Iris E. Jansen - Concepedia

Author

Iris E. Jansen

Also Known As

Deborah Janowitz, Frederic Brosseron, I Jansen, I. Jansen, I.E., Jansen, Iris E Jansen, Iris E. Jansen, Iris Jansen, Iris E. Jansen, Irshaad Jansen

148

Publications

17.5K

Citations

H-Index

Concepts

All Affiliations

Amsterdam Neuroscience Vrije Universiteit Amsterdam German Center for Neurodegenerative Diseases University College London Amsterdam University Medical Centers

About

Iris E. Jansen is an author at Amsterdam Neuroscience specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	20	7.4K
2	Public Health	5	5	1.3K
3	Social Sciences	5	5	503
4	Health Sciences	3	3	161
5	Engineering	1	1	108

Iris E. Jansen

Publications

12.7K

Citations

H-Index

Page 1

	Year	Citations
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD Alan E. Renton, Elisa Majounie, Adrian J. Waite, Neuron ChromatinNeurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderGenetics	2011	4.4K
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
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease Douglas P. Wightman, Iris E. Jansen, Jeanne E. Savage, Nature Genetics Genome-wide Association StudyNeurodegenerative DiseasesAlzheimer's DiseaseMedicineGenetics	2021	1K
A saturated map of common genetic variants associated with human height Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Nature	2022	827
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease Laurie Robak, Iris E. Jansen, Jeroen van Rooij, Brain GeneticsGenetic EpidemiologyVariant BurdenDisease Gene IdentificationGenome-wide Association Study	2017	440
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy Suzanne Lesage, Valérie Drouet, Elisa Majounie, The American Journal of Human Genetics Cell AutophagyMitophagyMitochondrial FunctionGeneticsAutophagy	2016	427
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases Aree Witoelar, Iris E. Jansen, Yunpeng Wang, JAMA Neurology	2017	367
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores Itziar de Rojas, Sonia Moreno–Grau, Niccoló Tesi, Nature Communications	2021	320
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's Ganqiang Liu, Brendon Boot, Joseph J. Locascio, Annals of Neurology	2016	268
Pathophysiological subtypes of Alzheimer’s disease based on cerebrospinal fluid proteomics Betty M. Tijms, Johan Gobom, Lianne M. Reus, Brain Subtype 1Neurochemical BiomarkersSocial SciencesProteomic TechnologyDisease Heterogeneity	2020	212

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