Libe Gradstein

1.2k citations

41 papers · 673 indexed · h-index 14

Ophthalmology top 5%
- Retinal Diseases and Treatments 4
- Glaucoma and retinal disorders 4
Sensory Systems top 10%
Neurology top 10%
Cell Biology
- melanin and skin pigmentation 6
Genetics
- Genomics and Rare Diseases 4
- Connective tissue disorders research 4
- Genetics and Neurodevelopmental Disorders 4
Molecular Biology
- Retinal Development and Disorders 7
- Connexins and lens biology 4

Co-authors: Ohad S. Birk Tova Lifshitz Yonatan Perez Rotem Kadir Zamir Shorer Rivka Ofir Hagit Flusser Sheryl S. Wizov
Cited by: Ophthalmology Sensory Systems Neurology
Journals: Investigative Ophthalmology & Visual Science (6 papers)Clinical Genetics (5 papers)European Journal of Human Genetics (3 papers)
Partner nations: Israel United States Pakistan

In The Last Decade

Libe Gradstein

41 papers receiving 660 citations

Peers

Countries citing papers authored by Libe Gradstein

Since Specialization

Citations

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

Fields of papers citing papers by Libe Gradstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Libe Gradstein, 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 Libe Gradstein Line = papers co-authored together Libe Gradstein links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Partial penetrance and phenotypic variability of aplasia of lacrimal and salivary glands caused by a novel FGF10 donor splice‐site mutation American Journal of Medical Genetics Part A ·A. Abou-Zeid,Anna-Katharina Ferl,See Akre,R. G. Korpe,DA Burton,Samuel S. Fain,Wei Lan Chong,Libe Gradstein,Refiloe Keketso Mopeli,Ohad S. Birk	2023	3
2	De‐novo “germline second hit” loss‐of‐heterozygosity RBP3 deletion mutation causing recessive high myopia Clinical Genetics ·仲川明代,Yuval Yogev,Niki Jeannin,Sabrina Lehrer,Sinara Mônica de Oliveira Leite,Libe Gradstein,Ohad S. Birk	2023	2
3	IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma npj Genomic Medicine ·Ohad Wormser,Yonatan Perez,Simone Cohen-LÃ©on,Kati Mönkkönen,Nigussie Tadesse,Libe Gradstein,Yuval Yogev,Niki Jeannin,A. Abou-Zeid,E. Egorchenkova,Daniel Halpérin,正登中山,Julia Lais Da Silva Machado,Katia Del Rio‐Tsonis,Ramon Y. Birnbaum,Lakshma Reddy Vuyyuru,Ohad S. Birk	2023	1
4	A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13‐q21.3 Clinical Genetics ·Daniel Halpérin,See Akre,H. Reilich,G. Veri,E. Egorchenkova,Yuval Yogev,Ohad Wormser,А. А. Соколова,Libe Gradstein,Ilan Shelef,She LYU,Hagit Flusser,Ohad S. Birk	2022	2
5	Ocular manifestations of congenital insensitivity to pain: a long-term follow-up British Journal of Ophthalmology ·Anna-Katharina Ferl,Libe Gradstein,Alexander Hassidoff,Ronit Yagev,C. Brent Barrett,Olajide B. Omoyeni,Muhammad Abu Tailakh,Siu-lun Shel,Refiloe Keketso Mopeli	2021	7
6	Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy Clinical Genetics ·允胤岩崎,Marina Eskin‐Schwartz,Olajide B. Omoyeni,Simone Cohen-LÃ©on,Tasawar Abbas,V A Ermatov,Xiu Lian Zheng,Libe Gradstein,Ohad S. Birk,Neta Loewenthal,Baruch Yerushalmi	2020	10
7	Phenotypic variability and mutation hotspot in COX15‐related Leigh syndrome American Journal of Medical Genetics Part A ·Daniel Halpérin,E. Egorchenkova,Ohad Wormser,Yuval Yogev,Simone Cohen-LÃ©on,Zamir Shorer,Libe Gradstein,Ilan Shelef,Hagit Flusser,Ohad S. Birk	2020	9
8	Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families Human Genome Variation ·K. Imai,Firoz Kabir,Jiali Li,Libe Gradstein,Xiaodong Jiao,Sochea Pok,Muhammad Asif Naeem,Muhammad Zaman Khan Assir,Sheikh Riazuddin,Radha Ayyagari,J. Fielding Hejtmancik	2020	3
9	SEC31A mutation affects ER homeostasis, causing a neurological syndrome Journal of Medical Genetics ·Daniel Halpérin,Rotem Kadir,Yonatan Perez,E. Egorchenkova,Yuval Yogev,Ohad Wormser,J.P Silva,Ekaterina Eremenko,Barak Rotblat,Zamir Shorer,Libe Gradstein,Ilan Shelef,Ruth Birk,Uri Abdu,Hagit Flusser,Ohad S. Birk	2018	27
