Adeline Vanderver

14.6k citations

149 papers · 3.5k indexed · 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

Immunology 38
- interferon and immune responses 36
Clinical Biochemistry 12

Co-authors: Marjo S. van der Knaap Geneviève Bernard Raphael Schiffmann Nicole I. Wolf Guy Helman Cas Simons Simona Orcesi Bernard Brais
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

#	Work
1	Experiences and Hope in Caregivers of Children With Aicardi Goutières Syndrome Journal of Child Neurology ·Francesco Gavazzi, Ashley E. Martin, Anjana Sevagamoorthy, Ylenia Vaia, Ariel Vincent, Sarah Woidill, Russell D’Aiello, Sara B. DeMauro, Scott A. Lorch, Adeline Vanderver, Laura Adang	2025	0
2	Single Large-Scale Mitochondrial Deletion Syndromes: Neuroimaging Phenotypes and Longitudinal Progression in Pediatric Patients American Journal of Neuroradiology ·Cesar Alves, Maria Camilla Rossi‐Espagnet, Francisco A. Perez, Amirreza Manteghinejad, James T. Peterson, Rebecca Ganetzky, Antonio Napolitano, Francesco Grassi, Ibrahim George‐Sankoh, Harun Yıldız, Colleen Muraresku, Marni J. Falk, Diego Martinelli, Daniela Longo, Adeline Vanderver, Carlo Gandolfo, Russell P. Saneto, Amy Goldstein, Arastoo Vossough	2025	1
3	Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders Molecular Genetics and Metabolism ·Anthony Cheung, Erminia Di Pietro, Catherine Argyriou, Eric Bareke, Yasmin D’Souza, Ratna Dua Puri, P Muhammed Shabeer, Rebecca Ganetzky, Amy B. Goldstein, Adeline Vanderver, Shruthi Mohan, Jacek Majewski, Christine Yergeau, Nancy Braverman	2025	0
4	Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease American Journal of Neuroradiology ·Thaís Armangue, Matthew T. Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L. Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek‐Andrews, Amy Waldman, Adeline Vanderver	2024	0
5	Utility of genome sequencing in exome‐negative pediatric patients with neurodevelopmental phenotypes American Journal of Medical Genetics Part A ·Tomoki Nomakuchi, Eden Yitna Teferedegn, Dong Li, Kayla Muirhead, Holly Dubbs, Jacqueline Leonard, Colleen Muraresku, Emily Sergio, Kaley Arnold, Amy Pizzino, Cara Skraban, Elaine H. Zackai, Kai Wang, Rebecca Ganetzky, Adeline Vanderver, Rebecca C. Ahrens‐Nicklas, Elizabeth Bhoj	2024	0
6	Characterization of Fine Motor and Visual Motor Skills in Aicardi-Goutières Syndrome Journal of Child Neurology ·Stacy V. Cusack, Francesco Gavazzi, Isabella Peixoto de Barcelos, Nicholson Modesti, Sarah Woidill, Brielle Formanowski, Sara B. DeMauro, Scott A. Lorch, Ariel Vincent, Abbas F. Jawad, Timothy Estilow, Allan M. Glanzman, Adeline Vanderver, Laura Adang	2024	0
7	Practical Approach to Longitudinal Neurologic Care of Adults With X-Linked Adrenoleukodystrophy and Adrenomyeloneuropathy Neurology Genetics ·Alexandra B. Kornbluh, Aaron Baldwin, Ali Fatemi, Adeline Vanderver, Laura Adang, Keith Van Haren, Jacinda B. Sampson, Florian Eichler, Reza Sadjadi, Marc Engelen, Jennifer Orthmann‐Murphy	2024	3
8	Neurodegenerative disease after hematopoietic stem cell transplantation in metachromatic leukodystrophy Annals of Clinical and Translational Neurology ·Murtadha L. Al‐Saady, Shanice Beerepoot, Bonnie C. Plug, Marjolein Breur, Hristina Galabova, Petra J. W. Pouwels, Jaap Jan Boelens, Caroline A. Lindemans, Peter M. van Hasselt, Ulrich Matzner, Adeline Vanderver, Marianna Bugiani, Marjo S. van der Knaap, Nicole I. Wolf	2023	6
9	Novel SLC13A3 Variants and Cases of Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation and Literature Review Neurology Genetics ·Kristen N. Wong, Lorenzo D. Botto, Miao He, Peter R. Baker, Adeline Vanderver, Joshua L. Bonkowsky	2023	1
