Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Retinoblastoma
2015368 citationsFrancis L. Munier et al.profile →
IC3D Classification of Corneal Dystrophies—Edition 2
2015323 citationsJayne S. Weiss, Hans Ulrik Møller et al.Corneaprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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Countries citing papers authored by Francis L. Munier
Since
Specialization
Citations
This map shows the geographic impact of Francis L. Munier'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 Francis L. Munier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francis L. Munier more than expected).
Fields of papers citing papers by Francis L. Munier
This network shows the impact of papers produced by Francis L. Munier. 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 Francis L. Munier. The network helps show where Francis L. Munier may publish in the future.
Co-authorship network of co-authors of Francis L. Munier
This figure shows the co-authorship network connecting the top 25 collaborators of Francis L. Munier.
A scholar is included among the top collaborators of Francis L. Munier 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 Francis L. Munier. Francis L. Munier is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Vaclavik, Veronika, Francis L. Munier, Franz Josef Holzer, et al.. (2019). Novel compound heterozygote mutations in CYP2U1 can cause maculopathy with or without neurological signs of hereditary spastic paraplegia HSP56. Investigative Ophthalmology & Visual Science. 60(9). 2930–2930.1 indexed citations
5.
Munier, Francis L., Marie‐Claire Gaillard, Christina Stathopoulos, et al.. (2016). Concomitant first line intra-arterial (IAC) and intra-vitreal (IVC) chemotherapy with melphalan for unilateral group D retinoblastoma (Rb) with diffuse vitreous seeding at presentation. Investigative Ophthalmology & Visual Science. 57(12). 3682–3682.
6.
Weiss, Jayne S., Hans Ulrik Møller, Anthony J. Aldave, et al.. (2015). IC3D Classification of Corneal Dystrophies—Edition 2. Cornea. 34(2). 117–159.323 indexed citations breakdown →
7.
Munier, Francis L., Marie‐Claire Gaillard, Sarah Decembrini, & Maja Beck‐Popovic. (2015). Aqueous seeding: fall of the ultimate intraocular retinoblastoma sanctuary by a new in situ chemotherapy technique. Investigative Ophthalmology & Visual Science. 56(7). 1663–1663.6 indexed citations
8.
Vaclavik, Veronika, Francis L. Munier, Daniel F. Schorderet, & Hoai Viet Tran. (2015). Mutation in EYS gene causes variable expressivity, ranging from Leber Congenital Amaurosis to adult onset Retinitis Pimentosa. Autofluorescence Study.. Investigative Ophthalmology & Visual Science. 56(7). 2894–2894.2 indexed citations
Uffer, S., et al.. (2008). Cryptic Optic Nerve Involvement With Tumor-Free Papillary and Peripapillary Area in a Group D Retinoblastoma Following Chemoreduction. Investigative Ophthalmology & Visual Science. 49(13). 15–15.1 indexed citations
14.
Héon, Elise, Christina Gerth‐Kahlert, Yesmino Elia, & Francis L. Munier. (2007). Ocular Phenotype Comparison Between Patients With Bardet-Biedl Syndrome With Identified BBS1 and BBS10 Mutations. Investigative Ophthalmology & Visual Science. 48(13). 3698–3698.1 indexed citations
Cottet, Sandra, Tatiana Favez, Francisca Maurer, et al.. (2005). Targeted Silencing of RPE65 in the Retinal Pigment Epithelial Cell Line ARPE–19 Using Lentivirus–Mediated siRNA Delivery. Investigative Ophthalmology & Visual Science. 46(13). 3054–3054.1 indexed citations
17.
Favez, Tatiana, et al.. (2004). Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients. Investigative Ophthalmology & Visual Science. 45(13). 2453–2453.1 indexed citations
18.
Munier, Francis L., et al.. (2004). A second family with X–linked retinitis pigmentosa mapping to the RP24 locus. Investigative Ophthalmology & Visual Science. 45(13). 5092–5092.1 indexed citations
19.
Munier, Francis L., et al.. (2003). Autosomal Dominant Congenital Nuclear Cataract Associated with delG91 in CRYBA3/A1. Investigative Ophthalmology & Visual Science. 44(13). 1259–1259.1 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.