Marian A. Kroos

5.0k citations

88 papers · 3.6k indexed · h-index 36

Co-authors: Arnold Reuser Ans T. van der Ploeg M M Hermans Marianne Hoogeveen‐Westerveld J. Van Beeumen Ben A. Oostra A. G. A. Bijvoet Rob Willemsen
Topics: Lysosomal Storage Disorders Research (76 papers)Glycogen Storage Diseases and Myoclonus (56 papers)Carbohydrate Chemistry and Synthesis (48 papers)
Cited by: Rheumatology Physiology Organic Chemistry
Journals: Journal of Biological Chemistry Journal of Clinical Investigation The EMBO Journal
Partner nations: Netherlands United Kingdom Japan

In The Last Decade

Marian A. Kroos

88 papers receiving 3.5k citations

Peers

Countries citing papers authored by Marian A. Kroos

Since Specialization

Citations

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

Fields of papers citing papers by Marian A. Kroos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marian A. Kroos. 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 Marian A. Kroos. The network helps show where Marian A. Kroos may publish in the future.

Co-authorship network of co-authors of Marian A. Kroos

This figure shows the co-authorship network connecting the top 25 collaborators of Marian A. Kroos. A scholar is included among the top collaborators of Marian A. Kroos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marian A. Kroos. Marian A. Kroos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays 2019 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),Marianne Hoogeveen‐Westerveld,Marian A. Kroos,Sirpa Ala‐Mello,Olga Amaral,Clara Sá-Miranda,Irene Mavridou,Helen Michelakakis,K Naess,Frans W. Verheijen,Lies H. Hoefsloot,Trijnie Dijkhuizen,(unknown),(unknown),Ans T. van der Ploeg,W.W.M. Pim Pijnappel,Jasper J. Saris,Dicky Halley	8
2	Childhood Pompe disease: clinical spectrum and genotype in 31 patients 2016 ·Orphanet Journal of Rare Diseases ·Carine I. van Capelle,Jan C. van der Meijden,Johanna M. P. van den Hout,Jaak Jaeken,Martina Baethmann,Thomas Voit,Marian A. Kroos,Terry G. J. Derks,M. Estela Rubio‐Gozalbo,Michèl A.A.P. Willemsen,Robin Lachmann,Eugen Mengel,Helen Michelakakis,J. C. de Jongste,Arnold Reuser,Ans T. van der Ploeg	47
3	Identification and Characterization of Aberrant Splicing in Pompe Disease Using a Generic Approach 2015 ·Journal of Neuromuscular Diseases ·Atze J. Bergsma,Marian A. Kroos,Marianne Hoogeveen‐Westerveld,Dicky Halley,Ans T. van der Ploeg,W.W.M. Pim Pijnappel	1
4	T.P.19 2014 ·Neuromuscular Disorders ·Juna M. de Vries,(unknown),Marianne Hoogeveen‐Westerveld,Stephan C.A. Wens,Marian A. Kroos,Michelle E. Kruijshaar,Pieter A. van Doorn,Ans T. van der Ploeg,W.W.M. Pim Pijnappel	1
5	Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study 2012 ·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,(unknown),Jan J.G.M. Verschuuren,Arnold Reuser,Ans T. van der Ploeg,Pieter A. van Doorn	111
6	The genotype–phenotype correlation in Pompe disease 2012 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marian A. Kroos,Marianne Hoogeveen‐Westerveld,Ans van der Ploeg,Arnold Reuser	93
7	Remarkably low fibroblast acid α-glucosidase activity in three adults with Pompe disease 2012 ·Molecular Genetics and Metabolism ·Stephan C.A. Wens,Marian A. Kroos,Juna M. de Vries,Marianne Hoogeveen‐Westerveld,Mark Wijgerde,Pieter A. van Doorn,Ans T. van der Ploeg,Arnold Reuser	4
8	Identification and Functional Characterization of GAA Mutations in Colombian Patients Affected by Pompe Disease 2012 ·JIMD Reports ·(unknown),Heidi Mateus,Dora Janeth Fonseca,Marian A. Kroos,(unknown),Juan Fernando Mejía,(unknown),Arnold Reuser,Paul Laissue	10
9	Improved assay for differential diagnosis between Pompe disease and acid α-glucosidase pseudodeficiency on dried blood spots 2011 ·Molecular Genetics and Metabolism ·(unknown),(unknown),(unknown),Kimitoshi Nakamura,Fumio Endo,Torayuki Okuyama,Hiroaki Takeuchi,Marian A. Kroos,Frans W. Verheijen,Arnold Reuser,Toshika Okumiya	24
