Veerle Van Gerwen

2.0k citations

18 papers · 884 indexed · h-index 11

Cellular and Molecular Neuroscience top 5%
Molecular Biology
Cell Biology top 5%
Radiology, Nuclear Medicine and Imaging top 10%
Neurology top 5%

Co-authors: Vincent Timmerman Peter De Jonghe Els De Vriendt Nathalie Verpoorten An Jacobs Kristien Verhoeven Michaela Auer‐Grumbach Hans‐Peter Hartung
Topics: Hereditary Neurological Disorders (8 papers)Corneal Surgery and Treatments (7 papers)Connexins and lens biology (3 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Cell Biology
Journals: Brain Neurology The American Journal of Human Genetics
Partner nations: Belgium Netherlands Austria

In The Last Decade

Veerle Van Gerwen

18 papers receiving 866 citations

Peers

Countries citing papers authored by Veerle Van Gerwen

Since Specialization

Citations

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

Fields of papers citing papers by Veerle Van Gerwen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veerle Van Gerwen. 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 Veerle Van Gerwen. The network helps show where Veerle Van Gerwen may publish in the future.

Co-authorship network of co-authors of Veerle Van Gerwen

This figure shows the co-authorship network connecting the top 25 collaborators of Veerle Van Gerwen. A scholar is included among the top collaborators of Veerle Van Gerwen 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 Veerle Van Gerwen. Veerle Van Gerwen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Belgian Endothelial Surgical Transplant of the Cornea (BEST cornea) protocol: clinical and patient-reported outcomes of Ultra-Thin Descemet Stripping Automated Endothelial Keratoplasty (UT-DSAEK) versus Descemet Membrane Endothelial Keratoplasty (DMEK) – a multicentric, randomised, parallel group pragmatic trial in corneal endothelial decompensation 2023 ·BMJ Open ·Sorcha Ní Dhubhghaill,(unknown),Ilse Claerhout,(unknown),(unknown),(unknown),Manon Huizing,(unknown),(unknown),Silke Oellerich,(unknown),(unknown),Bert Van den Bogerd,Veerle Van Gerwen,(unknown),Robert P. L. Wisse,Kristien Wouters,Bernard Duchesne,Carina Koppen	1
2	The importance of the epithelial fibre cell interface to lens regeneration in an in vivo rat model and in a human bag-in-the-lens (BiL) sample 2021 ·Experimental Eye Research ·Weiju Wu,Noemi Lois,Alan R. Prescott,Adrian P. Brown,Veerle Van Gerwen,Marie‐José Tassignon,Shane A. Richards,Christopher D. Saunter,Miguel Jarrı́n,Roy A. Quinlan	4
3	Pterygium Pathology: A Prospective Case-Control Study on Tear Film Cytokine Levels 2019 ·Mediators of Inflammation ·(unknown),Michel Haagdorens,Ella Roelant,J. Rozema,(unknown),Veerle Van Gerwen,(unknown),Veva De Groot,Sorcha Ní Dhubhghaill,Carina Koppen,Nadia Zakaria	15
4	Corneal epithelial restoration after penetrating keratoplasty in repeated failed cultivated limbal stem cell grafts 2019 ·VUBIR (Vrije Universiteit Brussel) ·(unknown),Carina Koppen,Veerle Van Gerwen,Marie‐José Tassignon,Sorcha Ní Dhubhghaill	3
5	Proteomic analysis of posterior capsular plaques in congenital unilateral cataract 2018 ·Acta Ophthalmologica ·Jan Van Looveren,Veerle Van Gerwen,(unknown),Kris Laukens,Geert Baggerman,Marie‐José Tassignon	3
6	A method for quantifying limbal stem cell niches using OCT imaging 2017 ·British Journal of Ophthalmology ·Michel Haagdorens,(unknown),J. Rozema,Veerle Van Gerwen,(unknown),Sorcha Ní Dhubhghaill,Marie‐José Tassignon,Nadia Zakaria	24
7	Xeno-Free Cultivation of Mesenchymal Stem Cells From the Corneal Stroma 2017 ·Investigative Ophthalmology & Visual Science ·(unknown),Sorcha Ní Dhubhghaill,Veerle Van Gerwen,Nadia Zakaria	16
8	Immunohistochemical characteristics of the vitreolenticular interface in congenital unilateral posterior cataract 2016 ·Journal of Cataract & Refractive Surgery ·Jan Van Looveren,Veerle Van Gerwen,Jean‐Pierre Timmermans,Marie‐José Tassignon	7
