Eva Nelis

7.8k citations

73 papers · 4.2k · h-index 31

Impact in

Cellular and Molecular Neuroscience top 0.2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 0.5%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders

Papers in

Cellular and Molecular Neuroscience 60
- Hereditary Neurological Disorders 60
- Genetic Neurodegenerative Diseases 24
Molecular Biology 25
- Signaling Pathways in Disease 8

Co-authors: Christine Van Broeckhoven (51 shared papers)Vincent Timmerman (47 shared papers)Peter De Jonghe (36 shared papers)Peter Raeymaekers (3 shared papers)Neva E. Haites (3 shared papers)James R. Lupski (7 shared papers)A. Löfgren (12 shared papers)J. J. Martin (2 shared papers)
Journals: Human Mutation (11 papers)Neurology (8 papers)Neuromuscular Disorders (7 papers)Journal of Medical Genetics (5 papers)Annals of Neurology (3 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-authors

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

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

20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) Neuromuscular Disorders ·Peter Raeymaekers, Vincent Timmerman, Eva Nelis, Peter De Jonghe, J.E Hoogenduk, Frank Baas, David F. Barker, J. J. Martin, Marianne de Visser, Pieter A. Bolhuis, Christine Van Broeckhoven	1991	477
2	Estimation of the Mutation Frequenciesin Charcot-Marie-Tooth Disease Type 1and Hereditary Neuropathy withLiability to Pressure Palsies:A European Collaborative Study European Journal of Human Genetics ·Eva Nelis, Christine Van Broeckhoven	1996	327
3	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, K.L. Chen, S. Wang, K. Ben Othman, Bryan R. Cullen, Robin J. Leach, C. Oliver Hanemann, Peter De Jonghe, Peter Raeymaekers, G-J.B. van Ommen, J-J. Martin, Hans Werner Müller, Jeffery M. Vance, Kenneth H. Fischbeck, Christine Van Broeckhoven	1992	314
4	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, Calvin Wheeler, David R. Witt, Adria Bodell, Eva Nelis, Christine Van Broeckhoven, James R. Lupski	1996	287
5	The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype Brain ·Peter De Jonghe, Vincent Timmerman, C. Ceuterick, Eva Nelis, Els De Vriendt, A. Löfgren, Anina Vercruyssen, Christine Verellen, Lionel Van Maldergem, J. J. Martin, Christine Van Broeckhoven	1999	175
6	Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies Human Mutation ·Eva Nelis, Neva E. Haites, Christine Van Broeckhoven	1999	173
7	Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E Annals of Neurology ·Peter De Jonghe, Irina Mersivanova, Eva Nelis, Jurgen Del‐Favero, Jean‐Jacques Martin, Christine Van Broeckhoven, Oleg V. Evgrafov, Vincent Timmerman	2001	163
8	Human Meiotic Recombination Products Revealed by Sequencing a Hotspot for Homologous Strand Exchange in Multiple HNPP Deletion Patients The American Journal of Human Genetics ·Lawrence T. Reiter, Philip J. Hastings, Eva Nelis, Peter De Jonghe, Christine Van Broeckhoven, James R. Lupski	1998	132
9	Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. Journal of Medical Genetics ·Peter Raeymaekers, Vincent Timmerman, Eva Nelis, Wim Van Hul, Peter De Jonghe, Jean‐Jacques Martin, Christine Van Broeckhoven	1992	125
10	Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype Neurology ·Vincent Timmerman, Peter De Jonghe, C. Ceuterick, Els De Vriendt, A. Löfgren, Eva Nelis, Laura E. Warner, James R. Lupski, J. J. Martin, Christine Van Broeckhoven	1999	121
11	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
12	Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease Neurology ·Anneke Gabreëls-Festen, Jessica E. Hoogendijk, P.H.S. Meijerink, F.J.M. Gabreëls, Pieter A. Bolhuis, Sylvia E. C. van Beersum, Tanja Kulkens, Eva Nelis, F.G.I. Jennekens, M. Visser, Baziel G.M. van Engelen, Christine Van Broeckhoven, Edwin C.M. Mariman	1996	116
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	115
14	Mutations in GDAP1 Neurology ·Eva Nelis, Sevim Erdem‐Özdamar, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou, 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	2002	111
15	Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis Human Molecular Genetics ·Francesc Palau, Ann Löfgren, Peter De Jonghe, S Bort, Eva Nelis, Teresa Sevilla, Jean‐Jacques Martin, Juan J. Vílchez, Félix Prieto, Christine Van Broeckhoven	1993	103
16	Charcot-Marie-Tooth disease and related peripheral neuropathies. PubMed ·Peter De Jonghe, Vincent Timmerman, Eva Nelis, J. J. Martin, Christine Van Broeckhoven	1997	96
17	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	91
18	Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene Human Genetics ·Eva Nelis, Vincent Timmerman, Peter De Jonghe, Antoon Vandenberghe, Danielle Pham-Dinh, André Dautigny, Jean‐Jacques Martin, Christine Van Broeckhoven	1994	89
19	Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients Human Mutation ·Irina Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Е. Л. Дадали, В. П. Федотов, Eva Nelis, Ann L�fgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov	2000	67
20	Linkage and mutation analysis of Charcot‐Marie‐Tooth neuropathy type 2 families with chromosomes 1p35‐p36 and Xq13 Neurology ·Vincent Timmerman, Peter De Jonghe, Petra Spoelders, Sandra Simokovic, A. Löfgren, Eva Nelis, Jeffery M. Vance, Jean‐Jacques Martin, Christine Van Broeckhoven	1996	66

About Eva Nelis

Eva Nelis is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, 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 (60 papers), Genetic Neurodegenerative Diseases (24 papers), Neurological diseases and metabolism (16 papers), Botulinum Toxin and Related Neurological Disorders (9 papers), Signaling Pathways in Disease (8 papers), Cellular Mechanics and Interactions (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Toxin Mechanisms and Immunotoxins (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.5k citations), Neurology (1.1k citations), Neurology (1.1k citations), Cell Biology (732 citations) and Genetics (262 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.

Explore authors with similar magnitude of impact

Eva Nelis

Impact in

Papers in i

In The Last Decade

Eva Nelis

Peers

Countries citing papers authored by Eva Nelis

Fields of papers citing papers by Eva Nelis

All Works

About Eva Nelis

Explore authors with similar magnitude of impact

Papers in