Talya Dor

744 total citations
16 papers, 388 citations indexed

About

Talya Dor is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Talya Dor has authored 16 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Genetics. Recurrent topics in Talya Dor's work include Muscle Physiology and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Talya Dor is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Talya Dor collaborates with scholars based in Israel, United States and Germany. Talya Dor's co-authors include Simon Edvardson, Avraham Shaag, Orly Elpeleg, Itai Berger, Gregory J. Hannon, Pramod Thekkat, Emily Hodges, Shamir Zenvirt, Yaniv Erlich and Giora Landesberg and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Genome Research.

In The Last Decade

Talya Dor

14 papers receiving 383 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Talya Dor Israel	8	176	109	97	69	60	16	388
Lauren Brady Canada	17	360 2.0×	102 0.9×	120 1.2×	57 0.8×	33 0.6×	40	558
Riccardo Berutti Germany	12	215 1.2×	78 0.7×	175 1.8×	46 0.7×	24 0.4×	29	502
Jacomijn P. Dijksterhuis Sweden	8	438 2.5×	94 0.9×	73 0.8×	57 0.8×	37 0.6×	10	574
Chiara Aiello Italy	16	397 2.3×	110 1.0×	41 0.4×	64 0.9×	80 1.3×	34	583
Takashi Kurashige Japan	15	260 1.5×	124 1.1×	36 0.4×	73 1.1×	63 1.1×	58	593
Veronika Karcagi Hungary	13	461 2.6×	79 0.7×	101 1.0×	79 1.1×	22 0.4×	32	616
Sinan Çomu Türkiye	8	165 0.9×	91 0.8×	87 0.9×	62 0.9×	39 0.7×	15	404
Bader Alhaddad Germany	15	331 1.9×	69 0.6×	174 1.8×	24 0.3×	43 0.7×	29	516
Alejandra Catenaccio Chile	9	208 1.2×	141 1.3×	48 0.5×	61 0.9×	39 0.7×	13	398
Carola Hedberg‐Oldfors Sweden	15	335 1.9×	47 0.4×	152 1.6×	40 0.6×	32 0.5×	42	570

Countries citing papers authored by Talya Dor

Since Specialization

Citations

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

Fields of papers citing papers by Talya Dor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Talya Dor

This figure shows the co-authorship network connecting the top 25 collaborators of Talya Dor. A scholar is included among the top collaborators of Talya 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 Talya Dor. Talya 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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16 of 16 papers shown

Ben-Moshe, Zohar, Joel Reiter, Talya Dor, et al.. (2024). A deleterious variant of INTS1 leads to disrupted sleep–wake cycles. Disease Models & Mechanisms. 17(8).

Molnár, Mária Judit, Léna Szabó, Oana Aurelia Vladâcenco, et al.. (2024). Essential components of an effective transition from paediatric to adult neurologist care for adolescents with Duchenne muscular dystrophy; a consensus derived using the Delphi methodology in Eastern Europe, Greece and Israel. Orphanet Journal of Rare Diseases. 19(1). 260–260.

Cohen, Yuval, et al.. (2023). Inhibition of nonsense-mediated mRNA decay may improve stop codon read-through therapy for Duchenne muscular dystrophy. Human Molecular Genetics. 32(15). 2455–2463. 9 indexed citations

Abu‐Libdeh, Abdulsalam, et al.. (2023). Growth hormone therapy for children with Duchenne muscular dystrophy and glucocorticoid induced short stature. Growth Hormone & IGF Research. 72-73. 101558–101558. 5 indexed citations

Dor, Talya, Adi Tovin, Odelia Pisanty, et al.. (2022). A Zebrafish Model for a Rare Genetic Disease Reveals a Conserved Role for FBXL3 in the Circadian Clock System. International Journal of Molecular Sciences. 23(4). 2373–2373. 4 indexed citations

Ben‐Sasson, Shmuel A., et al.. (2021). Safety and clinical outcome of tamoxifen in Duchenne muscular dystrophy. Neuromuscular Disorders. 31(9). 803–813. 10 indexed citations

Dor, Talya, et al.. (2021). Growth Hormone Therapy for Children With Duchenne Muscular Dystrophy and Glucocorticoid Induced Short Stature. Journal of the Endocrine Society. 5(Supplement_1). A715–A715. 1 indexed citations

Lehmann‐Werman, Roni, Judith Magenheim, Joshua Moss, et al.. (2018). Monitoring liver damage using hepatocyte-specific methylation markers in cell-free circulating DNA. JCI Insight. 3(12). 95 indexed citations

Daum, Hagit, et al.. (2017). Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancy. Neuromuscular Disorders. 27(10). 947–950. 7 indexed citations

10.

Edvardson, Simon, Haibo Wang, Talya Dor, et al.. (2015). Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization. Neurogenetics. 17(1). 25–30. 7 indexed citations

11.

Aharoni, Sharon, Susan Treves, Michal Becker‐Cohen, et al.. (2013). Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation. PLoS ONE. 8(7). e69296–e69296. 10 indexed citations

12.

Dor, Talya, Yuval Cinnamon, Laure Raymond, et al.. (2013). KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. Journal of Medical Genetics. 51(2). 137–142. 50 indexed citations

13.

Berger, Itai, Talya Dor, Jonatan Halvardson, et al.. (2012). Intractable epilepsy of infancy due to homozygous mutation in the EFHC1 gene. Epilepsia. 53(8). 1436–1440. 12 indexed citations

14.

Erlich, Yaniv, Simon Edvardson, Emily Hodges, et al.. (2011). Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Genome Research. 21(5). 658–664. 134 indexed citations

15.

Berger, Itai, et al.. (2010). Paediatric Hashimoto encephalopathy, refractory epilepsy and immunoglobulin treatment – unusual case report and review of the literature. Acta Paediatrica. 99(12). 1903–1905. 42 indexed citations

16.

Edvardson, Simon & Talya Dor. (2008). [Referral letters to the pediatric emergency department].. PubMed. 147(7). 602–4, 663. 2 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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