Elizabeth Spellacy

777 total citations
19 papers, 604 citations indexed

About

Elizabeth Spellacy is a scholar working on Physiology, Molecular Biology and Rheumatology. According to data from OpenAlex, Elizabeth Spellacy has authored 19 papers receiving a total of 604 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 5 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Elizabeth Spellacy's work include Lysosomal Storage Disorders Research (10 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Metabolism and Genetic Disorders (3 papers). Elizabeth Spellacy is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Metabolism and Genetic Disorders (3 papers). Elizabeth Spellacy collaborates with scholars based in United Kingdom and United States. Elizabeth Spellacy's co-authors include R. W. E. Watts, Robert M. Shull, Elizabeth F. Neufeld, George Constantopoulos, Dorothy A. Gibbs, Jennifer Allsop, G Slavin, R O McKeran, Clara W. Hall and R. Gayman Helman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Pathology and British Journal of Ophthalmology.

In The Last Decade

Elizabeth Spellacy

19 papers receiving 576 citations

Peers

Elizabeth Spellacy
A. H. Fensom United Kingdom
F. A. Beemer Netherlands
Shu-Chuan Chiang Taiwan
R J Desnick United States
E. Young United Kingdom
R O McKeran United Kingdom
Yasutsugu Chinen Japan
Motomichi Kosuga Japan
Ed Wraith United Kingdom
M D Crawfurd United Kingdom
A. H. Fensom United Kingdom
Elizabeth Spellacy
Citations per year, relative to Elizabeth Spellacy Elizabeth Spellacy (= 1×) peers A. H. Fensom

Countries citing papers authored by Elizabeth Spellacy

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth Spellacy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Spellacy

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

All Works

19 of 19 papers shown
1.
Watts, R. W. E., et al.. (1986). Lesch‐nyhan syndrome: Growth delay, testicular atrophy and a partial failure of the 11β‐hydroxylation of steroids. Journal of Inherited Metabolic Disease. 10(3). 210–223. 19 indexed citations
2.
Friedmann, I., Elizabeth Spellacy, Julie Crow, & R. W. E. Watts. (1985). Histopathological studies of the temporal bones in Hurler's disease [Mucopolysaccharidosis (MPS) IH]. The Journal of Laryngology & Otology. 99(1). 29–42. 23 indexed citations
3.
Watts, R. W. E., Elizabeth Spellacy, & John H. Adams. (1985). Neuropathological and clinical correlations in hurler disease. Journal of Inherited Metabolic Disease. 9(3). 261–272. 12 indexed citations
4.
Shull, Robert M., et al.. (1984). Morphologic and biochemical studies of canine mucopolysaccharidosis I.. PubMed. 114(3). 487–95. 69 indexed citations
5.
Crow, Jesse C., et al.. (1983). Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantation.. Journal of Clinical Pathology. 36(4). 415–430. 19 indexed citations
6.
Spellacy, Elizabeth, Robert M. Shull, George Constantopoulos, & Elizabeth F. Neufeld. (1983). A canine model of human alpha-L-iduronidase deficiency.. Proceedings of the National Academy of Sciences. 80(19). 6091–6095. 66 indexed citations
7.
8.
Gibbs, Dorothy A., et al.. (1982). A clinical trial of fibroblast transplantation for the treatment of mucopolysaccharidoses. Journal of Inherited Metabolic Disease. 6(2). 62–81. 18 indexed citations
9.
Shull, Robert M., et al.. (1982). Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.. PubMed. 109(2). 244–8. 77 indexed citations
10.
Watts, R. W. E., Elizabeth Spellacy, B. E. Kendall, G. du Boulay, & Dorothy A. Gibbs. (1981). Computed tomography studies on patients with mucopolysaccharidoses. Neuroradiology. 21(1). 9–23. 35 indexed citations
11.
Spellacy, Elizabeth, Dorothy A. Gibbs, & R. W. E. Watts. (1981). A Newly Recognized Syndrome of Connective Tissue Dysplasia in Siblings (Previously Described as a Variant of Morquio Disease). QJM. 50(200). 377–415. 4 indexed citations
12.
13.
Spellacy, Elizabeth, et al.. (1980). The treatment of lysosomal storage diseases by fibroblast transplantation: some preliminary observations.. PubMed. 16(1). 457–74. 13 indexed citations
14.
Spellacy, Elizabeth, James L. Kennerley Bankes, Jesse C. Crow, et al.. (1980). Glaucoma in a case of Hurler disease.. British Journal of Ophthalmology. 64(10). 773–778. 42 indexed citations
15.
Spellacy, Elizabeth, et al.. (1979). Problems in the Behavioural Treatment of Self‐injury in the Lesch‐Nyhan Syndrome. Developmental Medicine & Child Neurology. 21(6). 795–800. 18 indexed citations
16.
Watts, R. W. E., R. A. Chalmers, Dorothy A. Gibbs, et al.. (1979). Studies on Some Possible Biochemical Treatments of Primary Hyperoxaluria. QJM. 48(190). 259–72. 20 indexed citations
17.
Spellacy, Elizabeth, R. W. E. Watts, & S.K. Goolamali. (1979). Trimethylaminuria. Journal of Inherited Metabolic Disease. 2(4). 85–88. 20 indexed citations
18.
Chalmers, R. A. & Elizabeth Spellacy. (1979). A Method for the Pre- and Post-Natal Detection of Defects of Isovalerate Metabolism. Clinical Science. 57(3). 24P–24P. 3 indexed citations
19.
Wootton, Richard, et al.. (1978). Skeletal Blood Flow in Paget's Disease of Bone and its Response to Calcitonin Therapy. Clinical Science. 54(1). 69–74. 48 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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