George Feldman

2.8k total citations · 1 hit paper
25 papers, 2.0k citations indexed

About

George Feldman is a scholar working on Molecular Biology, Rheumatology and Surgery. According to data from OpenAlex, George Feldman has authored 25 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Rheumatology and 8 papers in Surgery. Recurrent topics in George Feldman's work include Heterotopic Ossification and Related Conditions (7 papers), Hip disorders and treatments (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). George Feldman is often cited by papers focused on Heterotopic Ossification and Related Conditions (7 papers), Hip disorders and treatments (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). George Feldman collaborates with scholars based in United States, United Kingdom and Germany. George Feldman's co-authors include Eileen M. Shore, Frederick S. Kaplan, J. M. Connor, Roger Smith, James T. Triffitt, Maximilian Muenke, Martine LeMerrer, Jon Andoni Urtizberea, Rolf Morhart and Tae‐Joon Cho and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

George Feldman

25 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

2006 866 citations Eileen M. Shore, Meiqi Xu et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
George Feldman United States	18	887	881	695	611	354	25	2.0k
Martine LeMerrer France	14	665 0.7×	935 1.1×	725 1.0×	698 1.1×	296 0.8×	20	1.9k
Motomi Enomoto‐Iwamoto United States	18	786 0.9×	1.2k 1.3×	290 0.4×	146 0.2×	83 0.2×	21	1.9k
Michael C. Naski United States	22	1.9k 2.2×	370 0.4×	863 1.2×	239 0.4×	56 0.2×	29	2.7k
Michael N. Wosczyna United States	9	844 1.0×	371 0.4×	230 0.3×	148 0.2×	110 0.3×	12	1.3k
M. Le Merrer France	23	983 1.1×	320 0.4×	919 1.3×	164 0.3×	52 0.1×	93	1.8k
Allan J. Richards United Kingdom	30	893 1.0×	417 0.5×	1.9k 2.7×	158 0.3×	42 0.1×	81	2.9k
Kuber T. Sampath United States	18	1.3k 1.5×	338 0.4×	285 0.4×	65 0.1×	80 0.2×	30	1.9k
James O’Sullivan United Kingdom	22	1.4k 1.6×	198 0.2×	510 0.7×	111 0.2×	76 0.2×	40	2.0k
Branka Dabovic United States	23	1.1k 1.2×	168 0.2×	693 1.0×	375 0.6×	35 0.1×	32	2.0k
Luitgard M. Neumann Germany	20	708 0.8×	97 0.1×	1.0k 1.5×	208 0.3×	65 0.2×	46	1.7k

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-authorship network of co-authors of George Feldman

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

All Works

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20 of 20 papers shown

Feldman, George, et al.. (2024). Geranylgeraniol (GGOH), incorporated into a bone cement pellet promotes osteoclast function and healing in a model of medication-related osteonecrosis of the jaw. Journal of Oral Biology and Craniofacial Research. 14(2). 126–132. 3 indexed citations

Feldman, George, et al.. (2024). Medication-related osteonecrosis of the jaw (MRONJ) systemic review: mevalonate pathway mechanisms explored. Oral Surgery Oral Medicine Oral Pathology and Oral Radiology. 138(4). 475–483. 4 indexed citations

Wang, Mark L., Jolanta Fertala, Andrzej Steplewski, et al.. (2021). Circulating inflammatory cytokines alter transcriptional activity within fibrotic tissue of Dupuytren's disease patients. Journal of Orthopaedic Research®. 40(3). 738–749. 4 indexed citations

Kumar, Gaurav, et al.. (2020). iSeqQC: a tool for expression-based quality control in RNA sequencing. BMC Bioinformatics. 21(1). 56–56. 12 indexed citations

Feldman, George, et al.. (2017). A murine model for developmental dysplasia of the hip: ablation of CX3CR1 affects acetabular morphology and gait. Journal of Translational Medicine. 15(1). 233–233. 23 indexed citations

Feldman, George, et al.. (2014). Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX3CR1 in a Large Multi-Generation Family. The Journal of Arthroplasty. 29(9). 238–241. 20 indexed citations

Feldman, George, et al.. (2011). Variable Expression and Incomplete Penetrance of Developmental Dysplasia of the Hip. The Journal of Arthroplasty. 27(4). 527–532. 23 indexed citations

Feldman, George, Paul C. Billings, Rajesh V. Patel, et al.. (2007). Over‐expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: A new syndrome. American Journal of Medical Genetics Part A. 143A(7). 699–706. 19 indexed citations

Shore, Eileen M., Meiqi Xu, George Feldman, et al.. (2006). A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics. 38(5). 525–527. 866 indexed citations breakdown →

10.

Shore, Eileen M., George Feldman, Meiqi Xu, & Frederick S. Kaplan. (2005). The Genetics of Fibrodysplasia Ossificans Progressiva. Clinical Reviews in Bone and Mineral Metabolism. 3(3-4). 201–204. 85 indexed citations

11.

Ahn, Jaimo, et al.. (2003). Exoneration of NF-??B Dysregulation in Fibrodysplasia Ossificans Progressiva. Clinical Orthopaedics and Related Research. 406. 205–213. 2 indexed citations

12.

Ahn, Jaimo, et al.. (2003). Exoneration of NF-kappaB dysregulation in fibrodysplasia ossificans progressiva.. PubMed. 205–13. 3 indexed citations

13.

Feldman, George, M. Le Merrer, Michel Fardeau, et al.. (2000). Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP). Clinical Genetics. 58(4). 291–298. 44 indexed citations

14.

Feldman, George, Ming Li, Margrit Urbanek, et al.. (2000). Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31. The American Journal of Human Genetics. 66(1). 128–135. 74 indexed citations

15.

Gaudenz, Karin, Erich Roessler, Nandita Quaderi, et al.. (1998). Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain. The American Journal of Human Genetics. 63(3). 703–710. 57 indexed citations

16.

Feldman, George, Dolores Saavedra, Nathaniel H. Robin, et al.. (1997). A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22. Human Molecular Genetics. 6(11). 1937–1941. 28 indexed citations

17.

Quaderi, Nandita, Susann Schweiger, Karin Gaudenz, et al.. (1997). Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nature Genetics. 17(3). 285–291. 283 indexed citations

18.

Robin, Nathaniel H., George Feldman, Rosanna Weksberg, et al.. (1995). Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2. Nature Genetics. 11(4). 459–461. 83 indexed citations

19.

Hehr, Andreas, George Feldman, Nathaniel H. Robin, et al.. (1995). Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome. Human Molecular Genetics. 4(3). 323–328. 184 indexed citations

20.

Robin, Nathaniel H., George Feldman, Peter Lorenz, et al.. (1994). REPORTS. Human Molecular Genetics. 3(12). 2153–2158. 40 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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