J. E. Wraith

7.7k citations

71 papers · 5.6k indexed · 2 hit papers · h-index 35

Physiology top 0.5%
- Lysosomal Storage Disorders Research 51
Genetics top 0.5%
Rheumatology top 0.5%
- Glycogen Storage Diseases and Myoclonus 12
Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 12
Hematology top 2%
Epidemiology
- Trypanosoma species research and implications 19
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 13
Cell Biology
- Cellular transport and secretion 10
Psychiatry and Mental health
- Child Nutrition and Feeding Issues 7
Pathology and Forensic Medicine
- Biomedical Research and Pathophysiology 4

Co-authors: Robert Wynn Ilaria Bellantuono Leslie J. Fairbairn Joseph Muenzer L. Clarke M. Baxter Marc C. Patterson Simon N. Jowitt
Cited by: Physiology Genetics Rheumatology
Journals: Journal of Inherited Metabolic Disease (16 papers)PLoS ONE (5 papers)Molecular Genetics and Metabolism (4 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

J. E. Wraith

71 papers receiving 5.5k citations

Hit Papers

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Peers

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

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

#	Work
1	Thoracolumbar Kyphosis in Treated Mucopolysaccharidosis 1 (Hurler Syndrome) Spine ·李为萍,Raphael H. Sacho,Cai Chunqi,J. E. Wraith,解福泉,Natalia Semina	2014	24
2	Assessment of Sleep in Children with Mucopolysaccharidosis Type III PLoS ONE ·邓吉牛,Jin Eun Hyun,Saskia Heckters,孙元鹏,Dougal Julian Hare,J. E. Wraith,Simon Jones,Brian Bigger,Kia Langford‐Smith,Maria Mercè Canal	2014	32
3	Signal One and Two Blockade Are Both Critical for Non-Myeloablative Murine HSCT across a Major Histocompatibility Complex Barrier PLoS ONE ·Kia Langford‐Smith,Ornella Ru,Alex Langford-Smith,Fiona L. Wilkinson,Simon Jones,J. E. Wraith,Robert Wynn,Brian Bigger	2013	5
4	Neuropathology in Mouse Models of Mucopolysaccharidosis Type I, IIIA and IIIB PLoS ONE ·Fiona L. Wilkinson,Rebecca Holley,Kia Langford‐Smith,S Badrinath,Aiyin Liao,Alex Langford-Smith,Jonathan D. Cooper,Simon Jones,J. E. Wraith,Robert Wynn,Catherine L.R. Merry,Brian Bigger	2012	145
5	Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler's syndrome after pharmacological enzyme replacement therapy Haematologica ·Rahmawaty Antu,Brian Bigger,健治金行,Jean Mercer,Karen Tylee,Heather J. Church,Denise Bonney,Simon Jones,J. E. Wraith,Robert Wynn	2012	40
6	Genistein Improves Neuropathology and Corrects Behaviour in a Mouse Model of Neurodegenerative Metabolic Disease PLoS ONE ·Marcelina Malinowska,Fiona L. Wilkinson,Kia Langford‐Smith,Alex Langford-Smith,Jillian R. Brown,Brett E. Crawford,Marie T. Vanier,Grzegorz Grynkiewicz,Robert Wynn,J. E. Wraith,Grzegorz Węgrzyn,Brian Bigger	2010	115
7	Circadian rhythm and suprachiasmatic nucleus alterations in the mouse model of mucopolysaccharidosis IIIB Behavioural Brain Research ·Maria Mercè Canal,Fiona L. Wilkinson,Jonathan D. Cooper,J. E. Wraith,Robert Wynn,Brian Bigger	2010	24
8	Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: α-glucosaminide N-acetyltransferase (HGSNAT) gene Human Mutation ·Matthew Feldhammer,Stéphanie Durand,Lenka Mrázová,S. C. TEWARI,Rachel Laframboise,Robert Steinfeld,J. E. Wraith,Helen Michelakakis,Otto P. van Diggelen,Martin Hřebı́ček,Stanislav Kmoch,Alexey V. Pshezhetsky	2009	45
9	Genistein reduces lysosomal storage in peripheral tissues of mucopolysaccharide IIIB mice Molecular Genetics and Metabolism ·Marcelina Malinowska,Fiona L. Wilkinson,William Bennett,Kia Langford‐Smith,Frédéric Libaud,Joanna Jakóbkiewicz‐Banecka,Robert Wynn,J. E. Wraith,Grzegorz Węgrzyn,Brian Bigger	2009	82
10	Spiral analysis in Niemann‐Pick disease type C Movement Disorders ·Annie Hsu,Panida Piboolnurak,A Floyd,Qiping Yu,J. E. Wraith,Marc C. Patterson,Seth L. Pullman	2009	26
