Eva Nelis

7.8k total citations
73 papers, 4.2k citations indexed

About

Eva Nelis is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Eva Nelis has authored 73 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Cellular and Molecular Neuroscience, 26 papers in Molecular Biology and 18 papers in Cell Biology. Recurrent topics in Eva Nelis's work include Hereditary Neurological Disorders (62 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (17 papers). Eva Nelis is often cited by papers focused on Hereditary Neurological Disorders (62 papers), Genetic Neurodegenerative Diseases (28 papers) and Neurological diseases and metabolism (17 papers). Eva Nelis collaborates with scholars based in Belgium, United States and Germany. Eva Nelis's 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 and has published in prestigious journals such as Neuron, Nature Genetics and Brain.

In The Last Decade

Eva Nelis

70 papers receiving 4.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Eva Nelis Belgium 31 3.5k 1.4k 1.3k 1.2k 806 73 4.2k
Michaela Auer‐Grumbach Austria 35 2.1k 0.6× 924 0.7× 1.1k 0.8× 1.8k 1.5× 1.2k 1.4× 78 4.1k
Jamïlé Hazan France 21 1.3k 0.4× 386 0.3× 745 0.6× 532 0.5× 504 0.6× 38 1.9k
James A. Trofatter United States 25 885 0.3× 1.8k 1.3× 286 0.2× 1.5k 1.3× 521 0.6× 54 3.7k
Els De Vriendt Belgium 21 1.1k 0.3× 363 0.3× 440 0.3× 769 0.7× 549 0.7× 40 1.8k
Zhaohui Shao United States 24 1.4k 0.4× 321 0.2× 448 0.3× 2.7k 2.3× 230 0.3× 30 4.5k
Alanna E. McCall United States 15 2.6k 0.7× 753 0.6× 192 0.1× 3.1k 2.6× 201 0.2× 21 3.6k
Laura Lillien United States 24 1.5k 0.4× 154 0.1× 382 0.3× 2.2k 1.9× 343 0.4× 35 3.7k
Mireille Cossée France 22 1.9k 0.5× 572 0.4× 126 0.1× 2.6k 2.2× 437 0.5× 62 3.0k
Giorgia Dina Italy 21 1.2k 0.3× 376 0.3× 513 0.4× 1.1k 0.9× 401 0.5× 32 2.5k
K. H. Fischbeck United States 16 1.2k 0.3× 421 0.3× 235 0.2× 1.4k 1.2× 230 0.3× 20 2.1k

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 of co-authors of Eva Nelis

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

All Works

20 of 20 papers shown
1.
Baets, Jonathan, Ines Dierick, Chantal Ceuterick‐de Groote, et al.. (2009). Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity. Neuromuscular Disorders. 19(2). 172–175. 8 indexed citations
2.
Claeys, Kristl G., Stephan Züchner, Marina Kennerson, et al.. (2009). Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy. Brain. 132(7). 1741–1752. 62 indexed citations
3.
Gallardo, Eugénia, Kristl G. Claeys, Eva Nelis, et al.. (2008). Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation. Journal of Neurology. 255(7). 986–992. 31 indexed citations
4.
Barišić, Nina, Kristl G. Claeys, Maja Sirotković-Skerlev, et al.. (2008). Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation. Annals of Human Genetics. 72(3). 416–441. 119 indexed citations
5.
Goossens, D., Lotte Moens, Eva Nelis, et al.. (2008). Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing. Human Mutation. 30(3). 472–476. 50 indexed citations
6.
Schirmacher, Anja, Bernd Ringelstein, Peter Young, et al.. (2004). Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy. Muscle & Nerve. 29(4). 601–604. 1 indexed citations
7.
Verhoeven, Kristien, Peter De Jonghe, Tom Van de Putte, et al.. (2003). Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10. The American Journal of Human Genetics. 73(4). 926–932. 90 indexed citations
8.
Nelis, Eva, Luciano Merlini, Nina Barišić, et al.. (2003). Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. Neuromuscular Disorders. 13(9). 720–728. 37 indexed citations
9.
Jonghe, Peter De, Eva Nelis, Jurgen Del‐Favero, et al.. (2001). Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E. Annals of Neurology. 49(2). 245–249. 163 indexed citations
10.
Jonghe, Peter De, Vincent Timmerman, Eva Nelis, et al.. (1999). A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype. Archives of Neurology. 56(10). 1283–1283. 7 indexed citations
11.
Stögbauer, Florian, Heiko Wiebusch, Vincent Timmerman, et al.. (1998). Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome. Neuroscience Letters. 240(1). 1–4. 14 indexed citations
12.
Rautenstrauß, Bernd, Christina Fuchs, Arif B. Ekici, et al.. (1998). Assay of transfection rate in insect cells on a single cell level. Genetic Analysis Biomolecular Engineering. 14(3). 103–104. 2 indexed citations
13.
14.
Nelis, Eva, Vincent Timmerman, Ann Löfgren, et al.. (1997). Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations. Human Mutation. 9(1). 47–52. 30 indexed citations
15.
Warner, Laura E., Max J. Hilz, Stanley H. Appel, et al.. (1996). Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination. Neuron. 17(3). 451–460. 288 indexed citations
16.
Timmerman, Vincent, Peter De Jonghe, A. Löfgren, et al.. (1996). Linkage and mutation analysis of Charcot‐Marie‐Tooth neuropathy type 2 families with chromosomes 1p35‐p36 and Xq13. Neurology. 46(5). 1311–1311. 66 indexed citations
17.
Latour, Philippe, Eva Nelis, André Dautigny, et al.. (1995). Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B. Human Mutation. 6(1). 50–54. 31 indexed citations
18.
Bellone, Emilia, Eva Nelis, Paola Mandich, et al.. (1995). Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding. Neuroscience Letters. 194(1-2). 136–138. 3 indexed citations
19.
Timmerman, Vincent, Eva Nelis, Wim Van Hul, et al.. (1992). The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication. Nature Genetics. 1(3). 171–175. 312 indexed citations
20.
Timmerman, Vincent, Eva Nelis, Peter De Jonghe, et al.. (1992). Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree. Journal of the Neurological Sciences. 109(1). 41–48. 26 indexed citations

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

Breakdown of academic impact, for papers by Michaela Auer‐Grumbach Breakdown of academic impact, for papers by Jamïlé Hazan Breakdown of academic impact, for papers by James A. Trofatter Breakdown of academic impact, for papers by Els De Vriendt Breakdown of academic impact, for papers by Zhaohui Shao Breakdown of academic impact, for papers by Alanna E. McCall Breakdown of academic impact, for papers by Laura Lillien Breakdown of academic impact, for papers by Mireille Cossée Breakdown of academic impact, for papers by Giorgia Dina Breakdown of academic impact, for papers by K. H. Fischbeck
Rankless by CCL
2026