Emma Bedoukian

1.5k total citations
31 papers, 375 citations indexed

About

Emma Bedoukian is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Emma Bedoukian has authored 31 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Emma Bedoukian's work include Retinal Development and Disorders (9 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Emma Bedoukian is often cited by papers focused on Retinal Development and Disorders (9 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Emma Bedoukian collaborates with scholars based in United States, Belgium and United Kingdom. Emma Bedoukian's co-authors include Ian D. Krantz, Matthew A. Deardorff, Tomás S. Alemán, Cara Skraban, Xiaosong Zhu, Bart P. Leroy, Alisha Wilkens, E. Bryan Crenshaw, E Schwartz and Kinga M. Bujakowska and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and The Journal of Pediatrics.

In The Last Decade

Emma Bedoukian

30 papers receiving 372 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Bedoukian United States 13 238 119 61 56 36 31 375
Tobias Eisenberger Germany 11 437 1.8× 165 1.4× 75 1.2× 175 3.1× 15 0.4× 14 531
Lise Larrieu France 15 485 2.0× 75 0.6× 259 4.2× 56 1.0× 24 0.7× 17 586
Samer Khateb Israel 16 525 2.2× 147 1.2× 67 1.1× 178 3.2× 11 0.3× 43 662
Ersan Kalay Türkiye 13 316 1.3× 109 0.9× 228 3.7× 6 0.1× 52 1.4× 24 527
Jean-Louis Dufier France 8 236 1.0× 19 0.2× 90 1.5× 120 2.1× 10 0.3× 8 342
Pavan K. Kommareddi United States 8 114 0.5× 47 0.4× 84 1.4× 5 0.1× 37 1.0× 12 330
Greta Gillies Australia 9 302 1.3× 216 1.8× 62 1.0× 3 0.1× 11 0.3× 13 481
Saima Riazuddin Pakistan 2 275 1.2× 34 0.3× 168 2.8× 5 0.1× 18 0.5× 3 449
Zippora Brownstein Israel 14 363 1.5× 45 0.4× 327 5.4× 7 0.1× 139 3.9× 25 620
Zohreh Fattahi Iran 12 300 1.3× 112 0.9× 158 2.6× 2 0.0× 36 1.0× 36 459

Countries citing papers authored by Emma Bedoukian

Since Specialization
Citations

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

Fields of papers citing papers by Emma Bedoukian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Bedoukian

