Bärbel Felder

2.6k total citations
3 papers, 127 citations indexed

About

Bärbel Felder is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Bärbel Felder has authored 3 papers receiving a total of 127 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Public Health, Environmental and Occupational Health. Recurrent topics in Bärbel Felder's work include Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper) and Congenital heart defects research (1 paper). Bärbel Felder is often cited by papers focused on Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper) and Congenital heart defects research (1 paper). Bärbel Felder collaborates with scholars based in Germany, United Kingdom and Austria. Bärbel Felder's co-authors include Gabriele Schmötzer, Annemarie Poustka, Claudia Schuster, Fritz Poustka, Sabine M. Klauck, Ruth Wellenreuther, Hannelore Breitenbach‐Koller, Ingo Schupp, Anja Kolb‐Kokocinski and Andreas G. Chiocchetti and has published in prestigious journals such as Molecular Psychiatry, European Journal of Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Bärbel Felder

3 papers receiving 127 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bärbel Felder Germany 3 87 74 24 15 9 3 127
M.P. Botella Spain 5 80 0.9× 79 1.1× 33 1.4× 6 0.4× 7 0.8× 7 135
Candace Muss United States 3 58 0.7× 114 1.5× 29 1.2× 13 0.9× 8 0.9× 3 149
Taimoor I. Sheikh Canada 7 77 0.9× 82 1.1× 32 1.3× 7 0.5× 12 1.3× 11 135
Lucia Grillo Italy 8 103 1.2× 118 1.6× 31 1.3× 20 1.3× 13 1.4× 11 185
Meron Azage United States 4 81 0.9× 91 1.2× 11 0.5× 10 0.7× 7 0.8× 6 129
Marie‐Laure Vuillaume France 10 74 0.9× 90 1.2× 29 1.2× 29 1.9× 3 0.3× 16 138
Catherine Vincent‐Delorme France 8 100 1.1× 105 1.4× 8 0.3× 20 1.3× 17 1.9× 11 166
Stephanie Karch Germany 8 101 1.2× 50 0.7× 10 0.4× 11 0.7× 23 2.6× 8 146
Carmen Esmer Mexico 5 116 1.3× 157 2.1× 46 1.9× 33 2.2× 7 0.8× 16 225
Alfonso Caro‐Llopis Spain 7 102 1.2× 132 1.8× 16 0.7× 16 1.1× 8 0.9× 14 190

Countries citing papers authored by Bärbel Felder

Since Specialization
Citations

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

Fields of papers citing papers by Bärbel Felder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bärbel Felder

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

All Works

3 of 3 papers shown
1.
Felder, Bärbel, Bernhard Radlwimmer, Axel Benner, et al.. (2009). FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. American Journal of Medical Genetics Part A. 149A(5). 952–959. 30 indexed citations
2.
Klauck, Sabine M., Bärbel Felder, Anja Kolb‐Kokocinski, et al.. (2006). Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. Molecular Psychiatry. 11(12). 1073–1084. 78 indexed citations
3.
Felder, Bärbel, et al.. (2002). Evaluation of BMP4 and its specific inhibitor NOG as candidates in human neural tube defects (NTDs). European Journal of Human Genetics. 10(11). 753–756. 19 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

Breakdown of academic impact, for papers by M.P. Botella Breakdown of academic impact, for papers by Candace Muss Breakdown of academic impact, for papers by Taimoor I. Sheikh Breakdown of academic impact, for papers by Lucia Grillo Breakdown of academic impact, for papers by Meron Azage Breakdown of academic impact, for papers by Marie‐Laure Vuillaume Breakdown of academic impact, for papers by Catherine Vincent‐Delorme Breakdown of academic impact, for papers by Stephanie Karch Breakdown of academic impact, for papers by Carmen Esmer Breakdown of academic impact, for papers by Alfonso Caro‐Llopis
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