Eyal Banin - Publications, H-index & Citations

Eyal Banin

hebrew university of jerusalem

54H指数

321论文数

10.0K被引数

收录论文 116

发表时间

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans KHDC4基因中的纯合移码变异与人类综合征性遗传性视网膜疾病相关

Clinical Genetics

IF2.3

2026-10-01

OAAI

Asodu Sandeep Sarma; Neta Barnoy; Prakadeeswari Gopalakrishnan; Keren Dichter; Rotem Mizrachi; Manar Salameh; Eyal Banin; Dror Sharon; Adi Inbal; Samer Khateb

Temporal vision adaptation and restoration in achromatopsia 色盲中的时间视觉适应与恢复

iScience

IF4.1

2026-08-01

PREAI

McKyton, Ayelet; Bick, Atira; Elul, Deena; Abulafia, Ruth; Ohana, Devora Marks; Nahmany, Einav; Banin, Eyal; Levin, Netta

PRCD-associated retinitis pigmentosa in dogs and humans PRCD相关性色素性视网膜炎在犬和人类中

Experimental Eye Research

IF2.7

2026-05-08

OAAI

Valerie L. Dufour; Yu Sato; Alexander Sumaroka; Raghavi Sudharsan; Eyal Banin; Yinxi Yu; Ana Ripolles-Garcia; Jennifer Kwok; Tomas S. Alleman; Gui-Shuang Ying; Dror Sharon; Artur V. Cideciyan; William A. Beltran; Gustavo D. Aguirre

Bilateral fulminant Aspergillus endophthalmitis complicating chimeric antigen receptor T-cell therapy for refractory multiple myeloma 双侧暴发性曲霉菌性眼内炎，并发难治性多发性骨髓瘤的嵌合抗原受体T细胞疗法

Taiwan Journal of Ophthalmology

IF1.2

2026-05-01

PREAI

Shmueli, Or; Tiosano, Liran; Luski, Shahar; Elias, Shlomo; Grisariu, Sigal; Avni, Batia; Zimran, Eran; Lebel, Eyal; Asherie, Nathalie; Kfir-Erenfeld, Shlomit; Stepensky, Polina; Estrella, Fernando; Banin, Eyal; Amer, Radgonde

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa U4和U6 snRNA基因的新生和遗传显性变异导致色素性视网膜炎