10	Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities 2008 ·Journal of the Neurological Sciences ·Nadine A. M. E. van der Beek,Osama Soliman,Carine I. van Capelle,Marcel L. Geleijnse,W. B. Vletter,Marian A. Kroos,Arnold Reuser,Ingrid M.E. Frohn-Mulder,Pieter A. van Doorn,Ans T. van der Ploeg	23
11	A new diagnostic assay for glycogen storage disease type II in mixed leukocytes 2005 ·Molecular Genetics and Metabolism ·Toshika Okumiya,J. L. M. Keulemans,Marian A. Kroos,Nadine A. M. E. van der Beek,(unknown),Hiroaki Takeuchi,Otto P. van Diggelen,Arnold Reuser	58
12	Glycogen storage disease type II: Genetic and biochemical analysis of novel mutations in infantile patients from Turkish ancestry 1998 ·Human Mutation ·M M Hermans,Marian A. Kroos,Jan A. M. Smeitink,Ans T. van der Ploeg,Wim J. Kleijer,Arnold Reuser	18
13	Two extremes of the clinical spectrum of glycogen storage disease type II in one family: A matter of genotype 1997 ·Human Mutation ·Marian A. Kroos,(unknown),Otto P. van Diggelen,Wim J. Kleijer,Arnold Reuser	17
14	Mutation Detection in Glycogen Storage Disease Type II by RT-PCR and Automated Sequencing 1997 ·Biochemical and Biophysical Research Communications ·M M Hermans,Dik van Leenen,Marian A. Kroos,Arnold Reuser	21
15	Expression of cDNA-encoded human acid α-glucosidase in milk of transgenic mice 1996 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·A. G. A. Bijvoet,Marian A. Kroos,Frank Pieper,Herman A. de Boer,Arnold Reuser,Ans T. van der Ploeg,Martin Ph. Verbeet	23
16	Homozygous deletion of exon 18 leads to degradation of the lysosomal α‐glucosidase precursor and to the infantile form of glycogen storage disease type II 1996 ·Clinical Genetics ·(unknown),Marian A. Kroos,(unknown),Jan A. M. Smeitink,Wim J. Kleijer,Hans Kristian Ploos van Amstel,Arnold Reuser	7
17	Glycogenosis type II (acid maltase deficiency) 1995 ·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	132
18	Genotype‐phenotype correlation in adult‐onset acid maltase deficiency 1995 ·Annals of Neurology ·John H. J. Wokke,Margreet G.E.M. Ausems,Marie‐José H. van den Boogaard,Elly F. Ippel,(unknown),Marian A. Kroos,(unknown),F.G.I. Jennekens,Arnold Reuser,Hans Kristian Ploos van Amstel	60
19	Intravenous administration of phosphorylated acid alpha-glucosidase leads to uptake of enzyme in heart and skeletal muscle of mice. 1991 ·Journal of Clinical Investigation ·Ans T. van der Ploeg,Marian A. Kroos,Rob Willemsen,Nicolaas H. C. Brons,Arnold Reuser	63
20	Rat Heart Perfusion as Model System for Enzyme Replacement Therapy in Glycogenosis Type II 1990 ·Pediatric Research ·Ans T. van der Ploeg,(unknown),Rob Willemsen,Marian A. Kroos,Maarten J. J. E. Loonen,J.F. Koster,Arnold Reuser	10

About Marian A. Kroos

Marian A. Kroos is a scholar working on Rheumatology, Physiology and Organic Chemistry, having authored 88 papers that have together received 3.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (76 papers), Glycogen Storage Diseases and Myoclonus (56 papers) and Carbohydrate Chemistry and Synthesis (48 papers). The work is most often cited by research in Rheumatology (1.9k citations), Physiology (2.8k citations) and Organic Chemistry (1.2k citations). Marian A. Kroos has collaborated with scholars based in Netherlands, United Kingdom and Japan. Frequent co-authors include Arnold Reuser, Ans T. van der Ploeg, M M Hermans, Marianne Hoogeveen‐Westerveld, J. Van Beeumen, Ben A. Oostra, A. G. A. Bijvoet, Rob Willemsen, Martin Ph. Verbeet and J. M. Tager. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The EMBO Journal.

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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