J. E. Wraith

2.5k total citations
35 papers, 1.3k citations indexed

About

J. E. Wraith is a scholar working on Physiology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, J. E. Wraith has authored 35 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Physiology, 14 papers in Rheumatology and 12 papers in Clinical Biochemistry. Recurrent topics in J. E. Wraith's work include Lysosomal Storage Disorders Research (16 papers), Metabolism and Genetic Disorders (12 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). J. E. Wraith is often cited by papers focused on Lysosomal Storage Disorders Research (16 papers), Metabolism and Genetic Disorders (12 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). J. E. Wraith collaborates with scholars based in United Kingdom, United States and Switzerland. J. E. Wraith's co-authors include Maureen Cleary, J. H. Walter, F. White, J. P. R. Jenkins, David G. Hughes, Ashok Vellodi, Anupam Chakrapani, Kenneth L. Tyler, Brian Fowler and John H. Walter and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and The Journal of Pediatrics.

In The Last Decade

J. E. Wraith

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. E. Wraith United Kingdom	20	692	437	434	381	242	35	1.3k
Julian Raiman Canada	24	738 1.1×	334 0.8×	439 1.0×	559 1.5×	331 1.4×	58	1.5k
Agnieszka Jurecka Poland	21	649 0.9×	180 0.4×	293 0.7×	405 1.1×	446 1.8×	63	1.2k
Carolina Fischinger Moura de Souza Brazil	19	427 0.6×	362 0.8×	279 0.6×	507 1.3×	170 0.7×	110	1.2k
Serena Gasperini Italy	16	443 0.6×	185 0.4×	282 0.6×	223 0.6×	146 0.6×	64	880
C B Whitley United States	17	556 0.8×	122 0.3×	209 0.5×	287 0.8×	214 0.9×	30	970
Ana María Martins Brazil	21	1.2k 1.7×	113 0.3×	361 0.8×	251 0.7×	513 2.1×	101	1.4k
I Maire France	17	785 1.1×	82 0.2×	287 0.7×	341 0.9×	279 1.2×	85	1.2k
David Coman Australia	20	302 0.4×	302 0.7×	149 0.3×	583 1.5×	131 0.5×	79	1.2k
Nicole Muschol Germany	23	893 1.3×	84 0.2×	228 0.5×	291 0.8×	297 1.2×	93	1.3k
Ed Wraith United Kingdom	11	718 1.0×	82 0.2×	203 0.5×	149 0.4×	242 1.0×	24	910

Countries citing papers authored by J. E. Wraith

Since Specialization

Citations

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

Fields of papers citing papers by J. E. Wraith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. E. Wraith

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Muenzer, Joseph, Michael Beck, Christine M. Eng, et al.. (2010). Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome. Genetics in Medicine. 13(2). 95–101. 173 indexed citations

Wraith, J. E.. (2009). Enzyme replacement therapy for the management of the mucopolysaccharidoses. International Journal of Clinical Pharmacology and Therapeutics. 47 Suppl 1. S63–5. 19 indexed citations

Cox‐Brinkman, Josanne, Jaap Jan Boelens, J. E. Wraith, et al.. (2006). Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome. Bone Marrow Transplantation. 38(1). 17–21. 82 indexed citations

Wraith, J. E.. (2006). Limitations of enzyme replacement therapy: Current and future. Journal of Inherited Metabolic Disease. 29(2-3). 442–447. 70 indexed citations

Dumas, Helene M., et al.. (2004). Physical performance testing in mucopolysaccharidosis I: a pilot study. Pediatric Rehabilitation. 7(2). 125–131. 21 indexed citations

Suormala, Terttu, Matthias R. Baumgartner, David Coelho, et al.. (2004). The cblD Defect Causes Either Isolated or Combined Deficiency of Methylcobalamin and Adenosylcobalamin Synthesis. Journal of Biological Chemistry. 279(41). 42742–42749. 90 indexed citations

Roland, N.J., et al.. (2003). Hearing loss due to mannosidosis and otitis media with effusion. A case report and review of audiological assessments in children with otitis media with effusion. The Journal of Laryngology & Otology. 117(4). 307–309. 6 indexed citations

Johnson, Trevor N., Amin Rostami‐Hodjegan, Anupam Chakrapani, et al.. (2002). An indirect response model of homocysteine suppression by betaine: optimising the dosage regimen of betaine in homocystinuria. British Journal of Clinical Pharmacology. 54(2). 140–146. 22 indexed citations

Wraith, J. E.. (2001). Current topic: Ornithine carbamoyltransferase deficiency. Archives of Disease in Childhood. 84(1). 84–88. 35 indexed citations

10.

Chakrapani, Anupam, Maureen Cleary, & J. E. Wraith. (2001). Detection of inborn errors of metabolism in the newborn. Archives of Disease in Childhood Fetal & Neonatal. 84(3). F205–F210. 39 indexed citations

11.

Walter, J. H., J. E. Wraith, F. White, Craig A. Bridge, & J. E. Till. (1998). Strategies for the treatment of cystathionine β-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years. European Journal of Pediatrics. 157(S2). S71–S76. 69 indexed citations

12.

Hughes, David G., et al.. (1997). MRI of the brain and craniocervical junction in Morquio's disease. Neuroradiology. 39(5). 381–385. 53 indexed citations

13.

Fowler, Brian, et al.. (1997). Methionine and Serine Formation in Control and Mutant Human Cultured Fibroblasts: Evidence for Methyl Trapping and Characterization of Remethylation Defects. Pediatric Research. 41(1). 145–151. 30 indexed citations

14.

Hughes, David G., et al.. (1996). Magnetic resonance imaging of the brain, neck and cervical spine in mild hunter's syndrome (mucopolysaccharidoses type II). Clinical Radiology. 51(10). 719–723. 45 indexed citations

15.

Cleary, Maureen, et al.. (1995). Magnetic resonance imaging in phenylketonuria: Reversal of cerebral white matter change. The Journal of Pediatrics. 127(2). 251–255. 91 indexed citations

16.

Scott, Hamish S., Paul V. Nelson, Alan Cooper, et al.. (1992). Mucopolysaccharidosis type I (Hurler syndrome): Linkage disequilibrium indicates the presence of a major allele. Human Genetics. 88(6). 701–702. 15 indexed citations

17.

Cleary, Maureen & J. E. Wraith. (1991). Antenatal diagnosis of inborn errors of metabolism.. Archives of Disease in Childhood. 66(7 Spec No). 816–822. 2 indexed citations

18.

Cooper, Alan, Margaret J. Thornley, & J. E. Wraith. (1991). First‐trimester diagnosis of hunter syndrome: Very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus. Prenatal Diagnosis. 11(9). 731–735. 5 indexed citations

19.

O'Driscoll, J. B., M. H. Beck, M Lendon, J. E. Wraith, & I. B. Sardharwalla. (1990). Cutaneous presentation of sarcoidosis in an infant. Clinical and Experimental Dermatology. 15(1). 60–62. 3 indexed citations

20.

Wraith, J. E.. (1989). Diagnosis and management of inborn errors of metabolism.. Archives of Disease in Childhood. 64(10 Spec No). 1410–1415. 10 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.

Explore authors with similar magnitude of impact