1.Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies

作　　者：Avigail Beryozkin ;Elia Shevah ;Adva Kimchi 等

出　　处：Scientific Reports. 2015 ;5.doi:10.1038/srep13187

出版社：Springer Nature

文章 ID：113410329

文章详细全文下载
2.TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

作　　者：Alaa AlTalbishi ;Lina Zelinger ;Christina Zeitz 等

出　　处：Scientific Reports. 2019 ;9(1):1-6.doi:10.1038/s41598-019-46811-7

出版社：Springer Nature

文章 ID：244233670

文章详细全文下载
3.Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases

作　　者：Mor Hanany ;Carlo Rivolta ;Dror Sharon

出　　处：Proceedings of the National Academy of Sciences. 2020 ;117(5):2710-2716.doi:10.1073/pnas.1913179117

出版社：The National Academy of Sciences of the United States of America

文章 ID：243452277

文章详细全文下载
4.Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies

作　　者：Avigail Beryozkin ;Elia Shevah ;Adva Kimchi 等

出　　处：Scientific Reports. 2015 ;5(1).doi:10.1038/srep13187

出版社：Springer Nature

文章 ID：235882585

文章详细全文下载
5.Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE)

作　　者：Dror Sharon ;Seth Blackshaw ;Constance L. Cepko 等

出　　处：Proceedings of the National Academy of Sciences. 2002 ;99(1):315-320.doi:10.1073/pnas.012582799

出版社：The National Academy of Sciences of the United States of America

文章 ID：200563973

文章详细全文下载
6.A new mouse model for retinal degeneration due to Fam161a deficiency

作　　者：Avigail Beryozkin ;Chen Matsevich ;Alexey Obolensky 等

出　　处：Scientific Reports. 2021 ;11(1):2030.doi:10.1038/s41598-021-81414-1

出版社：Springer Nature

文章 ID：258489744

文章详细全文下载
7.Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

作　　者：Avigail Beryozkin ;Samer Khateb ;Carlos Alberto Idrobo-Robalino 等

出　　处：Scientific Reports. 2020 ;10(1).doi:10.1038/s41598-020-72028-0

出版社：Springer Nature

文章 ID：255832364

文章详细全文下载
8.Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

作　　者：Irene Perea-Romero ;Gema Gordo ;Ionut F. Iancu 等

出　　处：Scientific Reports. 2021 ;11.doi:10.1038/s41598-021-89275-4

出版社：Springer Nature

文章 ID：1032088054

文章详细

	有本地全文	7篇
	有全文链接	1篇

	Dror Sharon	8篇
	Eyal Banin	5篇
	Avigail Beryozkin	4篇
	Samer Khateb	4篇
	Itay Chowers	3篇

	Tamar Ben-Yosef	3篇
	Abraham Zlotogorski	2篇
	Adva Kimchi	2篇
	Alexey Obolensky	2篇
	Alexis Boleda	2篇
	Anand Swaroop	2篇
	Anat Blumenfeld	2篇
	Carlo Rivolta	2篇
	Csilla H. Lazar	2篇
	Eduard Averbuch	2篇
	Elia Shevah	2篇
	Frans P. M. Cremers	2篇
	Jacob Pe’er	2篇
	Liliana Mizrahi-Meissonnier	2篇
	Linn Gieser	2篇
	Michal Sagi	2篇
	Mor Hanany	2篇
	Ola Alimi-Kasem	2篇
	Rinki Ratnapriya	2篇
	Samuel G. Jacobson	2篇
	Tzipora Falik-Zaccai	2篇
	Yitzhak Hemo	2篇
	Alaa AlTalbishi	1篇
	Alfredo Santana	1篇
	Almudena Avila-Fernandez	1篇
	Ana Arteche	1篇
	Ana Bustamante-Aragones	1篇
	Ana Fontalba-Romero	1篇
	Andrea Martinez-Ramas	1篇
	Ascension Gimenez-Pardo	1篇
	Belen Gil-Fournier	1篇
	Belen Jimenez-Rolando	1篇
	Berta Almoguera	1篇
	Berta Rodriguez-Sanchez	1篇
	Blanca Garcia-Sandoval	1篇

	英国	6篇
	美国	2篇

全文

出版年度

作者

文章类型

来源期刊

学科主题

语种

国别/地区

检索条件:"( ( 高级检索(( ((AU:(("Dror Sharon")))) )) ) )"

	Scientific Reports	6篇
	Proceedings of the National Academy of Sciences	2篇

	2021	2篇
	2020	2篇
	2019	1篇
	2015	2篇
	2002	1篇