Simon Jones

10.5k citations

261 papers · 6.1k · h-index 44

Impact in

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

Papers in

Physiology 194
- Lysosomal Storage Disorders Research 191
Epidemiology 43
- Trypanosoma species research and implications 33

Co-authors: Robert Wynn (50 shared papers)Paul Harmatz (33 shared papers)Brian Bigger (41 shared papers)Roberto Giugliani (28 shared papers)Jean Mercer (33 shared papers)J. E. Wraith (15 shared papers)Christian J. Hendriksz (17 shared papers)Barbara K. Burton (24 shared papers)
Journals: Molecular Genetics and Metabolism (79 papers)Orphanet Journal of Rare Diseases (25 papers)Journal of Inherited Metabolic Disease (21 papers)PLoS ONE (6 papers)Genetics in Medicine (6 papers)
Partner nations: United Kingdom United States France

In The Last Decade

Simon Jones

248 papers receiving 6.0k citations

Peers

Countries citing papers authored by Simon Jones

Since Specialization

Citations

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

Fields of papers citing papers by Simon Jones

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Simon Jones, 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 Simon Jones Line = papers co-authored together Simon Jones 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 261 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure Orphanet Journal of Rare Diseases ·Minke H. de Ru, Jaap Jan Boelens, Anibh M. Das, Simon Jones, Johanna H. van der Lee, Nizar Mahlaoui, Eugen Mengel, Martin Offringa, Anne O’Meara, Rossella Parini, Attilio Rovelli, Karl‐Walter Sykora, Vassili Valayannopoulos, Ashok Vellodi, Robert Wynn, Frits A. Wijburg	2011	186
2	Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo‐controlled study Journal of Inherited Metabolic Disease ·Christian J. Hendriksz, Barbara K. Burton, Thomas R. Fleming, Paul Harmatz, Derralynn Hughes, Simon Jones, Hsiang‐Yu Lin, Eugen Mengel, Maurizio Scarpa, Vassili Valayannopoulos, Roberto Giugliani, (unknown), Peter Slasor, Debra L. Lounsbury, Wolfgang Dummer	2014	179
3	Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease Genetics in Medicine ·Yoav H. Messinger, Nancy J. Mendelsohn, William J. Rhead, David Dimmock, Eli Hershkovitz, Michael Champion, Simon Jones, Rebecca Olson, Amy White, Cara Wells, Deeksha Bali, Laura E. Case, Sarah P. Young, Amy S. Rosenberg, Priya S. Kishnani	2012	172
4	The value of feedback in teaching interviewing skills to medical students Psychological Medicine ·Peter Maguire, Philip Roe, David P. Goldberg, Simon Jones, Clive E. Hyde, Terry O'Dowd	1978	149
5	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	148
6	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	140
7	Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA Molecular Genetics and Metabolism ·Christian J. Hendriksz, Paul Harmatz, Michael Beck, Simon Jones, Tim Wood, Ralph Lachman, Curtis Gravance, T Orii, Shunji Tomatsu	2013	138
8	Hematopoietic Cell Transplantation for Mucopolysaccharidosis Patients Is Safe and Effective: Results after Implementation of International Guidelines Biology of Blood and Marrow Transplantation ·Mieke Aldenhoven, Simon Jones, Denise Bonney, Roisin Borrill, Mary Coussons, Jean Mercer, Marc Bierings, Birgitta Versluys, Peter M. van Hasselt, Frits A. Wijburg, Ans T. van der Ploeg, Robert Wynn, Jaap Jan Boelens	2015	126
9	The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects Molecular Genetics and Metabolism ·Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Carla E. M. Hollak, Peter Slasor, Celeste Decker	2013	114
10	Anaesthesia and airway management in mucopolysaccharidosis Journal of Inherited Metabolic Disease ·Robert Walker, Kumar G. Belani, Elizabeth Braunlin, Iain Bruce, Henrik Hack, Paul Harmatz, Simon Jones, Richard Rowe, Guirish A. Solanki, Barbara Valdemarsson	2012	101
11	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
12	Hematopoietic Stem Cell and Gene Therapy Corrects Primary Neuropathology and Behavior in Mucopolysaccharidosis IIIA Mice Molecular Therapy ·Alex Langford-Smith, Fiona L. Wilkinson, Kia Langford‐Smith, Rebecca Holley, Ana Sergijenko, Steven J. Howe, William Bennett, Simon Jones, JE Wraith, Catherine L.R. Merry, Robert Wynn, Brian Bigger	2012	89