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Bedoukian. A scholar is included among the top collaborators of Emma Bedoukian 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 Emma Bedoukian. Emma Bedoukian 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.
Sumaroka, Alexander, Tara C. Mitchell, Erin O'Neil, et al.. (2024). Anti-TRPM1 autoantibody-positive unilateral melanoma associated retinopathy (MAR) triggered by immunotherapy recapitulates functional and structural details of TRPM1-associated congenital stationary night blindness. American Journal of Ophthalmology Case Reports. 36. 102098–102098. 2 indexed citations
2.
Bedoukian, Emma, Danielle S. Burstein, J. William Gaynor, et al.. (2023). Diagnostic Yield of Exome Sequencing in Pediatric Cardiomyopathy. The Journal of Pediatrics. 265. 113808–113808. 3 indexed citations
3.
Izumi, Kosuke, Rebecca Ganetzky, Gerald Wertheim, et al.. (2023). Co-Occurrence of Pallister-Killian Syndrome and Burkitt Lymphoma in a Patient with Near-Normal Neurocognitive Development. Molecular Syndromology. 14(4). 303–309.
4.
Bedoukian, Emma, Erin O'Neil, Ian D. Krantz, et al.. (2022). Ocular Biomarkers of Riboflavin Transporter Deficiency. Journal of Neuro-Ophthalmology. 43(1). 110–115. 2 indexed citations
5.
Bedoukian, Emma, Xiaosong Zhu, Leona Serrano, Drew Scoles, & Tomás S. Alemán. (2022). NMNAT1-ASSOCIATED CONE-ROD DYSTROPHY: EVIDENCE FOR A SPECTRUM OF FOVEAL MALDEVELOPMENT.. PubMed. 16(3). 385–392. 4 indexed citations
6.
Jenkins, Zandra A., Tim Morgan, Grégory Gimenez, et al.. (2021). Exon skip‐inducing variants in FLNA in an attenuated form of frontometaphyseal dysplasia. American Journal of Medical Genetics Part A. 185(12). 3675–3682. 1 indexed citations
7.
Alemán, Tomás S., Leona Serrano, Emma Bedoukian, et al.. (2021). A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy. Clinical ophthalmology. Volume 15. 939–952. 20 indexed citations
8.
Srivastava, Siddharth, Erica L. Macke, Lindsay C. Swanson, et al.. (2021). Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental Disorder. Brain Sciences. 11(7). 931–931. 9 indexed citations
9.
Strong, Alanna, Dong Li, Frank Mentch, et al.. (2020). Ciliopathies: Coloring outside of the lines. American Journal of Medical Genetics Part A. 185(3). 687–694. 7 indexed citations
10.
Cohen, Jennifer L., Samantha A. Schrier Vergano, Alanna Strong, et al.. (2020). EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients. American Journal of Medical Genetics Part A. 182(12). 2926–2938. 18 indexed citations
11.
Ritter, Alyssa, Emma Bedoukian, Justin H. Berger, et al.. (2019). Clinical utility of exome sequencing in infantile heart failure. Genetics in Medicine. 22(2). 423–426. 13 indexed citations
12.
Ammar, Michael J., Katherine E. Uyhazi, Emma Bedoukian, et al.. (2019). ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPY. Retinal Cases & Brief Reports. 15(6). 694–701. 10 indexed citations
13.
Banka, Siddharth, Catherine Breen, Stephanie Barton, et al.. (2019). Genotype–phenotype specificity in Menke–Hennekam syndrome caused by missense variants in exon 30 or 31 of CREBBP. American Journal of Medical Genetics Part A. 179(6). 1058–1062. 16 indexed citations
14.
Guan, Qiaoning, Jorune Balciuniene, Kajia Cao, et al.. (2018). AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss. Genetics in Medicine. 20(12). 1600–1608. 27 indexed citations
15.
Bedoukian, Emma, et al.. (2018). Bohring‐Opitz syndrome caused by an ASXL1 mutation inherited from a germline mosaic mother. American Journal of Medical Genetics Part A. 176(5). 1249–1252. 16 indexed citations
16.
Ritter, Alyssa, Carey McDougall, Cara Skraban, et al.. (2018). Variable Clinical Manifestations of Xia‐Gibbs syndrome: Findings of Consecutively Identified Cases at a Single Children's Hospital. American Journal of Medical Genetics Part A. 176(9). 1890–1896. 24 indexed citations
17.
Edmondson, Andrew C., Emma Bedoukian, Matthew A. Deardorff, et al.. (2017). A human case of SLC35A3‐related skeletal dysplasia. American Journal of Medical Genetics Part A. 173(10). 2758–2762. 16 indexed citations
18.
Noon, Sarah E., E Schwartz, Alisha Wilkens, et al.. (2016). Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic. American Journal of Medical Genetics Part A. 170(10). 2523–2530. 36 indexed citations
19.
Ganetzky, Rebecca, Emma Bedoukian, Matthew A. Deardorff, & Can Fıçıcıoğlu. (2016). Argininosuccinic Acid Lyase Deficiency Missed by Newborn Screen. JIMD Reports. 34. 43–47. 4 indexed citations
20.
Bujakowska, Kinga M., Rosario Fernández‐Godino, Emily Place, et al.. (2016). Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. Genetics in Medicine. 19(6). 643–651. 40 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Tobias Eisenberger Breakdown of academic impact, for papers by Lise Larrieu Breakdown of academic impact, for papers by Samer Khateb Breakdown of academic impact, for papers by Ersan Kalay Breakdown of academic impact, for papers by Jean-Louis Dufier Breakdown of academic impact, for papers by Pavan K. Kommareddi Breakdown of academic impact, for papers by Greta Gillies Breakdown of academic impact, for papers by Saima Riazuddin Breakdown of academic impact, for papers by Zippora Brownstein Breakdown of academic impact, for papers by Zohreh Fattahi
Rankless by CCL
2026