9	Limbal Stem Cell Deficiency: Current Treatment Options and Emerging Therapies 2015 ·Stem Cells International ·Michel Haagdorens,(unknown),Veerle Van Gerwen,Sorcha Ní Dhubhghaill,Carina Koppen,Marie‐José Tassignon,Nadia Zakaria	130
10	A Novel Fish Scale Derived Scaffold for Ocular Reconstruction 2013 ·Investigative Ophthalmology & Visual Science ·(unknown),Nadia Zakaria,Veerle Van Gerwen,Shih-Cheng Chen,(unknown),(unknown),(unknown)	1
11	Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV 2005 ·Neuromuscular Disorders ·Nathalie Verpoorten,Kristl G. Claeys,Liesbet Deprez,An Jacobs,Veerle Van Gerwen,Lieven Lagae,Willem F. Arts,Linda De Meırleır,Kathelijn Keymolen,Chantal Ceuterick‐de Groote,Peter De Jonghe,Vincent Timmerman,Eva Nelis	25
12	Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene 2004 ·Neurology ·Nisrine Bissar‐Tadmouri,Eva Nelis,Stephan Züchner,Yeşim Parman,Feza Deymeer,(unknown),Peter De Jonghe,Veerle Van Gerwen,Vincent Timmerman,(unknown),Esra Battaloğlu	11
13	SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I 2004 ·Neurology ·K. Verhoeven,Katrien Coen,Els De Vriendt,Alice K. Jacobs,Veerle Van Gerwen,(unknown),A Pou-Serradell,(unknown),Vincent Timmerman,Peter De Jonghe	33
14	Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10 2003 ·The American Journal of Human Genetics ·Kristien Verhoeven,Peter De Jonghe,Tom Van de Putte,Eva Nelis,An Zwijsen,Nathalie Verpoorten,Els De Vriendt,An Jacobs,Veerle Van Gerwen,Annick Francis,C. Ceuterick,Danny Huylebroeck,Vincent Timmerman	90
15	Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy 2003 ·The American Journal of Human Genetics ·Kristien Verhoeven,Peter De Jonghe,Katrien Coen,Nathalie Verpoorten,Michaela Auer‐Grumbach,Jennifer M. Kwon,David Fitzpatrick,Eric Schmedding,Els De Vriendt,An Jacobs,Veerle Van Gerwen,Klaus Wagner,Hans‐Peter Hartung,Vincent Timmerman	351
16	Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? 2002 ·Brain ·Peter De Jonghe,Michaela Auer‐Grumbach,Joy Irobi,Klaus Wagner,Barbara Plecko,Marina Kennerson,Danqing Zhu,Els De Vriendt,Veerle Van Gerwen,Garth A. Nicholson,Hans‐Peter Hartung,Vincent Timmerman	57
17	Mutations in GDAP1 2002 ·Neurology ·Eva Nelis,Sevim Erdem‐Özdamar,Peter Van den Bergh,(unknown),C. Ceuterick,Veerle Van Gerwen,Ana Cuesta,Laia Pedrola,Francesc Palau,A.A.W.M. Gabreëls‐Festen,Christine Verellen,Ersin Tan,Mehmet Demirci,Christine Van Broeckhoven,Peter De Jonghe,Haluk Topaloğlu,Vincent Timmerman	110
18	Homozygosity mapping of families with recessive Charcot-Marie-Tooth neuropathies 2001 ·Eva Nelis,Joy Irobi,Els De Vriendt,Veerle Van Gerwen,Claudina Pérez-Novo,Haluk Topaloğlu,Michaela Auer‐Grumbach,Luciano Merlini,Marcello Villanova,Albena Jordanova,Peter De Jonghe,Vincent Timmerman	3

About Veerle Van Gerwen

Veerle Van Gerwen is a scholar working on Ophthalmology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging, having authored 18 papers that have together received 884 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (8 papers), Corneal Surgery and Treatments (7 papers) and Connexins and lens biology (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (413 citations), Neurology (158 citations) and Cell Biology (252 citations). Veerle Van Gerwen has collaborated with scholars based in Belgium, Netherlands and Austria. Frequent co-authors include Vincent Timmerman, Peter De Jonghe, Els De Vriendt, Nathalie Verpoorten, An Jacobs, Kristien Verhoeven, Michaela Auer‐Grumbach, Hans‐Peter Hartung, Klaus Wagner and Sorcha Ní Dhubhghaill. Their work appears in journals such as Brain, Neurology and The American Journal of Human Genetics.

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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