Nature Genetics

IF29

2026-01-09

OAAI

Mathieu Quinodoz; Kim Rodenburg; Zuzana Cvackova; Karolina Kaminska; Suzanne E. de Bruijn; Ana Belén Iglesias-Romero; Erica G. M. Boonen; Mukhtar Ullah; Nick Zomer; Marc Folcher; Jacques Bijon; Lara K. Holtes; Stephen H. Tsang; Zelia Corradi; K. Bailey Freund; Stefanida Shliaga; Daan M. Panneman; Rebekkah J. Hitti-Malin; Manir Ali; Ala’a AlTalbishi; Sten Andréasson; Georg Ansari; Gavin Arno; Galuh D. N. Astuti; Carmen Ayuso; Radha Ayyagari; Sandro Banfi; Eyal Banin; Tahsin Stefan Barakat; Mirella T. S. Barboni; Miriam Bauwens; Tamar Ben-Yosef; Virginie Bernard; David G. Birch; Pooja Biswas; Fiona Blanco-Kelly; Beatrice Bocquet; Camiel J. F. Boon; Kari Branham; Dominique Bremond-Gignac; Alexis Ceecee Britten-Jones; Kinga M. Bujakowska; Cyril Burin des Roziers; Elizabeth L. Cadena; Giacomo Calzetti; Francesca Cancellieri; Luca Cattaneo; Naomi Chadderton; Peter Charbel Issa; Luísa Coutinho-Santos; Stephen P. Daiger; Elfride De Baere; Marieke De Bruyne; Berta de la Cerda; John N. De Roach; Julie De Zaeytijd; Ronny Derks; Claire-Marie Dhaenens; Lubica Dudakova; Jacque L. Duncan; G. Jane Farrar; Nicolas Feltgen; Beau J. Fenner; Lidia Fernández-Caballero; Juliana M. Ferraz Sallum; Simone Gana; Alejandro Garanto; Jessica C. Gardner; Christian Gilissen; Roser Gonzàlez-Duarte; Kensuke Goto; Sam Griffiths-Jones; Tobias B. Haack; Lonneke Haer-Wigman; Alison J. Hardcastle; Takaaki Hayashi; Elise Héon; Lies H. Hoefsloot; Alexander Hoischen; Josephine P. Holtan; Carel B. Hoyng; Manuel Benjamin B. Ibanez; Chris F. Inglehearn; Takeshi Iwata; Brynjar O. Jensson; Kaylie Jones; Vasiliki Kalatzis; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C. W. Klaver; Krisztina Knézy; Robert K. Koenekoop; Susanne Kohl; Taro Kominami; Laura Kühlewein; Tina M. Lamey; Rina Leibu; Bart P. Leroy; Petra Liskova; Irma Lopez; Victor R. de J. López-Rodríguez; Quinten Mahieu; Omar A. Mahroo; Gaël Manes; Luke Mansard; M. Pilar Martín-Gutiérrez; Nelson Martins; Laura Mauring; Martin McKibbin; Terri L. McLaren; Isabelle Meunier; Michel Michaelides; José M. Millán; Kei Mizobuchi; Rajarshi Mukherjee; Zoltán Zsolt Nagy; Kornelia Neveling; Monika Ołdak; Michiel Oorsprong; Yang Pan; Anastasia Papachristou; Antonio Percesepe; Maximilian Pfau; Eric A. Pierce; Emily Place; Raj Ramesar; Francis Ramond; Florence Andrée Rasquin; Gillian I. Rice; Lisa Roberts; María Rodríguez-Hidalgo; Javier Ruiz-Ederra; Ataf H. Sabir; Ai Fujita Sajiki; Ana Isabel Sánchez-Barbero; Asodu Sandeep Sarma; Riccardo Sangermano; Cristina M. Santos; Margherita Scarpato; Hendrik P. N. Scholl; Dror Sharon; Sabrina G. Signorini; Francesca Simonelli; Ana Berta Sousa; Maria Stefaniotou; Kari Stefansson; Katarina Stingl; Akiko Suga; Patrick Sulem; Lori S. Sullivan; Viktória Szabó; Jacek P. Szaflik; Gita Taurina; Alberta A. H. J. Thiadens; Carmel Toomes; Viet H. Tran; Miltiadis K. Tsilimbaris; Pavlina Tsoka; Veronika Vaclavik; Marie Vajter; Sandra Valeina; Enza Maria Valente; Casey Valentine; Rebeca Valero; Sophie Valleix; Joseph van Aerschot; L. Ingeborgh van den Born; Mattias Van Heetvelde; Virginie J. M. Verhoeven; Andrea L. Vincent; Andrew R. Webster; Laura Whelan; Bernd Wissinger; Georgia G. Yioti; Kazutoshi Yoshitake; Juan C. Zenteno; Roberta Zeuli; Theresia Zuleger; Chaim Landau; Allan I. Jacob; Siying Lin; Frans P. M. Cremers; Winston Lee; Jamie M. Ellingford; David Stanek; Susanne Roosing; Carlo Rivolta

Measuring Rod-and Cone-Photoreceptor-Specific Vision in Inherited Retinal Diseases Using a Commercial Perimeter 使用商业视野计测量遗传性视网膜疾病中视杆细胞和视锥细胞特异性的视觉功能

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2025-10-01

OAAI

Wu, Vivian; Roman, Alejandro J.; Galsterer, Emma L.; Ansari, Georg; Erdinest, Inbar; Righetti, Giulia; Viarbitskaya, Iryna; Russell, Robert C.; Kim, Rebecca J.; Charlier, Jacques; Pfau, Kristina; Stingl, Krunoslav; Banin, Eyal; Pfau, Maximilian; Stingl, Katarina; Aleman, Tomas S.; Cideciyan, Artur, V

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy C19orf44基因的双等位基因无义变异导致一种独特的迟发性视网膜营养不良表型，其特征为斑片状黄斑周围脉络膜视网膜萎缩。

GENETICS IN MEDICINE

IF6.2

2025-06-01

OAAI

Ehrenberg, Miriam; Avraham, Maayan; Asodu, Sandeep Sarma; Moye, Abigail R.; Sangermano, Riccardo; Rizel, Leah; Ali-Nasser, Tahleel; Sher, Ifat; Gurwitz, David; Chao, Katherine R.; Rivera, Antonio; Webster, Andrew R.; Rivolta, Carlo; Newman, Hadas; Pras, Eran; Rotenstreich, Ygal; Banin, Eyal; Pierce, Eric A.; Zur, Dinah; Arno, Gavin; Bujakowska, Kinga M.; Lin, Siying; Sharon, Dror; Ben-Yosef, Tamar

