Paul W.J. van Vught

2.7k citations

22 papers · 1.0k indexed · h-index 14

Neurology top 2%
- Amyotrophic Lateral Sclerosis Research 20
- Neurological diseases and metabolism 9
- Parkinson's Disease Mechanisms and Treatments 2
Genetics top 2%
- Neurogenetic and Muscular Disorders Research 16
Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 20
- Neurological diseases and metabolism 9
- Parkinson's Disease Mechanisms and Treatments 2
Cellular and Molecular Neuroscience top 10%
- Hereditary Neurological Disorders 2
Molecular Biology
- Cancer-related gene regulation 3
- Kruppel-like factors research 3
Organic Chemistry
- Synthetic Organic Chemistry Methods 1

Co-authors: Jan H. Veldink Leonard H. van den Berg Michael A. van Es Philip Van Damme Marka van Blitterswijk John H. J. Wokke Hylke M. Blauw Helenius J. Schelhaas
Cited by: Neurology Genetics
Journals: PLoS ONE (1 paper)Neurology (5 papers)Human Molecular Genetics (1 paper)
Partner nations: Netherlands Belgium Sweden

In The Last Decade

Paul W.J. van Vught

22 papers receiving 1000 citations

Peers

Countries citing papers authored by Paul W.J. van Vught

Since Specialization

Citations

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

Fields of papers citing papers by Paul W.J. van Vught

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul W.J. van Vught. 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 Paul W.J. van Vught. The network helps show where Paul W.J. van Vught may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Paul W.J. van Vught, 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 Paul W.J. van Vught Line = papers co-authored together Paul W.J. van Vught links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis Neurology Genetics ·Jeroen W. Bos,Ewout J. N. Groen,Renske I. Wadman,Chantall A.D. Curial,Naomi N. Molleman,Marinka Zegers,Paul W.J. van Vught,Reinier Snetselaar,Raymon Vijzelaar,W. Ludo van der Pol,Leonard H. van den Berg	2021	1
2	Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study PLoS ONE ·Wouter van Rheenen,Frank P. Diekstra,Oliver Harschnitz,Henk-Jan Westeneng,Kristel R. van Eijk,Christiaan G. J. Saris,Ewout J. N. Groen,Michael A. van Es,Hylke M. Blauw,Paul W.J. van Vught,Jan H. Veldink,Leonard H. van den Berg	2018	38
3	Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Christiaan G. J. Saris,Ewout J. N. Groen,Paul W.J. van Vught,Michael A. van Es,Hylke M. Blauw,Jan H. Veldink,Leonard H. van den Berg	2013	13
4	Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients Neurobiology of Aging ·Marka van Blitterswijk,Anna M. Blokhuis,Michael A. van Es,Paul W.J. van Vught,Paulina A. Rowicka,Helenius J. Schelhaas,Anneke J. van der Kooi,Marianne de Visser,Jan H. Veldink,Leonard H. van den Berg	2012	11
5	Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3 Neurobiology of Aging ·Max Koppers,Ewout J. N. Groen,Paul W.J. van Vught,Wouter van Rheenen,Esther Witteveen,Michael A. van Es,R. Jeroen Pasterkamp,Leonard H. van den Berg,Jan H. Veldink	2012	14
6	NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis Human Molecular Genetics ·Hylke M. Blauw,Wouter van Rheenen,Max Koppers,Philip Van Damme,Stefan Waibel,Robin Lemmens,Paul W.J. van Vught,Thomas Meyer,Claudia Schulte,Thomas Gasser,Edwin Cuppen,R. Jeroen Pasterkamp,Wim Robberecht,Albert C. Ludolph,Jan H. Veldink,Leonard H. van den Berg	2012	35
7	Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients Neurobiology of Aging ·Marka van Blitterswijk,Paul W.J. van Vught,Michael A. van Es,Helenius J. Schelhaas,Anneke J. van der Kooi,Marianne de Visser,Jan H. Veldink,Leonard H. van den Berg	2011	50
8	VCP mutations in familial and sporadic amyotrophic lateral sclerosis Neurobiology of Aging ·Max Koppers,Marka van Blitterswijk,Lotte Vlam,Paulina A. Rowicka,Paul W.J. van Vught,Ewout J. N. Groen,Wim G.M. Spliet,Joo-Yeon Engelen-Lee,Helenius J. Schelhaas,Marianne de Visser,Anneke J. van der Kooi,W. Ludo van der Pol,R. Jeroen Pasterkamp,Jan H. Veldink,Leonard H. van den Berg	2011	108
9	UNC13A is a modifier of survival in amyotrophic lateral sclerosis Neurobiology of Aging ·Frank P. Diekstra,Paul W.J. van Vught,Wouter van Rheenen,Max Koppers,R. Jeroen Pasterkamp,Michael A. van Es,Helenius J. Schelhaas,Marianne de Visser,Wim Robberecht,Philip Van Damme,Peter M. Andersen,Leonard H. van den Berg,Jan H. Veldink	2011	84
