Jan Meuleman

890 citations

21 papers · 514 indexed · h-index 10

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

Co-authors: Jan Wijnholds Anna Malysheva Inge Versteeg Serge A. van de Pavert Jan Klooster Mathias W. Seeliger Albena Kantardzhieva Christiaan N. Levelt
Topics: Signaling Pathways in Disease (8 papers)Hereditary Neurological Disorders (8 papers)Neurological diseases and metabolism (6 papers)
Cited by: Ophthalmology Cell Biology Neurology
Journals: Journal of Neuroscience Neurology Journal of Cell Science
Partner nations: Belgium Germany Netherlands

In The Last Decade

Jan Meuleman

21 papers receiving 506 citations

Peers

Countries citing papers authored by Jan Meuleman

Since Specialization

Citations

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

Fields of papers citing papers by Jan Meuleman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jan Meuleman

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	A Single Amino Acid Substitution (Cys249Trp) in Crb1 Causes Retinal Degeneration and Deregulates Expression of Pituitary Tumor Transforming GenePttg1 2007 ·Journal of Neuroscience ·Serge A. van de Pavert,Jan Meuleman,Anna Malysheva,Wendy M. Aartsen,Inge Versteeg,Felix Tonagel,Willem Kamphuis,Chris J. McCabe,Mathias W. Seeliger,Jan Wijnholds	69
2	Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Müller glia cells 2006 ·Human Molecular Genetics ·(unknown),Wendy M. Aartsen,Jan Meuleman,Jan Klooster,Anna Malysheva,Inge Versteeg,Jean‐Pierre Arsanto,(unknown),Jan Wijnholds	90
3	Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy 2004 ·Muscle & Nerve ·(unknown),Anja Schirmacher,Bernd Ringelstein,Peter Young,Giles D. Watts,Jan Meuleman,Eva Nelis,Phillip F. Chance,Vincent Timmerman,Florian Stögbauer,Gregor Kuhlenbäumer	1
4	Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure 2004 ·Journal of Cell Science ·Serge A. van de Pavert,Albena Kantardzhieva,Anna Malysheva,Jan Meuleman,Inge Versteeg,Christiaan N. Levelt,Jan Klooster,(unknown),Mathias W. Seeliger,Penny Rashbass,André Le Bivic,Jan Wijnholds	207
5	Crumbs homologue 1 in polarity and blindness 2004 ·Biochemical Society Transactions ·Jan Meuleman,Serge A. van de Pavert,Jan Wijnholds	12
6	[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]. 2002 ·PubMed ·(unknown),(unknown),María J. Téllez,(unknown),A. Löfgren,Jan Meuleman,Vincent Timmerman,Peter De Jonghe,C. Ceuterick,J. J. Martin	3
7	Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous 2002 ·Journal of the Peripheral Nervous System ·Gregor Kuhlenbäumer,Jan Meuleman,Peter De Jonghe,(unknown),Peter Young,(unknown),Christine Van Broeckhoven,Vincent Timmerman,Florian Stögbauer	1
8	Hereditary neuralgic amyotrophy 2001 ·Neurogenetics ·Jan Meuleman,Vincent Timmerman,Christine Van Broeckhoven,Peter De Jonghe	10
9	A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies 2001 ·Neuromuscular Disorders ·Jan Meuleman,A Pou-Serradell,A. Löfgren,C. Ceuterick,J. J. Martin,Vincent Timmerman,Christine Van Broeckhoven,Peter De Jonghe	19
10	Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies 2001 ·Neuroreport ·Koen J. T. Venken,Jan Meuleman,Joy Irobi,C. Ceuterick,Rudolf Martini,Peter De Jonghe,Vincent Timmerman	2
11	Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous 2001 ·Journal of Neurology ·Gregor Kuhlenbäumer,Jan Meuleman,Peter De Jonghe,(unknown),(unknown),(unknown),Christine Van Broeckhoven,Vincent Timmerman,Florian Stögbauer	15
12	Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA) 2001 ·Human Genetics ·Jan Meuleman,(unknown),Dominique Audenaert,(unknown),(unknown),Peter R. Young,Florian St�gbauer,E. Bernd Ringelstein,Christine Van Broeckhoven,Peter De Jonghe,Vincent Timmerman	7
13	Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3. 2001 ·PubMed ·Joy Irobi,Eva Nelis,Jan Meuleman,Koen J. T. Venken,Peter De Jonghe,Christine Van Broeckhoven,Vincent Timmerman	1
14	Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3 2001 ·Annals of Human Genetics ·Joy Irobi,Eva Nelis,Jan Meuleman,Koen J. T. Venken,Peter De Jonghe,Christine Van Broeckhoven,Vincent Timmerman	2
15	The natural history of hereditary neuralgic amyotrophy in the Dutch population. 2000 ·Neuromuscular Disorders ·(unknown),Peter De Jonghe,(unknown),Johan A. K. Suykens,A.A.W.M. Gabreëls‐Festen,(unknown),(unknown),Gregor Kuhlenbäumer,(unknown),Jan Meuleman,A Pou-Serradell,(unknown),Andrea Schenone,Florian Stögbauer,Vincent Timmerman,Nens van Alfen,Baziel G.M. van Engelen,Christine Van Broeckhoven	3
16	Molecular genetics of inherited peripheral neuropathies: who are the actors? 2000 ·PubMed ·Jan Meuleman,Vincent Timmerman,Eva Nelis,(unknown)	5
17	A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes 1999 ·Genomics ·Gregor Kuhlenbäumer,Anja Schirmacher,Jan Meuleman,Fadel Tissir,Jurgen Del‐Favero,Florian Stögbauer,Peter Young,Bernd Ringelstein,Christine Van Broeckhoven,Vincent Timmerman	14
18	Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate Genes 1999 ·Annals of the New York Academy of Sciences ·Jan Meuleman,Gregor Kuhlenbäumer,Anja Schirmacher,Manfred Wehnert,Peter Young,Florian Stögbauer,E B Ringelstein,Christine Van Broeckhoven,Vincent Timmerman	2
19	Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c‐myb ET‐locus in two families with hereditary neuralgic amyotrophy (HNA) 1998 ·Annals of Human Genetics ·Gregor Kuhlenbäeumer,Jan Meuleman,Anja Schirmacher,(unknown),E B Ringelstein,M Wehnert,Maria Hoeltzenbein,Christine Van Broeckhoven,Vincent Timmerman	8
20	Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q 1997 ·Neurology ·Manfred Wehnert,Vincent Timmerman,(unknown),Jan Meuleman,Eva Nelis,Christine Van Broeckhoven	20

About Jan Meuleman

Jan Meuleman is a scholar working on Neurology, Cellular and Molecular Neuroscience and Cell Biology, having authored 21 papers that have together received 514 indexed citations. Recurring topics across this work include Signaling Pathways in Disease (8 papers), Hereditary Neurological Disorders (8 papers) and Neurological diseases and metabolism (6 papers). The work is most often cited by research in Ophthalmology (132 citations), Cell Biology (166 citations) and Neurology (65 citations). Jan Meuleman has collaborated with scholars based in Belgium, Germany and Netherlands. Frequent co-authors include Jan Wijnholds, Anna Malysheva, Inge Versteeg, Serge A. van de Pavert, Jan Klooster, Mathias W. Seeliger, Albena Kantardzhieva, Christiaan N. Levelt, Vincent Timmerman and Wendy M. Aartsen. Their work appears in journals such as Journal of Neuroscience, Neurology and Journal of Cell Science.

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.

Explore authors with similar magnitude of impact