Julie van der Zee - Concepedia

Author

Julie van der Zee

Also Known As

J van der Zee, J. V. Zee, J. Van Der Zee, J. van der ZEE, J. van der Zee, Julie Van Der Zee, Julie Van der Zee, Julie van der Zee, Julie van der Zee, van der Zee, Julie

212

Publications

12.1K

Citations

H-Index

Concepts

All Affiliations

University of Antwerp VIB-UAntwerp Center for Molecular Neurology ZNA Middelheim Hospital KU Leuven Antwerp University Hospital

About

Julie van der Zee is an author at University of Antwerp specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	27	4.4K
2	Social Sciences	5	5	281
3	Public Health	3	3	95
4	Natural Sciences	2	2	510
5	Biology	1	1	24

Julie van der Zee

Publications

9.5K

Citations

H-Index

Page 1

	Year	Citations
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 Marc Cruts, Ilse Gijselinck, Julie van der Zee, Nature Neurodegenerative DiseasesAlzheimer's DiseaseMendelian DisorderNull MutationsGenetic Disorder	2006	1.5K
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis Gernot Kleinberger, Yoshinori Yamanishi, Marc Suárez‐Calvet, Science Translational Medicine	2014	805
Perilipin ablation results in a lean mouse with aberrant adipocyte lipolysis, enhanced leptin production, and resistance to diet-induced obesity John T. Tansey, Carole Sztalryd, J. Gruia-Gray, Proceedings of the National Academy of Sciences	2001	727
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderMedicineGenetics	2011	625
Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins Kohji Mori, Thomas Arzberger, Friedrich A. Grässer, Acta Neuropathologica Sequence MotifDipeptide Repeat ProteinsNatural SciencesGeneticsGene Structure	2013	490
Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis Lenka Nosková, Viktor Stránecký, Hana Hartmannová, The American Journal of Human Genetics Linkage MappingNeurogenomicsGeneticsPathologyNeurochemical Biomarkers	2011	261
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Molecular Psychiatry	2015	245
Genetic contribution of <i>FUS</i> to frontotemporal lobar degeneration Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Neurology	2010	217
Serum biomarker for progranulin‐associated frontotemporal lobar degeneration Kristel Sleegers, Nathalie Brouwers, Philip Van Damme, Annals of Neurology	2009	204
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis Julia K Götzl, Kohji Mori, Katrin Fellerer, Acta Neuropathologica Developmental BiologyEpendymaAutophagyPathologyCell Death	2014	201

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