R Eldridge

2.6k total citations
44 papers, 1.9k citations indexed

About

R Eldridge is a scholar working on Neurology, Cellular and Molecular Neuroscience and Epidemiology. According to data from OpenAlex, R Eldridge has authored 44 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Neurology, 11 papers in Cellular and Molecular Neuroscience and 7 papers in Epidemiology. Recurrent topics in R Eldridge's work include Neurofibromatosis and Schwannoma Cases (11 papers), Neurological disorders and treatments (9 papers) and Botulinum Toxin and Related Neurological Disorders (8 papers). R Eldridge is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (11 papers), Neurological disorders and treatments (9 papers) and Botulinum Toxin and Related Neurological Disorders (8 papers). R Eldridge collaborates with scholars based in United States, Finland and Japan. R Eldridge's co-authors include R L Martuza, Janice A. Egeland, John A. Hostetler, Stanley Fahn, V A McKusick, Herbert Weingartner, V.A. McKusick, Dilys M. Parry, K Pulaski and M. MacCollin and has published in prestigious journals such as New England Journal of Medicine, The Lancet and JAMA.

In The Last Decade

R Eldridge

42 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R Eldridge United States	20	967	558	437	338	327	44	1.9k
Roswell Eldridge United States	26	1.4k 1.5×	594 1.1×	413 0.9×	226 0.7×	241 0.7×	40	2.3k
Eiichiro Uyama Japan	24	499 0.5×	244 0.4×	757 1.7×	286 0.8×	172 0.5×	85	1.8k
M Puranen Finland	17	848 0.9×	159 0.3×	234 0.5×	347 1.0×	266 0.8×	30	1.6k
Nathan Malamud United States	22	529 0.5×	307 0.6×	327 0.7×	81 0.2×	111 0.3×	27	1.7k
Ian Sutton Australia	20	814 0.8×	206 0.4×	352 0.8×	164 0.5×	224 0.7×	43	2.0k
Marcia Wilkinson United Kingdom	24	593 0.6×	160 0.3×	422 1.0×	67 0.2×	249 0.8×	49	2.4k
David Saperstein United States	21	1.4k 1.4×	463 0.8×	340 0.8×	360 1.1×	59 0.2×	60	2.2k
José Boucraut France	31	876 0.9×	224 0.4×	625 1.4×	282 0.8×	125 0.4×	97	2.8k
B. Eymard France	29	478 0.5×	336 0.6×	1.5k 3.4×	295 0.9×	153 0.5×	82	2.6k
Pierre Labauge France	23	1.2k 1.2×	146 0.3×	716 1.6×	344 1.0×	147 0.4×	119	2.4k

Countries citing papers authored by R Eldridge

Since Specialization

Citations

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

Fields of papers citing papers by R Eldridge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Eldridge

This figure shows the co-authorship network connecting the top 25 collaborators of R Eldridge. A scholar is included among the top collaborators of R Eldridge 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 R Eldridge. R Eldridge 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

Parry, Dilys M., M. MacCollin, Muriel I. Kaiser‐Kupfer, et al.. (1996). Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.. PubMed. 59(3). 529–39. 159 indexed citations

Schwankhaus, John D., David A. Katz, R Eldridge, S. Schlesinger, & Henry F. McFarland. (1994). Clinical and Pathological Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis. Archives of Neurology. 51(8). 757–766. 41 indexed citations

Parry, Dilys M., Muriel I. Kaiser‐Kupfer, J L Sherman, A. Pikus, & R Eldridge. (1991). Neurofibromatosis 2 (Bilateral Acoustic or Central Neurofibromatosis), a Treatable Cause of Deafness. Annals of the New York Academy of Sciences. 630(1). 305–307. 4 indexed citations

Eldridge, R. (1989). Neurofibromatosis Type 1 (Recklinghausen's Disease). American journal of diseases of children. 143(7). 833–833. 77 indexed citations

Martuza, R L & R Eldridge. (1988). Neurofibromatosis 2. New England Journal of Medicine. 318(11). 684–688. 337 indexed citations

Schwankhaus, John D., Nicholas J. Patronas, Robert H. Dorwart, et al.. (1988). Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy. Archives of Neurology. 45(9). 1004–1008. 33 indexed citations

Eldridge, R, et al.. (1987). Dementia of the Alzheimer type: clinical and family study of 22 twin pairs. Alzheimer Disease & Associated Disorders. 1(4). 263–263. 7 indexed citations

Eldridge, R, et al.. (1987). Dementia of the Alzheimer type. Neurology. 37(3). 359–359. 103 indexed citations

Iivanainen, M. & R Eldridge. (1987). Effect of phenytoin on the mental and physical function of patients with Baltic myoclonus epilepsy. Neurological Sciences. 8(4). 313–317. 5 indexed citations

10.

Brown, Ronald T., R. J. Polinsky, John D. Schwankhaus, et al.. (1987). Adrenergic dysfunction in hereditary adult‐onset leukodystrophy. Neurology. 37(8). 1421–1421. 14 indexed citations

11.

Batshaw, Mark L., et al.. (1985). Munchausen's Syndrome Simulating Torsion Dystonia. New England Journal of Medicine. 312(22). 1437–1439. 35 indexed citations

12.

Eldridge, R. (1981). Central neurofibromatosis with bilateral acoustic neuroma.. PubMed. 29. 57–65. 78 indexed citations

13.

Allen, Jeffrey C., et al.. (1974). Early-onset neuroma: genetic, clinical and nosologic aspects.. PubMed. 10(10). 171–84. 5 indexed citations

14.

Eldridge, R, et al.. (1973). Studies of catecholamine metabolism in two hereditary forms of dystonia.. PubMed. 98. 245–7.

15.

Eldridge, R, et al.. (1972). Superior intelligence in sighted retinoblastoma patients and their families.. Journal of Medical Genetics. 9(3). 331–335. 7 indexed citations

16.

Eldridge, R, et al.. (1970). Increased intelligence in recessively inherited torsion dystonia (dystonia musculorum deformans).. PubMed. 20(4). 410–410. 1 indexed citations

17.

Eldridge, R, et al.. (1970). Hearing Loss and Otitis Media on Guam. Archives of Otolaryngology - Head and Neck Surgery. 91(2). 148–153. 13 indexed citations

18.

Eldridge, R, et al.. (1969). Hereditary acoustic neuroma--clinical and genetic aspects in a large kindred.. PubMed. 94. 353–4. 1 indexed citations

19.

McKusick, V A, et al.. (1965). DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA.. PubMed. 116. 285–326. 209 indexed citations

20.

McKusick, V.A., R Eldridge, John A. Hostetler, & Janice A. Egeland. (1964). DWARFISM IN THE AMISH.. PubMed. 77. 151–68. 112 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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