J. E. Wraith

7.5k citations

84 papers · 5.0k · h-index 37

Impact in

Physiology top 0.2%
- Lysosomal Storage Disorders Research
Rheumatology top 0.5%
- Glycogen Storage Diseases and Myoclonus

Papers in

Physiology 65
- Lysosomal Storage Disorders Research 63
Epidemiology 19
- Trypanosoma species research and implications 18

Co-authors: Michael Beck (13 shared papers)Nathalie Guffon (10 shared papers)Roberto Giugliani (9 shared papers)Joseph Muenzer (5 shared papers)Ashok Vellodi (5 shared papers)Simon Jones (15 shared papers)MA Cleary (1 shared paper)Maurizio Scarpa (5 shared papers)
Journals: Journal of Inherited Metabolic Disease (16 papers)Archives of Disease in Childhood (10 papers)Molecular Genetics and Metabolism (8 papers)The Journal of Pediatrics (5 papers)Human Mutation (4 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

J. E. Wraith

82 papers receiving 4.9k citations

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-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 84 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome) Genetics in Medicine ·Joseph Muenzer, J. E. Wraith, Michael Beck, Roberto Giugliani, Paul Harmatz, Christine M. Eng, Ashok Vellodi, Rick Martin, Uma Ramaswami, Müge Güçsavaş‐Çalıkoğlu, Suresh Vijayaraghavan, S. Wendt, Antonio Puga, B. Ulbrich, Marwan Shinawi, Maureen Cleary, Diane Piper, Ann Marie Conway, Alan Kimura	2006	457
2	Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy European Journal of Pediatrics ·J. E. Wraith, Maurizio Scarpa, Michael Beck, Olaf A. Bodamer, Linda De Meırleır, Nathalie Guffon, Allan M. Lund, Gunilla Malm, Ans T. van der Ploeg, J Zeman	2007	367
3	Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study The Journal of Pediatrics ·Paul Harmatz, Roberto Giugliani, Ida Vanessa Döederlein Schwartz, Nathalie Guffon, Elisa Leão Teles, Clara Sá-Miranda, J. E. Wraith, Michael Beck, Laila Arash, Maurizio Scarpa, Zi‐Fan Yu, Janet Wittes, Kenneth I. Berger, Mary S. Newman, Ann M. Lowe, Emil Kakkis, Stuart J. Swiedler	2006	285
4	Long-term Efficacy and Safety of Laronidase in the Treatment of Mucopolysaccharidosis I PEDIATRICS ·L. Clarke, J. E. Wraith, Michael Beck, Edwin H. Kolodny, Gregory M. Pastores, Joseph Muenzer, David M. Rapoport, Kenneth I. Berger, Marisa Sidman, Emil Kakkis, Gerald F. Cox	2008	260
5	Enzyme Replacement Therapy in Patients Who Have Mucopolysaccharidosis I and Are Younger Than 5 Years: Results of a Multinational Study of Recombinant Human α-l-Iduronidase (Laronidase) PEDIATRICS ·J. E. Wraith, Michael Beck, Roderick Lane, Ans van der Ploeg, Elsa Shapiro, Yong Xue, Emil Kakkis, Nathalie Guffon	2007	193
6	Recommendations on the diagnosis and management of Niemann-Pick disease type C Molecular Genetics and Metabolism ·J. E. Wraith, Matthias R. Baumgartner, Bruno Bembi, Athanasios Covanis, Thierry Levade, Eugen Mengel, Mercè Pineda, Frédéric Sedel, Meral Topçu, Marie T. Vanier	2009	175
7	The MPS I registry: Design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I Molecular Genetics and Metabolism ·Gregory M. Pastores, Pamela Arn, Michael Beck, Joe T.R. Clarke, Nathalie Guffon, Paige Kaplan, Joseph Muenzer, Denise Norato, Elsa Shapiro, Janet A. Thomas, David Viskochil, J. E. Wraith	2007	160
8	Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase Molecular Genetics and Metabolism ·Paul Harmatz, Roberto Giugliani, Ida Vanessa Döederlein Schwartz, Nathalie Guffon, Elisa Leão Teles, Clara Sá-Miranda, J. E. Wraith, Michael Beck, Laila Arash, Maurizio Scarpa, David Ketteridge, John J. Hopwood, Barbara Plecko, Robert D. Steiner, Chester B. Whitley, Paige Kaplan, Zi-Fan Yu, Stuart J. Swiedler, Celeste Decker	2008	159
9	Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres Archives of Disease in Childhood ·Ashok Vellodi, Elisabeth Young, Alan Cooper, J. E. Wraith, Bryan Winchester, Cathy Meaney, Uma Ramaswami, Andrew Will	1997	154
10	Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure Bone Marrow Transplantation ·Jaap Jan Boelens, Robert Wynn, A. O’Meara, Paul Veys, (unknown), G Souillet, J. E. Wraith, Alain Fischer, Marina Cavazzana, Karl‐Walter Sykora, Petr Sedláček, Attilio Rovelli, Cuno S.P.M. Uiterwaal, N. M. Wulffraat	2007	152
