Libe Gradstein

1.2k total citations
41 papers, 673 citations indexed

About

Libe Gradstein is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Libe Gradstein has authored 41 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Ophthalmology. Recurrent topics in Libe Gradstein's work include Retinal Development and Disorders (7 papers), melanin and skin pigmentation (6 papers) and Genomics and Rare Diseases (4 papers). Libe Gradstein is often cited by papers focused on Retinal Development and Disorders (7 papers), melanin and skin pigmentation (6 papers) and Genomics and Rare Diseases (4 papers). Libe Gradstein collaborates with scholars based in Israel, United States and Pakistan. Libe Gradstein's co-authors include Ohad S. Birk, Tova Lifshitz, Yonatan Perez, Rotem Kadir, Zamir Shorer, Rivka Ofir, Jaime Levy, Sheryl S. Wizov, Robert Reinecke and Hagit Flusser and has published in prestigious journals such as Brain, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Libe Gradstein

41 papers receiving 660 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Libe Gradstein Israel 14 356 151 127 105 75 41 673
Yasuo Ouchi Japan 20 677 1.9× 176 1.2× 75 0.6× 61 0.6× 30 0.4× 34 1.0k
Stephen Sikkink United Kingdom 15 407 1.1× 88 0.6× 77 0.6× 83 0.8× 64 0.9× 20 892
Christian Hamel France 20 1.2k 3.5× 265 1.8× 323 2.5× 203 1.9× 52 0.7× 39 1.5k
Defne A. Amado United States 11 270 0.8× 93 0.6× 63 0.5× 24 0.2× 58 0.8× 22 548
Lejin Wang China 11 808 2.3× 221 1.5× 84 0.7× 83 0.8× 46 0.6× 18 1.2k
Matthew A. Lines Canada 19 634 1.8× 283 1.9× 92 0.7× 73 0.7× 17 0.2× 35 919
Katharina Steindl Switzerland 18 411 1.2× 323 2.1× 72 0.6× 52 0.5× 36 0.5× 50 698
Christel Vaché France 14 611 1.7× 102 0.7× 69 0.5× 53 0.5× 57 0.8× 24 799
Emma L. Baple United Kingdom 18 547 1.5× 373 2.5× 24 0.2× 137 1.3× 49 0.7× 59 902
Ajoy Vincent Canada 18 757 2.1× 216 1.4× 462 3.6× 134 1.3× 37 0.5× 68 1.0k

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 of co-authors of Libe Gradstein

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

All Works

20 of 20 papers shown
1.
2.
Wormser, Ohad, Yonatan Perez, Libe Gradstein, et al.. (2023). IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma. npj Genomic Medicine. 8(1). 22–22. 1 indexed citations
3.
Gradstein, Libe, et al.. (2023). 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. 191(11). 2768–2774. 3 indexed citations
4.
Yogev, Yuval, et al.. (2023). De‐novo “germline second hit” loss‐of‐heterozygosity RBP3 deletion mutation causing recessive high myopia. Clinical Genetics. 104(5). 571–576. 2 indexed citations
5.
Halpérin, Daniel, Yuval Yogev, Ohad Wormser, et al.. (2022). 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. 102(2). 123–129. 2 indexed citations
6.
Gradstein, Libe, et al.. (2021). Ocular manifestations of congenital insensitivity to pain: a long-term follow-up. British Journal of Ophthalmology. 106(9). 1217–1221. 7 indexed citations
7.
Eskin‐Schwartz, Marina, et al.. (2021). Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. Yearbook of pediatric endocrinology. 3 indexed citations
8.
Eskin‐Schwartz, Marina, et al.. (2020). Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. Clinical Genetics. 98(3). 303–307. 10 indexed citations
9.
Halpérin, Daniel, Ohad Wormser, Yuval Yogev, et al.. (2020). Phenotypic variability and mutation hotspot in COX15‐related Leigh syndrome. American Journal of Medical Genetics Part A. 182(6). 1506–1512. 9 indexed citations
10.
Halpérin, Daniel, Rotem Kadir, Yonatan Perez, et al.. (2018). SEC31A mutation affects ER homeostasis, causing a neurological syndrome. Journal of Medical Genetics. 56(3). 139–148. 27 indexed citations
11.
Perez, Yonatan, Zamir Shorer, Pauline Chabosseau, et al.. (2017). SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome. Brain. 140(4). 928–939. 71 indexed citations
12.
Beryozkin, Avigail, Gal Levy, Anat Blumenfeld, et al.. (2016). Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual. Investigative Ophthalmology & Visual Science. 57(3). 940–940. 12 indexed citations
13.
Volodarsky, Michael, Hava Lichtig, Tom Leibson, et al.. (2015). CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay. Human Molecular Genetics. 24(22). 6485–6491. 12 indexed citations
14.
Flusser, Hagit, Barak Markus, Zamir Shorer, et al.. (2014). A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European Journal of Human Genetics. 23(12). 1729–1734. 13 indexed citations
15.
Perez, Yonatan, Libe Gradstein, Hagit Flusser, et al.. (2013). Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation. European Journal of Human Genetics. 22(5). 703–706. 38 indexed citations
16.
Gradstein, Libe, Annika Pasanen, Rivka Ofir, et al.. (2011). High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2. The American Journal of Human Genetics. 89(3). 438–445. 81 indexed citations
17.
Gradstein, Libe, E. J. Fitzgibbon, J. Fielding Hejtmancik, et al.. (2006). Atypical Phenotype and Genotype in a Family With Suspected X–Linked Ocular Albinism. Investigative Ophthalmology & Visual Science. 47(13). 2508–2508. 1 indexed citations
18.
Gradstein, Libe, Edmond J. FitzGibbon, Ekaterini Tsilou, et al.. (2005). Eye Movement Abnormalities in Hermansky-Pudlak Syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 9(4). 369–378. 17 indexed citations
19.
Rabinowitz, R, Libe Gradstein, A Galil, Jaime Levy, & Tova Lifshitz. (2004). The ocular manifestations of Weissenbacher–Zweymuller syndrome. Eye. 18(12). 1258–1263. 7 indexed citations
20.
Gradstein, Libe, et al.. (1998). Relationships among visual acuity demands, convergence, and nystagmus in patients with manifest/latent nystagmus. Journal of American Association for Pediatric Ophthalmology and Strabismus. 2(4). 218–229. 12 indexed citations

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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