F. E. Stephens

677 total citations
12 papers, 266 citations indexed

About

F. E. Stephens is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, F. E. Stephens has authored 12 papers receiving a total of 266 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in F. E. Stephens's work include Genetic Neurodegenerative Diseases (2 papers), Mitochondrial Function and Pathology (2 papers) and Muscle Physiology and Disorders (2 papers). F. E. Stephens is often cited by papers focused on Genetic Neurodegenerative Diseases (2 papers), Mitochondrial Function and Pathology (2 papers) and Muscle Physiology and Disorders (2 papers). F. E. Stephens collaborates with scholars based in United States. F. E. Stephens's co-authors include Frank H. Tyler, Gerald T. Perkoff, David A. Dolowitz, Charles M. Woolf and Eldon J. Gardner and has published in prestigious journals such as Journal of Clinical Investigation, Annals of Internal Medicine and Cancer.

In The Last Decade

F. E. Stephens

11 papers receiving 184 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. E. Stephens United States	9	144	55	47	40	27	12	266
O. Vuia Germany	11	123 0.9×	65 1.2×	21 0.4×	6 0.1×	62 2.3×	56	376
Katrina A. Marsh United Kingdom	8	121 0.8×	82 1.5×	14 0.3×	28 0.7×	9 0.3×	10	319
S C Cwyfan-Hughes United Kingdom	11	138 1.0×	26 0.5×	70 1.5×	46 1.1×	19 0.7×	14	436
John C. Winkelmann United States	11	186 1.3×	36 0.7×	28 0.6×	21 0.5×	15 0.6×	13	390
S. H. M. Nyström Finland	8	85 0.6×	40 0.7×	14 0.3×	6 0.1×	17 0.6×	18	252
Achilles K. Papavasiliou United States	6	189 1.3×	64 1.2×	22 0.5×	26 0.7×	27 1.0×	7	368
Michiel J.R. van der Wielen Netherlands	6	176 1.2×	43 0.8×	71 1.5×	48 1.2×	6 0.2×	8	245
G. Said France	7	112 0.8×	79 1.4×	22 0.5×	6 0.1×	11 0.4×	17	302
G. C. Guazzi Italy	10	125 0.9×	52 0.9×	7 0.1×	12 0.3×	41 1.5×	26	273
Marius Kuhn Germany	10	107 0.7×	50 0.9×	34 0.7×	37 0.9×	9 0.3×	16	207

Countries citing papers authored by F. E. Stephens

Since Specialization

Citations

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

Fields of papers citing papers by F. E. Stephens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. E. Stephens. 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 F. E. Stephens. The network helps show where F. E. Stephens may publish in the future.

Co-authorship network of co-authors of F. E. Stephens

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

All Works

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12 of 12 papers shown

1.

Dolowitz, David A. & F. E. Stephens. (1961). LXIV Hereditary Nerve Deafness. Annals of Otology Rhinology & Laryngology. 70(3). 851–859. 11 indexed citations

2.

Perkoff, Gerald T., F. E. Stephens, & Frank H. Tyler. (1960). Chronic Hereditary Nephritis and Y-Chromosome Linkage: Reply to Graham.. PubMed. 12(3). 381–2. 5 indexed citations

3.

Stephens, F. E.. (1959). HEREDITARY MULTIPLE SEBACEOUS CYSTS. Journal of Heredity. 50(6). 299–301. 9 indexed citations

4.

Stephens, F. E., et al.. (1959). HEREDITARY MULTIPLE LIPOMATOSIS. Journal of Heredity. 50(2). 51–53. 14 indexed citations

5.

Stephens, F. E., Eldon J. Gardner, & Charles M. Woolf. (1958). A recheck of kindred 107, which has shown a high frequency of breast cancer. Cancer. 11(5). 967–972. 17 indexed citations

6.

Stephens, F. E.. (1954). Heredity counseling. Eugenics Quarterly. 1(4). 261–263.

7.

Stephens, F. E.. (1953). Inheritance of diseases primary in the muscles. The American Journal of Medicine. 15(4). 558–569. 4 indexed citations

8.

Dolowitz, David A., et al.. (1953). LVII Hereditary Hemorrhagic Telangiectasia. Annals of Otology Rhinology & Laryngology. 62(3). 642–651. 10 indexed citations

9.

Tyler, Frank H. & F. E. Stephens. (1951). STUDIES IN DISORDERS OF MUSCLE. IV. THE CLINICAL MANIFESTATIONS AND INHERITANCE OF CHILDHOOD PROGRESSIVE MUSCULAR DYSTROPHY. Annals of Internal Medicine. 35(1). 169–185. 24 indexed citations

10.

Stephens, F. E. & Frank H. Tyler. (1951). Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.. PubMed. 3(2). 111–25. 58 indexed citations

11.

Stephens, F. E., et al.. (1951). Partially sex-linked cominant inheritance of interstitial pyelonephritis.. PubMed. 3(4). 303–13. 23 indexed citations

12.

Tyler, Frank H., et al.. (1951). STUDIES IN DISORDERS OF MUSCLE. VII. CLINICAL MANIFESTATIONS AND INHERITANCE OF A TYPE OF PERIODIC PARALYSIS WITHOUT HYPOPOTASSEMIA 1. Journal of Clinical Investigation. 30(5). 492–502. 91 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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