F.P.M. Cremers

638 total citations
10 papers, 443 citations indexed

About

F.P.M. Cremers is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, F.P.M. Cremers has authored 10 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Ophthalmology and 2 papers in Genetics. Recurrent topics in F.P.M. Cremers's work include Retinal Development and Disorders (4 papers), Retinal Diseases and Treatments (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). F.P.M. Cremers is often cited by papers focused on Retinal Development and Disorders (4 papers), Retinal Diseases and Treatments (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). F.P.M. Cremers collaborates with scholars based in Netherlands, United States and Austria. F.P.M. Cremers's co-authors include Carel B. Hoyng, Janneke J.C. van Lith-Verhoeven, David Schlessinger, Anthony P. Monaco, David Lee Nelson, Andrea Ballabio, Mary J. van Schooneveld, Rando Allikmets, Meira R. Meltzer and Peter Gouras and has published in prestigious journals such as Neurology, Investigative Ophthalmology & Visual Science and British Journal of Ophthalmology.

In The Last Decade

F.P.M. Cremers

10 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F.P.M. Cremers Netherlands 8 377 243 83 55 45 10 443
Katsuhiro Hosono Japan 13 407 1.1× 197 0.8× 132 1.6× 64 1.2× 68 1.5× 45 507
Maigi Külm United States 6 297 0.8× 183 0.8× 39 0.5× 40 0.7× 31 0.7× 7 349
Margaret R. Starostik United States 7 340 0.9× 148 0.6× 102 1.2× 70 1.3× 32 0.7× 10 502
T. P. Dryja United States 7 320 0.8× 147 0.6× 57 0.7× 30 0.5× 64 1.4× 10 371
María González‐del Pozo Spain 13 408 1.1× 179 0.7× 123 1.5× 31 0.6× 46 1.0× 21 461
Tobias Eisenberger Germany 11 437 1.2× 175 0.7× 165 2.0× 51 0.9× 66 1.5× 14 531
T.J.R. van de Pol Netherlands 8 195 0.5× 95 0.4× 55 0.7× 29 0.5× 28 0.6× 11 243
Avril Kennan Ireland 11 542 1.4× 189 0.8× 66 0.8× 36 0.7× 102 2.3× 16 612
Marie Burstedt Sweden 15 463 1.2× 290 1.2× 50 0.6× 96 1.7× 75 1.7× 32 545
Ascensión Giménez Spain 9 335 0.9× 183 0.8× 64 0.8× 43 0.8× 34 0.8× 14 363

Countries citing papers authored by F.P.M. Cremers

Since Specialization
Citations

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

Fields of papers citing papers by F.P.M. Cremers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F.P.M. Cremers. 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 F.P.M. Cremers. The network helps show where F.P.M. Cremers may publish in the future.

Co-authorship network of co-authors of F.P.M. Cremers

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

All Works

10 of 10 papers shown
1.
Boon, Camiel J.F., Mary J. van Schooneveld, Janneke J.C. van Lith-Verhoeven, et al.. (2007). Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus. British Journal of Ophthalmology. 91(11). 1504–1511. 95 indexed citations
2.
López, I., Gerald A. Fishman, Julie Racine, et al.. (2005). The Phenotypes of Patients and Heterozygous Carriers With RDH12 Mutations Are Different From Those With RPE65 Mutations. Investigative Ophthalmology & Visual Science. 46(13). 528–528. 1 indexed citations
3.
Zernant, Jana, Maigi Külm, Amy Hutchinson, et al.. (2003). Genotyping microarray (gene chip) for theABCR(ABCA4) gene. Human Mutation. 22(5). 395–403. 202 indexed citations
4.
Cremers, F.P.M., et al.. (2003). Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea.. PubMed. 9. 138–43. 17 indexed citations
5.
6.
Lith-Verhoeven, Janneke J.C. van, et al.. (2002). Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13). Ophthalmic Genetics. 23(1). 1–12. 25 indexed citations
7.
Bom, Steven J. H., Henricus P. M. Kunst, P.L.M. Huygen, F.P.M. Cremers, & Cor W. R. J. Cremers. (1999). Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes. British Journal of Audiology. 33(5). 335–348. 20 indexed citations
8.
Maarel, Silvère M. van der, D. Olde Weghuis, I Huber, et al.. (1995). Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations. American Journal of Medical Genetics Part A. 64(1). 19. 1 indexed citations
9.
Nelson, David Lee, Andrea Ballabio, F.P.M. Cremers, Anthony P. Monaco, & David Schlessinger. (1995). Report of the sixth international workshop on X chromosome mapping 1995. Data Archiving and Networked Services (DANS). 71(4). 308–342. 64 indexed citations
10.
Schooneveld, Mary J. van, E. M. Bleeker‐Wagemakers, Rob Zwart, et al.. (1993). Kearns‐Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathy. Neurology. 43(1_part_1). 218–218. 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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