Susanne Roosing

3.9k total citations
68 papers, 1.9k citations indexed

About

Susanne Roosing is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Susanne Roosing has authored 68 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 25 papers in Ophthalmology and 19 papers in Genetics. Recurrent topics in Susanne Roosing's work include Retinal Development and Disorders (49 papers), Retinal Diseases and Treatments (22 papers) and RNA regulation and disease (10 papers). Susanne Roosing is often cited by papers focused on Retinal Development and Disorders (49 papers), Retinal Diseases and Treatments (22 papers) and RNA regulation and disease (10 papers). Susanne Roosing collaborates with scholars based in Netherlands, United States and United Kingdom. Susanne Roosing's co-authors include Frans P.M. Cremers, Carel B. Hoyng, Anneke I. den Hollander, Caroline C. W. Klaver, L. Ingeborgh van den Born, Alberta A. H. J. Thiadens, Mary J. van Schooneveld, Rob W.J. Collin, Elfride De Baere and Maria M. van Genderen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Susanne Roosing

59 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susanne Roosing Netherlands	24	1.6k	716	433	321	221	68	1.9k
Enrico Maria Surace Italy	33	2.1k 1.3×	653 0.9×	686 1.6×	364 1.1×	405 1.8×	55	2.6k
Gustavo D. Aguirre United States	26	2.2k 1.4×	929 1.3×	672 1.6×	233 0.7×	638 2.9×	88	2.5k
Donna S. Mackay United Kingdom	31	2.4k 1.5×	917 1.3×	897 2.1×	207 0.6×	241 1.1×	48	2.6k
Sara J. Bowne United States	27	2.4k 1.5×	1.0k 1.4×	487 1.1×	338 1.1×	430 1.9×	67	2.5k
Mary J. van Schooneveld Netherlands	27	1.9k 1.2×	1.3k 1.9×	347 0.8×	269 0.8×	282 1.3×	69	2.4k
Arne Nystuen United States	19	1.4k 0.9×	1.2k 1.6×	215 0.5×	706 2.2×	275 1.2×	28	2.3k
Lori S. Sullivan United States	30	2.9k 1.8×	1.2k 1.7×	612 1.4×	453 1.4×	574 2.6×	80	3.2k
Peter J. Francis United States	26	2.2k 1.4×	1.2k 1.7×	643 1.5×	170 0.5×	285 1.3×	52	2.9k
Brian P. Brooks United States	22	884 0.6×	253 0.4×	360 0.8×	390 1.2×	148 0.7×	73	1.4k
Nicole Weisschuh Germany	27	1.3k 0.8×	964 1.3×	377 0.9×	251 0.8×	124 0.6×	73	1.8k

Countries citing papers authored by Susanne Roosing

Since Specialization

Citations

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

Fields of papers citing papers by Susanne Roosing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanne Roosing

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

All Works

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20 of 20 papers shown

Cremers, Frans P.M., et al.. (2025). Minigene Splice Assays Allow Pathogenicity Reclassification of RPE65 Variants of Uncertain Significance. Genes. 16(9). 1022–1022.

Bruijn, Suzanne E. de, L. Ingeborgh van den Born, Ronny Derks, et al.. (2025). Long-read technologies identify a hidden LINE-1/ERV1 insertion in IQCB1 as causative variant for Senior-Løken syndrome. npj Genomic Medicine. 10(1). 33–33.

Obolensky, Alexey, Anand Swaroop, Susanne Roosing, et al.. (2025). Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration. JAMA Ophthalmology. 143(8). 692–692.

Khateb, Samer, et al.. (2024). A Leaky Deep Intronic Splice Variant in CLRN1 Is Associated with Non-Syndromic Retinitis Pigmentosa. Genes. 15(11). 1363–1363.

McKibbin, Martin, Susanne Roosing, Manir Ali, et al.. (2023). Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. Genes. 14(1). 191–191. 2 indexed citations

Bruijn, Suzanne E. de, Almudena Ávila‐Fernández, Marta Del Pozo‐Valero, et al.. (2023). ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease. Frontiers in Genetics. 14. 1234032–1234032. 5 indexed citations

Haarman, Annechien E. G., Caroline C. W. Klaver, Milly S. Tedja, et al.. (2023). Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing. SHILAP Revista de lepidopterología. 3(4). 100303–100303. 4 indexed citations

Obolensky, Alexey, Mingchu Xu, Yumei Li, et al.. (2022). Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily. Genetics in Medicine. 24(7). 1523–1535. 7 indexed citations

Duijkers, Lonneke, Michael Kwint, Hester Y. Kroes, et al.. (2022). The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner. Cells. 11(22). 3640–3640. 8 indexed citations

10.

Bruijn, Suzanne E. de, Chang Liu, Cris Lanting, et al.. (2020). A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss. Journal of Medical Genetics. 58(2). 96–104. 14 indexed citations

11.

Khan, Mubeen, Marta Del Pozo‐Valero, Stéphanie S. Cornelis, et al.. (2019). Identification of splice defects due to noncanonical splice site or deep-intronic variants in ABCA4.. eScholarship (California Digital Library).

12.

Khan, Mubeen, Marta Del Pozo‐Valero, Stéphanie S. Cornelis, et al.. (2019). Identification of splice defects due to noncanonical splice site or deep‐intronic variants in ABCA4. Human Mutation. 40(12). 2365–2376. 37 indexed citations

13.

Verbakel, Sanne K., B. Jeroen Klevering, Maria M. van Genderen, et al.. (2019). The identification of a RNA splice variant in TULP1 in two siblings with early‐onset photoreceptor dystrophy. Molecular Genetics & Genomic Medicine. 7(6). e660–e660. 12 indexed citations

14.

Runhart, Esmee H., Riccardo Sangermano, Stéphanie S. Cornelis, et al.. (2018). The CommonABCA4Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present intransWith Severe Variants. Investigative Ophthalmology & Visual Science. 59(8). 3220–3220. 65 indexed citations

15.

Biswas, Pooja, Kari Branham, Shyamanga Borooah, et al.. (2018). IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. Human Genetics. 137(6-7). 447–458. 11 indexed citations

16.

Albert, Sílvia, Riccardo Sangermano, Nathalie M. Bax, et al.. (2015). Towards the identification of deep-intronic ABCA4 mutations in Stargardt patients by using induced pluripotent stem cell-derived photoreceptor progenitor cells. Investigative Ophthalmology & Visual Science. 56(7). 3174–3174. 1 indexed citations

17.

Roosing, Susanne, Klaus Rohrschneider, Avigail Beryozkin, et al.. (2013). Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy. The American Journal of Human Genetics. 93(1). 110–117. 67 indexed citations

18.

Roosing, Susanne, L. Ingeborgh van den Born, Carel B. Hoyng, et al.. (2013). Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone Dysfunction. Ophthalmology. 120(6). 1239–1246. 29 indexed citations

19.

Roosing, Susanne, Alberta A. H. J. Thiadens, Renate C. Zekveld-Vroon, et al.. (2011). Is There Evidence For A Digenic Model In Stargardt Disease. Investigative Ophthalmology & Visual Science. 52(14). 5395–5395. 1 indexed citations

20.

Thiadens, Alberta A. H. J., Anneke I. den Hollander, Susanne Roosing, et al.. (2009). Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders. The American Journal of Human Genetics. 85(2). 240–247. 159 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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