Esmée Oussoren

1.2k citations

32 papers · 768 indexed · h-index 15

Co-authors: Ans T. van der Ploeg George J. G. Ruijter Marion M. Brands W.W.M. Pim Pijnappel Arnold Reuser Wim C.J. Hop Frank Baas P.A. Voûte
Topics: Lysosomal Storage Disorders Research (18 papers)Metabolism and Genetic Disorders (9 papers)Glycogen Storage Diseases and Myoclonus (8 papers)
Cited by: Physiology Clinical Biochemistry Rheumatology
Journals: Blood PLoS ONE Biochemical and Biophysical Research Communications
Partner nations: Netherlands United States Germany

In The Last Decade

Esmée Oussoren

32 papers receiving 752 citations

Peers

Countries citing papers authored by Esmée Oussoren

Since Specialization

Citations

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

Fields of papers citing papers by Esmée Oussoren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esmée Oussoren

This figure shows the co-authorship network connecting the top 25 collaborators of Esmée Oussoren. A scholar is included among the top collaborators of Esmée Oussoren 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 Esmée Oussoren. Esmée Oussoren 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	Social cognition, emotion regulation and social competence in classical galactosemia patients without intellectual disability 2024 ·Acta Neuropsychiatrica ·(unknown),Gert J. Geurtsen,Carla E. M. Hollak,Mirian C. H. Janssen,Janneke G. Langendonk,(unknown),Esmée Oussoren,Kim J. Oostrom,Annet M. Bosch	1
2	Analysis of urinary oligosaccharide excretion patterns by UHPLC/HRAM mass spectrometry for screening of lysosomal storage disorders 2023 ·Journal of Inherited Metabolic Disease ·Marne C. Hagemeijer,(unknown),(unknown),Edwin H. Jacobs,Johanna M. P. van den Hout,Esmée Oussoren,George J. G. Ruijter	5
3	Modeling cartilage pathology in mucopolysaccharidosis VI using iPSCs reveals early dysregulation of chondrogenic and metabolic gene expression 2022 ·Frontiers in Bioengineering and Biotechnology ·(unknown),(unknown),Esmée Oussoren,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Roberto Narcisi,(unknown)	4
4	Effect of Anti-Iduronate 2-Sulfatase Antibodies in Patients with Mucopolysaccharidosis Type II Treated with Enzyme Replacement Therapy 2022 ·The Journal of Pediatrics ·(unknown),Marianne Hoogeveen‐Westerveld,George J. G. Ruijter,(unknown),Esmée Oussoren,Ans T. van der Ploeg,W.W.M. Pim Pijnappel	1
5	Mucolipidosis type II and type III: a systematic review of 843 published cases 2021 ·Genetics in Medicine ·(unknown),(unknown),Martina Wilke,Serwet Demirdas,Nicole Muschol,Sandra Pohl,Jan C. van der Meijden,Dimitris Rizopoulos,Ans T. van der Ploeg,Esmée Oussoren	15
6	Using Out-of-Batch Reference Populations to Improve Untargeted Metabolomics for Screening Inborn Errors of Metabolism 2020 ·Metabolites ·(unknown),(unknown),Serwet Demirdas,Edwin H. Jacobs,Esmée Oussoren,Ans van der Ploeg,Margreet A. E. M. Wagenmakers,Robert M.W. Hofstra,Henk J. Blom,Marcel Reinders,George J. G. Ruijter	12
7	Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor 2020 ·Blood ·Saskia B. Wortmann,Johan L.K. Van Hove,Terry G. J. Derks,Nathalie Chevalier,Vijaya Knight,Andreas Koller,Esmée Oussoren,Johannes A. Mayr,Francjan J. van Spronsen,Florian B. Lagler,Sommer Gaughan,Emile Van Schaftingen,Maria Veiga‐da‐Cunha	93
8	A Generic Assay to Detect Aberrant ARSB Splicing and mRNA Degradation for the Molecular Diagnosis of MPS VI 2020 ·Molecular Therapy — Methods & Clinical Development ·(unknown),(unknown),(unknown),Esmée Oussoren,(unknown),Atze J. Bergsma,Ans T. van der Ploeg,W.W.M. Pim Pijnappel	8
9	Classical galactosemia: neuropsychological and psychosocial functioning beyond intellectual abilities 2020 ·Orphanet Journal of Rare Diseases ·(unknown),Kim J. Oostrom,(unknown),Carla E. M. Hollak,Mirian C. H. Janssen,Janneke G. Langendonk,Esmée Oussoren,M. Estela Rubio‐Gozalbo,Maaike de Vries,Gert J. Geurtsen,Annet M. Bosch	13