11	Miglustat in adult and juvenile patients with Niemann–Pick disease type C: Long-term data from a clinical trial Molecular Genetics and Metabolism ·J. E. Wraith, Darleen Vecchio, Elizabeth Jacklin, Larry A. Abel, Harbajan Chadha‐Boreham, Cecile Paquet Luzy, R. Giorgino, Marc C. Patterson	2009	144
12	Initial report from the Hunter Outcome Survey Genetics in Medicine ·J. E. Wraith, Michael Beck, Roberto Giugliani, Joe T.R. Clarke, Rick Martin, Joseph Muenzer	2008	142
13	Management of mucopolysaccharidosis type III. Archives of Disease in Childhood ·MA Cleary, J. E. Wraith	1993	136
14	Mortality and cause of death in mucopolysaccharidosis type II—a historical review based on data from the Hunter Outcome Survey (HOS) Journal of Inherited Metabolic Disease ·Simon Jones, Zsuzsanna Almássy, Michael Beck, Karen Burt, Joe T.R. Clarke, Roberto Giugliani, Christian J. Hendriksz, T Kroepfl, Lawrence A. Lavery, Shau‐Ping Lin, Gunilla Malm, Uma Ramaswami, Radka Tincheva, J. E. Wraith, (unknown)	2009	132
15	Development of a Suspicion Index to aid diagnosis of Niemann-Pick disease type C Neurology ·Frits A. Wijburg, F. Sedel, M. Pineda, Christian J. Hendriksz, Michael Fahey, Mark Walterfang, Marc C. Patterson, J. E. Wraith, Stefan Kolb	2012	110
16	Safety and Efficacy of Enzyme Replacement Therapy with Agalsidase Beta: An International, Open-label Study in Pediatric Patients with Fabry Disease The Journal of Pediatrics ·J. E. Wraith, Anna Tylki‐Szymańska, Nathalie Guffon, Yeong‐Hau H. Lien, Michel Tsimaratos, Ashok Vellodi, Dominique P. Germain	2007	108
17	Myeloid/Microglial Driven Autologous Hematopoietic Stem Cell Gene Therapy Corrects a Neuronopathic Lysosomal Disease Molecular Therapy ·Ana Sergijenko, Alex Langford-Smith, Ai Yin Liao, Claire E. Pickford, John McDermott, Gabriel Nowinski, Kia Langford‐Smith, Catherine L.R. Merry, Simon Jones, J. E. Wraith, Robert Wynn, Fiona L. Wilkinson, Brian Bigger	2013	101
18	SPINAL PROBLEMS IN MUCOPOLYSACCHARIDOSIS I (HURLER SYNDROME) Journal of Bone and Joint Surgery - British Volume ·Vickram J. Tandon, J. B. Williamson, R. A. Cowie, J. E. Wraith	1996	78
19	Idursulfase treatment of Hunter syndrome in children younger than 6 years: Results from the Hunter Outcome Survey Genetics in Medicine ·Joseph Muenzer, Michael Beck, Roberto Giugliani, Yasuyuki Suzuki, Anna Tylki‐Szymańska, Vassili Valayannopoulos, Ashok Vellodi, J. E. Wraith	2011	77
20	Safety and efficacy of enzyme replacement therapy in combination with hematopoietic stem cell transplantation in Hurler syndrome Genetics in Medicine ·Satkiran S. Grewal, Robert Wynn, José E. Abdenur, Barbara K. Burton, Maged I. Gharib, Claudia M. Haase, Robert J. Hayashi, Shalini Shenoy, David Sillence, George E. Tiller, Martha Dudek, Annet van Royen‐Kerkhof, J. E. Wraith, Paul Woodard, Guy Young, Nico Wulffraat, Chester B. Whitley, Charles Peters	2005	75

About J. E. Wraith

J. E. Wraith is a scholar working on Physiology, Epidemiology, Rheumatology, Organic Chemistry and Molecular Biology, having authored 84 papers that have together received 5.0k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (63 papers), Trypanosoma species research and implications (18 papers), Glycogen Storage Diseases and Myoclonus (12 papers), Metabolism and Genetic Disorders (9 papers), Carbohydrate Chemistry and Synthesis (9 papers), Child Nutrition and Feeding Issues (7 papers), Biomedical Research and Pathophysiology (5 papers) and Autoimmune and Inflammatory Disorders Research (5 papers). The work is most often cited by research in Physiology (4.2k citations), Rheumatology (942 citations), Epidemiology (1.4k citations), Hematology (357 citations) and Cell Biology (494 citations). J. E. Wraith has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Michael Beck, Nathalie Guffon, Roberto Giugliani, Joseph Muenzer, Ashok Vellodi, Simon Jones, MA Cleary, Maurizio Scarpa, Emil Kakkis and Paul Harmatz. Their work appears in journals such as Journal of Inherited Metabolic Disease, Archives of Disease in Childhood, Molecular Genetics and Metabolism, The Journal of Pediatrics and Human Mutation.

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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J. E. Wraith

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