Lina Zelinger

1.2k citations
19 papers · 733 · h-index 15

Impact in

  • Ophthalmology top 2%
    • Retinal Diseases and Treatments
  • Molecular Biology
    • Retinal Development and Disorders
    • CRISPR and Genetic Engineering
    • RNA regulation and disease

Papers in

  • Molecular Biology 15
    • Retinal Development and Disorders 12
    • RNA regulation and disease 3
    • Connexins and lens biology 2
  • Ophthalmology 8
    • Retinal Diseases and Treatments 8
Co-authors
Eyal Banin (15 shared papers)Dror Sharon (14 shared papers)Anand Swaroop (6 shared papers)Avigail Beryozkin (5 shared papers)Liliana Mizrahi‐Meissonnier (3 shared papers)Saul Merin (4 shared papers)Alexey Obolensky (4 shared papers)Dikla Bandah‐Rozenfeld (3 shared papers)
Journals
Investigative Ophthalmology & Visual Science (5 papers)The American Journal of Human Genetics (3 papers)Ophthalmology (2 papers)iScience (1 paper)Scientific Reports (1 paper)
Partner nations
IsraelUnited StatesGermany

In The Last Decade

Lina Zelinger

19 papers receiving 722 citations

Peers

Lina Zelinger
Comparison fields: 5 of 60
  • Ophthalmology 246
  • Molecular Biology 653
  • Sensory Systems 42
  • Cellular and Molecular Neuroscience 135
  • Cell Biology 109
Replace Elena Marrocco with:
Elena Marrocco Italy
Britta Baumann Germany
Drew Everhart United States
Marina Garcia Garrido Germany
Karina E Guziewicz United States
Samer Khateb Israel
Elisabeth M. Bleeker‐Wagemakers Netherlands
Christian Hamel France
N. L. Hawes United States
Aline Antonio France
Lina Zelinger relative to Elena Marrocco Italy Elena Marrocco's profile →
Citations per field
00.5×1.5×2×2.5×
Elena Marrocco · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Lina Zelinger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lina Zelinger Line = papers co-authored together Lina Zelinger links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1
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 ·Lina Zelinger, Eyal Banin, Alexey Obolensky, Liliana Mizrahi‐Meissonnier, Avigail Beryozkin, Dikla Bandah‐Rozenfeld, Shahar Frenkel, Tamar Ben‐Yosef, Saul Merin, Sharon Schwartz, Artur V. Cideciyan, Samuel G. Jacobson, Dror Sharon
201193
2
NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors
Cell Reports ·Jung-Woong Kim, Hyun‐Jin Yang, Matthew J. Brooks, Lina Zelinger, Gökhan Karakülah, Norimoto Gotoh, Alexis Boleda, Linn Gieser, Felipe Giuste, D. Thad Whitaker, Ashley Walton, Rafael Villasmil, Jennifer J. Barb, Peter J. Munson, Koray Dogan Kaya, Vijender Chaitankar, Tiziana Cogliati, Anand Swaroop
201691
3
Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia
Molecular Therapy ·Eyal Banin, E. Gootwine, Alexey Obolensky, Raaya Ezra-Elia, Ayala Ejzenberg, Lina Zelinger, Hen Honig, Alexander Rosov, Esther Yamin, Dror Sharon, Edward Averbukh, William W. Hauswirth, Ron Ofri
201587
4
Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy
The American Journal of Human Genetics ·Susanne Roosing, Klaus Rohrschneider, Avigail Beryozkin, Dror Sharon, Nicole Weisschuh, Jennifer Staller, Susanne Kohl, Lina Zelinger, Theo Peters, Kornelia Neveling, Tim M. Strom, L. Ingeborgh van den Born, Carel B. Hoyng, Caroline C. W. Klaver, Ronald Roepman, Bernd Wissinger, Eyal Banin, Frans P.M. Cremers, Anneke I. den Hollander
201367
5
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome
Journal of Medical Genetics ·Samer Khateb, Lina Zelinger, Liliana Mizrahi‐Meissonnier, Carmen Ayuso, Robert K. Koenekoop, Uri Laxer, Menachem Gross, Eyal Banin, Dror Sharon
201466
6
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia
Ophthalmology ·Lina Zelinger, Artur V. Cideciyan, Susanne Kohl, Sharon Schwartz, Ada Rosenmann, Dalia Eli, Alexander Sumaroka, Alejandro J. Román, Xunda Luo, Cassondra Brown, Boris Rosin, Anat Blumenfeld, Bernd Wissinger, Samuel G. Jacobson, Eyal Banin, Dror Sharon
201553
7
Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa
The American Journal of Human Genetics ·Alice E. Davidson, Nele Schwarz, Lina Zelinger, Gabriele Stern-Schneider, Amelia Shoemark, Benjamin Spitzbarth, Menachem Gross, Uri Laxer, Jacob Sosna, Panagiotis I. Sergouniotis, Naushin Waseem, Robert Wilson, Richard Kahn, Vincent Plagnol, Uwe Wolfrum, Eyal Banin, Alison J. Hardcastle, Michael E. Cheetham, Dror Sharon, Andrew R. Webster
201352
8
Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping
Investigative Ophthalmology & Visual Science ·Avigail Beryozkin, Lina Zelinger, Dikla Bandah‐Rozenfeld, Elia Shevach, Anat Harel, Tim Matthias Storm, Michal Sagi, Dalia Eli, Saul Merin, Eyal Banin, Dror Sharon
201444
9
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 ·Samer Khateb, Lina Zelinger, Tamar Ben‐Yosef, Saul Merin, Ornit Crystal‐Shalit, Menachem Gross, Eyal Banin, Dror Sharon
201227
10
Mutations inCRB1are a Relatively Common Cause of Autosomal Recessive Early-Onset Retinal Degeneration in the Israeli and Palestinian Populations
Investigative Ophthalmology & Visual Science ·Avigail Beryozkin, Lina Zelinger, Dikla Bandah‐Rozenfeld, Anat Harel, Tim A. Strom, Saul Merin, Itay Chowers, Eyal Banin, Dror Sharon
201326
11
Whole Exome Sequencing Reveals GUCY2D as a Major Gene Associated With Cone and Cone-Rod Dystrophy in Israel
Investigative Ophthalmology & Visual Science ·Csilla H. Lazar, Mousumi Mutsuddi, Adva Kimchi, Lina Zelinger, Liliana Mizrahi‐Meissonnier, Devorah Marks-Ohana, Alexis Boleda, Rinki Ratnapriya, Dror Sharon, Anand Swaroop, Eyal Banin
201425
12
RNA Biology in Retinal Development and Disease
Trends in Genetics ·Lina Zelinger, Anand Swaroop
201824
13
Cone Dystrophy with Supernormal Rod Response
Ophthalmology ·Lina Zelinger, Bernd Wissinger, Dalia Eli, Susanne Kohl, Dror Sharon, Eyal Banin
201317
14
Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL
Investigative Ophthalmology & Visual Science ·Lina Zelinger, Gökhan Karakülah, Vijender Chaitankar, Jung-Woong Kim, Hyun‐Jin Yang, Matthew J. Brooks, Anand Swaroop
201716
15
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
Scientific Reports ·Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, Karen Hendler, Prasanthi Namburi, Isabelle Audo, Ruth Sheffer, Claudia Yahalom, Samer Khateb, Eyal Banin, Dror Sharon
201915
16
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 ·Csilla H. Lazar, Adva Kimchi, Prasanthi Namburi, Mousumi Mutsuddi, Lina Zelinger, Avigail Beryozkin, Shiran Ben-Simhon, Alexey Obolensky, Ziva Ben‐Neriah, Zohar Argov, Eli Pikarsky, Yakov Fellig, Devorah Marks-Ohana, Rinki Ratnapriya, Eyal Banin, Dror Sharon, Anand Swaroop
201514
17
An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews
Human Genetics ·Lina Zelinger, Alexander Greenberg, Susanne Kohl, Eyal Banin, Dror Sharon
201010
18
Ultra-rare complement factor 8 coding variants in families with age-related macular degeneration
iScience ·Lina Zelinger, Tammy M. Martin, Jayshree Advani, Laura Campello, Milton A. English, Alan Kwong, Claire Weber, Jennifer K Maykoski, Yuri V. Sergeev, Robert N. Fariss, Emily Y. Chew, Michael L. Klein, Anand Swaroop
20235
19
GENE THERAPY IN A SHEEP MODEL OF CNGA3 ACHROMATOPSIA
Investigative Ophthalmology & Visual Science ·Eyal Banin, Alexey Obolensky, Ayala Ejzenberg, Lina Zelinger, Raaya Ezra-Elia, Alexander Rosov, Edward Averbukh, E. Gootwine, Ron Ofri, William W. Hauswirth
20141

About Lina Zelinger

Lina Zelinger is a scholar working on Molecular Biology, Ophthalmology, Cell Biology, Genetics and Cellular and Molecular Neuroscience, having authored 19 papers that have together received 733 indexed citations. Recurring topics across this work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers), Photoreceptor and optogenetics research (4 papers), melanin and skin pigmentation (3 papers), RNA regulation and disease (3 papers), Connexins and lens biology (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Cellular transport and secretion (2 papers). The work is most often cited by research in Ophthalmology (246 citations), Molecular Biology (653 citations), Sensory Systems (42 citations), Cellular and Molecular Neuroscience (135 citations) and Cell Biology (109 citations). Lina Zelinger has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Eyal Banin, Dror Sharon, Anand Swaroop, Avigail Beryozkin, Liliana Mizrahi‐Meissonnier, Saul Merin, Alexey Obolensky, Dikla Bandah‐Rozenfeld, Menachem Gross and Samer Khateb. Their work appears in journals such as Investigative Ophthalmology & Visual Science, The American Journal of Human Genetics, Ophthalmology, iScience and Scientific Reports.

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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