Manar Salameh - Hadassah University Medical Center, The Hebrew University of Jerusalem

基本信息

浏览量：1

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 11 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Variants in the AGBL5 Gene Are Responsible for Autosomal Recessive Retinitis Pigmentosa with Hearing Loss

EUROPEAN JOURNAL OF HUMAN GENETICS (2024)

引用0浏览0WOSNATURE引用

Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes

Maria Abu Elasal, Samira Mousa,Manar Salameh,Anat Blumenfeld,Samer Khateb,Eyal Banin,Dror Sharon

GENESno. 7 (2024)

引用0浏览0WOS引用

Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice

Alaa Abu-Diab,Prakadeeswari Gopalakrishnan,Chen Matsevich, Marije de Jong,Alexey Obolensky,Ayat Khalaileh,Manar Salameh,Ayala Ejzenberg,Menachem Gross,Eyal Banin,Dror Sharon,Samer Khateb

TRANSLATIONAL VISION SCIENCE & TECHNOLOGY（2023）

引用4浏览0WOS引用

Gene Augmentation Therapy Attenuates Retinal Degeneration in a Knockout Mouse Model of Fam161a Retinitis Pigmentosa

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

MOLECULAR THERAPY（2023）

引用4浏览0WOS引用

Whole Genome Sequencing for USH2A-associated Disease Reveals Several Pathogenic Deep-Intronic Variants That Are Amenable to Splice Correction

Janine Reurink,Nicole Weisschuh,Alejandro Garanto,Adrian Dockery,L. Ingeborgh van den Born,Isabelle Fajardy,Lonneke Haer-Wigman,Susanne Kohl,Bernd Wissinger,G. Jane Farrar,Tamar Ben-Yosef,Fatma Kivrak Pfiffner,Wolfgang Berger,Marianna E. Weener,Lubica Dudakova,Petra Liskova,Dror Sharon,Manar Salameh, Ashley Offenheim,Elise Heon,Giorgia Girotto,Paolo Gasparini,Anna Morgan,Arthur A. Bergen,Jacoline B. ten Brink,Caroline C. W. Klaver,Lisbeth Tranebjaerg,Nanna D. Rendtorff,Sascha Vermeer,Jeroen J. Smits,Ronald J. E. Pennings,Marco Aben,Jaap Oostrik,Galuh D. N. Astuti,Jordi Corominas Galbany,Hester Y. Kroes,Milan Phan,Wendy A. G. van Zelst-Stams,Alberta A. H. J. Thiadens,Joke B. G. M. Verheij,Mary J. van Schooneveld,Suzanne E. de Bruijn,Catherina H. Z. Li,Carel B. Hoyng,Christian Gilissen,Lisenka E. L. M. Vissers,Frans P. M. Cremers,Hannie Kremer,Erwin van Wijk,Susanne Roosing

HUMAN GENETICS AND GENOMICS ADVANCESno. 2 (2023)

引用12浏览0WOS引用

A Deep Intronic Substitution in CNGB3 is One of the Major Causes of Achromatopsia among Jewish Patients

Hamzah Aweidah,Manar Salameh,Claudia Yahalom,Anat Blumenfeld,Michal Macarov,Nicole Weisschuh,Susanne Kohl,Eyal Banin,Dror Sharon

PubMed（2021）

引用1浏览0WOS引用

ABCA4 C.859-25A>g, a Frequent Palestinian Founder Mutation Associated with Retinal Dystrophy, Results in Multiple Splice Defects

Manar Salameh,Zelia Corradi,Mubeen Khan,Ajoy Vincent,Elise Heon,Rebekkah Hitti-Malin,Yahya AlSwaiti,Eyal Banin,Claire-Marie Dhaenens,Dror Sharon,Alaa AlTalbishi,Frans Cremers

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2021）

引用0浏览0引用

Clinical Characterization and Genotype-Phenotype Correlation in RPGRIP1 Patients with Autosomal Recessive Early Onset Retinal Degeneration

Avigail Beryozkin,Hamzah Aweidah, Roque Daniel Carrero-Valenzuela,Manar Salameh,Myriam Berman,Oscar Iguzquiza,Samer Khateb,Tamar Ben-Yosef,Dror Sharon,Eyal Banin

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2021）

引用0浏览0引用

Resolving the Dark Matter of ABCA4 for 1054 Stargardt Disease Probands Through Integrated Genomics and Transcriptomics

Mubeen Khan,Stéphanie S. Cornelis,Marta Del Pozo-Valero,Laura Whelan,Esmee H. Runhart,Ketan Mishra, Femke Bults,Yahya AlSwaiti,Alaa AlTalbishi,Elfride De Baere,Sandro Banfi,Eyal Banin,Miriam Bauwens,Tamar Ben-Yosef,Camiel J. F. Boon,L. Ingeborgh van den Born,Sabine Defoort,Aurore Devos,Adrian Dockery,Lubica Dudakova,Ana Fakin,G. Jane Farrar,Juliana Maria Ferraz Sallum,Kaoru Fujinami,Christian Gilissen,Damjan Glavač,Michael B. Gorin,Jacquie Greenberg,Takaaki Hayashi,Ymkje M. Hettinga,Alexander Hoischen,Carel B. Hoyng,Karsten Hufendiek,Herbert Jägle,Smaragda Kamakari,Marianthi Karali,Ulrich Kellner,Caroline C. W. Klaver,Bohdan Kousal,Tina M. Lamey,Ian M. MacDonald,Anna Matynia,Terri L. McLaren,Marcela D. Mena,Isabelle Meunier, Rianne Miller,Hadas Newman, Buhle Ntozini,Monika Oldak,Marc Pieterse,Osvaldo L. Podhajcer,Bernard Puech,Raj Ramesar,Klaus Rüther,Manar Salameh,Mariana Vallim Salles,Dror Sharon,Francesca Simonelli,Georg Spital,Marloes Steehouwer,Jacek P. Szaflik,Jennifer A. Thompson,Caroline Thuillier,Anna M. Tracewska,Martine van Zweeden,Andrea L. Vincent,Xavier Zanlonghi,Petra Liskova,Heidi Stöhr,John N. De Roach,Carmen Ayuso,Lisa Roberts,Bernhard H. F. Weber,Claire‐Marie Dhaenens,Frans P. M. Cremers

Genetics in Medicine（2020）

引用110浏览0WOS引用

110

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn