Lina Zelinger

1.2k citations
21 papers · 749 · h-index 15

Impact in

Papers in

  • Molecular Biology 15
    • Retinal Development and Disorders 13
    • Connexins and lens biology 2
    • RNA regulation and disease 2
  • Ophthalmology 5
    • Retinal Diseases and Treatments 5
Co-authors
Eyal Banin (15 shared papers)Dror Sharon (14 shared papers)Anand Swaroop (7 shared papers)Avigail Beryozkin (5 shared papers)Saul Merin (4 shared papers)Liliana Mizrahi‐Meissonnier (3 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)Blood (1 paper)Cell Reports (1 paper)
Partner nations
IsraelUnited StatesGermany

In The Last Decade

Lina Zelinger

19 papers receiving 738 citations

Peers

Lina Zelinger
Comparison fields: 5 of 58
  • Ophthalmology 165
  • Sensory Systems 43
  • Molecular Biology 618
  • Cellular and Molecular Neuroscience 113
  • Cell Biology 99
Replace Elena Marrocco with:
Elena Marrocco Italy
Elisabeth M. Bleeker‐Wagemakers Netherlands
Karina E Guziewicz United States
Marina Garcia Garrido Germany
Corinne Leowski France
Samer Khateb Israel
Jillian N. Pearring United States
Sakae Ikeda 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

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1
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
201694
2
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
201194
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
201588
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
201368
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
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
201355
7
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
201554
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
201445
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
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
201426
11
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
12
RNA Biology in Retinal Development and Disease
Trends in Genetics ·Lina Zelinger, Anand Swaroop
201824
13
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
201918
14
Cone Dystrophy with Supernormal Rod Response
Ophthalmology ·Lina Zelinger, Bernd Wissinger, Dalia Eli, Susanne Kohl, Dror Sharon, Eyal Banin
201317
15
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
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
20236
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
20
Loss of paired immunoglobin-like type 2 receptor B gene associated with age-related macular degeneration impairs photoreceptor function in mouse retina
Human Molecular Genetics ·Partha Narayan Dey, Nivedita Singh, Lina Zelinger, Zachary Batz, Jacob Nellissery, Noor D. White, Haohua Qian, Tiansen Li, Robert N. Fariss, Lijin Dong, Anand Swaroop
20240

About Lina Zelinger

Lina Zelinger is a scholar working on Molecular Biology, Ophthalmology, Cell Biology, Cellular and Molecular Neuroscience and Genetics, having authored 21 papers that have together received 749 indexed citations. Recurring topics across this work include Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (5 papers), Photoreceptor and optogenetics research (3 papers), Cellular transport and secretion (2 papers), melanin and skin pigmentation (2 papers), Connexins and lens biology (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Ophthalmology (165 citations), Sensory Systems (43 citations), Molecular Biology (618 citations), Cellular and Molecular Neuroscience (113 citations) and Cell Biology (99 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, Saul Merin, Liliana Mizrahi‐Meissonnier, Alexey Obolensky, Dikla Bandah‐Rozenfeld, Menachem Gross and Susanne Kohl. Their work appears in journals such as Investigative Ophthalmology & Visual Science, The American Journal of Human Genetics, Ophthalmology, Blood and Cell 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Elena MarroccoBreakdown of academic impact, for papers by Elisabeth M. Bleeker‐WagemakersBreakdown of academic impact, for papers by Karina E GuziewiczBreakdown of academic impact, for papers by Marina Garcia GarridoBreakdown of academic impact, for papers by Corinne LeowskiBreakdown of academic impact, for papers by Samer KhatebBreakdown of academic impact, for papers by Jillian N. PearringBreakdown of academic impact, for papers by Sakae IkedaBreakdown of academic impact, for papers by Aline Antonio