Lina Zelinger

1.2k total citations
19 papers, 733 citations indexed

About

Lina Zelinger is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Lina Zelinger has authored 19 papers receiving a total of 733 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Ophthalmology and 5 papers in Cell Biology. Recurrent topics in Lina Zelinger's work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (4 papers). Lina Zelinger is often cited by papers focused on Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (4 papers). Lina Zelinger collaborates with scholars based in Israel, United States and Germany. Lina Zelinger's co-authors include Dror Sharon, Eyal Banin, Anand Swaroop, Avigail Beryozkin, Saul Merin, Liliana Mizrahi‐Meissonnier, Alexey Obolensky, Dikla Bandah‐Rozenfeld, Menachem Gross and Samer Khateb and has published in prestigious journals such as PLoS ONE, Scientific Reports and Ophthalmology.

In The Last Decade

Lina Zelinger

19 papers receiving 722 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lina Zelinger Israel 15 653 246 183 135 109 19 733
Elena Marrocco Italy 18 839 1.3× 184 0.7× 261 1.4× 153 1.1× 56 0.5× 27 969
Karina E Guziewicz United States 13 676 1.0× 354 1.4× 147 0.8× 157 1.2× 87 0.8× 26 762
Drew Everhart United States 6 651 1.0× 248 1.0× 180 1.0× 205 1.5× 77 0.7× 8 696
Corinne Leowski France 7 806 1.2× 500 2.0× 182 1.0× 165 1.2× 104 1.0× 7 858
Nele Schwarz United Kingdom 12 840 1.3× 174 0.7× 211 1.2× 250 1.9× 176 1.6× 14 931
Britta Baumann Germany 16 936 1.4× 429 1.7× 123 0.7× 146 1.1× 156 1.4× 23 1.0k
Christian Hamel France 9 851 1.3× 461 1.9× 123 0.7× 283 2.1× 108 1.0× 14 972
Melanie M. Sohocki United States 14 1.0k 1.6× 501 2.0× 177 1.0× 267 2.0× 160 1.5× 18 1.1k
Jillian N. Pearring United States 13 676 1.0× 134 0.5× 167 0.9× 345 2.6× 173 1.6× 19 775
Henri Leinonen United States 15 515 0.8× 133 0.5× 84 0.5× 202 1.5× 70 0.6× 32 704

Countries citing papers authored by Lina Zelinger

Since Specialization
Citations

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

Fields of papers citing papers by Lina Zelinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lina Zelinger

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

All Works

19 of 19 papers shown
1.
Zelinger, Lina, Tammy M. Martin, Jayshree Advani, et al.. (2023). Ultra-rare complement factor 8 coding variants in families with age-related macular degeneration. iScience. 26(4). 106417–106417. 5 indexed citations
2.
Zelinger, Lina, Christina Zeitz, Karen Hendler, et al.. (2019). TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations. Scientific Reports. 9(1). 12047–12047. 15 indexed citations
3.
Zelinger, Lina & Anand Swaroop. (2018). RNA Biology in Retinal Development and Disease. Trends in Genetics. 34(5). 341–351. 24 indexed citations
4.
Zelinger, Lina, Gökhan Karakülah, Vijender Chaitankar, et al.. (2017). Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL. Investigative Ophthalmology & Visual Science. 58(11). 4422–4422. 16 indexed citations
5.
Kim, Jung-Woong, Hyun‐Jin Yang, Matthew J. Brooks, et al.. (2016). NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors. Cell Reports. 17(9). 2460–2473. 91 indexed citations
6.
Zelinger, Lina, Artur V. Cideciyan, Susanne Kohl, et al.. (2015). Genetics and Disease Expression in the CNGA3 Form of Achromatopsia. Ophthalmology. 122(5). 997–1007. 53 indexed citations
7.
Banin, Eyal, E. Gootwine, Alexey Obolensky, et al.. (2015). Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia. Molecular Therapy. 23(9). 1423–1433. 87 indexed citations
8.
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
9.
Banin, Eyal, Alexey Obolensky, Lina Zelinger, et al.. (2014). GENE THERAPY IN A SHEEP MODEL OF CNGA3 ACHROMATOPSIA. Investigative Ophthalmology & Visual Science. 55(13). 4566–4566. 1 indexed citations
10.
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
11.
Beryozkin, Avigail, Lina Zelinger, Dikla Bandah‐Rozenfeld, et al.. (2014). Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping. Investigative Ophthalmology & Visual Science. 55(2). 1149–1149. 44 indexed citations
12.
Khateb, Samer, Lina Zelinger, Liliana Mizrahi‐Meissonnier, et al.. (2014). A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome. Journal of Medical Genetics. 51(7). 460–469. 66 indexed citations
13.
Davidson, Alice E., Nele Schwarz, Lina Zelinger, et al.. (2013). Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa. The American Journal of Human Genetics. 93(2). 321–329. 52 indexed citations
14.
Roosing, Susanne, Klaus Rohrschneider, Avigail Beryozkin, et al.. (2013). Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy. The American Journal of Human Genetics. 93(1). 110–117. 67 indexed citations
15.
Zelinger, Lina, et al.. (2013). Cone Dystrophy with Supernormal Rod Response. Ophthalmology. 120(11). 2338–2343. 17 indexed citations
16.
Beryozkin, Avigail, Lina Zelinger, Dikla Bandah‐Rozenfeld, et al.. (2013). Mutations inCRB1are a Relatively Common Cause of Autosomal Recessive Early-Onset Retinal Degeneration in the Israeli and Palestinian Populations. Investigative Ophthalmology & Visual Science. 54(3). 2068–2068. 26 indexed citations
17.
Khateb, Samer, Lina Zelinger, Tamar Ben‐Yosef, et al.. (2012). Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa with Late-Onset Hearing Loss. PLoS ONE. 7(12). e51566–e51566. 27 indexed citations
18.
Zelinger, Lina, Eyal Banin, Alexey Obolensky, et al.. (2011). A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews. The American Journal of Human Genetics. 88(2). 207–215. 93 indexed citations
19.
Zelinger, Lina, Alexander Greenberg, Susanne Kohl, Eyal Banin, & Dror Sharon. (2010). An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews. Human Genetics. 128(3). 261–267. 10 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Elena Marrocco Breakdown of academic impact, for papers by Karina E Guziewicz Breakdown of academic impact, for papers by Drew Everhart Breakdown of academic impact, for papers by Corinne Leowski Breakdown of academic impact, for papers by Nele Schwarz Breakdown of academic impact, for papers by Britta Baumann Breakdown of academic impact, for papers by Christian Hamel Breakdown of academic impact, for papers by Melanie M. Sohocki Breakdown of academic impact, for papers by Jillian N. Pearring Breakdown of academic impact, for papers by Henri Leinonen
Rankless by CCL
2026