Christine Van Broeckhoven

Author

Also Known As

A. Lofgren, An De Bruyn, B. Rautenstrauss, Broeckhoven, Christine Van, C Van Broeckhoven, C van Broeckhoven, C. Broeckhoven, C. V. Broeckhoven, C. VAN BROECKHOVEN, C. Van Broeckhoven

1.2K

Publications

93.4K

Citations

141

H-Index

272

Concepts

All Affiliations

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

About

Christine Van Broeckhoven is an author at University of Antwerp specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	87	305	37.1K
2	Public Health	22	28	3.8K
3	Health Sciences	17	20	2.9K
4	Natural Sciences	16	21	1.5K
5	Engineering	9	9	586

Christine Van Broeckhoven

551

Publications

65.5K

Citations

123

H-Index

Page 1

	Year	Citations
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Denise Harold, Richard Abraham, Paul Hollingworth, Nature Genetics Genome-wide Association StudyDisease HeterogeneityNeurodegenerative DiseasesAlzheimer's DiseaseGenetics	2009	3.4K
NanoPack: visualizing and processing long-read sequencing data Wouter De Coster, Svenn D’Hert, Darrin T. Schultz, Bioinformatics	2018	3.1K
New insights into the genetic etiology of Alzheimer’s disease and related dementias Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Nature Genetics	2022	2.3K
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
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang, PLoS ONE	2014	1.4K
Atherosclerosis, apolipoprotein E, and prevalence of dementia and Alzheimer's disease in the Rotterdam Study Albert Hofman, Alewijn Ott, Monique M.B. Breteler, The Lancet Alzheimer's DiseaseAgingAtherosclerosisDementiaVascular Dementia	1997	1.4K
The <i>C9orf72</i> GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS Kohji Mori, Shih‐Ming Weng, Thomas Arzberger, Science	2013	1.3K
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans, The American Journal of Human Genetics NeurophysiologyGenetic DisorderGeneticsNeuroscienceMolecular Neurobiology	2001	1.3K
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions Gert Van Goethem, Bart Dermaut, A. Löfgren, Nature Genetics Ocular DiseaseOphthalmologyGenetic DisorderGeneticsPathology	2001	831
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis Gernot Kleinberger, Yoshinori Yamanishi, Marc Suárez‐Calvet, Science Translational Medicine	2014	805

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