Adeline Vanderver

14.6k citations

149 papers · 3.5k · h-index 33

Impact in

Neurology top 2%
- Neuroinflammation and Neurodegeneration Mechanisms
Molecular Biology top 2%
- RNA regulation and disease
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- Mitochondrial Function and Pathology

Papers in

Molecular Biology 114
- RNA regulation and disease 89
- RNA Research and Splicing 38
- RNA modifications and cancer 20
- RNA and protein synthesis mechanisms 20
- Mitochondrial Function and Pathology 13
Immunology 38
- interferon and immune responses 36

Co-authors: Marjo S. van der Knaap (29 shared papers)Geneviève Bernard (27 shared papers)Raphael Schiffmann (23 shared papers)Nicole I. Wolf (19 shared papers)Guy Helman (26 shared papers)Cas Simons (20 shared papers)Simona Orcesi (10 shared papers)Bernard Brais (8 shared papers)
Journals: Molecular Genetics and Metabolism (18 papers)Journal of Child Neurology (14 papers)Neurology (12 papers)Pediatric Neurology (8 papers)Brain (4 papers)
Partner nations: United States Netherlands Italy

In The Last Decade

Adeline Vanderver

131 papers receiving 3.5k citations

Peers

Countries citing papers authored by Adeline Vanderver

Since Specialization

Citations

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

Fields of papers citing papers by Adeline Vanderver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 149 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Ubiquitous L1 Mosaicism in Hippocampal Neurons Cell ·Kyle R. Upton, Daniel J. Gerhardt, J. Samuel Jesuadian, Sandra R. Richardson, Francisco J. Sánchez‐Luque, Gabriela O. Bodea, Adam D. Ewing, Carmen Salvador‐Palomeque, Marjo S. van der Knaap, Paul M. Brennan, Adeline Vanderver, Geoffrey J. Faulkner	2015	235
2	Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy The American Journal of Human Genetics ·Geneviève Bernard, Éliane Chouery, Maria Lisa Putorti, Martine Tétreault, Asako Takanohashi, Giovanni A. Carosso, I Clément, Odile Boespflug‐Tanguy, Diana Rodriguez, Valérie Delague, Joelle Abou Ghoch, Nadine Jalkh, Imen Dorboz, Sébastien Fribourg, Martin Teichmann, André Mégarbané, Raphael Schiffmann, Adeline Vanderver, Bernard Brais	2011	181
3	Magnetic resonance imaging pattern recognition in hypomyelinating disorders Brain ·Marjan E. Steenweg, Adeline Vanderver, Susan Blasér, Alberto Bizzi, Tom J. de Koning, Grazia M.S. Mancini, Wessel N. van Wieringen, Frederik Barkhof, Nicole I. Wolf, Marjo S. van der Knaap	2010	180
4	Case definition and classification of leukodystrophies and leukoencephalopathies Molecular Genetics and Metabolism ·Adeline Vanderver, Morgan Prust, Davide Tonduti, Fanny Mochel, Heather M. Hussey, Guy Helman, James Garbern, Florian Eichler, Pierre Labauge, Patrick Aubourg, Diana Rodriguez, Marc C. Patterson, Johan L.K. Van Hove, Johanna Schmidt, Nicole I. Wolf, Odile Boespflug‐Tanguy, Raphael Schiffmann, Marjo S. van der Knaap	2015	157
5	A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies Molecular Genetics and Metabolism ·Sumit Parikh, Geneviève Bernard, Richard J. Leventer, Marjo S. van der Knaap, Johan Van Hove, Amy Pizzino, Nathan H. McNeill, Guy Helman, Cas Simons, Johanna Schmidt, William B. Rizzo, Marc C. Patterson, Ryan J. Taft, Adeline Vanderver	2014	123
6	Recessive Mutations in POLR3B, Encoding the Second Largest Subunit of Pol III, Cause a Rare Hypomyelinating Leukodystrophy The American Journal of Human Genetics ·Martine Tétreault, Karine Choquet, Simona Orcesi, Davide Tonduti, Umberto Balottin, Martin Teichmann, Sébastien Fribourg, Raphael Schiffmann, Bernard Brais, Adeline Vanderver, Geneviève Bernard	2011	110
7	Hypomyelinating leukodystrophies: Translational research progress and prospects Annals of Neurology ·Petra J. W. Pouwels, Adeline Vanderver, Geneviève Bernard, Nicole I. Wolf, Steffi F. Dreha‐Kulczewksi, Sean Deoni, Enrico Bertini, Alfried Kohlschütter, William D. Richardson, Charles ffrench‐Constant, Wolfgang Köhler, David H. Rowitch, A. James Barkovich	2014	107
8	Comprehensive Immunophenotyping of Cerebrospinal Fluid Cells in Patients with Neuroimmunological Diseases The Journal of Immunology ·Sungpil Han, Yen Chih Lin, Tianxia Wu, Alan D. Salgado, Ina Mexhitaj, Simone C. Wuest, Elena Romm, Joan Ohayon, Raphaela Goldbach‐Mansky, Adeline Vanderver, Adriana Marques, Camilo Toro, Peter R. Williamson, Irene Cortese, Bibiana Bielekova	2014	98
9	Adulthood leukodystrophies Nature Reviews Neurology ·Wolfgang Köhler, Julian Curiel, Adeline Vanderver	2018	88
10	ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism Journal of Medical Genetics ·Sacha Ferdinandusse, Kim D. Falkenberg, Janet Koster, P. A. W. Mooyer, Richard O. Jones, Carlo W.T. van Roermund, Amy Pizzino, Michael Schrader, Ronald J. A. Wanders, Adeline Vanderver, Hans R. Waterham	2016	87
