum Disorder Research (5 papers), Mitochondrial Function and Pathology (2 papers), Ubiquitin and proteasome pathways (2 papers), Sphingolipid Metabolism and Signaling (1 paper), Pancreatic function and diabetes (1 paper), Lipid metabolism and biosynthesis (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (303 citations), Cognitive Neuroscience (148 citations), Molecular Biology (226 citations), Cellular and Molecular Neuroscience (54 citations) and Endocrine and Autonomic Systems (17 citations). Glenda M. Espinal has collaborated with scholars based in United States, Thailand and Colombia. Frequent co-authors include Paul J. Hagerman, Randi Jenssen Hagerman, Flora Tassone, Isaac N. Pessah, Kyoungmi Kim, Craig H. Warden, Blythe P Durbin-Johnson, Dalyir I. Pretto, Susan Hulsizer and Sally Chiu. Their work appears in journals such as Physiological Genomics, Annals of the New York Academy of Sciences, Frontiers in Genetics, Brain Communications and Molecular Brain.

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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