J. E. Wraith

2.5k citations

35 papers · 1.3k indexed · h-index 20

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Rheumatology top 2%
- Folate and B Vitamins Research
- Glycogen Storage Diseases and Myoclonus

Papers in ⓘ

Clinical Biochemistry 12
- Metabolism and Genetic Disorders 12
Rheumatology 14
- Glycogen Storage Diseases and Myoclonus 8
- Folate and B Vitamins Research 6

Co-authors: Maureen Cleary (5 shared papers)J. H. Walter (3 shared papers)F. White (3 shared papers)J. P. R. Jenkins (3 shared papers)David G. Hughes (2 shared papers)Ashok Vellodi (2 shared papers)Anupam Chakrapani (3 shared papers)Kenneth L. Tyler (1 shared paper)
Journals: Journal of Inherited Metabolic Disease (10 papers)Archives of Disease in Childhood (3 papers)The Journal of Pediatrics (2 papers)Neuroradiology (1 paper)Clinical and Experimental Dermatology (1 paper)
Partner nations: United Kingdom United States Switzerland

In The Last Decade

J. E. Wraith

35 papers receiving 1.2k citations

Peers

Replace Julian Raiman with:

Julian Raiman Canada

Agnieszka Jurecka Poland

Carolina Fischinger Moura de Souza Brazil

Stephanie Austin United States

Serena Gasperini Italy

Hélène Ogier France

C B Whitley United States

I Maire France

Ana María Martins Brazil

David Kronn United States

J. E. Wraith relative to Julian Raiman Canada Julian Raiman's profile →

Citations per field

00.5×1.5×

Julian Raiman · 1×

×1.3 437/334

CB

×1.0 434/439

RHEUM

×0.9 692/738

PHYSI

×0.8 62/77

BIOCH

×1.1 118/108

PMH

Citations per year

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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-authors

