Mor Hanany

775 total citations
12 papers, 448 citations indexed

About

Mor Hanany is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Mor Hanany has authored 12 papers receiving a total of 448 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Mor Hanany's work include Retinal Development and Disorders (12 papers), Cellular transport and secretion (4 papers) and Retinal Diseases and Treatments (4 papers). Mor Hanany is often cited by papers focused on Retinal Development and Disorders (12 papers), Cellular transport and secretion (4 papers) and Retinal Diseases and Treatments (4 papers). Mor Hanany collaborates with scholars based in Israel, Netherlands and United Kingdom. Mor Hanany's co-authors include Dror Sharon, Carlo Rivolta, Eyal Banin, Avigail Beryozkin, Prakadeeswari Gopalakrishnan, Shay Ben‐Aroya, Erez Y. Levanon, Tamar Ben‐Yosef, Samer Khateb and Sari Lieberman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Progress in Retinal and Eye Research.

In The Last Decade

Mor Hanany

12 papers receiving 443 citations

Peers

Countries citing papers authored by Mor Hanany

Since Specialization

Citations

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

Fields of papers citing papers by Mor Hanany

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mor Hanany

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	Simultaneous Detection of Common Founder Mutations Using a Cost-Effective Deep Sequencing Panel 2024 ·Genes ·(unknown), Mor Hanany, (unknown), Itay Chowers, Tamar Ben‐Yosef, Samer Khateb, Eyal Banin, Dror Sharon	1
2	An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy 2023 ·Translational Vision Science & Technology ·Mor Hanany, (unknown), (unknown), Avigail Beryozkin, (unknown), Dror Sharon	5
3	Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations 2023 ·Cold Spring Harbor Perspectives in Medicine ·Mor Hanany, (unknown), Tamar Ben‐Yosef, Dror Sharon	17
4	Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily 2022 ·Genetics in Medicine ·(unknown), (unknown), Alexey Obolensky, (unknown), Mingchu Xu, Yumei Li, (unknown), Prakadeeswari Gopalakrishnan, Menachem Gross, Boris Rosin, Mor Hanany, Andrew R. Webster, (unknown), Robert K. Koenekoop, Rui Chen, Gavin Arno, Ora Schueler‐Furman, Susanne Roosing, Eyal Banin, Dror Sharon	7
5	SENIOR–LØKEN SYNDROME 2021 ·Retina ·Claudia Yahalom, Oded Volovelsky, (unknown), (unknown), (unknown), (unknown), Mor Hanany, Muhammad Imran Khan, Frans P.M. Cremers, Irene Anteby, Eyal Banin, Dror Sharon, Samer Khateb	11
6	Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities 2021 ·Progress in Retinal and Eye Research ·(unknown), (unknown), Prakadeeswari Gopalakrishnan, Avigail Beryozkin, Mor Hanany, Erez Y. Levanon, Eyal Banin, Shay Ben‐Aroya, Dror Sharon	102
7	Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations 2020 ·Scientific Reports ·Avigail Beryozkin, Samer Khateb, (unknown), Muhammad Imran Khan, Frans P.M. Cremers, Alexey Obolensky, Mor Hanany, Eedy Mezer, Itay Chowers, Hadas Newman, Tamar Ben‐Yosef, Dror Sharon, Eyal Banin	15
8	Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases 2020 ·Proceedings of the National Academy of Sciences ·Mor Hanany, Carlo Rivolta, Dror Sharon	228
9	Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children 2020 ·European Journal of Ophthalmology ·(unknown), Karen Hendler, Eyal Banin, Mor Hanany, (unknown), Hadas Mechoulam, Vardiella Meiner, Yoav Parag, Dror Sharon, (unknown), Claudia Yahalom	6
10	Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variants 2019 ·Journal of Medical Genetics ·Mor Hanany, Dror Sharon	22
11	Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population 2018 ·European Journal of Human Genetics ·Mor Hanany, (unknown), (unknown), Anat Blumenfeld, Hadas Newman, Eran Pras, Ohad Wormser, Ohad S. Birk, Libe Gradstein, Eyal Banin, Tamar Ben‐Yosef, Dror Sharon	13
12	Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data 2016 ·Journal of Medical Genetics ·Samer Khateb, Mor Hanany, (unknown), Avigail Beryozkin, (unknown), (unknown), (unknown), Liliana Mizrahi‐Meissonnier, Sari Lieberman, Tamar Ben‐Yosef, Eyal Banin, Dror Sharon	21

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