Fernando Arena

703 total citations
8 papers, 477 citations indexed

About

Fernando Arena is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Fernando Arena has authored 8 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Fernando Arena's work include Genetics and Neurodevelopmental Disorders (6 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (2 papers). Fernando Arena is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (2 papers). Fernando Arena collaborates with scholars based in United States, Norway and Italy. Fernando Arena's co-authors include Charles E. Schwartz, Melanie May, Herbert A. Lubs, Lisbeth Tranebjærg, Roger E. Stevenson, Roger E. Stevenson, Gumersindo Fontán, David Vetrie, Stephanie Smith and Elaine Kendall and has published in prestigious journals such as Nature Genetics, Journal of Medical Genetics and American Journal of Medical Genetics.

In The Last Decade

Fernando Arena

7 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fernando Arena United States	7	352	171	96	60	57	8	477
Greta Gillies Australia	9	302 0.9×	216 1.3×	32 0.3×	62 1.0×	56 1.0×	13	481
Aifen Yang China	13	320 0.9×	33 0.2×	43 0.4×	64 1.1×	25 0.4×	25	423
Petra Laššuthová Czechia	13	193 0.5×	103 0.6×	17 0.2×	42 0.7×	176 3.1×	34	411
Lise Larrieu France	15	485 1.4×	75 0.4×	18 0.2×	259 4.3×	64 1.1×	17	586
Shino Shimada Japan	15	315 0.9×	318 1.9×	33 0.3×	3 0.1×	68 1.2×	36	545
Nora Overlack Germany	10	638 1.8×	123 0.7×	15 0.2×	244 4.1×	92 1.6×	13	726
Antonio Vitobello France	13	446 1.3×	212 1.2×	11 0.1×	10 0.2×	79 1.4×	36	595
Gerald Nyakatura Germany	7	585 1.7×	221 1.3×	13 0.1×	24 0.4×	266 4.7×	11	694
Eleonora Di Gregorio Italy	17	389 1.1×	170 1.0×	16 0.2×	4 0.1×	134 2.4×	32	569
Dominique Ducroq France	17	1.2k 3.3×	246 1.4×	14 0.1×	54 0.9×	182 3.2×	20	1.3k

Countries citing papers authored by Fernando Arena

Since Specialization

Citations

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

Fields of papers citing papers by Fernando Arena

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Arena

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Howell, R. J. S., Lisa K. Marengo, Andrew Dixon, et al.. (2024). Epidemiology of Macrocephaly in the Texas Birth Defects Registry, 1999–2019. Birth Defects Research. 116(11). e2415–e2415.

2.

Verma, Mukesh, et al.. (2006). Genetic and Epigenetic Biomarkers in Cancer. Molecular Diagnosis & Therapy. 10(1). 1–15. 23 indexed citations

3.

Lubs, Herbert A., et al.. (1999). X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. American Journal of Medical Genetics. 85(3). 236–242. 23 indexed citations

4.

Lubs, Herbert A., Fatima Abidi, Jo‐Ann Blaymore Bier, et al.. (1999). XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28. American Journal of Medical Genetics. 85(3). 243–248. 54 indexed citations

5.

Jin, Hongjian, Melanie May, Lisbeth Tranebjærg, et al.. (1996). A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness. Nature Genetics. 14(2). 177–180. 199 indexed citations

6.

Tranebjærg, Lisbeth, Charles E. Schwartz, Sten Andréasson, et al.. (1995). A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.. Journal of Medical Genetics. 32(4). 257–263. 136 indexed citations

7.

Schwartz, Charles E., Melanie May, Tim H.‐M. Huang, et al.. (1992). MRX8: An X‐linked mental retardation condition with linkage to Xq21. American Journal of Medical Genetics. 43(1-2). 467–474. 16 indexed citations

8.

Neri, Giovanni, Pietro Chiurazzi, Fernando Arena, Herbert A. Lubs, & Ian A. Glass. (1992). XLMR genes: Update 1992. American Journal of Medical Genetics. 43(1-2). 373–382. 26 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.

Explore authors with similar magnitude of impact