Eva Nelis

7.8k citations

73 papers · 4.2k indexed · h-index 31

Cellular and Molecular Neuroscience top 0.2%
- Hereditary Neurological Disorders 62
- Genetic Neurodegenerative Diseases 28
Neurology top 0.5%
- Neurological diseases and metabolism 17
- Botulinum Toxin and Related Neurological Disorders 10
Neurology top 0.5%
- Neurological diseases and metabolism 17
- Botulinum Toxin and Related Neurological Disorders 10
Cell Biology top 1%
- Cellular Mechanics and Interactions 7
- Hippo pathway signaling and YAP/TAZ 4
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 6
Molecular Biology
- Signaling Pathways in Disease 9

Co-authors: Christine Van Broeckhoven Vincent Timmerman Peter De Jonghe Peter Raeymaekers Neva E. Haites James R. Lupski A. Löfgren J. J. Martin
Cited by: Cellular and Molecular Neuroscience Neurology Cell Biology
Journals: Human Mutation (11 papers)Neurology (8 papers)Neuromuscular Disorders (7 papers)
Partner nations: Belgium United States Germany

In The Last Decade

Eva Nelis

70 papers receiving 4.1k citations

Peers

Countries citing papers authored by Eva Nelis

Since Specialization

Citations

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

Fields of papers citing papers by Eva Nelis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity Neuromuscular Disorders ·Jonathan Baets,Ines Dierick,Chantal Ceuterick‐de Groote,Jenneke van den Ende,N. Hayashi,Saheed Abidemi Bukola,Wim Robberecht,Eva Nelis,Vincent Timmerman,Peter De Jonghe	2009	8
2	Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy Brain ·Kristl G. Claeys,Stephan Züchner,Marina Kennerson,José Berciano,Abel Garcı́a Garcı́a,K. Verhoeven,Elsdon Storey,John Merory,H.M.E. Bienfait,Martin Lammens,Eva Nelis,Jonathan Baets,Els De Vriendt,Zwi Berneman,Ilse De Veuster,Jeffery M. Vance,Garth A. Nicholson,Vincent Timmerman,Peter De Jonghe	2009	62
3	Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation Journal of Neurology ·Eugénia Gallardo,Kristl G. Claeys,Eva Nelis,Abel Garcı́a Garcı́a,Ana Canga,Onofre Combarros,Vincent Timmerman,Peter De Jonghe,José Berciano	2008	31
4	Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation Annals of Human Genetics ·Nina Barišić,Kristl G. Claeys,Maja Sirotković-Skerlev,A. Löfgren,Eva Nelis,Peter De Jonghe,Vincent Timmerman	2008	119
5	Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing Human Mutation ·D. Goossens,Lotte Moens,Eva Nelis,An‐Sofie Lenaerts,下園美保子,G. N. Nastas,Bruno S. Frey,Guido Kopal,Peter De Jonghe,Peter De Rijk,Jurgen Del‐Favero	2008	50
6	Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy Muscle & Nerve ·Bishwajit Ganguly,Anja Schirmacher,Bernd Ringelstein,Peter Young,Giles D. Watts,Jan Meuleman,Eva Nelis,Phillip F. Chance,Vincent Timmerman,Florian Stögbauer,Gregor Kuhlenbäumer	2004	1
7	Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10 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	2003	90
8	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease Neuromuscular Disorders ·Yiğit Özbek,Eva Nelis,Luciano Merlini,Nina Barišić,Rim Amouri,C. Ceuterick,Jean‐Jacques Martin,Vincent Timmerman,Fayçal Hentati,Peter De Jonghe	2003	37
9	Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E Annals of Neurology ·Peter De Jonghe,Jorge Eugenio de Jesús Mora-Tordecillas,Eva Nelis,Jurgen Del‐Favero,Jean‐Jacques Martin,Christine Van Broeckhoven,Oleg V. Evgrafov,Vincent Timmerman	2001	163
10	A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype Archives of Neurology ·Peter De Jonghe,Vincent Timmerman,Eva Nelis,Els De Vriendt,Ann Löfgren,C. Ceuterick,N. Hayashi,Christine Van Broeckhoven	1999	7
11	Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome Neuroscience Letters ·Florian Stögbauer,Cortney Simons,Heiko Wiebusch,Vincent Timmerman,Gregor Kuhlenbäumer,Eva Nelis,E. Bernd Ringelstein,SABRİYE KARADENİZLİ TAŞKIN,Gerd Assmann,Christine Van Broeckhoven,Harald Funke	1998	14
