Marian A. Kroos

5.0k citations

88 papers · 3.6k indexed · h-index 36

Rheumatology top 0.2%
- Glycogen Storage Diseases and Myoclonus 56
Physiology top 0.5%
- Lysosomal Storage Disorders Research 76
Organic Chemistry top 2%
- Carbohydrate Chemistry and Synthesis 48
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 5
Physiology top 2%
- Lysosomal Storage Disorders Research 76
Epidemiology
- Trypanosoma species research and implications 12
Molecular Biology
- Glycosylation and Glycoproteins Research 10
- Biochemical and Molecular Research 10
Cell Biology
- Cellular transport and secretion 7

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
Cited by: Rheumatology Physiology Organic Chemistry
Journals: Journal of Biological Chemistry (5 papers)Journal of Clinical Investigation (2 papers)The EMBO Journal (1 paper)
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

The 25 scholars most cited alongside Marian A. Kroos, 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 Marian A. Kroos Line = papers co-authored together Marian A. Kroos links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays European Journal of Human Genetics ·Ineke Labrijn-Marks,Galhana M. Somers‐Bolman,Stijn L. M. In ’t Groen,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,Marloes Benjamins,Hannerieke J. M. van den Hout,Ans T. van der Ploeg,W.W.M. Pim Pijnappel,Jasper J. Saris,Dicky Halley	2019	8
2	Childhood Pompe disease: clinical spectrum and genotype in 31 patients 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	2016	47
3	Identification and Characterization of Aberrant Splicing in Pompe Disease Using a Generic Approach 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	2015	1
4	T.P.19 Neuromuscular Disorders ·Juna M. de Vries,Esther Kuperus,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	2014	1
5	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
6	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
7	Remarkably low fibroblast acid α-glucosidase activity in three adults with Pompe disease 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	2012	4
8	Identification and Functional Characterization of GAA Mutations in Colombian Patients Affected by Pompe Disease JIMD Reports ·Monica Y. Niño,Heidi Mateus,Dora Janeth Fonseca,Marian A. Kroos,Sandra Yaneth Ospina,Juan Fernando Mejía,Alfredo Uribe,Arnold Reuser,Paul Laissue	2012	10
9	Improved assay for differential diagnosis between Pompe disease and acid α-glucosidase pseudodeficiency on dried blood spots Molecular Genetics and Metabolism ·Shohei Shigeto,Tatsuya Katafuchi,Yuya Okada,Kimitoshi Nakamura,Fumio Endo,Torayuki Okuyama,Hiroaki Takeuchi,Marian A. Kroos,Frans W. Verheijen,Arnold Reuser,Toshika Okumiya	2011	24
10	Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities 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	2008	23
11	A new diagnostic assay for glycogen storage disease type II in mixed leukocytes Molecular Genetics and Metabolism ·Toshika Okumiya,J. L. M. Keulemans,Marian A. Kroos,Nadine A. M. E. van der Beek,Marijke A. Boer,Hiroaki Takeuchi,Otto P. van Diggelen,Arnold Reuser	2005	58
12	Glycogen storage disease type II: Genetic and biochemical analysis of novel mutations in infantile patients from Turkish ancestry Human Mutation ·M M Hermans,Marian A. Kroos,Jan A. M. Smeitink,Ans T. van der Ploeg,Wim J. Kleijer,Arnold Reuser	1998	18
13	Two extremes of the clinical spectrum of glycogen storage disease type II in one family: A matter of genotype Human Mutation ·Marian A. Kroos,Magna Van der Kraan,Otto P. van Diggelen,Wim J. Kleijer,Arnold Reuser	1997	17
14	Mutation Detection in Glycogen Storage Disease Type II by RT-PCR and Automated Sequencing Biochemical and Biophysical Research Communications ·M M Hermans,Dik van Leenen,Marian A. Kroos,Arnold Reuser	1997	21
15	Expression of cDNA-encoded human acid α-glucosidase in milk of transgenic mice 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	1996	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 Clinical Genetics ·Margreet G. E. M. Ausems,Marian A. Kroos,Magna Van der Kraan,Jan A. M. Smeitink,Wim J. Kleijer,Hans Kristian Ploos van Amstel,Arnold Reuser	1996	7
17	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
18	Genotype‐phenotype correlation in adult‐onset acid maltase deficiency Annals of Neurology ·John H. J. Wokke,Margreet G.E.M. Ausems,Marie‐José H. van den Boogaard,Elly F. Ippel,Otto van Diggelen,Marian A. Kroos,M. Boer,F.G.I. Jennekens,Arnold Reuser,Hans Kristian Ploos van Amstel	1995	60
19	Intravenous administration of phosphorylated acid alpha-glucosidase leads to uptake of enzyme in heart and skeletal muscle of mice. Journal of Clinical Investigation ·Ans T. van der Ploeg,Marian A. Kroos,Rob Willemsen,Nicolaas H. C. Brons,Arnold Reuser	1991	63
20	Rat Heart Perfusion as Model System for Enzyme Replacement Therapy in Glycogenosis Type II Pediatric Research ·Ans T. van der Ploeg,A M M van der Kraaij,Rob Willemsen,Marian A. Kroos,Maarten J. J. E. Loonen,J.F. Koster,Arnold Reuser	1990	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), Carbohydrate Chemistry and Synthesis (48 papers), Trypanosoma species research and implications (12 papers), Glycosylation and Glycoproteins Research (10 papers), Biochemical and Molecular Research (10 papers), Cellular transport and secretion (7 papers) and Metabolism and Genetic Disorders (5 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.

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