Delphine Blain

681 total citations
24 papers, 432 citations indexed

About

Delphine Blain is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Delphine Blain has authored 24 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Radiology, Nuclear Medicine and Imaging and 12 papers in Genetics. Recurrent topics in Delphine Blain's work include Ocular Disorders and Treatments (10 papers), Retinal Development and Disorders (9 papers) and Retinal and Macular Surgery (7 papers). Delphine Blain is often cited by papers focused on Ocular Disorders and Treatments (10 papers), Retinal Development and Disorders (9 papers) and Retinal and Macular Surgery (7 papers). Delphine Blain collaborates with scholars based in United States and France. Delphine Blain's co-authors include Brian P. Brooks, Stefano Bertuzzi, Kerry Goetz, Santa J. Tumminia, Robert B. Hufnagel, Andrea Gropman, Wadih M. Zein, Donald W. Hadley, Joan C. Han and Daniel Pineda‐Alvarez and has published in prestigious journals such as SHILAP Revista de lepidopterología, Ophthalmology and American Journal of Ophthalmology.

In The Last Decade

Delphine Blain

24 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Delphine Blain United States 10 275 189 119 90 59 24 432
Cristina Villanueva‐Mendoza Mexico 12 223 0.8× 145 0.8× 84 0.7× 74 0.8× 35 0.6× 34 361
K. Kozlowski Canada 8 330 1.2× 128 0.7× 108 0.9× 70 0.8× 46 0.8× 10 427
Irina Balikova Belgium 12 179 0.7× 243 1.3× 57 0.5× 34 0.4× 29 0.5× 30 392
Oscar F. Chacón‐Camacho Mexico 12 348 1.3× 211 1.1× 156 1.3× 60 0.7× 43 0.7× 62 533
Elena Schiff United Kingdom 10 300 1.1× 107 0.6× 134 1.1× 40 0.4× 54 0.9× 29 418
Åsa Blixt Sweden 7 372 1.4× 164 0.9× 95 0.8× 101 1.1× 42 0.7× 9 463
Hannah Verdin Belgium 14 317 1.2× 268 1.4× 69 0.6× 23 0.3× 26 0.4× 29 467
Luísa Coutinho Santos Portugal 7 219 0.8× 161 0.9× 141 1.2× 66 0.7× 36 0.6× 11 372
Raúl Ayala-Ramírez Mexico 9 209 0.8× 152 0.8× 194 1.6× 88 1.0× 23 0.4× 12 324
Britta Fiebig Germany 13 489 1.8× 134 0.7× 260 2.2× 88 1.0× 45 0.8× 21 622

Countries citing papers authored by Delphine Blain

Since Specialization
Citations

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

Fields of papers citing papers by Delphine Blain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Blain

This figure shows the co-authorship network connecting the top 25 collaborators of Delphine Blain. A scholar is included among the top collaborators of Delphine Blain 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 Delphine Blain. Delphine Blain 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.
Benson, Matthew D., Delphine Blain, Denise Cunningham, et al.. (2023). RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3′-end of ORF15. Investigative Ophthalmology & Visual Science. 64(12). 19–19. 3 indexed citations
2.
Duong, Dat, Amy Turriff, Delphine Blain, et al.. (2022). Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal Hypoplasia. SHILAP Revista de lepidopterología. 3(1). 100225–100225. 8 indexed citations
3.
Guan, Bin, Laryssa A. Huryn, Andrew B. Hughes, et al.. (2022). Early-Onset TIMP3-Related Retinopathy Associated With Impaired Signal Peptide. JAMA Ophthalmology. 140(7). 730–730. 3 indexed citations
4.
Cukras, Catherine A., Emily Y. Chew, Yuri V. Sergeev, et al.. (2022). Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies. Genes. 13(5). 925–925. 7 indexed citations
5.
Blain, Delphine, et al.. (2021). Review of evidence for environmental causes of uveal coloboma. Survey of Ophthalmology. 67(4). 1031–1047. 7 indexed citations
6.
Goetz, Kerry, Bin Guan, Ehsan Ullah, et al.. (2020). Genotype-phenotype associations in a large PRPH2-related retinopathy cohort. Investigative Ophthalmology & Visual Science. 61(7). 2421–2421. 1 indexed citations
7.
Varela, Malena Daich, Laryssa A. Huryn, Robert B. Hufnagel, et al.. (2020). Ocular and Systemic Findings in Adults with Uveal Coloboma. Ophthalmology. 127(12). 1772–1774. 6 indexed citations
8.
Goetz, Kerry, Bin Guan, Ehsan Ullah, et al.. (2020). Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort. Human Mutation. 41(9). 1528–1539. 27 indexed citations
9.
Hufnagel, Robert B., et al.. (2020). Retinoschisis associated with Kearns-Sayre syndrome. Ophthalmic Genetics. 41(5). 497–500. 5 indexed citations
10.
Turriff, Amy, Delphine Blain, Morgan Similuk, et al.. (2019). Motivations and Decision Making Processes of Men With X-linked Retinoschisis Considering Participation in an Ocular Gene Therapy Trial. American Journal of Ophthalmology. 204. 90–96. 7 indexed citations
11.
12.
Sullivan, Lori S., Sara J. Bowne, Delphine Blain, et al.. (2013). Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 54(9). 6255–6255. 64 indexed citations
13.
Huynh, Nancy, Delphine Blain, Tanya Glaser, et al.. (2013). Systemic Diagnostic Testing in Patients With Apparently Isolated Uveal Coloboma. American Journal of Ophthalmology. 156(6). 1159–1168.e4. 9 indexed citations
14.
Brooks, Brian P., A. Thompson, Janine A. Clayton, et al.. (2011). Ocular Manifestations of Trichothiodystrophy. Ophthalmology. 118(12). 2335–2342. 21 indexed citations
15.
Solomon, Benjamin D., Daniel Pineda‐Alvarez, Joan Z. Balog, et al.. (2009). Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia. American Journal of Medical Genetics Part A. 149A(11). 2543–2546. 73 indexed citations
16.
Blain, Delphine. (2007). Molecular Diagnosis and Genetic Counseling in Ophthalmology. Archives of Ophthalmology. 125(2). 196–196. 13 indexed citations
17.
Gradstein, Libe, E. J. Fitzgibbon, J. Fielding Hejtmancik, et al.. (2006). Atypical Phenotype and Genotype in a Family With Suspected X–Linked Ocular Albinism. Investigative Ophthalmology & Visual Science. 47(13). 2508–2508. 1 indexed citations
18.
Tang, Johnny, Parag A. Gokhale, Steven E. Brooks, Delphine Blain, & Brian P. Brooks. (2006). Increased Corneal Thickness In Patients With Ocular Coloboma. Journal of American Association for Pediatric Ophthalmology and Strabismus. 10(2). 175–177. 7 indexed citations
19.
Blain, Delphine, et al.. (2006). Uveal coloboma: clinical and basic science update. Current Opinion in Ophthalmology. 17(5). 447–470. 99 indexed citations
20.
Brooks, Brian P., Jeanne Meck, Bassem R. Haddad, et al.. (2006). Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature. BMC Medical Genetics. 7(1). 2–2. 13 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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