Tine Van Dyck

1.0k total citations
6 papers, 472 citations indexed

About

Tine Van Dyck is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Tine Van Dyck has authored 6 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Psychiatry and Mental health, 2 papers in Genetics and 1 paper in Molecular Biology. Recurrent topics in Tine Van Dyck's work include Epilepsy research and treatment (5 papers), Migraine and Headache Studies (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Tine Van Dyck is often cited by papers focused on Epilepsy research and treatment (5 papers), Migraine and Headache Studies (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Tine Van Dyck collaborates with scholars based in Belgium, Brazil and Croatia. Tine Van Dyck's co-authors include Liesbet Deprez, Peter De Jonghe, Arvid Suls, Kristl G. Claeys, Lieve Claes, Dominique Audenaert, Tine Deconinck, Laurence Claes, Lieven Lagae and Wim Van Paesschen and has published in prestigious journals such as Neurology, Epilepsia and Human Mutation.

In The Last Decade

Tine Van Dyck

6 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tine Van Dyck Belgium	6	332	188	179	156	61	6	472
Maéva Langouët United States	8	164 0.5×	253 1.3×	114 0.6×	226 1.4×	43 0.7×	9	462
Liri Jin China	11	151 0.5×	141 0.8×	140 0.8×	60 0.4×	62 1.0×	34	391
Evan E. Eichler United States	2	150 0.5×	338 1.8×	142 0.8×	270 1.7×	24 0.4×	3	538
Bree Hodgson Australia	11	429 1.3×	400 2.1×	286 1.6×	335 2.1×	109 1.8×	15	792
Amedeo Bianchi Italy	15	289 0.9×	167 0.9×	168 0.9×	230 1.5×	103 1.7×	32	507
Cassie L. Albury Australia	8	204 0.6×	66 0.4×	24 0.1×	111 0.7×	16 0.3×	12	337
Stephen W. Briggs United States	7	107 0.3×	140 0.7×	129 0.7×	72 0.5×	59 1.0×	7	312
Miriam Kessi China	11	158 0.5×	160 0.9×	117 0.7×	143 0.9×	50 0.8×	34	440
Gregorio Pineda Spain	5	252 0.8×	118 0.6×	131 0.7×	156 1.0×	97 1.6×	6	408
Paola Nobili Italy	11	150 0.5×	108 0.6×	186 1.0×	28 0.2×	49 0.8×	19	362

Countries citing papers authored by Tine Van Dyck

Since Specialization

Citations

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

Fields of papers citing papers by Tine Van Dyck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tine Van Dyck

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

All Works

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6 of 6 papers shown

1.

Claes, Lieve, Liesbet Deprez, Arvid Suls, et al.. (2009). TheSCN1Avariant database: a novel research and diagnostic tool. Human Mutation. 30(10). E904–E920. 103 indexed citations

2.

Deprez, Liesbet, Sarah Weckhuysen, Tine Deconinck, et al.. (2007). Epilepsy as part of the phenotype associated with ATP1A2 mutations. Epilepsia. 49(3). 500–508. 80 indexed citations

3.

Deprez, Liesbet, Kristel Peeters, Wim Van Paesschen, et al.. (2007). Familial occipitotemporal lobe epilepsy and migraine with visual aura. Neurology. 68(23). 1995–2002. 55 indexed citations

4.

Audenaert, Dominique, E Schwartz, Kristl G. Claeys, et al.. (2006). A novel GABRG2 mutation associated with febrile seizures. Neurology. 67(4). 687–690. 128 indexed citations

5.

Suls, Arvid, Kristl G. Claeys, D. Goossens, et al.. (2006). Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients. Human Mutation. 27(9). 914–920. 90 indexed citations

6.

Deprez, Liesbet, Lieve Claes, Kristl G. Claeys, et al.. (2005). Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation. Human Genetics. 118(5). 618–625. 16 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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