Christer Nilsson - Concepedia

Author

Christer Nilsson

Lund University ORCID

Also Known As

C Nilsson, C. Nilsson, CHRISTER NILSSON, Christer C. Nilsson, Christer Nilsson, Erik Stomrud, Nilsson, Christer

228

Publications

4.9K

Citations

H-Index

Concepts

All Affiliations

Lund University Karolinska Institutet Uppsala University Karolinska University Hospital Inserm

About

Christer Nilsson is an author at Lund University specializing in medicine, neurology, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	661
2	Engineering	5	5	235
3	Health Sciences	4	4	95
4	Public Health	4	4	267
5	Social Sciences	1	1	37

Christer Nilsson

Publications

4.7K

Citations

H-Index

Page 1

	Year	Citations
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria Günter U. Höglinger, Gesine Respondek, María Stamelou, Movement Disorders	2017	2.2K
Phenotypic variation in a large Swedish pedigree due to <i>SNCA</i> duplication and triplication Julia Fuchs, Christer Nilsson, Jennifer M. Kachergus, Neurology	2007	397
Genomic investigation of α‐synuclein multiplication and parkinsonism Owen A. Ross, Adam Braithwaite, Lisa Skipper, Annals of Neurology	2008	339
Characterization and prognostic features of secondary acute myeloid leukemia in a population‐based setting: <scp>A</scp> report from the <scp>S</scp>wedish <scp>A</scp>cute <scp>L</scp>eukemia <scp>R</scp>egistry Erik Hulegårdh, Christer Nilsson, Vladimir Lazarević, American Journal of Hematology	2014	271
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska, The Lancet Neurology Neurodegenerative DiseasesGenetic DisorderGeneticsGenetic EpidemiologySequencing Study	2018	159
Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research Selina Wray, Matthew W. Self, Patrick A. Lewis, PLoS ONE EngineeringMutation-defined Cell LinesDisease Gene IdentificationNeurobiology Of DiseaseMendelian Disorder	2012	141
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy Max‐Joseph Grimm, Gesine Respondek, María Stamelou, Movement Disorders	2019	139
Large-scale replication and heterogeneity in Parkinson disease genetic loci Manu Sharma, John P. A. Ioannidis, Jan Aasly, Neurology	2012	130
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group Christoph Kamm, D G Healy, N Quinn, Brain Fmr1 PremutationsNeurological DisorderMultiple System AtrophyGenetic EpidemiologyDiagnosis	2005	107
Expression levels of long non-coding RNAs are prognostic for AML outcome Arvind Singh Mer, Johan Lindberg, Christer Nilsson, Journal of Hematology & Oncology	2018	97

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