Roxane Van Heurck

675 total citations
7 papers, 377 citations indexed

About

Roxane Van Heurck is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Roxane Van Heurck has authored 7 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Roxane Van Heurck's work include Metabolism and Genetic Disorders (2 papers), Heavy Metal Exposure and Toxicity (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Roxane Van Heurck is often cited by papers focused on Metabolism and Genetic Disorders (2 papers), Heavy Metal Exposure and Toxicity (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Roxane Van Heurck collaborates with scholars based in Belgium, Switzerland and United States. Roxane Van Heurck's co-authors include Pierre Vanderhaeghen, Angéline Bilheu, Adèle Herpoel, Ikuo Suzuki, Marta Wojno, Julian Chéron, David Gacquer, Devesh Kumar, Vincent Detours and Franck Polleux and has published in prestigious journals such as Cell, Neuron and Neurology.

In The Last Decade

Roxane Van Heurck

6 papers receiving 374 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roxane Van Heurck Belgium	6	259	82	82	75	51	7	377
Barbara K. Stepien Germany	8	294 1.1×	104 1.3×	90 1.1×	59 0.8×	35 0.7×	13	432
Yuh-Man Sun United Kingdom	14	452 1.7×	138 1.7×	56 0.7×	113 1.5×	36 0.7×	20	642
Naosuke Hoshina Japan	8	142 0.5×	71 0.9×	39 0.5×	54 0.7×	23 0.5×	9	240
Wendy Chang United States	4	302 1.2×	204 2.5×	97 1.2×	60 0.8×	36 0.7×	5	383
Katarzyna J. Radomska Sweden	10	169 0.7×	50 0.6×	29 0.4×	126 1.7×	44 0.9×	18	397
Juliette Pouch France	9	162 0.6×	84 1.0×	23 0.3×	20 0.3×	30 0.6×	11	336
С. В. Саложин Russia	10	507 2.0×	124 1.5×	45 0.5×	159 2.1×	43 0.8×	20	668
Jennifer E. Bestman United States	11	407 1.6×	146 1.8×	49 0.6×	72 1.0×	32 0.6×	16	600
Caroline Dubacq France	10	207 0.8×	88 1.1×	24 0.3×	46 0.6×	14 0.3×	17	380
Michael Molinek United Kingdom	10	335 1.3×	90 1.1×	149 1.8×	102 1.4×	10 0.2×	11	569

Countries citing papers authored by Roxane Van Heurck

Since Specialization

Citations

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

Fields of papers citing papers by Roxane Van Heurck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roxane Van Heurck. 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 Roxane Van Heurck. The network helps show where Roxane Van Heurck may publish in the future.

Co-authorship network of co-authors of Roxane Van Heurck

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

All Works

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7 of 7 papers shown

1.

Heurck, Roxane Van, Eva Hammar, Dorothée Ville, et al.. (2025). Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathy. European Journal of Paediatric Neurology. 56. 97–103.

2.

Heurck, Roxane Van, Jérôme Bonnefont, Marta Wojno, et al.. (2022). CROCCP2 acts as a human-specific modifier of cilia dynamics and mTOR signaling to promote expansion of cortical progenitors. Neuron. 111(1). 65–80.e6. 24 indexed citations

3.

Heurck, Roxane Van, Emmanuelle Ranza, Lina Quteineh, et al.. (2021). Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss. Genes. 12(8). 1277–1277. 13 indexed citations

4.

Suzuki, Ikuo, David Gacquer, Roxane Van Heurck, et al.. (2018). Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation. Cell. 173(6). 1370–1384.e16. 255 indexed citations

5.

Depondt, Chantal, Simona Donatello, Nicolas Simonis, et al.. (2014). Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations. Neurology. 82(19). 1749–1750. 28 indexed citations

6.

Heurck, Roxane Van, M. C. Payen, Stéphane De Wit, & Nathan Clumeck. (2013). EPIDEMIOLOGY OF MDR-TB IN A BELGIAN INFECTIOUS DISEASES UNIT: A 15 YEARS REVIEW. Acta Clinica Belgica. 68(5). 321–324. 5 indexed citations

7.

Boom, Alain, Michèle Authelet, Robert Dedecker, et al.. (2008). Bimodal modulation of tau protein phosphorylation and conformation by extracellular Zn2+ in human-tau transfected cells. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(6). 1058–1067. 52 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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