Danit Oz-Levi

1.6k total citations
7 papers, 401 citations indexed

About

Danit Oz-Levi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Danit Oz-Levi has authored 7 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Cell Biology. Recurrent topics in Danit Oz-Levi's work include Hereditary Neurological Disorders (3 papers), Autophagy in Disease and Therapy (2 papers) and Endoplasmic Reticulum Stress and Disease (2 papers). Danit Oz-Levi is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Autophagy in Disease and Therapy (2 papers) and Endoplasmic Reticulum Stress and Disease (2 papers). Danit Oz-Levi collaborates with scholars based in Israel, United States and Austria. Danit Oz-Levi's co-authors include Doron Lancet, Tsippi Iny Stein, Tsviya Olender, Frida Belinky, Marilyn Safran, Eugene Kolker, Bernd Mayer, Noam Nativ, Paul Perco and Iris Bahir and has published in prestigious journals such as The American Journal of Human Genetics, Autophagy and JCI Insight.

In The Last Decade

Danit Oz-Levi

6 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Danit Oz-Levi Israel	6	195	77	73	62	55	7	401
Akari Minami Japan	10	201 1.0×	45 0.6×	40 0.5×	52 0.8×	13 0.2×	14	383
Yung-Feng Liao Taiwan	14	255 1.3×	56 0.7×	26 0.4×	24 0.4×	61 1.1×	20	504
Marianna Fantin Italy	11	261 1.3×	21 0.3×	75 1.0×	19 0.3×	22 0.4×	12	464
Ping‐Chang Kuo United States	16	358 1.8×	53 0.7×	33 0.5×	32 0.5×	18 0.3×	33	695
Charlene D. McWhinney United States	9	357 1.8×	20 0.3×	70 1.0×	62 1.0×	27 0.5×	13	597
Adriana Sumoza‐Toledo Mexico	10	224 1.1×	44 0.6×	47 0.6×	11 0.2×	42 0.8×	17	714
Leena Patel United States	4	330 1.7×	84 1.1×	111 1.5×	16 0.3×	31 0.6×	5	535
Manini Bhatt India	3	236 1.2×	73 0.9×	21 0.3×	28 0.5×	29 0.5×	4	448
Junfang Teng China	12	130 0.7×	37 0.5×	38 0.5×	14 0.2×	14 0.3×	30	335

Countries citing papers authored by Danit Oz-Levi

Since Specialization

Citations

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

Fields of papers citing papers by Danit Oz-Levi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danit Oz-Levi. 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 Danit Oz-Levi. The network helps show where Danit Oz-Levi may publish in the future.

Co-authorship network of co-authors of Danit Oz-Levi

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

All Works

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7 of 7 papers shown

1.

Elefant, Naama, Danit Oz-Levi, Neil J. Ball, et al.. (2024). Talin1 dysfunction is genetically linked to systemic capillary leak syndrome. JCI Insight. 9(24).

2.

Rappaport, Noa, Simon Fishilevich, Ron Nudel, et al.. (2017). Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect. BioMedical Engineering OnLine. 16(S1). 72–72. 68 indexed citations

3.

Heimer, Gali, Danit Oz-Levi, Eran Eyal, et al.. (2015). TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability. European Journal of Paediatric Neurology. 20(1). 69–79. 27 indexed citations

4.

Ekhilevitch, Nina, Alina Kurolap, Danit Oz-Levi, et al.. (2015). Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita. Clinical Genetics. 90(1). 84–89. 12 indexed citations

5.

Oz-Levi, Danit, et al.. (2013). TECPR2. Autophagy. 9(5). 801–802. 13 indexed citations

6.

Oz-Levi, Danit, Bruria Ben‐Zeev, Elizabeth K. Ruzzo, et al.. (2012). Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis. The American Journal of Human Genetics. 91(6). 1065–1072. 106 indexed citations

7.

Stelzer, Gil, Tsippi Iny Stein, Naomi Rosen, et al.. (2011). In-silico human genomics with GeneCards. Human Genomics. 5(6). 709–709. 175 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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