10	Generation of three induced pluripotent stem cell lines from individuals with Aicardi-Goutières syndrome caused by a c.3019G>A (p.G1007R) autosomal dominant pathogenic variant in ADAR1 Stem Cell Research ·Luis Garcia, Carlos Dominguez Gonzalez, Alyssa Gagne, Jean Ann McGuire, Deborah L. French, Asako Takanohashi, (unknown), Adeline Vanderver, Sunetra Sase	2023	1
11	Therapy Trial Design in Vanishing White Matter Neurology Genetics ·Marjo S. van der Knaap, Joshua L. Bonkowsky, Adeline Vanderver, Raphael Schiffmann, Ingeborg Krägeloh‐Mann, Enrico Bertini, Geneviève Bernard, Seyed Ali Fatemi, Nicole I. Wolf, Elise F. Saunier-Vivar, Robert Rauner, Hanka Dekker, Pieter van Bokhoven, Peter M. van de Ven, Prisca S. Leferink	2022	11
12	Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III–related leukodystrophy and Feingold syndrome Molecular Case Studies ·Kayla Muirhead, Amanda Clause, Zinayida Schlachetzki, Holly Dubbs, Denise Perry, R. Tanner Hagelstrom, Ryan J. Taft, Adeline Vanderver	2021	2
13	Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features Pediatric Neurology ·Cara Piccoli, Nowa Bronner, Francesco Gavazzi, Holly Dubbs, Micaela De Simone, Valentina De Giorgis, Simona Orcesi, Elisa Fazzi, Jessica Galli, Silvia Masnada, Davide Tonduti, Costanza Varesio, Adeline Vanderver, Arastoo Vossough, Laura Adang	2020	17
14	Brain white matter abnormalities associated with copy number variants American Journal of Medical Genetics Part A ·Nitzan Vigdorovich, Liat Ben‐Sira, Lubov Blumkin, Ronit Precel, Ifat Nezer, Keren Yosovich, Zachary Cross, Adeline Vanderver, Dorit Lev, Tally Lerman‐Sagie, Ayelet Zerem	2019	6
15	Aicardi goutières syndrome is associated with pulmonary hypertension Molecular Genetics and Metabolism ·Laura Adang, David B. Frank, Ahmed Gilani, Asako Takanohashi, Nicole Ulrick, Abigail Collins, Zachary Cross, Csaba Galambos, Guy Helman, Usama Kanaan, Stephanie Keller, Dawn M. Simon, Omar Sherbini, Brian D. Hanna, Adeline Vanderver	2018	32
16	Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement Molecular Genetics and Metabolism ·Rebecca C. Ahrens‐Nicklas, Lars Schlotawa, Andrea Ballabio, Nicola Brunetti‐Pierri, Mauricio De Castro, Thomas Dierks, Florian Eichler, Can Fıçıcıoğlu, Alan Finglas, Jutta Gaertner, Brian Kirmse, Joerg Klepper, Marcus Lee, Amber Olsen, Giancarlo Parenti, Arastoo Vossough, Adeline Vanderver, Laura Adang	2018	27
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	Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy Annals of Neurology ·Stefanie Perrier, Laurence Gauquelin, Martine Tétreault, Luan T. Tran, Neil Webb, Myriam Srour, Joshua R. Mitchell, Catherine Brunel‐Guitton, Jacek Majewski, Long Long, S Keller, Michael J. Gambello, Cas Simons, Adeline Vanderver, Geneviève Bernard	2017	0
19	Autosomal Dominant Leukodystrophy with Autonomic Disease Norah Nahhas, Parisa Sabet Rasekh, Adeline Vanderver, Quasar Saleem Padiath	2016	7
20	CSF and Blood Levels of GFAP in Alexander Disease eNeuro ·Paige L. Jany, Guillermo Agosta, William Benko, Jens C. Eickhoff, Stephanie Keller, Wolfgang Köehler, David M. Koeller, Soe Mar, Sakkubai Naidu, Jayne Ness, Davide Pareyson, Deborah L. Renaud, Ettore Salsano, Raphael Schiffmann, Julie Simon, Adeline Vanderver, Florian Eichler, Marjo S. van der Knaap, Albee Messing	2015	31

About Adeline Vanderver

Adeline Vanderver is a scholar working on Immunology, Clinical Biochemistry, Molecular Biology, Neurology and Rheumatology, 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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