Joyce E. Fox

2.9k total citations
43 papers, 1.6k citations indexed

About

Joyce E. Fox is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joyce E. Fox has authored 43 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joyce E. Fox's work include Metabolism and Genetic Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (6 papers). Joyce E. Fox is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (6 papers). Joyce E. Fox collaborates with scholars based in United States, Canada and Italy. Joyce E. Fox's co-authors include C C Reynolds, David R. Phillips, Wayne A. Fenton, Betty Leung, José A. López, Arthur L. Horwich, J K Boyles, León E. Rosenberg, Rima Rozen and Julie De Backer and has published in prestigious journals such as Nature, New England Journal of Medicine and Journal of Biological Chemistry.

In The Last Decade

Joyce E. Fox

42 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joyce E. Fox United States 20 505 498 434 334 233 43 1.6k
Hiroshi Kaito Japan 27 939 1.9× 300 0.6× 406 0.9× 307 0.9× 139 0.6× 110 2.3k
Wakako Yamada Japan 14 661 1.3× 100 0.2× 353 0.8× 354 1.1× 84 0.4× 19 1.7k
Jacob van den Born Netherlands 17 485 1.0× 104 0.2× 173 0.4× 104 0.3× 255 1.1× 23 1.3k
Noëlynn Oliver United States 25 1.2k 2.5× 263 0.5× 43 0.1× 147 0.4× 187 0.8× 41 2.2k
Tamotsu Miyazaki Japan 19 424 0.8× 70 0.1× 315 0.7× 266 0.8× 598 2.6× 88 1.5k
Alexander Sandra United States 19 832 1.6× 221 0.4× 96 0.2× 106 0.3× 277 1.2× 38 1.5k
Tohru Ikuta United States 20 680 1.3× 115 0.2× 542 1.2× 63 0.2× 104 0.4× 48 1.6k
Mitsuru Hara Japan 22 440 0.9× 160 0.3× 44 0.1× 339 1.0× 337 1.4× 70 1.6k
GEORGE LAMSON United States 22 1.0k 2.1× 379 0.8× 37 0.1× 182 0.5× 149 0.6× 24 2.4k
Luciano Baronciani Italy 22 194 0.4× 368 0.7× 1.1k 2.5× 151 0.5× 318 1.4× 84 1.8k

Countries citing papers authored by Joyce E. Fox

Since Specialization
Citations

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

Fields of papers citing papers by Joyce E. Fox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joyce E. Fox

This figure shows the co-authorship network connecting the top 25 collaborators of Joyce E. Fox. A scholar is included among the top collaborators of Joyce E. Fox 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 Joyce E. Fox. Joyce E. Fox 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
1.
2.
Frank, Graeme R., Joyce E. Fox, Elena G. Bochukova, et al.. (2013). Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency. Molecular Genetics and Metabolism. 110(1-2). 191–194. 45 indexed citations
3.
Simpson, Terri, et al.. (2012). Screening for Mycobacterium tuberculosis Using an Interferon-Gamma Release Assay. Journal of Public Health Management and Practice. 18(4). E19–E25. 4 indexed citations
4.
Simpson, Terri, et al.. (2012). Quantitative and qualitative QuantiFERON®-TB Gold In-Tube results among groups with varying risks of exposure to tuberculosis. Heart & Lung. 41(6). 553–561. 12 indexed citations
5.
DiMaio, Miriam S., Joyce E. Fox, & Maurice J. Mahoney. (2010). Prenatal Diagnosis: Cases & Clinical Challenges. 2 indexed citations
6.
Coucke, Paul, Andy Willaert, Marja W. Wessels, et al.. (2006). Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome. Nature Genetics. 38(4). 452–457. 246 indexed citations
7.
Edwards, Paul C., et al.. (2004). Bilateral central giant cell granulomas of the mandible in an 8-year-old girl with Noonan syndrome (Noonan-like/multiple giant cell lesion syndrome). Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 99(3). 334–340. 34 indexed citations
8.
Zaslav, Ann‐Leslie, et al.. (2004). Prenatal diagnosis of trisomy 3 mosaicism. Prenatal Diagnosis. 24(9). 693–696. 19 indexed citations
9.
Zaslav, Ann‐Leslie, et al.. (2003). Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4. American Journal of Medical Genetics Part A. 126A(4). 420–422. 2 indexed citations
10.
Zaslav, Ann‐Leslie, et al.. (2000). Prenatal diagnosis of trisomy 4 mosaicism. American Journal of Medical Genetics. 95(4). 381–384. 11 indexed citations
11.
Edelmann, Lisa, Elizabeth Spiteri, Rosalie Goldberg, et al.. (1999). A Common Breakpoint on 11q23 in Carriers of the Constitutional t(11;22) Translocation. The American Journal of Human Genetics. 65(6). 1608–1616. 46 indexed citations
12.
Zaslav, Ann‐Leslie, et al.. (1999). Mosaicism with a normal cell line and an unbalanced structural rearrangement. American Journal of Medical Genetics. 82(1). 15–19. 15 indexed citations
13.
Pletcher, Beth A., Joyce E. Fox, Robert A. Boxer, et al.. (1996). Four sibs with arterial tortuosity: Description and review of the literature. American Journal of Medical Genetics. 66(2). 121–128. 40 indexed citations
14.
Fox, Joyce E., et al.. (1995). Infant with mos45,X/46,XY/47,XYY/48,XYYY: Genetic and clinical findings. The American Journal of Human Genetics. 59(4). 435–440.
15.
Worley, Kim C., Jeffrey A. Towbin, David F. Barker, et al.. (1992). Identification of new markers in Xp21 between DXS28 (C7) and DMD. Genomics. 13(4). 957–961. 25 indexed citations
16.
Maytal, Joseph, Alan Shanske, Joyce E. Fox, S Lipper, & Lydia Eviatar. (1991). Duchenne Muscular Dystrophy in a Girl Identified by Dystrophin Deficiency. Neuropediatrics. 22(3). 163–165. 2 indexed citations
17.
Heimler, Audrey, et al.. (1991). Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities in sibs. American Journal of Medical Genetics. 39(2). 192–195. 35 indexed citations
18.
Fox, Joyce E., et al.. (1988). Trisomy 18 with Cantrell pentalogy in a stillborn infant. American Journal of Medical Genetics. 31(2). 391–394. 36 indexed citations
19.
Rozen, Rima, Joyce E. Fox, Adelle M. Hack, et al.. (1986). DNA analysis for ornithine transcarbamylase deficiency. Journal of Inherited Metabolic Disease. 9(S1). 49–57. 20 indexed citations
20.
Fox, Joyce E., et al.. (1985). 820 ADDITIONAL RESTRICTION FRAGMENT LENGTH POLYMORPHISMS (RFLS)FOR DETECTION OF ORNITHINE TRANSCARBAMYLASE (OTC) DEFICIENCY. Pediatric Research. 19(4). 247A–247A. 1 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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