Birgit Neophytou

646 total citations
5 papers, 195 citations indexed

About

Birgit Neophytou is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Birgit Neophytou has authored 5 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Physiology and 2 papers in Genetics. Recurrent topics in Birgit Neophytou's work include Machine Learning in Bioinformatics (1 paper), Muscle metabolism and nutrition (1 paper) and Magnesium in Health and Disease (1 paper). Birgit Neophytou is often cited by papers focused on Machine Learning in Bioinformatics (1 paper), Muscle metabolism and nutrition (1 paper) and Magnesium in Health and Disease (1 paper). Birgit Neophytou collaborates with scholars based in Austria, Netherlands and Germany. Birgit Neophytou's co-authors include Francisco J. Arjona, Karl P. Schlingmann, Anke L. Lameris, Stephan Rust, Georg Christoph Korenke, Joost G.J. Hoenderop, René J.M. Bindels, Jeroen H. F. de Baaij, Erwin van Wijk and Martin Konrad and has published in prestigious journals such as PLoS Genetics, Epilepsia and Molecular Genetics and Metabolism.

In The Last Decade

Birgit Neophytou

5 papers receiving 194 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Birgit Neophytou Austria 4 72 62 53 33 31 5 195
Ananya De United States 8 136 1.9× 26 0.4× 80 1.5× 14 0.4× 6 0.2× 15 292
M. van Raak Netherlands 9 260 3.6× 20 0.3× 52 1.0× 8 0.2× 13 0.4× 11 322
Maurice Stanley Australia 7 35 0.5× 36 0.6× 39 0.7× 14 0.4× 9 0.3× 10 232
Juan Zapata‐Muñoz Spain 5 161 2.2× 19 0.3× 26 0.5× 6 0.2× 7 0.2× 7 305
Junko Muroi Japan 12 228 3.2× 8 0.1× 33 0.6× 172 5.2× 39 1.3× 19 439
Haiba Kaul Pakistan 11 207 2.9× 29 0.5× 22 0.4× 68 2.1× 10 0.3× 33 320
Mark T. Clunes United Kingdom 10 109 1.5× 11 0.2× 108 2.0× 11 0.3× 8 0.3× 17 320
J. Byeong United States 8 160 2.2× 7 0.1× 27 0.5× 9 0.3× 12 0.4× 14 301
Peter Aulkemeyer Germany 9 93 1.3× 7 0.1× 19 0.4× 20 0.6× 15 0.5× 15 295
Romina Burla Italy 13 256 3.6× 19 0.3× 92 1.7× 28 0.8× 22 0.7× 21 350

Countries citing papers authored by Birgit Neophytou

Since Specialization
Citations

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

Fields of papers citing papers by Birgit Neophytou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Neophytou

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

All Works

5 of 5 papers shown
1.
Arjona, Francisco J., Jeroen H. F. de Baaij, Karl P. Schlingmann, et al.. (2014). CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia. PLoS Genetics. 10(4). e1004267–e1004267. 92 indexed citations
2.
Reinthaler, Eva M., Dennis Lal, Wiktor Jurkowski, et al.. (2014). Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy. Epilepsia. 55(8). e89–93. 40 indexed citations
3.
Freilinger, Michael, Dagmar Csaicsich, Klaus Arbeiter, et al.. (2011). 2FC1.3 Plasmapheresis in pediatric neurology: indications, methods and outcome. European Journal of Paediatric Neurology. 15. S18–S18. 1 indexed citations
4.
Mercimek‐Mahmutoglu, Saadet, Gajja S. Salomons, Birgit Neophytou, et al.. (2009). Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometry. Molecular Genetics and Metabolism. 96(4). 273–275. 16 indexed citations
5.
Seidl, Rainer, Daniela Prayer, Birgit Neophytou, et al.. (2006). Central nervous system‐related permanent consequences in patients with Langerhans cell histiocytosis. Pediatric Blood & Cancer. 48(1). 50–56. 46 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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