Elfride De Baere

12.2k total citations
153 papers, 4.4k citations indexed

About

Elfride De Baere is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Elfride De Baere has authored 153 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 106 papers in Molecular Biology, 60 papers in Genetics and 43 papers in Ophthalmology. Recurrent topics in Elfride De Baere's work include Retinal Development and Disorders (62 papers), Retinal Diseases and Treatments (31 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers). Elfride De Baere is often cited by papers focused on Retinal Development and Disorders (62 papers), Retinal Diseases and Treatments (31 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers). Elfride De Baere collaborates with scholars based in Belgium, United States and Netherlands. Elfride De Baere's co-authors include Bart P. Leroy, Frauke Coppieters, Reiner A. Veitia, Diane Beysen, Hannah Verdin, Steve Lefever, Frans P.M. Cremers, Carel B. Hoyng, Filomeen Haerynck and Debby Bogaert and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS ONE.

In The Last Decade

Elfride De Baere

145 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elfride De Baere Belgium	39	3.1k	1.8k	986	478	400	153	4.4k
Lies H. Hoefsloot Netherlands	45	3.7k 1.2×	1.7k 0.9×	543 0.6×	532 1.1×	160 0.4×	136	6.6k
Mireille Claustres France	46	4.3k 1.4×	1.8k 1.0×	300 0.3×	328 0.7×	126 0.3×	221	8.2k
Lisbeth Tranebjærg Denmark	43	3.6k 1.2×	2.3k 1.2×	156 0.2×	577 1.2×	362 0.9×	163	6.7k
Patrick Calvas France	31	2.1k 0.7×	1.4k 0.8×	915 0.9×	91 0.2×	124 0.3×	104	3.9k
Marianne Schwartz Denmark	40	3.2k 1.0×	1.2k 0.6×	284 0.3×	482 1.0×	124 0.3×	116	4.9k
Hélène Dollfus France	42	4.8k 1.6×	3.0k 1.6×	1.2k 1.2×	275 0.6×	102 0.3×	178	6.7k
Karen Brøndum‐Nielsen Denmark	34	2.3k 0.7×	2.0k 1.1×	214 0.2×	102 0.2×	141 0.4×	137	4.1k
Anthony T. Moore United Kingdom	45	5.9k 1.9×	1.6k 0.9×	2.3k 2.3×	473 1.0×	134 0.3×	107	8.0k
A. Westerveld Netherlands	44	4.3k 1.4×	1.4k 0.7×	274 0.3×	287 0.6×	122 0.3×	153	6.1k
Joël Zlotogora Israel	35	1.9k 0.6×	2.0k 1.1×	103 0.1×	234 0.5×	222 0.6×	170	5.0k

Countries citing papers authored by Elfride De Baere

Since Specialization

Citations

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

Fields of papers citing papers by Elfride De Baere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elfride De Baere. 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 Elfride De Baere. The network helps show where Elfride De Baere may publish in the future.

Co-authorship network of co-authors of Elfride De Baere

This figure shows the co-authorship network connecting the top 25 collaborators of Elfride De Baere. A scholar is included among the top collaborators of Elfride De Baere 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 Elfride De Baere. Elfride De Baere 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

Schooneveld, Mary J. van, Roselie M.H. Diederen, Astrid S. Plomp, et al.. (2025). Pseudocolobomatous autosomal dominant atrophic maculopathy (PADAM). Ophthalmic Genetics. 46(5). 468–473.

Merle, David A., Spyridon Dimopoulos, Susanne Kohl, et al.. (2025). Short-Term Outcomes of Pediatric Patients With Mild Autosomal Recessive RPE65-Associated Retinal Dystrophy Treated With Voretigene Neparvovec. Translational Vision Science & Technology. 14(8). 8–8. 1 indexed citations

McKibbin, Martin, Suzanne E. de Bruijn, Andrea L. Vincent, et al.. (2025). Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 66(6). 19–19.

Ligneul, Clémence, C Chatelain, Christophe Barrea, et al.. (2025). Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice. Molecular Autism. 16(1). 14–14.

