Adeline Vanderver

14.6k total citations
149 papers, 3.5k citations indexed

About

Adeline Vanderver is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Adeline Vanderver has authored 149 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 114 papers in Molecular Biology, 38 papers in Immunology and 19 papers in Epidemiology. Recurrent topics in Adeline Vanderver's work include RNA regulation and disease (89 papers), RNA Research and Splicing (38 papers) and interferon and immune responses (36 papers). Adeline Vanderver is often cited by papers focused on RNA regulation and disease (89 papers), RNA Research and Splicing (38 papers) and interferon and immune responses (36 papers). Adeline Vanderver collaborates with scholars based in United States, Netherlands and Italy. Adeline Vanderver's co-authors include Marjo S. van der Knaap, Geneviève Bernard, Raphael Schiffmann, Nicole I. Wolf, Guy Helman, Cas Simons, Simona Orcesi, Johanna Schmidt, Wolfgang Köhler and Bernard Brais and has published in prestigious journals such as Cell, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Adeline Vanderver

131 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adeline Vanderver United States 33 2.6k 571 442 373 320 149 3.5k
Marianna Bugiani Netherlands 34 2.5k 1.0× 361 0.6× 691 1.6× 273 0.7× 325 1.0× 134 3.9k
Tayfun Özçelık Türkiye 30 1.5k 0.6× 405 0.7× 175 0.4× 859 2.3× 317 1.0× 59 3.1k
Hoa Nguyen United States 19 1.6k 0.6× 904 1.6× 1.2k 2.7× 685 1.8× 131 0.4× 31 3.4k
Wia Baron Netherlands 33 1.8k 0.7× 534 0.9× 615 1.4× 154 0.4× 484 1.5× 79 3.3k
Patrick Küry Germany 34 1.4k 0.5× 434 0.8× 633 1.4× 173 0.5× 111 0.3× 119 3.2k
Fabrizio Mainiero Italy 32 1.1k 0.4× 822 1.4× 206 0.5× 140 0.4× 742 2.3× 52 3.2k
Carmen Ruiz de Almodóvar Germany 30 1.7k 0.7× 402 0.7× 434 1.0× 110 0.3× 624 1.9× 55 3.3k
Alfredo Brusco Italy 32 2.2k 0.9× 223 0.4× 196 0.4× 799 2.1× 188 0.6× 141 3.3k
Mary G. Sweeney United Kingdom 34 2.8k 1.1× 189 0.3× 324 0.7× 290 0.8× 337 1.1× 71 4.0k
Elena Brambilla Italy 26 1.3k 0.5× 716 1.3× 857 1.9× 145 0.4× 89 0.3× 62 3.8k

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-authorship network of co-authors of Adeline Vanderver

This figure shows the co-authorship network connecting the top 25 collaborators of Adeline Vanderver. A scholar is included among the top collaborators of Adeline Vanderver 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 Adeline Vanderver. Adeline Vanderver 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.
Gavazzi, Francesco, Ashley E. Martin, Sarah Woidill, et al.. (2025). Experiences and Hope in Caregivers of Children With Aicardi Goutières Syndrome. Journal of Child Neurology. 40(7). 543–554.
2.
Cheung, Anthony, Erminia Di Pietro, Eric Bareke, et al.. (2025). Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders. Molecular Genetics and Metabolism. 145(1). 109080–109080.
3.
Alves, Cesar, Maria Camilla Rossi‐Espagnet, Francisco A. Perez, et al.. (2025). Single Large-Scale Mitochondrial Deletion Syndromes: Neuroimaging Phenotypes and Longitudinal Progression in Pediatric Patients. American Journal of Neuroradiology. 46(6). 1272–1281. 1 indexed citations
4.
Nomakuchi, Tomoki, Dong Li, Holly Dubbs, et al.. (2024). Utility of genome sequencing in exome‐negative pediatric patients with neurodevelopmental phenotypes. American Journal of Medical Genetics Part A. 194(12). e63817–e63817.
5.
Whitehead, Matthew T., Davide Tonduti, Laura Farina, et al.. (2024). Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. American Journal of Neuroradiology. 45(6). 769–772.
6.
Gavazzi, Francesco, Isabella Peixoto de Barcelos, Sarah Woidill, et al.. (2024). Characterization of Fine Motor and Visual Motor Skills in Aicardi-Goutières Syndrome. Journal of Child Neurology. 39(3-4). 147–154.
7.
Fatemi, Ali, Adeline Vanderver, Laura Adang, et al.. (2024). Practical Approach to Longitudinal Neurologic Care of Adults With X-Linked Adrenoleukodystrophy and Adrenomyeloneuropathy. Neurology Genetics. 10(5). e200192–e200192. 3 indexed citations
8.
Beerepoot, Shanice, Marjolein Breur, Petra J. W. Pouwels, et al.. (2023). Neurodegenerative disease after hematopoietic stem cell transplantation in metachromatic leukodystrophy. Annals of Clinical and Translational Neurology. 10(7). 1146–1159. 6 indexed citations
9.
Botto, Lorenzo D., et al.. (2023). Novel SLC13A3 Variants and Cases of Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation and Literature Review. Neurology Genetics. 9(6). e200101–e200101. 1 indexed citations
10.
Knaap, Marjo S. van der, Joshua L. Bonkowsky, Adeline Vanderver, et al.. (2022). Therapy Trial Design in Vanishing White Matter. Neurology Genetics. 8(2). e657–e657. 11 indexed citations
11.
Gavazzi, Francesco, Holly Dubbs, Valentina De Giorgis, et al.. (2020). Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features. Pediatric Neurology. 115. 1–6. 17 indexed citations
12.
Ben‐Sira, Liat, Keren Yosovich, Adeline Vanderver, et al.. (2019). Brain white matter abnormalities associated with copy number variants. American Journal of Medical Genetics Part A. 182(1). 93–103. 6 indexed citations
13.
Ahrens‐Nicklas, Rebecca C., Lars Schlotawa, Andrea Ballabio, et al.. (2018). Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. Molecular Genetics and Metabolism. 123(3). 337–346. 27 indexed citations
14.
Adang, Laura, David B. Frank, Ahmed Gilani, et al.. (2018). Aicardi goutières syndrome is associated with pulmonary hypertension. Molecular Genetics and Metabolism. 125(4). 351–358. 32 indexed citations
15.
Curiel, Julian, Guillermo Rodríguez Bey, Asako Takanohashi, et al.. (2017). TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. 26(22). 4506–4518. 53 indexed citations
16.
Tétreault, Martine, Luan T. Tran, Myriam Srour, et al.. (2017). Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy. Annals of Neurology. 82.
17.
Vanderver, Adeline, et al.. (2016). Autosomal Dominant Leukodystrophy with Autonomic Disease. 7 indexed citations
18.
Agosta, Guillermo, William Benko, Jens C. Eickhoff, et al.. (2015). CSF and Blood Levels of GFAP in Alexander Disease. eNeuro. 2(5). ENEURO.0080–15.2015. 31 indexed citations
19.
Steenweg, Marjan E., Adeline Vanderver, Berten Ceulemans, et al.. (2012). Novel Infantile-Onset Leukoencephalopathy With High Lactate Level and Slow Improvement. Archives of Neurology. 69(6). 718–22. 9 indexed citations
20.
Tétreault, Martine, Karine Choquet, Simona Orcesi, et al.. (2011). Recessive Mutations in POLR3B, Encoding the Second Largest Subunit of Pol III, Cause a Rare Hypomyelinating Leukodystrophy. The American Journal of Human Genetics. 89(5). 652–655. 110 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.

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