Elena Schiff

1.6k total citations
29 papers, 418 citations indexed

About

Elena Schiff is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Elena Schiff has authored 29 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Ophthalmology. Recurrent topics in Elena Schiff's work include Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (6 papers) and Lysosomal Storage Disorders Research (6 papers). Elena Schiff is often cited by papers focused on Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (6 papers) and Lysosomal Storage Disorders Research (6 papers). Elena Schiff collaborates with scholars based in United Kingdom, United States and Israel. Elena Schiff's co-authors include Andrew R. Webster, Gavin Arno, Mariya Moosajee, Nikolas Pontikos, Omar A. Mahroo, Michel Michaelides, Genevieve Wright, Samantha Malka, Gideon Bach and Neringa Jurkutė and has published in prestigious journals such as Gastroenterology, International Journal of Molecular Sciences and Ophthalmology.

In The Last Decade

Elena Schiff

26 papers receiving 412 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Schiff United Kingdom 10 300 134 107 57 54 29 418
Bert Eussen Netherlands 11 317 1.1× 241 1.8× 92 0.9× 56 1.0× 28 0.5× 18 569
Riccardo Sangermano United States 10 529 1.8× 205 1.5× 74 0.7× 37 0.6× 99 1.8× 20 603
Anh-Chi N. Le United States 6 436 1.5× 61 0.5× 70 0.7× 41 0.7× 47 0.9× 6 489
Silvio Alessandro Di Gioia Switzerland 10 333 1.1× 83 0.6× 126 1.2× 12 0.2× 74 1.4× 14 425
Britta Fiebig Germany 13 489 1.6× 260 1.9× 134 1.3× 11 0.2× 45 0.8× 21 622
Claudia Busse United Kingdom 10 161 0.5× 61 0.5× 50 0.5× 16 0.3× 34 0.6× 35 324
Jenina Capasso United States 12 238 0.8× 113 0.8× 103 1.0× 8 0.1× 22 0.4× 36 316
Luísa Coutinho Santos Portugal 7 219 0.7× 141 1.1× 161 1.5× 14 0.2× 36 0.7× 11 372
Jan Liebelt Australia 10 291 1.0× 61 0.5× 156 1.5× 8 0.1× 28 0.5× 20 449

Countries citing papers authored by Elena Schiff

Since Specialization
Citations

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

Fields of papers citing papers by Elena Schiff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Schiff

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Schiff. A scholar is included among the top collaborators of Elena Schiff 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 Elena Schiff. Elena Schiff 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.
Schiff, Elena, Siying Lin, José S. Pulido, et al.. (2025). Comparison of inherited retinal disease genes covered by two comprehensive genetic testing panels and a widely used online resource. Eye. 39(5). 1009–1010. 1 indexed citations
2.
Lin, Siying, Anthony G. Robson, Dorothy Thompson, et al.. (2024). Non‐syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activity. Clinical Genetics. 106(4). 505–511. 1 indexed citations
3.
Lin, Siying, Gavin Arno, Anthony G. Robson, et al.. (2024). Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathy. Eye. 39(5). 951–957.
4.
5.
Varela, Malena Daich, Elena Schiff, Samantha Malka, et al.. (2024). PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum Disease. Investigative Ophthalmology & Visual Science. 65(2). 38–38.
6.
Lin, Siying, Nikolas Pontikos, Malena Daich Varela, et al.. (2024). Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort. Ophthalmology Retina. 8(7). 699–709. 14 indexed citations
7.
Schiff, Elena, Samantha Malka, Vijay Tailor, et al.. (2022). Prospective study of pediatric patients presenting with idiopathic infantile nystagmus—Management and molecular diagnostics. Frontiers in Genetics. 13. 977806–977806. 5 indexed citations
8.
Schiff, Elena, Genevieve Wright, Naushin Waseem, et al.. (2022). Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1. Investigative Ophthalmology & Visual Science. 63(9). 14–14. 6 indexed citations
9.
10.
Schiff, Elena, Vijay Tailor, Hwei Wuen Chan, et al.. (2021). Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia. International Journal of Molecular Sciences. 22(3). 1130–1130. 11 indexed citations
11.
Pontikos, Nikolas, Gavin Arno, Neringa Jurkutė, et al.. (2020). Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom. Ophthalmology. 127(10). 1384–1394. 152 indexed citations
12.
Khan, Mubeen, Gavin Arno, Ana Fakin, et al.. (2020). Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease. Molecular Therapy — Nucleic Acids. 21. 412–427. 57 indexed citations
13.
Ba‐Abbad, Rola, Anthony G. Robson, Omar A. Mahroo, et al.. (2020). A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophy. Eye. 35(5). 1482–1489. 6 indexed citations
14.
Schiff, Elena, Matthew Frampton, Francesca Semplici, et al.. (2018). Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease. Human Genetics. 137(9). 723–734. 7 indexed citations
15.
Schiff, Elena, Matthew Frampton, Francesca Semplici, et al.. (2018). A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population. Digestive Diseases and Sciences. 63(11). 3049–3057. 10 indexed citations
16.
Levine, Adam P., Nikolas Pontikos, Elena Schiff, et al.. (2016). Genetic Complexity of Crohn’s Disease in Two Large Ashkenazi Jewish Families. Gastroenterology. 151(4). 698–709. 42 indexed citations
17.
Zeigler, M., et al.. (1998). Niemann Pick Disease type A in Israeli Arabs: 677delT, a common novel single mutation. Mutations in brief no. 161. Online.. Human Mutation. 12(2). 136. 8 indexed citations
18.
Schiff, Elena, Joël Zlotogora, Dvorah Abeliovich, M. Zeigler, & Gideon Bach. (1994). Hunter syndrome among Jews in Israel. Biomedicine & Pharmacotherapy. 48(8-9). 381–384. 5 indexed citations
19.
Schiff, Elena, et al.. (1994). Mutation analysis of Jewish hunter patients in Israel. Human Mutation. 4(4). 263–270. 18 indexed citations
20.
Schiff, Elena, Gideon Bach, Joël Zlotogora, & Dvorah Abeliovich. (1993). Combined enzymatic and linkage analysis for heterozygote detection in Hunter syndrome: Identification of an apparent case of germinal mosaicism. American Journal of Medical Genetics. 47(6). 837–842. 9 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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