Talia Dor

473 total citations
7 papers, 346 citations indexed

About

Talia Dor is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology. According to data from OpenAlex, Talia Dor has authored 7 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Rheumatology. Recurrent topics in Talia Dor's work include Prenatal Substance Exposure Effects (2 papers), Folate and B Vitamins Research (2 papers) and RNA modifications and cancer (1 paper). Talia Dor is often cited by papers focused on Prenatal Substance Exposure Effects (2 papers), Folate and B Vitamins Research (2 papers) and RNA modifications and cancer (1 paper). Talia Dor collaborates with scholars based in Israel, United States and Mexico. Talia Dor's co-authors include Itai Berger, Gil Goldzweig, Yoram Nevo, Orly Elpeleg, Kenneth Walsh, Laura E. Benjamin, Thuy L. Phung, Ann M. Dvořàk, Ichiro Shiojima and Jing Sun and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Medical Genetics and Muscle & Nerve.

In The Last Decade

Talia Dor

7 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Talia Dor Israel	7	165	84	63	61	42	7	346
Gabrielle Gold‐von Simson United States	12	172 1.0×	52 0.6×	25 0.4×	28 0.5×	21 0.5×	39	561
Janet Jones United States	13	225 1.4×	130 1.5×	52 0.8×	55 0.9×	39 0.9×	15	692
Heidi Mateus Colombia	11	165 1.0×	119 1.4×	54 0.9×	21 0.3×	31 0.7×	32	362
Tsung-Ming Chen Taiwan	14	237 1.4×	56 0.7×	49 0.8×	28 0.5×	8 0.2×	19	510
Lauren J. Mills United States	13	159 1.0×	82 1.0×	31 0.5×	47 0.8×	17 0.4×	32	391
I. Desguerre France	12	194 1.2×	69 0.8×	98 1.6×	23 0.4×	64 1.5×	37	400
Mark Wardle United Kingdom	15	177 1.1×	56 0.7×	70 1.1×	85 1.4×	14 0.3×	35	972
J. P. M. Evans United Kingdom	11	82 0.5×	85 1.0×	81 1.3×	47 0.8×	58 1.4×	15	536
Raidah Albaradie Saudi Arabia	11	248 1.5×	103 1.2×	95 1.5×	11 0.2×	64 1.5×	48	531
Aude Charollais France	9	170 1.0×	137 1.6×	37 0.6×	36 0.6×	144 3.4×	19	428

Countries citing papers authored by Talia Dor

Since Specialization

Citations

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

Fields of papers citing papers by Talia Dor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Talia Dor

This figure shows the co-authorship network connecting the top 25 collaborators of Talia Dor. A scholar is included among the top collaborators of Talia Dor 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 Talia Dor. Talia Dor 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.

Tenenbaum, Ariel, et al.. (2020). Fetal alcohol spectrum disorder among pre-adopted and foster children. BMC Pediatrics. 20(1). 275–275. 13 indexed citations

2.

Stepensky, Polina, Katherine H. Kim, Omar Abuzaitoun, et al.. (2017). Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome. Journal of Medical Genetics. 54(8). 558–566. 82 indexed citations

3.

Guen, Vincent J., Simon Edvardson, Aviva Fattal‐Valevski, et al.. (2017). A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness. American Journal of Medical Genetics Part A. 176(1). 92–98. 18 indexed citations

4.

Dor, Talia, Yakov Fellig, Sharon Eylon, et al.. (2015). Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1). Muscle & Nerve. 53(4). 564–569. 35 indexed citations

5.

Tenenbaum, Ariel, et al.. (2011). Fetal alcohol spectrum disorder in Israel: increased prevalence in an at-risk population.. PubMed. 13(12). 725–9. 14 indexed citations

6.

Berger, Itai, Talia Dor, Yoram Nevo, & Gil Goldzweig. (2008). Attitudes Toward Attention-Deficit Hyperactivity Disorder (ADHD) Treatment: Parents' and Children's Perspectives. Journal of Child Neurology. 23(9). 1036–1042. 66 indexed citations

7.

Sun, Jing, Thuy L. Phung, Ichiro Shiojima, et al.. (2004). Microvascular patterning is controlled by fine-tuning the Akt signal. Proceedings of the National Academy of Sciences. 102(1). 128–133. 118 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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