13	A phase 1/2 study of intrathecal heparan-N-sulfatase in patients with mucopolysaccharidosis IIIA Molecular Genetics and Metabolism ·Simon Jones, Catherine Breen, Fiona Heap, Stewart Rust, Jessica de Ruijter, Evelien Tump, Jan Pieter Marchal, Luying Pan, Yongchang Qiu, Jou-Ku Chung, Nitin Nair, Patrick Haslett, Ann Barbier, Frits A. Wijburg	2016	87
14	Clinical Effect And Safety Profile of Recombinant Human Lysosomal Acid Lipase in Patients With Cholesteryl Ester Storage Disease Hepatology ·Manisha Balwani, Catherine Breen, Gregory M. Enns, Patrick Deegan, Tomáš Honzík, Simon Jones, John P. Kane, Vĕra Malinová, Reena Sharma, Eveline O. Stock, Vassili Valayannopoulos, Ed Wraith, Jennifer M. Burg, Stephen Eckert, Eugene Schneider, Anthony Quinn	2013	83
15	The role of enzyme replacement therapy in severe Hunter syndrome—an expert panel consensus European Journal of Pediatrics ·Joseph Muenzer, Olaf A. Bodamer, Barbara K. Burton, L. Clarke, Gudrun Schulze Frenking, Roberto Giugliani, Simon Jones, María Verónica Muñoz Rojas, Maurizio Scarpa, Michael Beck, Paul Harmatz	2011	79
16	Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiency Molecular Genetics and Metabolism ·Melissa Wasserstein, Simon Jones, Handrean Soran, George A. Díaz, Natalie Lippa, Beth L. Thurberg, Kerry Culm-Merdek, Elias Shamiyeh, Haig Inguilizian, Gerald F. Cox, Ana Cristina Puga	2015	78
17	Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux–Lamy syndrome)—10‐year follow‐up of patients who previously participated in an MPS VI survey study American Journal of Medical Genetics Part A ·Roberto Giugliani, Christina Lampe, Nathalie Guffon, David Ketteridge, Elisa Leão Teles, J. E. Wraith, Simon Jones, Cheri Piscia‐Nichols, Ping Lin, Adrian Quartel, Paul Harmatz	2014	73
18	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	71
19	The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families Brain ·Helen Tuppen, Vanessa Hogan, Langping He, Emma L. Blakely, Lisa Worgan, Mazhor Aldosary, Gabriele Saretzki, Charlotte L. Alston, Andrew A. M. Morris, Michael A. Clarke, Simon Jones, Anita Devlin, Sahar Mansour, Zofia M. Chrzanowska‐Lightowlers, David R. Thorburn, Robert McFarland, Robert W. Taylor	2010	71
20	Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency The American Journal of Human Genetics ·Siddharth Banka, Henk J. Blom, John H. Walter, Majid Aziz, Jill Urquhart, Christopher M. Clouthier, Gillian Rice, Arjan P.M. de Brouwer, Emma Hilton, Grace Vassallo, Andrew Will, Desirée E.C. Smith, Yvo M. Smulders, Ron A. Wevers, Robert Steinfeld, Simon Heales, Yanick J. Crow, Joelle N. Pelletier, Simon Jones, William G. Newman	2011	69

About Simon Jones

Simon Jones is a scholar working on Physiology, Epidemiology, Rheumatology, Molecular Biology and Hematology, having authored 261 papers that have together received 6.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (191 papers), Glycogen Storage Diseases and Myoclonus (34 papers), Trypanosoma species research and implications (33 papers), Biomedical Research and Pathophysiology (18 papers), Child Nutrition and Feeding Issues (14 papers), Autoimmune and Inflammatory Disorders Research (14 papers), Metabolism and Genetic Disorders (13 papers) and Family and Disability Support Research (13 papers). The work is most often cited by research in Physiology (4.3k citations), Rheumatology (919 citations), Physiology (217 citations), Epidemiology (1.3k citations) and Clinical Biochemistry (274 citations). Simon Jones has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Robert Wynn, Paul Harmatz, Brian Bigger, Roberto Giugliani, Jean Mercer, J. E. Wraith, Christian J. Hendriksz, Barbara K. Burton, Frits A. Wijburg and Rossella Parini. Their work appears in journals such as Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Journal of Inherited Metabolic Disease, PLoS ONE and Genetics in Medicine.

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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