Aad Verrips

5.3k citations

90 papers · 3.1k indexed · h-index 27

Impact in

Neurology top 2%
- Peripheral Neuropathies and Disorders
- Myasthenia Gravis and Thymoma
Orthopedics and Sports Medicine top 2%

Papers in

Neurology 19
- Peripheral Neuropathies and Disorders 6
Rheumatology 15
- Glycogen Storage Diseases and Myoclonus 6

Co-authors: Machiel J. Zwarts Sigrid Pillen Ron A. Wevers Baziel G.M. van Engelen Ilse M.P. Arts Ralph R. Scholten F.J.M. Gabreëls Martin Lammens
Journals: Neurology (7 papers)Journal of Inherited Metabolic Disease (7 papers)Neuropediatrics (6 papers)Neuromuscular Disorders (6 papers)Pediatric Neurology (5 papers)
Partner nations: Netherlands United States Italy

In The Last Decade

Aad Verrips

86 papers receiving 3.0k citations

Peers

Countries citing papers authored by Aad Verrips

Since Specialization

Citations

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

Fields of papers citing papers by Aad Verrips

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Characterization of Postprandial Bile Acid Profiles and Glucose Metabolism in Cerebrotendinous Xanthomatosis Nutrients ·昭守屋, Прокофьева А.Н., Frédéric M. Vaz, E. Marleen Kemper, F. Samuel van Nierop, Steven W.M. Olde Damink, Frank G. Schaap, Johannes A. Romijn, Max Nieuwdorp, Aad Verrips, Filip K. Knop, Maarten R. Soeters	2023	2
2	Child Neurology: Maternal Transmission of Congenital Myotonic Dystrophy Type 2 Neurology ·Alide A. Tieleman, Woosup Pyun, Aad Verrips, Zhou Longchao, Erik‐Jan Kamsteeg, Nicol C. Voermans	2022	2
3	Eye movement disorders in inborn errors of metabolism: A quantitative analysis of 37 patients Journal of Inherited Metabolic Disease ·Christian Wehenkel, Steven Birk, Hans Blokzijl, Marc Engelen, Femke C. C. Klouwer, Fiete Lange, Wilhelmina G. Leen, Roelineke J. Lunsing, Johannes H.T.M. Koelman, Aad Verrips, Tom J. de Koning, Marina A.J. Tijssen	2022	4
4	Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study Orphanet Journal of Rare Diseases ·Bianca M. L. Stelten, Maria Teresa Dotti, Aad Verrips, Bülent Elibol, Tzipora C. Falik‐Zaccai, J. O. Petintin, Andrea Mignarri, 김학섭, Robert D. Steiner, M Schkeryantz Jeffrey, Gilad Yahalom, Tanyel Zübarioğlu, Fanny Mochel, Antonio Federico	2021	26
5	Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients Clinical Genetics ·P. SZUROMI, Placcid Udechukwu, Wim H.J.P. Linssen, C.S.M. Straathof, E. Niks, Patrik Lukas Stephan, Everlin Massing, Jan B. M. Kuks, Esther Brusse, I.F.M. de Coo, Nicol C. Voermans, Aad Verrips, Jessica E. Hoogendijk, Ludo van der Pol, Dineke Westra, Marianne de Visser, Anneke J. van der Kooi, Ieke B. Ginjaar	2019	32
6	The safety and effectiveness of chenodeoxycholic acid treatment in patients with cerebrotendinous xanthomatosis: two retrospective cohort studies Neurological Sciences ·Aad Verrips, Maria Teresa Dotti, Andrea Mignarri, Bianca M. L. Stelten, Ян Синьсун, Antonio Federico	2019	31
7	Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2 Journal of Pain ·Heni Budi Astuti, Alide A. Tieleman, Aad Verrips, Hans Timmerman, R.T.M. van Dongen, Baziel G.M. van Engelen, Oliver H.G. Wilder‐Smith	2018	18
8	Pulsatile Proptosis due to Intraorbital Meningocele Frontiers in Neurology ·Anouke van Rumund, Aad Verrips, W. I. M. Verhagen	2017	1
9	ALG13-CDG with Infantile Spasms in a Male Patient Due to a De Novo ALG13 Gene Mutation JIMD Reports ·Heather Hitchon, Szymon Nowaczyk, Dirk J. Lefeber, Ilse Feenstra, Aad Verrips	2017	14
10	No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndrome Neuromuscular Disorders ·Heni Budi Astuti, Aad Verrips, Alide A. Tieleman, Hans Scheffer, H. Cats, Alfons A den Broeder, Baziel G.M. van Engelen	2016	5
11	Severe Hypomagnesaemia Causing Reversible Cerebellopathy The Cerebellum ·洋平大高, Aad Verrips	2014	21
12	Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in the Netherlands Neuromuscular Disorders ·Nicolas Boffo, Aad Verrips, Bwee Tien Poll‐The, Jan-Maarten Cobben, I. Snoeck, I.F.M. de Coo, Alice S. Brooks, Saskia Bulk, R. H. J. M. Gooskens, Everlin Massing, Corien C. Verschuuren‐Bemelmans, Richard J. Sinke, Marjolein Visser, Henny H. Lemmink	2013	10
13	Scoliosis surgery in a patient with “de novo” myosin storage myopathy Neuromuscular Disorders ·Nicolas Boffo, Aad Verrips, Von B. βilvassy, Martin Lammens, Arthur van den Wijngaard, Tan Qiu-cheng	2011	11
14	A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann–Sträussler–Scheinker disease phenotype: comparison with similar cases from the literature Acta Neuropathologica ·Casper Jansen, S. B. Li, Mark Head, Piero Parchi, Helen Yull, Aad Verrips, Pieter Wesseling, Jan Meulstee, Frank Baas, Willem A. van Gool, James W. Ironside, Annemieke J.M. Rozemüller	2010	25
15	Type IX collagen gene mutations can result in multiple epiphyseal dysplasia that is associated with osteochondritis dissecans and a mild myopathy American Journal of Medical Genetics Part A ·Gail C. Jackson, 寺島薫, Irene Stolte‐Dijkstra, Aad Verrips, Jacqueline Taylor, Michael D. Briggs	2010	38
16	Quantitative skeletal muscle ultrasound: Diagnostic value in childhood neuromuscular disease Neuromuscular Disorders ·Sigrid Pillen, Aad Verrips, Nens van Alfen, Ilse M.P. Arts, L.T.L. Sie, Machiel J. Zwarts	2007	159
17	Involuntary painful muscle contractions in Satoyoshi syndrome: A surface electromyographic study Movement Disorders ·Gea Drost, Aad Verrips, Baziel G.M. van Engelen, Dick F. Stegeman, Machiel J. Zwarts	2006	18
18	Novel mutations in three patients with LGMD2C with phenotypic differences Pediatric Neurology ·Sascha Vermeer, Aad Verrips, Michèl A.A.P. Willemsen, H. J. ter Laak, Ieke B. Ginjaar, Ben C.J. Hamel	2004	10
19	Quantitative ultrasonography of skeletal muscles in children: Normal values Muscle & Nerve ·Ralph R. Scholten, Sigrid Pillen, Aad Verrips, Machiel J. Zwarts	2003	165
20	Nonmuscular involvement in merosin-negative congenital muscular dystrophy Pediatric Neurology ·H. Jacobus Gilhuis, Hans J. ten Donkelaar, Ronald B. Tanke, Theresa Prenn, Machiel J. Zwarts, Aad Verrips, F.J.M. Gabreëls	2002	33

