Rik Hendrickx - Concepedia

Concepedia

Author

Rik Hendrickx

University of Antwerp ORCID

Also Known As

Hendrickx, R, Hendrickx, Rik, R Hendrickx, R. Hendrickx, R.J.B.M. Hendrickx, R.J.H. Hendrickx, Rik Hendrickx

39

Publications

1.1K

Citations

11

H-Index

30

Concepts

All Affiliations

University of Antwerp Antwerp University Hospital VIB-UAntwerp Center for Molecular Neurology Christian-Albrechts-Universität zu Kiel University of Southern Denmark

RH

About

Rik Hendrickx is an author at University of Antwerp specializing in medicine, genetics, and metabolic syndrome.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	452
2	Social Sciences	2	2	290
3	Health Sciences	1	1	15
4	Natural Sciences	1	1	10
5	Biochemistry	1	1	10

Rik Hendrickx

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12

Publications

1.1K

Citations

11

H-Index

	Year	Citations
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, The American Journal of Human Genetics Chd2 CauseDravet SyndromeMolecular NeuroscienceNeurobiology Of DiseaseGenetic Disorder	2013	219
Extending the <i>KCNQ2</i> encephalopathy spectrum Sarah Weckhuysen, Vanja Ivanović, Rik Hendrickx, Neurology	2013	218
<i>GRIN2B</i> mutations in west syndrome and intellectual disability with focal epilepsy Johannes R. Lemke, Rik Hendrickx, Kirsten Geider, Annals of Neurology	2013	209
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients Carolien G. F. de Kovel, Eva H. Brilstra, Marjan J. A. van Kempen, Molecular Genetics & Genomic Medicine	2016	89
Milky spots in the mouse omentum may play an important role in the origin of peritoneal macrophages Josien F.A.M. Wijffels, Rik Hendrickx, Joke J. E. Steenbergen, Research in Immunology InflammationPathogenesisImmunologyAutophagyPathology	1992	86
Reduction of seizure frequency after epilepsy surgery in a patient with <scp><i>STXBP1</i></scp> encephalopathy and clinical description of six novel mutation carriers Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, Epilepsia Neurological DisorderGeneticsWest SyndromeGenetic EpidemiologyClinical Neurology	2013	71
Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity Doreen Zegers, Sigri Beckers, Rik Hendrickx, International Journal of Obesity ObesityMetabolic SyndromeChildhood ObesityMetabolic DisorderGenetic Disorder	2013	51
Loss of synaptic Zn2+ transporter function increases risk of febrile seizures Michael S. Hildebrand, A. Marie Phillips, Saul A. Mullen, Scientific Reports	2015	46
PRRT2 mutations: exploring the phenotypical boundaries Tania Djémié, Sarah Weckhuysen, Per Holmgren, Journal of Neurology Neurosurgery & Psychiatry	2013	29
Evaluation of a pan-Leishmania SL RNA qPCR assay for parasite detection in laboratory-reared and field-collected sand flies and reservoir hosts Myrthe Pareyn, Rik Hendrickx, Nigatu Girma, Parasites & Vectors	2020	16

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