Ceroni, Fabiola, Richard Holt, Елена А. Сорокина, et al.. (2024). Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development. Nature Communications. 15(1). 9245–9245. 2 indexed citations

Caspers, Laure, Marieke De Bruyne, Elfride De Baere, et al.. (2024). INHERITED RETINAL DISEASE GENE PANEL IN POSTERIOR OR PANUVEITIS WITH DYSTROPHIC FEATURES. Retina. 45(3). 509–521.

Pozo‐Valero, Marta Del, et al.. (2024). Autozygome‐guided exome‐first study in a consanguineous cohort with early‐onset retinal disease uncovers an isolated RIMS2 phenotype and a retina‐enriched RIMS2 isoform. Clinical Genetics. 106(2). 127–139. 1 indexed citations

Terryn, Wim, et al.. (2024). INTERMEDIATE UVEITIS IN COMMON VARIABLE IMMUNODEFICIENCY ASSOCIATED WITH A HETEROZYGOUS VARIANT IN THE TNFRSF13B GENE. Retinal Cases & Brief Reports. 19(5). 644–646.

Beyens, Aude, Kathleen Claes, Elfride De Baere, et al.. (2023). HRAS ‐related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects. Clinical Genetics. 103(6). 709–713. 1 indexed citations

10.

Potorac, Iulia, Olivier Malaise, Corinne Fasquelle, et al.. (2023). The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndrome and Premature Ovarian Insufficiency. Journal of Clinical Medicine. 12(3). 990–990. 4 indexed citations

11.

Štingl, Katarína, Britta Baumann, Pietro De Angeli, et al.. (2022). Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International Journal of Molecular Sciences. 23(12). 6868–6868. 4 indexed citations

12.

Bever, Yolande van, Hennie T. Brüggenwirth, Katja P. Wolffenbuttel, et al.. (2020). Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development. Journal of Medical Genetics. 57(9). 581–589. 10 indexed citations

13.

Naert, Thomas, Toon Rosseel, Dario Priem, et al.. (2020). Functional characterization of a Xenopus tropicalis knockout and a human cellular model of RCBTB1-associated inherited retinal disease shows involvement of RCBTB1 in the cellular response to oxidative stress. Investigative Ophthalmology & Visual Science. 61(7). 1125–1125. 1 indexed citations

14.

Mayer, Anja K., Muhammad Mahajnah, Mervyn G. Thomas, et al.. (2019). Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus. Brain. 142(6). 1528–1534. 25 indexed citations

15.

Sánchez, Mayka, et al.. (2017). Functional characterization of a novel non-coding mutation “Ghent +49A > G” in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome. Scientific Reports. 7(1). 18025–18025. 5 indexed citations

16.

Bogaert, Debby, Mélissa Dullaers, Hye Sun Kuehn, et al.. (2017). Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes. Scientific Reports. 7(1). 3702–3702. 22 indexed citations

17.

Thiadens, Alberta A. H. J., Renate C. Zekveld-Vroon, Bart P. Leroy, et al.. (2012). Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy. Ophthalmology. 119(4). 819–826. 93 indexed citations

18.

Coppieters, Frauke, Elise Héon, Igor Cima, et al.. (2009). Exploring the Role of Genes of the Retinal Transcription Network in Retinal Degeneration. Investigative Ophthalmology & Visual Science. 50(13). 3745–3745. 1 indexed citations

19.

Cotton, Richard G.H., Arleen D. Auerbach, A. F. Brown, et al.. (2007). A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases. Human Mutation. 28(10). 931–932. 9 indexed citations

20.

Gross, Coleman, Elfride De Baere, Annie Lo, Wenhan Chang, & Ludwine Messiaen. (2001). Cloning and Characterization of Human WDR10 , a Novel Gene Located at 3q21 Encoding a WD-Repeat Protein That Is Highly Expressed in Pituitary and Testis. DNA and Cell Biology. 20(1). 41–52. 14 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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