Csilla H. Lazar

462 total citations
6 papers, 250 citations indexed

About

Csilla H. Lazar is a scholar working on Molecular Biology, Ophthalmology and Infectious Diseases. According to data from OpenAlex, Csilla H. Lazar has authored 6 papers receiving a total of 250 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Ophthalmology and 1 paper in Infectious Diseases. Recurrent topics in Csilla H. Lazar's work include Retinal Development and Disorders (3 papers), Connexins and lens biology (2 papers) and Retinal Diseases and Treatments (2 papers). Csilla H. Lazar is often cited by papers focused on Retinal Development and Disorders (3 papers), Connexins and lens biology (2 papers) and Retinal Diseases and Treatments (2 papers). Csilla H. Lazar collaborates with scholars based in Israel, United States and Romania. Csilla H. Lazar's co-authors include Eyal Banin, Anand Swaroop, Paul A. Sieving, Shobi Veleri, Bo Chang, Rinki Ratnapriya, Dror Sharon, Mousumi Mutsuddi, Lina Zelinger and Prasanthi Namburi and has published in prestigious journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science and Human Mutation.

In The Last Decade

Csilla H. Lazar

6 papers receiving 250 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Csilla H. Lazar Israel	4	216	86	65	52	23	6	250
Raquel Pérez-Carro Spain	10	278 1.3×	139 1.6×	37 0.6×	72 1.4×	25 1.1×	12	299
Tomokazu Takeuchi Japan	11	265 1.2×	144 1.7×	48 0.7×	35 0.7×	42 1.8×	28	319
Ryan A. Kelley United States	10	325 1.5×	70 0.8×	116 1.8×	70 1.3×	32 1.4×	15	365
Marion Neuillé France	8	244 1.1×	81 0.9×	131 2.0×	28 0.5×	20 0.9×	12	276
Marcela Mena Spain	6	251 1.2×	100 1.2×	51 0.8×	53 1.0×	26 1.1×	8	331
Marina França Dias Brazil	3	290 1.3×	125 1.5×	77 1.2×	51 1.0×	34 1.5×	6	337
Charlotte Reiff Germany	6	161 0.7×	63 0.7×	55 0.8×	15 0.3×	27 1.2×	6	183
R. Barhoum Spain	6	299 1.4×	97 1.1×	108 1.7×	56 1.1×	28 1.2×	6	396
Julio C. Corral-Serrano Netherlands	6	216 1.0×	52 0.6×	46 0.7×	48 0.9×	23 1.0×	7	240
Nicola Glöckle Germany	6	270 1.3×	138 1.6×	103 1.6×	82 1.6×	20 0.9×	6	359

Countries citing papers authored by Csilla H. Lazar

Since Specialization

Citations

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

Fields of papers citing papers by Csilla H. Lazar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Csilla H. Lazar. 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 Csilla H. Lazar. The network helps show where Csilla H. Lazar may publish in the future.

Co-authorship network of co-authors of Csilla H. Lazar

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

All Works

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6 of 6 papers shown

1.

Jakab, Endre, et al.. (2019). Screening of mecI Gene in Staphylococcus Strains Isolated in Transylvania Region of Romania. Microbial Drug Resistance. 25(5). 639–643. 2 indexed citations

2.

Sharon, Dror, Prasanthi Namburi, Rinki Ratnapriya, et al.. (2016). Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients. Investigative Ophthalmology & Visual Science. 57(12). 3153–3153. 1 indexed citations

3.

Namburi, Prasanthi, Rinki Ratnapriya, Samer Khateb, et al.. (2016). Bi-allelic Truncating Mutations in CEP78 , Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. The American Journal of Human Genetics. 99(3). 777–784. 23 indexed citations

4.

Veleri, Shobi, Csilla H. Lazar, Bo Chang, et al.. (2015). Biology and therapy of inherited retinal degenerative disease: insights from mouse models. Disease Models & Mechanisms. 8(2). 109–129. 185 indexed citations

5.

Lazar, Csilla H., Prasanthi Namburi, Mousumi Mutsuddi, et al.. (2015). Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations inALMS1andDYSF. Human Mutation. 36(9). 836–841. 14 indexed citations

6.

Lazar, Csilla H., Mousumi Mutsuddi, Lina Zelinger, et al.. (2014). Whole Exome Sequencing Reveals GUCY2D as a Major Gene Associated With Cone and Cone-Rod Dystrophy in Israel. Investigative Ophthalmology & Visual Science. 56(1). 420–430. 25 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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