Eyby Leon

1.1k total citations
29 papers, 379 citations indexed

About

Eyby Leon is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Eyby Leon has authored 29 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Clinical Biochemistry. Recurrent topics in Eyby Leon's work include Metabolism and Genetic Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Mitochondrial Function and Pathology (4 papers). Eyby Leon is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Mitochondrial Function and Pathology (4 papers). Eyby Leon collaborates with scholars based in United States, Spain and India. Eyby Leon's co-authors include Jullianne Diaz, Alina Khromykh, Ramaswamy K. Iyer, Joseph G. Vockley, John E. Niederhuber, Rajiv Baveja, Dale L. Bodian, Anna Lehman, J. R. Ashworth and Ermelinda Santos Silva and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and The American Journal of Human Genetics.

In The Last Decade

Eyby Leon

27 papers receiving 369 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Eyby Leon United States 9 263 104 60 41 32 29 379
Eri Imagawa Japan 13 250 1.0× 170 1.6× 31 0.5× 24 0.6× 29 0.9× 30 418
Alina Kurolap Israel 12 150 0.6× 118 1.1× 28 0.5× 55 1.3× 61 1.9× 42 399
Emily Spencer United States 11 208 0.8× 214 2.1× 21 0.3× 17 0.4× 22 0.7× 15 489
Christina Rudduck Australia 14 233 0.9× 111 1.1× 37 0.6× 31 0.8× 12 0.4× 26 442
Chin-To Fong United States 9 198 0.8× 95 0.9× 84 1.4× 108 2.6× 17 0.5× 9 450
Y T Chen United States 11 187 0.7× 193 1.9× 58 1.0× 41 1.0× 13 0.4× 11 769
Amy Knight Johnson United States 12 196 0.7× 164 1.6× 16 0.3× 15 0.4× 32 1.0× 16 396
Marjan M. Nezarati Canada 10 232 0.9× 198 1.9× 15 0.3× 23 0.6× 38 1.2× 17 447
Maya Chopra United States 11 151 0.6× 174 1.7× 20 0.3× 31 0.8× 51 1.6× 25 406
Yu Ding China 12 219 0.8× 170 1.6× 38 0.6× 22 0.5× 19 0.6× 38 359

Countries citing papers authored by Eyby Leon

Since Specialization
Citations

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

Fields of papers citing papers by Eyby Leon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eyby Leon

This figure shows the co-authorship network connecting the top 25 collaborators of Eyby Leon. A scholar is included among the top collaborators of Eyby Leon 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 Eyby Leon. Eyby Leon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Leon, Eyby, Natasha Shur, Kimberly A. Chapman, et al.. (2024). Death associated with brain herniation in classical MSUD patients from underrepresented populations. Molecular Genetics and Metabolism. 141(4). 108297–108297.
2.
Kousa, Youssef A., et al.. (2023). Pearls & Oy-sters: Delayed Response to Pyridoxine in Pyridoxine-Dependent Epilepsy. Neurology. 101(18). e1828–e1832. 4 indexed citations
3.
Leon, Eyby, Veronica Gomez‐Lobo, Maureen Monaghan, et al.. (2023). P227: De novo GATA4 deletion in a 46,XX boy with hypospadias and pulmonic valve stenosis. SHILAP Revista de lepidopterología. 1(1). 100255–100255.
4.
Ekong, Udeme D., Nada Yazigi, Karim Khan, et al.. (2022). Domino liver transplantation: Expanding the liver donor pool to the pediatric recipient. Liver Transplantation. 28(12). 1947–1950. 2 indexed citations
5.
Leon, Eyby, et al.. (2022). ALDH1A2‐related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway. American Journal of Medical Genetics Part A. 191(1). 90–99. 7 indexed citations
6.
Diaz, Jullianne, et al.. (2021). Pure Distal 7q Duplication: Describing a Macrocephalic Neurodevelopmental Syndrome, Case Report and Review of the Literature. Molecular Syndromology. 12(3). 159–168. 2 indexed citations
7.
Leon, Eyby, Jullianne Diaz, Hanne Hove, et al.. (2020). Unique skeletal manifestations in patients with Primrose syndrome. European Journal of Medical Genetics. 63(8). 103967–103967. 6 indexed citations
8.
Diaz, Jullianne, et al.. (2019). MAP1B related syndrome: Case presentation and review of literature. American Journal of Medical Genetics Part A. 179(9). 1703–1708. 9 indexed citations
9.
Alston, Charlotte L., Mike T. Veling, Juliana Heidler, et al.. (2019). Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency. The American Journal of Human Genetics. 106(1). 92–101. 40 indexed citations
10.
Diaz, Jullianne, et al.. (2018). Presentation of a recurrent FMR1 missense mutation (R138Q) in an affected female. 3(3-4). 139–144. 4 indexed citations
11.
Beck, David B., Kristina Cusmano‐Ozog, Nickie Andescavage, & Eyby Leon. (2018). Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction. PubMed. 3(1). 45–48. 10 indexed citations
12.
Crippa, Beatrice Letizia, et al.. (2015). Biochemical abnormalities in Pearson syndrome. American Journal of Medical Genetics Part A. 167(3). 621–628. 28 indexed citations
13.
Khromykh, Alina, Benjamin D. Solomon, Dale L. Bodian, et al.. (2015). Diagnosis of D-Bifunctional Protein Deficiency through Whole-Genome Sequencing: Implications for Cost-Effective Care. Molecular Syndromology. 6(3). 141–146. 6 indexed citations
14.
Lehman, Anna, Dale L. Bodian, J. R. Ashworth, et al.. (2014). Mutations in NOTCH1 Cause Adams-Oliver Syndrome. The American Journal of Human Genetics. 95(3). 275–284. 136 indexed citations
15.
Johnston, Jennifer J., Julie C. Sapp, Cynthia J. Curry, et al.. (2013). Expansion of the TARP syndrome phenotype associated with de novo mutations and mosaicism. American Journal of Medical Genetics Part A. 164(1). 120–128. 30 indexed citations
16.
Christensen, Robert D., Hassan M. Yaish, Eyby Leon, Martha Sola‐Visner, & Pankaj B. Agrawal. (2013). A de novo T73I Mutation in <b><i>PTPN11</i></b> in a Neonate with Severe and Prolonged Congenital Thrombocytopenia and Noonan Syndrome. Neonatology. 104(1). 1–5. 12 indexed citations
17.
Leon, Eyby, Seema M. Jamal, Ying Zou, & Jeff M. Milunsky. (2011). Partial trisomy 8 mosaicism due to a pseudoisodicentric chromosome 8. American Journal of Medical Genetics Part A. 155(7). 1740–1744. 5 indexed citations
18.
Leon, Eyby, Ying Zou, & Jeff M. Milunsky. (2010). Mosaic down syndrome in a patient with low‐level mosaicism detected by microarray. American Journal of Medical Genetics Part A. 152A(12). 3154–3156. 14 indexed citations
19.
Leon, Eyby, et al.. (2010). Computer-mediated emotional regulation: Detection of emotional changes using non-parametric cumulative sum. PubMed. 2010. 1109–1112. 5 indexed citations
20.
Leon, Eyby, et al.. (2007). Pallister–Killian syndrome: tetrasomy of 12pter→12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome. Clinical Genetics. 72(5). 434–440. 5 indexed citations

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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