Arnold Reuser

12.0k citations
196 papers · 8.8k · 1 hit paper · h-index 54

Impact in

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

Papers in

  • Physiology 161
    • Lysosomal Storage Disorders Research 158
  • Rheumatology 87
    • Glycogen Storage Diseases and Myoclonus 87
Co-authors
Ans T. van der Ploeg (73 shared papers)Marian A. Kroos (74 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 (17 shared papers)
Journals
Journal of Inherited Metabolic Disease (11 papers)Molecular Genetics and Metabolism (11 papers)Orphanet Journal of Rare Diseases (10 papers)Human Mutation (9 papers)Neuromuscular Disorders (9 papers)
Partner nations
NetherlandsUnited StatesUnited Kingdom

In The Last Decade

Arnold Reuser

194 papers receiving 8.4k citations

Arnold Reuser's Hit Papers

Pompe's disease 2008 · 560 citations
5600+6+12Years since publication100200300400500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2008 The Lancet

Peers

Arnold Reuser
Comparison fields: 5 of 116
  • Physiology 6.3k
  • Rheumatology 3.2k
  • Physiology 313
  • Clinical Biochemistry 442
  • Organic Chemistry 1.9k
Replace Steven U. Walkley with:
Steven U. Walkley United States
M. Elleder Czechia
John W. Callahan Canada
Gideon Bach Israel
J S O′Brien United States
Alexey V. Pshezhetsky Canada
Anu Jalanko Finland
Xingxuan He United States
Marjan Huizing United States
Alasdair M. Gilfillan United States
Arnold Reuser relative to Steven U. Walkley United States Steven U. Walkley's profile →
Citations per field
00.5×2×4×7.0×
Steven U. Walkley · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 196 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 →		2008560
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
2003436
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
1982318
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
1993283
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
2004181
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
1988156
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
1993147
8
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
2001146
9
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
1991144
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
1995142
11
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
2005141
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
2003126
13
Characterization of the human lysosomal α-glucosidase gene
Biochemical Journal ·Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Arnold Reuser, Ben A. Oostra
1990114
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
2012113
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
2008111
16
Biochemical, immunological, and cell genetic studies in glycogenosis type II.
PubMed ·Arnold Reuser, J.F. Koster, A. T. Hoogeveen, H. Galjaard
1978110
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
1999104
18
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
2012100
19
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
1985100
20
Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
Human Genetics ·R. A. Barneveld, W. Keiizer, F. P. W. Tegelaers, Edward I. Ginns, Ad Geurts van Kessel, Roscoe O. Brady, J. A. Barranger, J. M. Tager, H. Galjaard, A. Westerveld, Arnold Reuser
198393

About Arnold Reuser

Arnold Reuser is a scholar working on Physiology, Rheumatology, Organic Chemistry, Molecular Biology and Cell Biology, having authored 196 papers that have together received 8.8k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (158 papers), Glycogen Storage Diseases and Myoclonus (87 papers), Carbohydrate Chemistry and Synthesis (62 papers), Cellular transport and secretion (21 papers), Glycosylation and Glycoproteins Research (20 papers), Trypanosoma species research and implications (19 papers), Biochemical and Molecular Research (16 papers) and Child Nutrition and Feeding Issues (16 papers). The work is most often cited by research in Physiology (6.3k citations), Rheumatology (3.2k citations), Physiology (313 citations), Clinical Biochemistry (442 citations) and Organic Chemistry (1.9k 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 Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Human Mutation and Neuromuscular Disorders.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Steven U. WalkleyBreakdown of academic impact, for papers by M. EllederBreakdown of academic impact, for papers by John W. CallahanBreakdown of academic impact, for papers by Gideon BachBreakdown of academic impact, for papers by J S O′BrienBreakdown of academic impact, for papers by Alexey V. PshezhetskyBreakdown of academic impact, for papers by Anu JalankoBreakdown of academic impact, for papers by Xingxuan HeBreakdown of academic impact, for papers by Marjan HuizingBreakdown of academic impact, for papers by Alasdair M. Gilfillan