D. Goossens - Concepedia

Author

D. Goossens

Also Known As

D GOOSSENS, D Goossens, D Goossens*, D. A. Goossens, D. GOOSSENS, D. Goossens, D. J. A. Goossens, D. J. Goossens, Dennis Goossens, Dirk Goossens

112

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

University of Antwerp VIB-UAntwerp Center for Molecular Neurology Antwerp University Hospital Vlaams Instituut voor Biotechnologie Inserm

About

D. Goossens is an author at University of Antwerp specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	21	2K
2	Engineering	1	1	67
3	Health Sciences	1	1	28
4	Natural Sciences	1	1	37
5	Public Health	1	1	193

D. Goossens

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck, Brain Genomic App DuplicationCerebral Amyloid AngiopathyGeneticsGene Locus DuplicationsNeurochemical Biomarkers	2006	404
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 Arvid Suls, Peter Dedeken, Karolien Goffin, Brain Neurological DisorderGlucose UptakeSocial SciencesGenetic AnalysisParoxysmal Exercise-induced Dyskinesia	2008	340
Mutations in SEPT9 cause hereditary neuralgic amyotrophy Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceGenetic DisorderGenetics	2005	259
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis Yurii S. Aulchenko, Ilse A Hoppenbrouwers, Sreeram V. Ramagopalan, Nature Genetics Disease SusceptibilityGenetic DisorderGeneticsGenetic EpidemiologyGenetic Variation	2008	193
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease Yukihide Momozawa, Myriam Mni, Kayo Nakamura, Nature Genetics InflammationImmunologyPathologyAutoimmunityImmune System	2010	186
Clinical spectrum of early-onset epileptic encephalopathies associated with <i>STXBP1</i> mutations Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren, Neurology	2010	167
<i>TP53</i> Outperforms Other Androgen Receptor Biomarkers to Predict Abiraterone or Enzalutamide Outcome in Metastatic Castration-Resistant Prostate Cancer Bram De Laere, Steffi Oeyen, Markus Mayrhofer, Clinical Cancer Research	2018	161
Mutations in <i>SACS</i> cause atypical and late-onset forms of ARSACS Jonathan Baets, Tine Deconinck, Kaat Smets, Neurology	2010	133
Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients Arvid Suls, Kristl G. Claeys, D. Goossens, Human Mutation	2006	115
Progranulin locus deletion in frontotemporal dementia Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Human Mutation	2007	94

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