Inge Cuppen

1.9k citations

41 papers · 934 indexed · h-index 18

Genetics top 1%
- Neurogenetic and Muscular Disorders Research 25
Surgery top 10%
- Congenital Anomalies and Fetal Surgery 16
Molecular Biology
- RNA modifications and cancer 10
- Mitochondrial Function and Pathology 2
Microbiology
Speech and Hearing top 10%
Public Health, Environmental and Occupational Health
- Spinal Dysraphism and Malformations 7
Pediatrics, Perinatology and Child Health
- Fetal and Pediatric Neurological Disorders 5
- Prenatal Screening and Diagnostics 3
Psychiatry and Mental health
- Child Nutrition and Feeding Issues 2

Co-authors: W. Ludo van der Pol Renske I. Wadman Camiel A. Wijngaarde Louise Otto Marloes Stam Bart Bartels Fay‐Lynn Asselman Ruben P. A. van Eijk
Cited by: Genetics Surgery Molecular Biology
Journals: Journal of Neuromuscular Diseases (4 papers)Orphanet Journal of Rare Diseases (3 papers)Neurology (3 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Inge Cuppen

40 papers receiving 909 citations

Peers

Countries citing papers authored by Inge Cuppen

Since Specialization

Citations

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

Fields of papers citing papers by Inge Cuppen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Swallowing Problems in Spinal Muscular Atrophy Types 2 and 3: A Clinical, Videofluoroscopic and Ultrasound Study Journal of Neuromuscular Diseases ·Osorio Resendiz,Rutger A. J. Nievelstein,Ruben P. A. van Eijk,Fay‐Lynn Asselman,Corrie E. Erasmus,Inge Cuppen,Arnold J. N. Bittermann,Ellen Gerrits,W. Ludo van der Pol,L. van den Engel–Hoek	2023	9
2	Lung function decline preceding chronic respiratory failure in spinal muscular atrophy: a national prospective cohort study Orphanet Journal of Rare Diseases ·Esther S. Veldhoen,Camiel A. Wijngaarde,Ruben P. A. van Eijk,Fay‐Lynn Asselman,Chen Xiao-b,Louise Otto,Marloes Stam,Inge Cuppen,Renske I. Wadman,Lizbeth Johanna Chicaiza Guachi,Erik H.J. Hulzebos,José Subires Antúnez,Bart Bartels,Л. Г. Пасєка,Michael A. Gaytant,Cornelis K. van der Ent,W. Ludo van der Pol	2023	5
3	Longitudinal prospective cohort study to assess peripheral motor function with extensive electrophysiological techniques in patients with Spinal Muscular Atrophy (SMA): the SMA Motor Map protocol BMC Neurology ·Pitterman Martin,H. Stephan Goedee,Hessel Franssen,Fay‐Lynn Asselman,Bart Bartels,Inge Cuppen,Ruben P. A. van Eijk,Boudewijn T.H.M. Sleutjes,W. Ludo van der Pol,Renske I. Wadman	2023	5
4	Monitoring Nusinersen Treatment Effects in Children with Spinal Muscular Atrophy with Quantitative Muscle MRI Journal of Neuromuscular Diseases ·Louise Otto,Martijn Froeling,Ruben P. A. van Eijk,Renske I. Wadman,Inge Cuppen,後藤毅,Bart Bartels,Fay‐Lynn Asselman,Jeroen Hendrikse,W. Ludo van der Pol	2023	7
5	Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatment European Journal of Paediatric Neurology ·Bernd Kracke,Inge Cuppen,Shiwei Sui,Patrick Attard,Diane Lanteigne,Fay‐Lynn Asselman,Renske I. Wadman,Edward F. Knol,W. Ludo van der Pol,Ewout J. N. Groen	2022	8
6	Population-based assessment of nusinersen efficacy in children with spinal muscular atrophy: a 3-year follow-up study Brain Communications ·Bernd Kracke,Inge Cuppen,Ruben P. A. van Eijk,Camiel A. Wijngaarde,Marja Schoenmakers,後藤毅,Bart Bartels,Esther S. Veldhoen,Pablo De-Santiago-López,Ewout J. N. Groen,Fay‐Lynn Asselman,Renske I. Wadman,W. Ludo van der Pol	2022	23
7	Natural history of respiratory muscle strength in spinal muscular atrophy: a prospective national cohort study Orphanet Journal of Rare Diseases ·Esther S. Veldhoen,Camiel A. Wijngaarde,Erik H.J. Hulzebos,Roelie M. Wösten‐van Asperen,Renske I. Wadman,Ruben P. A. van Eijk,高黎力,Marloes Stam,Louise Otto,Inge Cuppen,Bernd Kracke,Assouik Jamal,Bart Bartels,Michael A. Gaytant,Cornelis K. van der Ent,W. Ludo van der Pol	2022	19
8	Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome Journal of Clinical Investigation ·Andres Ramirez-Martinez,Yichi Zhang,Marie-José van den Boogaard,John McAnally,Валентина Крамаренко,Andreas C. Chai,Francesco Chemello,Isreal Tamari,Inge Cuppen,Martin Elferink,Robert J.J. van Es,Nard G. Janssen,A. Jahangiri,Ning Liu,Rhonda Bassel‐Duby,Richard H. van Jaarsveld,Eric N. Olson	2022	17
9	Parents’ perspectives on nusinersen treatment for children with spinal muscular atrophy Developmental Medicine & Child Neurology ·张燃,Carin D. Schröder,Marjolijn Ketelaar,W. Ludo van der Pol,Inge Cuppen,Sha Yi-xian,Fay‐Lynn Asselman,Maarten J. Fischer,Johanna M. A. Visser‐Meily,Marijke C. Kars	2021	8
