Leila Tiab

616 total citations
14 papers, 451 citations indexed

About

Leila Tiab is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Leila Tiab has authored 14 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Ophthalmology and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Leila Tiab's work include Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Retinal and Macular Surgery (2 papers). Leila Tiab is often cited by papers focused on Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Retinal and Macular Surgery (2 papers). Leila Tiab collaborates with scholars based in Switzerland, United States and Germany. Leila Tiab's co-authors include Daniel F. Schorderet, Francis L. Munier, Marie‐Claire Gaillard, Pascal Escher, Léonidas Zografos, François‐Xavier Borruat, Béatrice E. Frueh, Richard K. Forster, J. Fielding Hejtmancik and Yuri V. Sergeev and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and American Journal of Ophthalmology.

In The Last Decade

Leila Tiab

14 papers receiving 444 citations

Peers

Leila Tiab
Lue Xiang China
Dhani Tracey‐White United Kingdom
Jean‐Jacques De Laey Belgium
Richard A Axton United Kingdom
Ellen A.W. Blokland Netherlands
Tasneem P. Sharma United States
Anneke I. den Hollander Netherlands
Daniela Sanges Italy
F. Beby France
Birgit Lorenz Germany
Lue Xiang China
Leila Tiab
Citations per year, relative to Leila Tiab Leila Tiab (= 1×) peers Lue Xiang

Countries citing papers authored by Leila Tiab

Since Specialization
Citations

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

Fields of papers citing papers by Leila Tiab

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leila Tiab

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

All Works

14 of 14 papers shown
1.
Vaclavik, Veronika, Leila Tiab, Young Joo Sun, et al.. (2022). NewCOL6A6Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family. Investigative Ophthalmology & Visual Science. 63(3). 23–23. 3 indexed citations
2.
Schorderet, Daniel F., et al.. (2014). IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies—A Price Comparison with Sanger Sequencing. Advances in experimental medicine and biology. 171–176. 3 indexed citations
3.
Tiab, Leila, et al.. (2013). A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.. PubMed. 19. 829–34. 7 indexed citations
4.
Schorderet, Daniel F., Alexandra Iouranova, Tatiana Favez, Leila Tiab, & Pascal Escher. (2012). IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies. BioMed Research International. 2013. 1–9. 20 indexed citations
5.
Lisch, Walter, Anthony J. Bron, Francis L. Munier, et al.. (2012). Franceschetti Hereditary Recurrent Corneal Erosion. American Journal of Ophthalmology. 153(6). 1073–1081.e4. 17 indexed citations
6.
Bouyacoub, Yosra, Leila Tiab, Ahmed Rebaï, et al.. (2010). Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. Journal of Human Genetics. 56(1). 22–28. 13 indexed citations
7.
Vaclavik, Veronika, Marie‐Claire Gaillard, Leila Tiab, Daniel F. Schorderet, & Francis L. Munier. (2010). Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.. PubMed. 16. 467–75. 21 indexed citations
8.
Michaelides, Michel, Marie‐Claire Gaillard, Pascal Escher, et al.. (2010). ThePROM1Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy. Investigative Ophthalmology & Visual Science. 51(9). 4771–4771. 83 indexed citations
9.
Schorderet, Daniel F., et al.. (2008). Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome. The American Journal of Human Genetics. 82(5). 1178–1184. 59 indexed citations
10.
Escher, Pascal, Peter Gouras, Raphaël Roduit, et al.. (2008). Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family. Human Mutation. 30(3). 342–351. 56 indexed citations
11.
Tiab, Leila, Lie Chen, Laurent Kappeler, et al.. (2008). A novel dominant mutation of the Na v 1.4 α-subunit domain I leading to sodium channel myotonia. Neurology. 71(21). 1669–1675. 21 indexed citations
12.
Schorderet, Daniel F., Leila Tiab, Marie‐Claire Gaillard, et al.. (2007). Novel mutations in FRMD7 in X-linked congenital nystagmus. Human Mutation. 28(5). 525–525. 35 indexed citations
13.
Tiab, Leila, Xiaodong Jiao, Francis L. Munier, et al.. (2005). Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy. The American Journal of Human Genetics. 77(1). 54–63. 94 indexed citations
14.
Tiab, Leila, et al.. (2004). Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients. Ophthalmic Genetics. 25(4). 241–246. 19 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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