12	Assay of transfection rate in insect cells on a single cell level Genetic Analysis Biomolecular Engineering ·Bernd Rautenstrauß,Christina Fuchs,Arif B. Ekici,Eva Nelis,Christine Van Broeckhoven,Thomas Liehr	1998	2
13	Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies Human Genetics ·S Bort,Eva Nelis,Vincent Timmerman,Teresa Sevilla,A Cruz-Martı́nez,Francisco Martı́nez,José M. Millán,Javier Arpa,Juan J. Vílchez,Félix Prieto,Christine Van Broeckhoven,Francesc Palau	1997	114
14	Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations Human Mutation ·Eva Nelis,Francis,Vincent Timmerman,Ann Löfgren,H. Backhovens,Peter De Jonghe,N. Hayashi,Christine Van Broeckhoven	1997	30
15	Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination Neuron ·Laura E. Warner,Max J. Hilz,Stanley H. Appel,James M. Killian,Edwin H. Kolodny,George Karpati,Stirling Carpenter,Gordon V. Watters,Yoshifumi Kitadate,David R. Witt,Adria Bodell,Eva Nelis,Christine Van Broeckhoven,James R. Lupski	1996	288
16	Linkage and mutation analysis of Charcot‐Marie‐Tooth neuropathy type 2 families with chromosomes 1p35‐p36 and Xq13 Neurology ·Vincent Timmerman,Peter De Jonghe,Xinjin Fu,Francis,A. Löfgren,Eva Nelis,Jeffery M. Vance,Jean‐Jacques Martin,Christine Van Broeckhoven	1996	66
17	Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B Human Mutation ·Philippe Latour,Mateus Augusto dos Santos Baruel,Eva Nelis,Dermot McGeown,J. Barendregt,M. Bouhoun Ali,B. Sung,André Dautigny,Danielle Pham-Dinh,G Chazot,M. Boucherat,Christine Van Broeckhoven,Antoon Vandenberghe	1995	31
18	Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding Neuroscience Letters ·Moses Kabuu,Emilia Bellone,Eva Nelis,Paola Mandich,Angelo Schenone,Gianluigi Mancardi,Christine Van Broeckhoven,M. Abbruzzese,Franco Ajmar	1995	3
19	The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication Nature Genetics ·Vincent Timmerman,Eva Nelis,Wim Van Hul,Bart W. Nieuwenhuijsen,E Lehmann-Franken,S. Wang,Hyo sang Kim,Bryan R. Cullen,Robin J. Leach,C. Oliver Hanemann,Peter De Jonghe,Peter Raeymaekers,Mestri Agustini Ni Nyoman,John Palle Ngunde,Hans Werner Müller,Jeffery M. Vance,Kenneth H. Fischbeck,Christine Van Broeckhoven	1992	312
20	Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree Journal of the Neurological Sciences ·Vincent Timmerman,Viorel Filer,Eva Nelis,Peter De Jonghe,L. Muylle,C. Ceuterick,Jean‐Jacques Martin,Christine Van Broeckhoven	1992	26

About Eva Nelis

Eva Nelis is a scholar working on Cellular and Molecular Neuroscience, Neurology, Microbiology, Cell Biology and Neurology, having authored 73 papers that have together received 4.2k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (62 papers), Genetic Neurodegenerative Diseases (28 papers), Neurological diseases and metabolism (17 papers), Botulinum Toxin and Related Neurological Disorders (10 papers), Signaling Pathways in Disease (9 papers), Cellular Mechanics and Interactions (7 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.5k citations), Neurology (1.3k citations), Neurology (1.4k citations), Cell Biology (806 citations) and Genetics (289 citations). Eva Nelis has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Christine Van Broeckhoven, Vincent Timmerman, Peter De Jonghe, Peter Raeymaekers, Neva E. Haites, James R. Lupski, A. Löfgren, J. J. Martin, Pieter A. Bolhuis and C. Ceuterick. Their work appears in journals such as Human Mutation, Neurology, Neuromuscular Disorders, Journal of Medical Genetics and Annals of 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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