10	Prevalence of Bladder and Bowel Dysfunction in Duchenne Muscular Dystrophy Using the Childhood Bladder and Bowel Dysfunction Questionnaire Life ·K. Park,Imelda J. M. de Groot,Johanna M. Fock,Sylvia Klinkenberg,Desiree Vrijens,Anita Vreugdenhil,M. J. Dozio,Inge Cuppen,Bregje Jaeger,E. Niks,İrem Okman Koçoğlu,EzzatKhamis Amine,Frans Feron,Catharina G. Faber,Jos G.M. Hendriksen,Johan S.H. Vles	2021	10
11	Assessment of motor unit loss in patients with spinal muscular atrophy Clinical Neurophysiology ·Boudewijn T.H.M. Sleutjes,Camiel A. Wijngaarde,Renske I. Wadman,Louise Otto,Fay‐Lynn Asselman,Inge Cuppen,Leonard H. van den Berg,W. Ludo van der Pol,H. Stephan Goedee	2020	25
12	Natural history of lung function in spinal muscular atrophy Orphanet Journal of Rare Diseases ·Camiel A. Wijngaarde,Esther S. Veldhoen,Ruben P. A. van Eijk,Marloes Stam,Louise Otto,Fay‐Lynn Asselman,Roelie M. Wösten‐van Asperen,Erik H.J. Hulzebos,Assouik Jamal,Bart Bartels,Inge Cuppen,Renske I. Wadman,Leonard H. van den Berg,Cornelis K. van der Ent,W. Ludo van der Pol	2020	63
13	Deep intronic TIMMDC1 variant delays diagnosis of rapidly progressive complex I deficiency European Journal of Medical Genetics ·María Loreto Callejo-Goena,Debby M.E.I. Hellebrekers,Rutger A. J. Nievelstein,Peter M. van Hasselt,Richard H. van Jaarsveld,Inge Cuppen,Renske Oegema	2020	2
14	Protocol for a phase II, monocentre, double-blind, placebo-controlled, cross-over trial to assess efficacy of pyridostigmine in patients with spinal muscular atrophy types 2–4 (SPACE trial) BMJ Open ·Marloes Stam,Renske I. Wadman,Camiel A. Wijngaarde,Bart Bartels,Maria A Caruso,Louise Otto,H. Stephan Goedee,X. Liu,Janke F. de Groot,Marja Schoenmakers,Inge Cuppen,Leonard H. van den Berg,W. Ludo van der Pol	2018	32
15	Small Biparietal Diameter and Head Circumference Are Part of the Phenotype instead of Independent Prognostic Markers in Fetuses with Spinal Dysraphism Fetal Diagnosis and Therapy ·Inge Cuppen,Dagmar de Bruijn,Sevda Mohammadzadeh,Jan J. Rotteveel,Michèl A.A.P. Willemsen,J. M. G. van Vugt,Jaco W. Pasman,Nel Roeleveld	2014	4
16	Sprengel’s deformity and spinal dysraphism: connecting the shoulder and the spine Child s Nervous System ·Jasper van Aalst,J.S.H. Vles,Inge Cuppen,Deborah Sival,E. Niks,Lodewijk W. van Rhijn,Maurice A. M. Van Steensel,Erwin M. J. Cornips	2013	4
17	Motor evoked potentials and compound muscle action potentials as prognostic tools for neonates with spina bifida European Journal of Paediatric Neurology ·Inge Cuppen,Sevda Mohammadzadeh,Jan J. Rotteveel,Reinier A. Mullaart,Nel Roeleveld,Jaco W. Pasman	2012	3
18	Influence of birth mode on early neurological outcome in infants with myelomeningocele European Journal of Obstetrics & Gynecology and Reproductive Biology ·Inge Cuppen,Alex J. Eggink,F.K. Lotgering,Jan J. Rotteveel,Reinier A. Mullaart,Nel Roeleveld	2011	13
19	Treatment for neonatal neuralgic amyotrophy European Journal of Paediatric Neurology ·И. В. Калиновская,Inge Cuppen,Nens van Alfen,Jan J. Rotteveel	2008	4
20	Broncholithiasis in an immune compromised boy with disseminated Mycobacteriumkansasii Pediatric Pulmonology ·Inge Cuppen,Wiel C.M. de Lange,Siebold S.N. de Graaf,D. Scott Dixon,C. Boetes,J.L. Yntema	2007	7

About Inge Cuppen

Inge Cuppen is a scholar working on Genetics, Microbiology, Surgery, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 41 papers that have together received 934 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (25 papers), Congenital Anomalies and Fetal Surgery (16 papers), RNA modifications and cancer (10 papers), Spinal Dysraphism and Malformations (7 papers), Fetal and Pediatric Neurological Disorders (5 papers), Prenatal Screening and Diagnostics (3 papers), Child Nutrition and Feeding Issues (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (661 citations), Surgery (472 citations), Molecular Biology (404 citations), Microbiology (4 citations) and Speech and Hearing (29 citations). Inge Cuppen has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include W. Ludo van der Pol, Renske I. Wadman, Camiel A. Wijngaarde, Louise Otto, Marloes Stam, Bart Bartels, Fay‐Lynn Asselman, Ruben P. A. van Eijk, Marja Schoenmakers and Henny H. Lemmink. Their work appears in journals such as Journal of Neuromuscular Diseases, Orphanet Journal of Rare Diseases, Neurology, European Journal of Paediatric Neurology and Brain 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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