George Feldman

2.8k citations
25 papers · 2.0k · 1 hit paper · h-index 18

Impact in

  • Rheumatology top 0.5%
    • Heterotopic Ossification and Related Conditions
  • Nephrology top 2%
    • Parathyroid Disorders and Treatments

Papers in

    • Congenital heart defects research 3
    • Heterotopic Ossification and Related Conditions 7
    • Bone Tumor Diagnosis and Treatments 4

George Feldman

25 papers receiving 2.0k citations

George Feldman's Hit Papers

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva 2006 · 874 citations
8740+6+13Years since publication250500750

Peers

George Feldman
Comparison fields: 5 of 78
  • Rheumatology 879
  • Nephrology 296
  • Genetics 649
  • Pulmonary and Respiratory Medicine 529
  • Genetics 165
Replace Martine LeMerrer with:
Martine LeMerrer France
Michael C. Naski United States
Kuber T. Sampath United States
Allan J. Richards United Kingdom
Mark S. Kronenberg United States
Andrew C. Lidral United States
James O’Sullivan United Kingdom
Yasuhiro Ishidou Japan
Hermann‐Josef Lüdecke Germany
Dražen Šošić United States
George Feldman relative to Martine LeMerrer France Martine LeMerrer's profile →
Citations per field
00.5×1.5×
Martine LeMerrer · 1×
Citations per year

Countries citing papers authored by George Feldman

Since Specialization
Citations

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

Fields of papers citing papers by George Feldman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside George Feldman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with George Feldman Line = papers co-authored together George Feldman links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Hit paper breakdown →
2006874
2 1997285
3 1995184
4 200586
5 199583
6 200074
7 199857
8 201347
9 200944
10 200043
11 199440
12
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.
199531
13 199728
14 201826
15 201723
16 201123
17 201420
18 200719
19 202012
20 20216

About George Feldman

George Feldman is a scholar working on Molecular Biology, Rheumatology, Surgery, Genetics and Pulmonary and Respiratory Medicine, having authored 25 papers that have together received 2.0k indexed citations. Recurring topics across this work include Heterotopic Ossification and Related Conditions (7 papers), Hip disorders and treatments (6 papers), Medical Imaging and Pathology Studies (5 papers), Bone Tumor Diagnosis and Treatments (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Orthopaedic implants and arthroplasty (4 papers), Congenital heart defects research (3 papers) and Craniofacial Disorders and Treatments (3 papers). The work is most often cited by research in Rheumatology (879 citations), Nephrology (296 citations), Genetics (649 citations), Pulmonary and Respiratory Medicine (529 citations) and Genetics (165 citations). George Feldman has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Eileen M. Shore, Frederick S. Kaplan, Roger Smith, J. M. Connor, James T. Triffitt, Maximilian Muenke, Jon Andoni Urtizberea, Martine LeMerrer, Patricia Delai and Matthew A. Brown. Their work appears in journals such as Human Molecular Genetics, Nature Genetics, The Journal of Arthroplasty, Journal of Orthopaedic Research® and Clinical Orthopaedics and Related Research.

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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