Arnold Reuser

12.0k citations

190 papers · 8.3k indexed · 1 hit paper · h-index 52

Impact in

Rheumatology top 0.1%
- Glycogen Storage Diseases and Myoclonus
Physiology top 0.1%
- Lysosomal Storage Disorders Research

Papers in ⓘ

Physiology 160
- Lysosomal Storage Disorders Research 157
Rheumatology 106
- Glycogen Storage Diseases and Myoclonus 106

Co-authors: Ans T. van der Ploeg (72 shared papers)Marian A. Kroos (72 shared papers)H. Galjaard (23 shared papers)A. T. Hoogeveen (14 shared papers)M M Hermans (19 shared papers)Pieter A. van Doorn (23 shared papers)Marianne Hoogeveen‐Westerveld (11 shared papers)Rob Willemsen (16 shared papers)
Journals: Molecular Genetics and Metabolism (11 papers)Journal of Inherited Metabolic Disease (11 papers)Orphanet Journal of Rare Diseases (10 papers)Neuromuscular Disorders (9 papers)Human Mutation (9 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Arnold Reuser

188 papers receiving 8.0k citations

Hit Papers

align trajectories log scale

Pompe's disease 2008 · 537 citations

Peers

Countries citing papers authored by Arnold Reuser

Since Specialization

Citations

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

Fields of papers citing papers by Arnold Reuser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Arnold Reuser, 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 Arnold Reuser Line = papers co-authored together Arnold Reuser 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 190 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Pompe's disease The Lancet ·Ans T. van der Ploeg, Arnold Reuser Hit paper breakdown →	2008	537
2	The Natural Course of Infantile Pompe’s Disease: 20 Original Cases Compared With 133 Cases From the Literature PEDIATRICS ·Hannerieke M.P. van den Hout, Wim Hop, Otto P. van Diggelen, Jan Smeıtınk, Gerrit Smit, Bwee Tien Poll‐The, H. D. Bakker, Maarten J. J. E. Loonen, Johannis B.C. de Klerk, Arnold Reuser, Ans T. van der Ploeg	2003	407
3	Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man. Proceedings of the National Academy of Sciences ·Alessandra d’Azzo, A. T. Hoogeveen, Arnold Reuser, Douglas N. Robinson, H. Galjaard	1982	284
4	Characterization and localization of the FMR-1 gene product associated with fragile X syndrome Nature ·Coleta Verheij, Cathy Bakker, Esther de Graaff, J. L. M. Keulemans, Rob Willemsen, Annemieke J.M.H. Verkerk, H. Galjaard, Arnold Reuser, A. T. Hoogeveen, Ben A. Oostra	1993	276
5	Enzyme replacement therapy in late‐onset Pompe's disease: A three‐year follow‐up Annals of Neurology ·Léon P. F. Winkel, Johanna M. P. van den Hout, Joep H. J. Kamphoven, Janus A. M. Disseldorp, Maaike Remmerswaal, Willem F. Arts, Maarten J. J. E. Loonen, Arnold G. Vulto, Pieter A. van Doorn, Gerard De Jong, Wim Hop, Gerrit Smit, Stuart K. Shapira, Marijke A. Boer, Arnold Reuser, Ans T. van der Ploeg, Otto P. van Diggelen	2004	161
6	Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex. The EMBO Journal ·L. H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Marian A. Kroos, J. Van Beeumen, Arnold Reuser, B. A. Oostra	1988	153
7	Structural and functional changes of lysosomal acid alpha-glucosidase during intracellular transport and maturation. Journal of Biological Chemistry ·H.A. Wisselaar, Marian A. Kroos, M M Hermans, J. Van Beeumen, Arnold Reuser	1993	143
8	Human lysosomal alpha-glucosidase. Characterization of the catalytic site Journal of Biological Chemistry ·M M Hermans, Marian A. Kroos, J. Van Beeumen, Ben A. Oostra, Arnold Reuser	1991	140
9	Disease severity in children and adults with Pompe disease related to age and disease duration Neurology ·M.L.C. Hagemans, Léon P. F. Winkel, Wim C.J. Hop, Arnold Reuser, Pieter A. van Doorn, Ans T. van der Ploeg	2005	133
10	Glycogenosis type II (acid maltase deficiency) Muscle & Nerve ·Arnold Reuser, Marian A. Kroos, M M Hermans, A. G. A. Bijvoet, Martin Ph. Verbeet, O. P. van Diggelen, Wim J. Kleijer, Ans T. van der Ploeg	1995	132
