David Fenstermacher

3.5k citations
23 papers · 1.6k indexed · 1 hit paper · h-index 12
Topics
Gene expression and cancer classification (4 papers)Molecular Biology Techniques and Applications (3 papers)Bioinformatics and Genomic Networks (3 papers)
Journals
Proceedings of the National Academy of SciencesNature GeneticsSHILAP Revista de lepidopterología

In The Last Decade

David Fenstermacher

23 papers receiving 1.6k citations

Hit Papers

A recurrent mutation in the BMP type I receptor ACVR1 cau...20062026201220192006250500750

Peers

David Fenstermacher
Comparison fields: 5 of 113
  • Molecular Biology 784
  • Rheumatology 653
  • Pulmonary and Respiratory Medicine 600
  • Genetics 324
  • Nephrology 279
Replace C Wooding with:
C Wooding United Kingdom
Stephan M. Tanner United States
Andreas Hadjisavvas Cyprus
Hidehiko Fujinaka Japan
H.-J. Gröne Germany
Akihiko Kudo Japan
E.B. Robson United Kingdom
Maki Moritani Japan
Mikiko Takahashi Japan
Omar Albagha United Kingdom
David Fenstermacher relative to C Wooding United Kingdom C Wooding's profile →
Citations per field
00.5×6.8×
C Wooding · 1×
Citations per year

Countries citing papers authored by David Fenstermacher

Since Specialization
Citations

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

Fields of papers citing papers by David Fenstermacher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Fenstermacher

This figure shows the co-authorship network connecting the top 25 collaborators of David Fenstermacher. A scholar is included among the top collaborators of David Fenstermacher 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 David Fenstermacher. David Fenstermacher 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
#WorkIndexed citations
1 24
2 17
3 9
4 19
5 2
6 1
7 3
8 77
9 21
10 2
11
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressivabreakdown →
866
12 8
13 1
14
Defining an Open Metadata Framework for Proteomics: The PROMIS Project
1
15 221
16 54
17 7
18 6
19 64
20 144

About David Fenstermacher

David Fenstermacher is a scholar working on Cancer Research, Statistics and Probability and Molecular Biology, having authored 23 papers that have together received 1.6k indexed citations. Recurring topics across this work include Gene expression and cancer classification (4 papers), Molecular Biology Techniques and Applications (3 papers) and Bioinformatics and Genomic Networks (3 papers). The work is most often cited by research in Rheumatology (653 citations), Nephrology (279 citations) and Pulmonary and Respiratory Medicine (600 citations). David Fenstermacher has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Sherif E. Gabriel, Richard C. Boucher, Eileen M. Shore, George Feldman, David L. Glaser, John Rogers, Martine LeMerrer, Rolf Morhart, Roger Smith and Frederick S. Kaplan. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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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