11	Lysosomal abnormalities in hereditary spastic paraplegia types SPG 15 and SPG 11 Annals of Clinical and Translational Neurology ·Benoît Renvoisé, Jaerak Chang, Rajat Singh, Sayuri Yonekawa, Edmond J. FitzGibbon, Ami Mankodi, Adeline Vanderver, Alice B. Schindler, Camilo Toro, William A. Gahl, Don J. Mahuran, Craig Blackstone, Tyler Mark Pierson	2014	82
12	Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype–phenotype correlation Brain ·Eline M. Hamilton, Emiel Polder, Adeline Vanderver, Sakkubai Naidu, Raphael Schiffmann, Kate Fisher, Ana Raguž, Luba Blumkin, Carola G.M. van Berkel, Quinten Waisfisz, Cas Simons, Ryan J. Taft, Truus E. M. Abbink, Nicole I. Wolf, Marjo S. van der Knaap	2014	77
13	Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism Journal of Medical Genetics ·Hussein Daoud, Martine Tétreault, William T. Gibson, Kether Guerrero, Ana S.A. Cohen, Janina Gburek‐Augustat, Matthis Synofzik, Bernard Brais, Cathy A. Stevens, Rocío Sánchez‐Carpintero, Cyril Goizet, Sakkubai Naidu, Adeline Vanderver, Geneviève Bernard	2013	70
14	Update on Leukodystrophies: A Historical Perspective and Adapted Definition Neuropediatrics ·Sietske H. Kevelam, Marjan E. Steenweg, Siddharth Srivastava, Guy Helman, Sakkubai Naidu, Raphael Schiffmann, Susan Blasér, Adeline Vanderver, Nicole I. Wolf, Marjo S. van der Knaap	2016	68
15	Therapies in Aicardi–Goutières syndrome Clinical & Experimental Immunology ·Yanick J. Crow, Adeline Vanderver, Simona Orcesi, Taco W. Kuijpers, Gillian Rice	2013	66
16	NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern Neurology ·Sietske H. Kevelam, Richard J. Rodenburg, Nicole I. Wolf, Patrick Ferreira, Roelineke J. Lunsing, Leo Nijtmans, Anne Mitchell, H Arroyo, D. Rating, Adeline Vanderver, Carola G.M. van Berkel, Truus E. M. Abbink, Peter Heutink, Marjo S. van der Knaap	2013	61
17	TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes Human Molecular Genetics ·Julian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, Marianna Bugiani, Xiaoqin Fu, Nicole I. Wolf, Bruce Nmezi, Raphael Schiffmann, Mona Bugaighis, Tyler Mark Pierson, Guy Helman, Cas Simons, Marjo S. van der Knaap, Judy Liu, Quasar Saleem Padiath, Adeline Vanderver	2017	53
18	Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome Neurology ·Roberta La Piana, C. Uggetti, Federico Roncarolo, Adeline Vanderver, Ivana Olivieri, Davide Tonduti, Guy Helman, Umberto Balottin, Elisa Fazzi, Yanick J. Crow, John Livingston, Simona Orcesi	2015	53
19	Identification of a Novel de Novo p.Phe932Ile KCNT1 Mutation in a Patient With Leukoencephalopathy and Severe Epilepsy Pediatric Neurology ·Adeline Vanderver, Cas Simons, Johanna Schmidt, Philip Pearl, Miriam Bloom, Bennett Lavenstein, David S. Miller, Sean M. Grimmond, Ryan J. Taft	2013	49
20	New-onset afebrile seizures in infants Neurology ·David T. Hsieh, Taeun Chang, Tammy N. Tsuchida, L. Gilbert Vezina, Adeline Vanderver, J. Siedel, Kathleen Brown, Madison M. Berl, Sally Stephens, Alex Zeitchick, William D. Gaillard	2010	49

About Adeline Vanderver

Adeline Vanderver is a scholar working on Molecular Biology, Immunology, Epidemiology, Rheumatology and Neurology, having authored 149 papers that have together received 3.5k indexed citations. Recurring topics across this work include RNA regulation and disease (89 papers), RNA Research and Splicing (38 papers), interferon and immune responses (36 papers), RNA modifications and cancer (20 papers), RNA and protein synthesis mechanisms (20 papers), Mitochondrial Function and Pathology (13 papers), Systemic Lupus Erythematosus Research (12 papers) and Lysosomal Storage Disorders Research (11 papers). The work is most often cited by research in Neurology (442 citations), Molecular Biology (2.6k citations), Clinical Biochemistry (227 citations), Immunology (571 citations) and Developmental Neuroscience (92 citations). Adeline Vanderver has collaborated with scholars based in United States, Netherlands and Italy. Frequent co-authors include Marjo S. van der Knaap, Geneviève Bernard, Raphael Schiffmann, Nicole I. Wolf, Guy Helman, Cas Simons, Simona Orcesi, Bernard Brais, Johanna Schmidt and Wolfgang Köhler. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Child Neurology, Neurology, Pediatric Neurology and Brain.

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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Adeline Vanderver

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Adeline Vanderver

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