The 25 scholars most cited alongside J. E. Wraith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J. E. Wraith Line = papers co-authored together J. E. Wraith links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome Genetics in Medicine ·Joseph Muenzer, Michael Beck, Christine M. Eng, Roberto Giugliani, Paul Harmatz, Rick Martin, Uma Ramaswami, Ashok Vellodi, J. E. Wraith, Maureen Cleary, Müge Güçsavaş‐Çalıkoğlu, Ana Cristina Puga, Marwan Shinawi, Birgit Ulbrich, Suresh Vijayaraghavan, Susanne Wendt, Anne Conway, Alexandra Rossi, David Whiteman, Alan Kimura	2010	173
2	Magnetic resonance imaging of the brain in phenylketonuria The Lancet ·Maureen Cleary, J. H. Walter, J. E. Wraith, Omar Abdulwahid AlAni, D Whittle, J. P. R. Jenkins, Kenneth L. Tyler	1994	126
3	Magnetic resonance imaging in phenylketonuria: Reversal of cerebral white matter change The Journal of Pediatrics ·Maureen Cleary, John H. Walter, J. E. Wraith, F. White, Kathryn Tyler, Jeremy P. R. Jenkins	1995	91
4	The cblD Defect Causes Either Isolated or Combined Deficiency of Methylcobalamin and Adenosylcobalamin Synthesis Journal of Biological Chemistry ·Terttu Suormala, Matthias R. Baumgartner, David Coelho, Petra Zavadáková, Viktor Kožich, Hans Georg Koch, Martin Berghaüser, J. E. Wraith, Alberto Burlina, A Sewell, Jürgen Herwig, Brian Fowler	2004	90
5	Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome Bone Marrow Transplantation ·Josanne Cox‐Brinkman, Jaap Jan Boelens, J. E. Wraith, A. O’Meara, Paul Veys, Frits A. Wijburg, N. M. Wulffraat, Robert Wynn	2006	82
6	Limitations of enzyme replacement therapy: Current and future Journal of Inherited Metabolic Disease ·J. E. Wraith	2006	70
7	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 ·J. H. Walter, J. E. Wraith, F. White, Craig A. Bridge, J. E. Till	1998	69
8	Treatment of infantile Pompe disease with alglucosidase alpha: the UK experience Journal of Inherited Metabolic Disease ·Anupam Chakrapani, Ashok Vellodi, Peter N. Robinson, Simon Jones, J. E. Wraith	2010	66
9	MRI of the brain and craniocervical junction in Morquio's disease Neuroradiology ·David G. Hughes, R. D. Chadderton, R. A. Cowie, J. E. Wraith, J. P. R. Jenkins	1997	53
10	Magnetic resonance imaging of the brain, neck and cervical spine in mild hunter's syndrome (mucopolysaccharidoses type II) Clinical Radiology ·V.J. Parsons, David G. Hughes, J. E. Wraith	1996	45
11	Detection of inborn errors of metabolism in the newborn Archives of Disease in Childhood Fetal & Neonatal ·Anupam Chakrapani, Maureen Cleary, J. E. Wraith	2001	39
12	Current topic: Ornithine carbamoyltransferase deficiency Archives of Disease in Childhood ·J. E. Wraith	2001	35
13	Methionine and Serine Formation in Control and Mutant Human Cultured Fibroblasts: Evidence for Methyl Trapping and Characterization of Remethylation Defects Pediatric Research ·Brian Fowler, C. Whitehouse, Fridel Wenzel, J. E. Wraith	1997	30
14	Velo‐cardio‐facial syndrome presenting as holoprosencephaly Clinical Genetics ·J. E. Wraith, M Super, G. H. Watson, Mark N. Phillips	1985	30
15	β‐Mannosidase deficiency in a female infant with epileptic encephalopathy Journal of Inherited Metabolic Disease ·Alan Cooper, J. E. Wraith, William Savage, Margaret J. Thornley, M. J. Noronha	1990	29
16	Poor cognitive outcome of eleven children with Sanfilippo syndrome after bone marrow transplantation and successful engraftment Kim Klein, William Krivit, Chester B. Whitley, Christina Peters, Valerie A. Cool, Michael Fuhrman, Pedro de Alarcón, Martin R. Klemperer, Lauren E. Miller, R.P. Nelson, J. Henslee-Downey, Pi-Nian Chang, J. E. Wraith, Lawrence A. Lockman, Elsa Shapiro	1995	26
17	Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type I Journal of Inherited Metabolic Disease ·Anbarasu Theodore Anbu, Jean Mercer, J. E. Wraith	2006	25
18	An indirect response model of homocysteine suppression by betaine: optimising the dosage regimen of betaine in homocystinuria British Journal of Clinical Pharmacology ·Angela Matthews, Trevor N. Johnson, Amin Rostami‐Hodjegan, Anupam Chakrapani, J. E. Wraith, Stuart J. Moat, James R. Bonham, Geoffrey T. Tucker	2002	22
19	Physical performance testing in mucopolysaccharidosis I: a pilot study Pediatric Rehabilitation ·Helene M. Dumas, Maria A. Fragala, Stephen M. Haley, Alison Skrinar, J. E. Wraith, Gerald F. Cox	2004	21
20	Enzyme replacement therapy for the management of the mucopolysaccharidoses International Journal of Clinical Pharmacology and Therapeutics ·J. E. Wraith	2009	19

About J. E. Wraith

J. E. Wraith is a scholar working on Clinical Biochemistry, Rheumatology, Physiology, Pediatrics, Perinatology and Child Health and Nephrology, having authored 35 papers that have together received 1.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (16 papers), Metabolism and Genetic Disorders (12 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Folate and B Vitamins Research (6 papers), Carbohydrate Chemistry and Synthesis (5 papers), Neonatal Health and Biochemistry (4 papers), Mitochondrial Function and Pathology (3 papers) and Trypanosoma species research and implications (3 papers). The work is most often cited by research in Clinical Biochemistry (437 citations), Rheumatology (434 citations), Physiology (692 citations), Biochemistry (62 citations) and Psychiatry and Mental health (118 citations). J. E. Wraith has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent 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. Their work appears in journals such as Journal of Inherited Metabolic Disease, Archives of Disease in Childhood, The Journal of Pediatrics, Neuroradiology and Clinical and Experimental Dermatology.

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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