11	Enzyme therapy for Pompe disease with recombinant human α‐glucosidase from rabbit milk Journal of Inherited Metabolic Disease ·Johanna M. P. van den Hout, Arnold Reuser, J. B. C. de Klerk, W.F.M. Arts, Jan Smeıtınk, Ans T. van der Ploeg	2001	129
12	Twenty-two novel mutations in the lysosomal ?-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II Human Mutation ·M M Hermans, Dik van Leenen, Marian A. Kroos, Clare Beesley, Ans T. van der Ploeg, Hitoshi Sakuraba, Ron A. Wevers, Wim Kleijer, Helen Michelakakis, Edwin P. Kirk, Janice M. Fletcher, N. U. Bosshard, Lina Basel‐Vanagaite, G. T. N. Besley, Arnold Reuser	2003	113
13	Characterization of the human lysosomal α-glucosidase gene Biochemical Journal ·Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Arnold Reuser, Ben A. Oostra	1990	113
14	Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study Orphanet Journal of Rare Diseases ·Nadine A. M. E. van der Beek, Juna M. de Vries, M.L.C. Hagemans, Wim C.J. Hop, Marian A. Kroos, John H. J. Wokke, Marianne de Visser, Baziel G.M. van Engelen, Jan B. M. Kuks, Anneke J. van der Kooi, Nicolette C. Notermans, Karin G. Faber, Jan J.G.M. Verschuuren, Arnold Reuser, Ans T. van der Ploeg, Pieter A. van Doorn	2012	111
15	Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating Human Mutation ·Marian A. Kroos, Robert J. Pomponio, Laura Van de Vliet, Rachel Palmer, Michael Phipps, Robert van der Helm, Dicky Halley, Arnold Reuser	2008	106
16	Biochemical, immunological, and cell genetic studies in glycogenosis type II. PubMed ·Arnold Reuser, J.F. Koster, A. T. Hoogeveen, H. Galjaard	1978	102
17	Human Acid -Glucosidase from Rabbit Milk Has Therapeutic Effect in Mice with Glycogen Storage Disease Type II Human Molecular Genetics ·A. G. A. Bijvoet, Hans Van Hirtum, Marian A. Kroos, Esther H. M. van de Kamp, Onard Schoneveld, P. Visser, Just P. J. Brakenhoff, M. Weggeman, E.J. van Corven, Ans T. van der Ploeg, Arnold Reuser	1999	95
18	Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II. Journal of Biological Chemistry ·Arnold Reuser, Marian A. Kroos, Ronald P.J. Oude Elferink, J. M. Tager	1985	94
19	The genotype–phenotype correlation in Pompe disease American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marian A. Kroos, Marianne Hoogeveen‐Westerveld, Ans van der Ploeg, Arnold Reuser	2012	93
20	Impact of enzyme replacement therapy on survival in adults with Pompe disease: results from a prospective international observational study Orphanet Journal of Rare Diseases ·Deniz Güngör, Michelle E. Kruijshaar, Iris Plug, Ralph B. D’Agostino, M.L.C. Hagemans, Pieter A. van Doorn, Arnold Reuser, Ans T. van der Ploeg	2013	90

About Arnold Reuser

Arnold Reuser is a scholar working on Physiology, Rheumatology, Organic Chemistry, Molecular Biology and Epidemiology, having authored 190 papers that have together received 8.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (157 papers), Glycogen Storage Diseases and Myoclonus (106 papers), Carbohydrate Chemistry and Synthesis (68 papers), Trypanosoma species research and implications (25 papers), Child Nutrition and Feeding Issues (21 papers), Cellular transport and secretion (21 papers), Glycosylation and Glycoproteins Research (19 papers) and Biochemical and Molecular Research (16 papers). The work is most often cited by research in Rheumatology (4.0k citations), Physiology (6.2k citations), Organic Chemistry (2.1k citations), Physiology (284 citations) and Clinical Biochemistry (418 citations). Arnold Reuser has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Ans T. van der Ploeg, Marian A. Kroos, H. Galjaard, A. T. Hoogeveen, M M Hermans, Pieter A. van Doorn, Marianne Hoogeveen‐Westerveld, Rob Willemsen, H.A. Wisselaar and M.L.C. Hagemans. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Neuromuscular Disorders 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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