10	Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease 2020 ·Molecular Therapy — Methods & Clinical Development ·(unknown),(unknown),(unknown),Esmée Oussoren,Ans T. van der Ploeg,W.W.M. Pim Pijnappel	63
11	Hip disease in Mucopolysaccharidoses and Mucolipidoses: A review of mechanisms, interventions and future perspectives 2020 ·Bone ·Esmée Oussoren,(unknown),Bianca Link,Jan C. van der Meijden,W.W.M. Pim Pijnappel,George J. G. Ruijter,Mirjam Langeveld,Ans T. van der Ploeg	10
12	Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcome 2020 ·Molecular Genetics and Metabolism ·(unknown),Anouk Schrantee,Matthan W.A. Caan,Carla E. M. Hollak,Mirian C. H. Janssen,Esmée Oussoren,Maaike C. de Vries,Stefan D. Roosendaal,Marc Engelen,Annet M. Bosch	9
13	A long term follow-up study of the development of hip disease in Mucopolysaccharidosis type VI 2017 ·Molecular Genetics and Metabolism ·Esmée Oussoren,J. H. J. M. Bessems,(unknown),Jan C. van der Meijden,(unknown),Iris Plug,Annick S. Devos,George J. G. Ruijter,Ans T. van der Ploeg,Mirjam Langeveld	8
14	A Multiplex Assay for the Diagnosis of Mucopolysaccharidoses and Mucolipidoses 2015 ·PLoS ONE ·Eveline J. Langereis,Tom Wagemans,Wim Kulik,Dirk J. Lefeber,Henk van Lenthe,Esmée Oussoren,Ans T. van der Ploeg,George J. G. Ruijter,Ron A. Wevers,Frits A. Wijburg,Naomi van Vlies	30
15	Genetic basis of alpha‐aminoadipic and alpha‐ketoadipic aciduria 2015 ·Journal of Inherited Metabolic Disease ·Jacob Hagen,Heleen te Brinke,Ronald J. A. Wanders,Alida C. Knegt,Esmée Oussoren,A. Jeannette M. Hoogeboom,George J. G. Ruijter,Daniel M. Becker,Karl Otfried Schwab,Ingo Franke,Marinus Durán,Hans R. Waterham,Jörn Oliver Sass,Sander M. Houten	44
16	Residual α-l-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients 2013 ·Molecular Genetics and Metabolism ·Esmée Oussoren,J. L. M. Keulemans,Otto P. van Diggelen,(unknown),(unknown),Ans T. van der Ploeg,George J. G. Ruijter	40
17	Up to five years experience with 11 mucopolysaccharidosis type VI patients 2013 ·Molecular Genetics and Metabolism ·Marion M. Brands,Esmée Oussoren,George J. G. Ruijter,(unknown),(unknown),Koen F. M. Joosten,Wim C.J. Hop,Iris Plug,Ans T. van der Ploeg	31
18	Mucopolysaccharidosis: Cardiologic features and effects of enzyme‐replacement therapy in 24 children with MPS I, II and VI 2012 ·Journal of Inherited Metabolic Disease ·Marion M. Brands,Ingrid M.E. Frohn-Mulder,M.L.C. Hagemans,Wim C.J. Hop,Esmée Oussoren,Willem A. Helbing,Ans T. van der Ploeg	60
19	Bone, joint and tooth development in mucopolysaccharidoses: Relevance to therapeutic options 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Esmée Oussoren,Marion M. Brands,George J. G. Ruijter,Ans T. van der Ploeg,Arnold Reuser	77
20	Molecular Cloning of Human MUC3 cDNA Reveals a Novel 59 Amino Acid Tandem Repeat Region 1997 ·Biochemical and Biophysical Research Communications ·B. Jan‐Willem van Klinken,(unknown),Esmée Oussoren,Hans A. Büller,Jan P. Dekker,Alexandra W. C. Einerhand	25

About Esmée Oussoren

Esmée Oussoren is a scholar working on Clinical Biochemistry, Physiology and Rheumatology, having authored 32 papers that have together received 768 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (18 papers), Metabolism and Genetic Disorders (9 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). The work is most often cited by research in Physiology (383 citations), Clinical Biochemistry (89 citations) and Rheumatology (166 citations). Esmée Oussoren has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Ans T. van der Ploeg, George J. G. Ruijter, Marion M. Brands, W.W.M. Pim Pijnappel, Arnold Reuser, Wim C.J. Hop, Frank Baas, P.A. Voûte, Erwin Pauws and Marjon van Groenigen. Their work appears in journals such as Blood, PLoS ONE and Biochemical and Biophysical Research Communications.

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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