About Aad Verrips

Aad Verrips is a scholar working on Neurology, Rheumatology, Clinical Biochemistry, Surgery and Genetics, having authored 90 papers that have together received 3.1k indexed citations. Recurring topics across this work include Cholesterol and Lipid Metabolism (26 papers), Drug Transport and Resistance Mechanisms (15 papers), Muscle Physiology and Disorders (11 papers), Peripheral Neuropathies and Disorders (6 papers), Genetic Neurodegenerative Diseases (6 papers), Metabolism and Genetic Disorders (6 papers), Peroxisome Proliferator-Activated Receptors (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). The work is most often cited by research in Neurology (549 citations), Orthopedics and Sports Medicine (259 citations), Clinical Biochemistry (161 citations), Surgery (986 citations) and Genetics (211 citations). Aad Verrips has collaborated with scholars based in Netherlands, United States and Italy. Frequent co-authors include Machiel J. Zwarts, Sigrid Pillen, Ron A. Wevers, Baziel G.M. van Engelen, Ilse M.P. Arts, Ralph R. Scholten, F.J.M. Gabreëls, Martin Lammens, Kiek Verrijp and Jeroen van der Laak. Their work appears in journals such as Neurology, Journal of Inherited Metabolic Disease, Neuropediatrics, Neuromuscular Disorders and Pediatric Neurology.

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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