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2025-04-01

OAAI

Kaminska, Karolina; Cancellieri, Francesca; Quinodoz, Mathieu; Moye, Abigail R.; Bauwens, Miriam; Lin, Siying; Janeschitz-Kriegl, Lucas; Hayman, Tamar; Barberan-Martinez, Pilar; Schlaeger, Regina; van den Broeck, Filip; Fernandez, Almudena Avila; Fernandez-Caballero, Lidia; Perea-Romero, Irene; Garcia-Garcia, Gema; Salom, David; Mazzola, Pascale; Zuleger, Theresia; Poths, Karin; Haack, Tobias B.; Jacob, Julie; Vermeer, Sascha; Terbeek, Frederique; Feltgen, Nicolas; Moulin, Alexandre P.; Koutroumanou, Louisa; Papadakis, George; Browning, Andrew C.; Madhusudhan, Savita; Granse, Lotta; Banin, Eyal; Sousa, Ana Berta; Santos, Luisa Coutinho; Kuehlewein, Laura; De Angeli, Pietro; Leroy, Bart P.; Mahroo, Omar A.; Sedgwick, Fay; Eden, James; Pfau, Maximilian; Andreasson, Sten; Scholl, Hendrik P. N.; Ayuso, Carmen; Millan, Jose M.; Sharon, Dror; Tsilimbaris, Miltiadis K.; Vaclavik, Veronika; Tran, Hoai, V; Ben-Yosef, Tamar; De Baere, Elfride; Webster, Andrew R.; Arno, Gavin; Sergouniotis, Panagiotis I.; Kohl, Susanne; Santos, Cristina; Rivolta, Carlo

Intact high-level visual functions in congenital rod-monochromacy

FRONTIERS IN NEUROSCIENCE

IF3.2

2024-09-27

OAAI

Shabat, Sheer; Mckyton, Ayelet; Elul, Deena; Marks Ohana, Devora; Nahmany, Einav; Banin, Eyal; Levin, Netta

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

BRITISH JOURNAL OF OPHTHALMOLOGY

IF3.5

2024-07-30

PREAI

Igelman, Austin D.; White, Elizabeth; Tayyib, Alaa; Everett, Lesley; Vincent, Ajoy; Heon, Elise; Zeitz, Christina; Michaelides, Michel; Mahroo, Omar A.; Katta, Mohamed; Webster, Andrew; Preising, Markus; Lorenz, Birgit; Khateb, Samer; Banin, Eyal; Sharon, Dror; Luski, Shahar; Van Den Broeck, Filip; Leroy, Bart Peter; De Baere, Elfride; Walraedt, Sophie; Stingl, Katarina; Kuehlewein, Laura; Kohl, Susanne; Reith, Milda; Fulton, Anne; Raghuram, Aparna; Meunier, Isabelle; Dollfus, Helene; Aleman, Tomas S.; Bedoukian, Emma C.; O'Neil, Erin C.; Krauss, Emily; Vincent, Andrea; Jordan, Charlotte; Iannaccone, Alessandro; Sen, Parveen; Sundaramurthy, Srilekha; Nagasamy, Soumittra; Balikova, Irina; Casteels, Ingele; Borooah, Shyamanga; Yassin, Shaden; Nagiel, Aaron; Schwartz, Hillary; Zanlonghi, Xavier; Gottlob, Irene; Mclean, Rebecca J.; Munier, Francis L.; Stephenson, Andrew; Sisk, Robert; Koenekoop, Robert; Wilson, Lorri B.; Fredrick, Douglas; Choi, Dongseok; Yang, Paul; Pennesi, Mark Edward

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration UBAP1L的功能丧失变异导致常染色体隐性视网膜变性

GENETICS IN MEDICINE

IF6.2

2024-06-01

PREAI

Han, Ji Hoon; Rodenburg, Kim; Hayman, Tamar; Calzetti, Giacomo; Kaminska, Karolina; Quinodoz, Mathieu; Marra, Molly; Wallerich, Sandrine; Allon, Gilad; Nagy, Zoltan Z.; Knezy, Krisztina; Li, Yumei; Chen, Rui; Barboni, Mirella Telles Salgueiro; Yang, Paul; Pennesi, Mark E.; van den Born, L. Ingeborgh; Varsanyi, Balazs; Szabo, Viktoria; Sharon, Dror; Banin, Eyal; Ben-Yosef, Tamar; Roosing, Susanne; Koenekoop, Robert K.; Rivolta, Carlo

Retinal Disorders

COLD SPRING HARBOR PERSPECTIVES IN MEDICINE

IF10.1

2024-04-02

PREAI

Sahel, Jose-Alain; Banin, Eyal; Bennett, Jean; Duncan, Jacque L.; Roska, Botond

Development and Evaluation of a New Self-Administered Near Visual Acuity Chart: Accuracy and Feasibility of Usage

JOURNAL OF CLINICAL MEDICINE

IF2.9

2024-04-02

OAAI

Ben-Eli, Hadas; Banin, Eyal; Levy, Jaime; Glik, Miryam; Afriat, Sarah; Magal, Yasmin; Harari, Rivka; Benyamin, Aviya; Shein, Shira; Chowers, Itay