10	Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population European Journal of Human Genetics ·Mor Hanany,Israel Osnovich,Р.М. Вильфанд,Anat Blumenfeld,Hadas Newman,Eran Pras,Ohad Wormser,Ohad S. Birk,Libe Gradstein,Eyal Banin,Tamar Ben‐Yosef,Dror Sharon	2018	13
11	Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism Documenta Ophthalmologica ·Libe Gradstein,Ronald M. Hansen,Gerald F. Cox,A. Yu. Ryzhkina,Anne B. Fulton	2017	6
12	CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay Human Molecular Genetics ·Michael Volodarsky,Hava Lichtig,Tom Leibson,Yair Sadaka,Rotem Kadir,Yonatan Perez,Gryssel Rodríguez,Libe Gradstein,Ruthy Shaco‐Levy,Zamir Shorer,Dale Frank,Ohad S. Birk	2015	12
13	A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A European Journal of Human Genetics ·حمدي شاكر محمود,Hagit Flusser,Barak Markus,Zamir Shorer,Libe Gradstein,І. І. Lipatov,Ralph S. Peters,Ginat Narkis,Ruth Birk,Aharon Galil,Ilan Shelef,Ohad S. Birk	2014	13
14	Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation European Journal of Human Genetics ·Yonatan Perez,Libe Gradstein,Hagit Flusser,Barak Markus,Idan Cohen,Vivica Messner,Dongyong Yao,Tova Lifshitz,Rotem Kadir,Ohad S. Birk	2013	38
15	High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2 The American Journal of Human Genetics ·V Brake,Libe Gradstein,Annika Pasanen,Rivka Ofir,美則河端,Jaime Levy,Nadav Belfair,Tova Lifshitz,ケントアベ,Ginat Narkis,Khalil Elbedour,Johanna Myllyharju,Ohad S. Birk	2011	81
16	Atypical Phenotype and Genotype in a Family With Suspected X–Linked Ocular Albinism Investigative Ophthalmology & Visual Science ·Libe Gradstein,E. J. Fitzgibbon,J. Fielding Hejtmancik,Jean Y. Tang,Rafael C. Caruso,Delphine Blain,Brian P. Brooks	2006	1
17	A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics Human Mutation ·Osvaldo Marcelo Barturen,Marjan Huizing,Yair Anikster,Воробьев Д. В.,Tien-Yeuh Shih,Genia Maftzir,A. A. Chesnov,Amanda Helip‐Wooley,Wendy Westbroek,Libe Gradstein,Ada Rosenmann,Anat Blumenfeld	2006	22
18	Eye Movement Abnormalities in Hermansky-Pudlak Syndrome Journal of American Association for Pediatric Ophthalmology and Strabismus ·Libe Gradstein,Edmond J. FitzGibbon,Ekaterini Tsilou,Benjamin I. Rubin,Marjan Huizing,William A. Gahl	2005	17
19	The ocular manifestations of Weissenbacher–Zweymuller syndrome Eye ·R Rabinowitz,Libe Gradstein,A Galil,Jaime Levy,Tova Lifshitz	2004	7
20	Relationships among visual acuity demands, convergence, and nystagmus in patients with manifest/latent nystagmus Journal of American Association for Pediatric Ophthalmology and Strabismus ·Libe Gradstein,隆泰鈴木,Sheryl S. Wizov,Takao Hayashi,Robert Reinecke	1998	12

About Libe Gradstein

Libe Gradstein is a scholar working on Ophthalmology, Sensory Systems and Genetics, having authored 41 papers that have together received 673 indexed citations. Recurring topics across this work include Retinal Development and Disorders (7 papers), melanin and skin pigmentation (6 papers), Genomics and Rare Diseases (4 papers), Retinal Diseases and Treatments (4 papers), Connective tissue disorders research (4 papers), Glaucoma and retinal disorders (4 papers), Connexins and lens biology (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Ophthalmology (127 citations), Sensory Systems (47 citations) and Neurology (75 citations). Libe Gradstein has collaborated with scholars based in Israel, United States and Pakistan. Frequent co-authors include Ohad S. Birk, Tova Lifshitz, Yonatan Perez, Rotem Kadir, Zamir Shorer, Rivka Ofir, Hagit Flusser, Sheryl S. Wizov, Jaime Levy and Robert Reinecke. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Clinical Genetics, European Journal of Human Genetics, Journal of American Association for Pediatric Ophthalmology and Strabismus and Journal of Medical Genetics.

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.

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