Dóra Nagy

631 total citations
29 papers, 462 citations indexed

About

Dóra Nagy is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Dóra Nagy has authored 29 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Neurology. Recurrent topics in Dóra Nagy's work include Amyotrophic Lateral Sclerosis Research (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Congenital heart defects research (2 papers). Dóra Nagy is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Congenital heart defects research (2 papers). Dóra Nagy collaborates with scholars based in Hungary, Austria and United States. Dóra Nagy's co-authors include P. D. Kushner, Takashi Kato, Márta Széll, Bernadett Csányi, K. Gyurkovits, Kathy Alderson, Kornélia Tripolszki, József I. Engelhardt, Péter Klivènyi and Ágnes Czibula and has published in prestigious journals such as International Journal of Molecular Sciences, CHEST Journal and Experimental Neurology.

In The Last Decade

Dóra Nagy

26 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dóra Nagy Hungary 13 191 100 89 78 73 29 462
Tatsuya Abe Japan 11 118 0.6× 57 0.6× 41 0.5× 29 0.4× 49 0.7× 53 475
Masakazu Kawajiri Japan 13 93 0.5× 176 1.8× 28 0.3× 37 0.5× 19 0.3× 46 408
S M Factor United States 9 111 0.6× 125 1.3× 19 0.2× 185 2.4× 36 0.5× 11 541
Alexandre Varella Giannetti Brazil 12 125 0.7× 94 0.9× 29 0.3× 23 0.3× 30 0.4× 44 437
H. Grehl Germany 12 245 1.3× 215 2.1× 32 0.4× 34 0.4× 38 0.5× 32 616
E Bernard France 15 227 1.2× 107 1.1× 115 1.3× 39 0.5× 12 0.2× 52 563
Raúl Juntas Morales France 10 128 0.7× 271 2.7× 85 1.0× 61 0.8× 53 0.7× 20 522
Cláudia Suemi Kamoi Kay Brazil 14 294 1.5× 236 2.4× 44 0.5× 68 0.9× 55 0.8× 70 624
M. Yahyaoui Morocco 11 115 0.6× 220 2.2× 25 0.3× 57 0.7× 22 0.3× 33 474

Countries citing papers authored by Dóra Nagy

Since Specialization
Citations

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

Fields of papers citing papers by Dóra Nagy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dóra Nagy

This figure shows the co-authorship network connecting the top 25 collaborators of Dóra Nagy. A scholar is included among the top collaborators of Dóra Nagy 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 Dóra Nagy. Dóra Nagy 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.
Nagy, Nikoletta, Dóra Nagy, Anita Varga, et al.. (2023). Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS. Current Issues in Molecular Biology. 45(7). 5293–5304. 1 indexed citations
2.
Nagy, Dóra, Katalin Farkas, Nikoletta Nagy, et al.. (2023). Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients. International Journal of Molecular Sciences. 24(8). 7401–7401. 2 indexed citations
3.
Nagy, Dóra, et al.. (2023). Long-Term Follow-Up of a Family with Retinal Dystrophy Caused by RPE65 Mutation. Case Reports in Ophthalmology. 14(1). 454–461. 1 indexed citations
4.
Nagy, Dóra, et al.. (2022). Spontaneous reshaping of vertebral fractures in an adolescent with osteogenesis imperfecta. Bone Reports. 16. 101595–101595. 3 indexed citations
5.
Czakó, Márta, Viktor Farkas, György Fekete, et al.. (2021). Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions. Frontiers in Genetics. 12. 673025–673025. 15 indexed citations
6.
Oláh, Judit, et al.. (2020). A Gorlin–Goltz-szindróma genetikai aspektusai. Orvosi Hetilap. 161(49). 2072–2077. 2 indexed citations
7.
Szakszon, Katalin, et al.. (2019). Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases. Journal of Biotechnology. 299. 86–95. 11 indexed citations
8.
Nagy, Dóra, Katalin Farkas, Lluı́s Armengol, et al.. (2019). Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature. European Journal of Medical Genetics. 63(4). 103800–103800. 6 indexed citations
9.
Tripolszki, Kornélia, Piyush Gampawar, Helena Schmidt, et al.. (2019). Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort. Frontiers in Genetics. 10. 732–732. 29 indexed citations
10.
Hoyk, Zsófia, Melinda Tóth, Nikolett Lénárt, et al.. (2018). Cerebrovascular Pathology in Hypertriglyceridemic APOB-100 Transgenic Mice. Frontiers in Cellular Neuroscience. 12. 380–380. 15 indexed citations
11.
Nagy, Dóra & Márta Széll. (2018). Congenitalis vitiumok genetikai heterogenitása és komplexitása. Orvosi Hetilap. 159(17). 661–670. 1 indexed citations
12.
Tripolszki, Kornélia, Bernadett Csányi, Dóra Nagy, et al.. (2017). Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis. Neurobiology of Aging. 53. 195.e1–195.e5. 18 indexed citations
13.
Nagy, Béla, Luka A. Clarke, Dóra Nagy, et al.. (2016). Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis. CHEST Journal. 150(3). 661–672. 49 indexed citations
14.
Nagy, Dóra, et al.. (2011). Comparison of lactase persistence polymorphism in ancient and present‐day Hungarian populations. American Journal of Physical Anthropology. 145(2). 262–269. 27 indexed citations
15.
Nagy, Dóra, et al.. (2009). Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians. European Journal of Clinical Nutrition. 63(7). 909–912. 26 indexed citations
16.
Nagy, Dóra, et al.. (2008). Effects of magnesium supplementation on the glutathione redox system in atopic asthmatic children. Inflammation Research. 57(6). 279–286. 22 indexed citations
17.
Gyurkovits, K., et al.. (2008). Toxocariasis associated with chronic cough in childhood: a longitudinal study in Hungary. Journal of Helminthology. 82(4). 357–363. 15 indexed citations
18.
Nagy, Dóra, et al.. (1995). Motor neuron-astrocyte interactions and levels of Cu, Zn superoxide dismutase in sporadic amyotrophic lateral sclerosis. Experimental Neurology. 131(2). 203–210. 44 indexed citations
19.
Nagy, Dóra, Takashi Kato, & P. D. Kushner. (1994). Reactive astrocytes are widespread in the cortical gray matter of amyotrophic lateral sclerosis. Journal of Neuroscience Research. 38(3). 336–347. 107 indexed citations
20.
Nagy, Dóra, et al.. (1993). Consequences of Reduced Cerebral Blood Flow in Brain Development. Experimental Neurology. 124(2). 326–342. 23 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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