10	Multifocal motor neuropathy is not associated with genetic variation in PTPN22, BANK1, Blk, FCGR2B, CD1A/E, and TAG‐1 genes Journal of the Peripheral Nervous System ·Lotte Vlam,Elisabeth A. Cats,Meinie Seelen,Paul W.J. van Vught,Leonard H. van den Berg,W. Ludo van der Pol	2011	5
11	Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2 Neurology ·Philip Van Damme,Jan H. Veldink,Marka van Blitterswijk,Anniek Corveleyn,Paul W.J. van Vught,Vincent Thijs,Bénédicte Dubois,Gert Matthijs,Leonard H. van den Berg,Wim Robberecht	2011	131
12	FUS Mutations in Familial Amyotrophic Lateral Sclerosis in the Netherlands Archives of Neurology ·Ewout J. N. Groen,Michael A. van Es,Paul W.J. van Vught,Wim G.M. Spliet,Jooyeon van Engelen-Lee,Marianne de Visser,John H. J. Wokke,Helenius J. Schelhaas,Roel A. Ophoff,Katsumi Fumoto,R. Jeroen Pasterkamp,Dennis Dooijes,Edwin Cuppen,Jan H. Veldink,Leonard H. van den Berg	2010	66
13	Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients BMC Genomics ·Christiaan G. J. Saris,Steve Horvath,Paul W.J. van Vught,Michael A. van Es,Hylke M. Blauw,Tova F Fuller,Peter Langfelder,Joseph DeYoung,John H. J. Wokke,Jan H. Veldink,Leonard H. van den Berg,Roel A. Ophoff	2009	139
14	DPP6 IS ASSOCIATED WITH SUSCEPTIBILITY TO PROGRESSIVE SPINAL MUSCULAR ATROPHY Neurology ·Michael A. van Es,Paul W.J. van Vught,G. van Kempen,Hylke M. Blauw,Jan H. Veldink,Leonard H. van den Berg	2009	8
15	Analysis ofFGGYas a risk factor for sporadic amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis ·Michael A. van Es,Paul W.J. van Vught,Jan H. Veldink,Peter M. Andersen,Anna Birve,Robin Lemmens,Simon Cronin,Anneke J. van der Kooi,Marianne de Visser,Helenius J. Schelhaas,Orla Hardiman,Jiannis Ragoussis,Diether Lambrechts,Wim Robberecht,John H. J. Wokke,Roel A. Ophoff,Leonard H. van den Berg	2009	14
16	Progranulin genetic variability contributes to amyotrophic lateral sclerosis Neurology ·Kristel Sleegers,Nathalie Brouwers,Sebastian Maurer‐Stroh,Michael A. van Es,Philip Van Damme,Paul W.J. van Vught,Julie van der Zee,Sally Serneels,Tim De Pooter,Marleen Van den Broeck,Marc Cruts,Joost Schymkowitz,Peter De Jonghe,Frédéric Rousseau,Leonard H. van den Berg,Wim Robberecht,Christine Van Broeckhoven	2008	128
17	Pharmacokinetics of riluzole: evidence for glucuronidation as a major metabolic pathway not associated with UGT1A1 genotype Biopharmaceutics & Drug Disposition ·H. J. M. van Kan,Leonard H. van den Berg,Geert Jan Groeneveld,R.J.H.M. van der Straaten,Paul W.J. van Vught,Loraine Lie‐A‐Huen,Henk‐Jan Guchelaar	2007	9
18	Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis Neuromuscular Disorders ·Paul W.J. van Vught,Joost Van Wijk,Ted Bradley,Dagmar Plasmans,Marja E. Jakobs,Jan H. Veldink,J.M.B.V. de Jong,Leonard H. van den Berg,Frank Baas	2007	5
19	The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population Archives of Neurology ·Nadia A. Sutedja,Richard J. Sinke,Paul W.J. van Vught,Michiel W. van der Linden,John H. J. Wokke,Cornelia M. van Duijn,Omer T. Njajou,Yvonne T. van der Schouw,Jan H. Veldink,Leonard H. van den Berg	2007	61
20	Lack of association between VEGF polymorphisms and ALS in a Dutch population Neurology ·Paul W.J. van Vught,Nadia A. Sutedja,Jan H. Veldink,B. Koeleman,Geert Jan Groeneveld,Cisca Wijmenga,Bernard M.J. Uitdehaag,J.M.B.V. de Jong,Frank Baas,John H. J. Wokke,Leonard H. van den Berg	2005	40

About Paul W.J. van Vught

Paul W.J. van Vught is a scholar working on Genetics, Neurology and Neurology, having authored 22 papers that have together received 1.0k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (20 papers), Neurogenetic and Muscular Disorders Research (16 papers), Neurological diseases and metabolism (9 papers), Cancer-related gene regulation (3 papers), Kruppel-like factors research (3 papers), Hereditary Neurological Disorders (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers) and Synthetic Organic Chemistry Methods (1 paper). The work is most often cited by research in Neurology (732 citations), Genetics (439 citations) and Neurology (254 citations). Paul W.J. van Vught has collaborated with scholars based in Netherlands, Belgium and Sweden. Frequent co-authors include Jan H. Veldink, Leonard H. van den Berg, Michael A. van Es, Leonard H. van den Berg, Philip Van Damme, Marka van Blitterswijk, John H. J. Wokke, Hylke M. Blauw, Helenius J. Schelhaas and Marianne de Visser. Their work appears in journals such as PLoS ONE, Neurology and Human Molecular 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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