Fine-tuning FAM161A gene augmentation therapy to restore retinal function 微调FAM161A基因增强疗法恢复视网膜功能

EMBO MOLECULAR MEDICINE

IF8.3

2024-03-19

OAAI

Arsenijevic, Yvan; Chang, Ning; Mercey, Olivier; El Fersioui, Younes; Koskiniemi-Kuendig, Hanna; Joubert, Caroline; Bemelmans, Alexis-Pierre; Rivolta, Carlo; Banin, Eyal; Sharon, Dror; Guichard, Paul; Hamel, Virginie; Kostic, Corinne

A pipeline for identifying guide RNA sequences that promote RNA editing of nonsense mutations that cause inherited retinal diseases

MOLECULAR THERAPY NUCLEIC ACIDS

IF6.1

2024-03-01

OAAI

Schneider, Nina; Steinberg, Ricky; Ben-David, Amit; Valensi, Johanna; David-Kadoch, Galit; Rosenwasser, Zohar; Banin, Eyal; Levanon, Erez Y.; Sharon, Dror; Ben-Aroya, Shay

Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population 最佳疾病: 以色列人群的全球突变回顾，基因型-表型相关性和患病率分析

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2024-02-27

OAAI

Beryozkin, Avigail; Sher, Ifat; Ehrenberg, Miriam; Zur, Dinah; Newman, Hadas; Gradstein, Libe; Simaan, Francis; Rotenstreich, Ygal; Goldenberg-Cohen, Nitza; Bahar, Irit; Blumenfeld, Anat; Rivera, Antonio; Rosin, Boris; Deitch-Harel, Iris; Perlman, Ido; Mechoulam, Hadas; Chowers, Itay; Leibu, Rina; Ben-Yosef, Tamar; Pras, Eran; Banin, Eyal; Sharon, Dror; Khateb, Samer

KCNV2-associated retinopathy: genotype-phenotype correlations-KCNV2 study group report 3 KCNV2-associated视网膜病变: 基因型-表型correlations-KCNV2研究组报告3

BRITISH JOURNAL OF OPHTHALMOLOGY

IF3.5

2023-10-18

OAAI

de Guimaraes, Thales A. C.; Georgiou, Michalis; Robson, Anthony G.; Fujinami, Kaoru; Vincent, Ajoy; Nasser, Fadi; Khateb, Samer; Mahroo, Omar A.; Pontikos, Nikolas; Vargas, Mauricio E.; Thiadens, Alberta A. H. J.; de Carvalho, Emanuel R.; Nguyen, Xuan-Than-An; Arno, Gavin; Fujinami-Yokokawa, Yu; Liu, Xiao; Tsunoda, Kazushige; Hayashi, Takaaki; Jimenez-Rolando, Belen; Martin-Merida, Maria Inmaculada; Avila-Fernandez, Almudena; Salas, Ester Carreno; Garcia-Sandoval, Blanca; Ayuso, Carmen; Sharon, Dror; Kohl, Susanne; Huckfeldt, Rachel M.; Banin, Eyal; Pennesi, Mark E.; Khan, Arif O.; Wissinger, Bernd; Webster, Andrew R.; Heon, Elise; Boon, Camiel J. F.; Zrenner, Eberhard; Michaelides, Michel

Achromatopsia-Visual Cortex Stability and Plasticity in the Absence of Functional Cones

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2023-10-17

OAAI

Molz, Barbara; Herbik, Anne; Baseler, Heidi A.; de Best, Peter; Raz, Noa; Gouws, Andre; Ahmadi, Khazar; Lowndes, Rebecca; Mclean, Rebecca J.; Gottlob, Irene; Kohl, Susanne; Choritz, Lars; Maguire, John; Kanowski, Martin; Kaesmann-Kellner, Barbara; Wieland, Ilse; Banin, Eyal; Levin, Netta; Morland, Antony B.; Hoffmann, Michael B.

Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes

JOURNAL OF MEDICAL GENETICS

IF3.7

2023-10-05

PREAI

Hayman, Tamar; Millo, Talya; Hendler, Karen; Chowers, Itay; Gross, Menachem; Banin, Eyal; Sharon, Dror

Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa

MOLECULAR THERAPY

IF12

2023-10-01

PREAI

Matsevich, Chen; Gopalakrishnan, Prakadeeswari; Chang, Ning; Obolensky, Alexey; Beryozkin, Avigail; Salameh, Manar; Kostic, Corinne; Sharon, Dror; Arsenijevic, Yvan; Banin, Eyal

研究方向