Linn Öijerstedt - Concepedia

Author

Linn Öijerstedt

Also Known As

Annabel Nelson, Benedetta Nacmias, Christin Andersson, David Tang-Wai, Hakan Thonberg, Jennifer Nicholas, Koen Poesen, Linn Öijerstedt, Michele Veldsman, Vesna Jelic

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Karolinska University Hospital Karolinska Institutet University College London University of Brescia UK Dementia Research Institute

LÖ

About

Linn Öijerstedt is an author at Karolinska University Hospital specializing in medicine, neurodegeneration, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	967
2	Public Health	3	3	293
3	Epidemiology	3	3	541
4	Health Sciences	1	1	296
5	Social Sciences	1	1	42

Linn Öijerstedt

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study Katrina Moore, Jennifer Nicholas, Murray Grossman, The Lancet Neurology Disease DurationNeurodegenerative DiseasesAlzheimer's DiseaseAgingGenetic Frontotemporal Dementia	2019	296
Neurofilament light chain: a biomarker for genetic frontotemporal dementia Lieke Meeter, Elise G.P. Dopper, Lize C. Jiskoot, Annals of Clinical and Translational Neurology	2016	263
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study David M. Cash, Martina Bocchetta, David L. Thomas, Neurobiology of Aging	2017	191
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study Emma L. van der Ende, Lieke Meeter, Jackie M. Poos, The Lancet Neurology Alzheimer's DiseaseGenetic Frontotemporal DementiaOphthalmologyDementiaMulticentre Cohort Study	2019	179
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD Cyril Pottier, Yingxue Ren, Ralph B. Perkerson, Acta Neuropathologica International Ftld-tdp Whole-genomeAutoimmune DiseaseImmune Cell DevelopmentMedicineGenetic Epidemiology	2019	123
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study Cyril Pottier, Xiaolai Zhou, Ralph B. Perkerson, The Lancet Neurology Genome-wide Association StudyPotential Genetic ModifiersDisease RiskGrn MutationsGenetic Disorder	2018	122
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis Ramita Dewan, Ruth Chia, Jinhui Ding, Neuron Amyotrophic Lateral SclerosisAlzheimer's DiseasePathologyDegenerative DiseaseFrontotemporal Dementia	2020	79
White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort Carole H. Sudre, Martina Bocchetta, David M. Cash, NeuroImage Clinical	2017	78
Altered levels of CSF proteins in patients with FTD, presymptomatic mutation carriers and non-carriers Julia Remnestål, Linn Öijerstedt, Abbe Ullgren, Translational Neurodegeneration	2020	71
Novel <scp>CSF</scp> biomarkers in genetic frontotemporal dementia identified by proteomics Emma L. van der Ende, Lieke Meeter, Christoph Stingl, Annals of Clinical and Translational Neurology	2019	67

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