Egill Briem

1.2k total citations
8 papers, 580 citations indexed

About

Egill Briem is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Egill Briem has authored 8 papers receiving a total of 580 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Egill Briem's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and RNA modifications and cancer (2 papers). Egill Briem is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and RNA modifications and cancer (2 papers). Egill Briem collaborates with scholars based in Italy, United States and Spain. Egill Briem's co-authors include Massimo Zeviani, Eleonora Lamantea, Valeria Tiranti, Laura Farina, Isabella Moroni, Marianna Bugiani, Graziella Uziel, Marco Spada, F. Carrara and Federica Invernizzi and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Biochimica et Biophysica Acta (BBA) - Bioenergetics.

In The Last Decade

Egill Briem

8 papers receiving 566 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Egill Briem Italy	8	437	341	111	75	46	8	580
M. DiRocco Italy	8	353 0.8×	244 0.7×	50 0.5×	64 0.9×	45 1.0×	11	497
Andrew A.M. Morris United Kingdom	11	701 1.6×	606 1.8×	39 0.4×	70 0.9×	48 1.0×	16	851
R. D. Scholem Australia	11	389 0.9×	423 1.2×	191 1.7×	54 0.7×	51 1.1×	12	589
J.M.F. Trijbels Netherlands	6	298 0.7×	239 0.7×	39 0.4×	53 0.7×	16 0.3×	7	413
Célia Nogueira Portugal	11	249 0.6×	216 0.6×	21 0.2×	117 1.6×	27 0.6×	36	385
Silvio Ferraris Italy	12	262 0.6×	198 0.6×	21 0.2×	27 0.4×	42 0.9×	12	370
Lucia Valente Italy	10	540 1.2×	251 0.7×	14 0.1×	85 1.1×	55 1.2×	11	644
Magdalena Pajdowska Poland	11	316 0.7×	209 0.6×	16 0.1×	25 0.3×	76 1.7×	22	422
Darius J. Adams United States	10	328 0.8×	328 1.0×	34 0.3×	64 0.9×	71 1.5×	17	464
Magalie Barth France	12	274 0.6×	171 0.5×	36 0.3×	23 0.3×	35 0.8×	32	378

Countries citing papers authored by Egill Briem

Since Specialization

Citations

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

Fields of papers citing papers by Egill Briem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Egill Briem

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

All Works

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8 of 8 papers shown

1.

Gerards, Mike, Lars Eijssen, Alexandra T.M. Hendrickx, et al.. (2006). Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients. Genetics in Medicine. 8(10). 620–627. 28 indexed citations

2.

Rocco, Maja Di, Ubaldo Caruso, Egill Briem, et al.. (2006). A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation. Molecular Genetics and Metabolism. 89(4). 395–397. 20 indexed citations

3.

Tiranti, Valeria, Egill Briem, Eleonora Lamantea, et al.. (2005). ETHE1 mutations are specific to ethylmalonic encephalopathy. Journal of Medical Genetics. 43(4). 340–346. 68 indexed citations

4.

Bugiani, Marianna, Federica Invernizzi, Egill Briem, et al.. (2004). Clinical and molecular findings in children with complex I deficiency. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1659(2-3). 136–147. 218 indexed citations

5.

Fetoni, V., Egill Briem, Franco Carrara, Marina Mora, & Massimo Zeviani. (2004). Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene. Neuromuscular Disorders. 14(11). 723–726. 21 indexed citations

6.

Tiranti, Valeria, Pio D’Adamo, Egill Briem, et al.. (2004). Ethylmalonic Encephalopathy Is Caused by Mutations in ETHE1, a Gene Encoding a Mitochondrial Matrix Protein. The American Journal of Human Genetics. 74(2). 239–252. 160 indexed citations

7.

Taylor, Robert W., Emma L. Blakely, Patrick F. Chinnery, et al.. (2003). Genotypes from patients indicate no paternal mitochondrial DNA contribution. Annals of Neurology. 54(4). 521–524. 58 indexed citations

8.

Arenas, Joaquı́n, Egill Briem, Wendy Hutchison, et al.. (2003). The V368i mutation in Twinkle does not segregate with adPEO. Annals of Neurology. 53(2). 278–278. 7 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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