11	Enzyme Replacement Therapy for Mucopolysaccharidoses: Opinions of Patients and Families The Journal of Pediatrics ·David Coman,Ian Hayes,Veronica Collins,Margaret Sahhar,J. E. Wraith,Martin B. Delatycki	2008	13
12	Mutational analysis of 105 mucopolysaccharidosis type VI patients Human Mutation ·Litsa Karageorgos,Doug A. Brooks,A.C. Pollard,Elizabeth Melville,Leanne K. Hein,Peter R. Clements,David Ketteridge,Stuart J. Swiedler,Michael Beck,Roberto Giugliani,Paul Harmatz,J. E. Wraith,Nathalie Guffon,Elisa Leão Teles,Clara Sá-Miranda,John J. Hopwood	2007	97
13	Substrate reduction therapy in Sandhoff disease: Evidence for improvement in nervous function in patients treated with miglustat Journal of Inherited Metabolic Disease ·Robin Lachmann,Nathan Wright,Jun Yuan,Henry McKeown,Michael F. Coleman,A. Miró Domínguez,Rowan Burnstein,Justine Gillard,Siân E. Harding,Frances M. Platt,J. E. Wraith,Timothy M. Cox	2006	4
14	Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) American Journal of Medical Genetics Part A ·Stuart J. Swiedler,Michael Beck,Yuxi Qiu,Roberto Giugliani,Ida Vanessa Döederlein Schwartz,Paul Harmatz,J. E. Wraith,Jane Roberts,David Ketteridge,John J. Hopwood,Nathalie Guffon,Clara Sá-Miranda,Elisa Leão Teles,Kenneth I. Berger,P. J. Sipling	2005	117
15	Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S) American Journal of Medical Genetics ·Olaf A. Bodamer,Heather J. Church,Alan Cooper,J. E. Wraith,C. Ronald Scott,Fernando Scaglia	2002	11
16	Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT): Cloning of the Human SCOT Gene, Tertiary Structural Modeling of the Human SCOT Monomer, and Characterization of Three Pathogenic Mutations Genomics ·Toshiyuki Fukao,Grant A. Mitchell,Xiang‐Qian Song,Haruki Nakamura,Sacha Kassovska‐Bratinova,Kenji E. Orii,J. E. Wraith,G. T. N. Besley,Ronald J. A. Wanders,Klary E. Niezen‐Koning,Gerard T. Berry,Michael Palmieri,Naomi Kondo	2000	45
17	Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene Nature Genetics ·Gerbert A. Jansen,Evgenii Nikolaevich Antonov,Sacha Ferdinandusse,Lodewijk IJlst,Anton O. Muijsers,Ola H. Skjeldal,Oddvar Stokke,C. Jakobs,G. T. N. Besley,J. E. Wraith,Ronald J. A. Wanders	1997	221
18	Geleophysic dysplasia American Journal of Medical Genetics ·J. E. Wraith,Agnes Bankier,C. W. Chow,David M. Danks,Greg J. Ghiardi	1990	15
19	Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conception European Journal of Pediatrics ·Carey J. Vaux,David Pitt,Guihai,J. E. Wraith,David M. Danks	1988	9
20	Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria European Journal of Pediatrics ·Eric Haan,R. D. Scholem,James Pitt,J. E. Wraith,Garry K. Brown	1987	10

About J. E. Wraith

J. E. Wraith is a scholar working on Physiology, Clinical Biochemistry, Rheumatology, Cell Biology and Epidemiology, having authored 71 papers that have together received 5.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (51 papers), Trypanosoma species research and implications (19 papers), Carbohydrate Chemistry and Synthesis (13 papers), Metabolism and Genetic Disorders (12 papers), Glycogen Storage Diseases and Myoclonus (12 papers), Cellular transport and secretion (10 papers), Child Nutrition and Feeding Issues (7 papers) and Biomedical Research and Pathophysiology (4 papers). The work is most often cited by research in Physiology (3.5k citations), Genetics (1.2k citations), Rheumatology (995 citations), Clinical Biochemistry (436 citations) and Hematology (468 citations). J. E. Wraith has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Robert Wynn, Ilaria Bellantuono, Leslie J. Fairbairn, Joseph Muenzer, L. Clarke, M. Baxter, Marc C. Patterson, Simon N. Jowitt, Darleen Vecchio and Larry A. Abel. Their work appears in journals such as Journal of Inherited Metabolic Disease, PLoS ONE, Molecular Genetics and Metabolism, Human Mutation and The Journal of Pediatrics.

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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