Hannu Laaksovirta - Concepedia

Author

Hannu Laaksovirta

Also Known As

H. Laaksovirta, Hannu Laaksovirta, Isabella Fogh, Letizia Mazzini, Marcella Zollino, Philip Van Damme, Richard W. Orrell, Stefan M. Pulst

Publications

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Helsinki University Hospital Folkhälsans Forskningscentrum National Institute on Aging National Institutes of Health

About

Hannu Laaksovirta is an author at University of Helsinki specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	6.1K
2	Health Sciences	1	1	29
3	Anesthesia	1	1	147
4	Immunology	1	1	27
5	Molecular Biology	1	1	4.4K

Hannu Laaksovirta

Publications

6.5K

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
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Elisa Majounie, Alan E. Renton, Kin Y. Mok, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisDementiaFrontotemporal DementiaNeuroscience	2012	1.2K
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Hannu Laaksovirta, Terhi Peuralinna, Jennifer C. Schymick, The Lancet Neurology Genome-wide Association StudyAmyotrophic Lateral SclerosisChromosome 9P21Mendelian DisorderGenetic Disorder	2010	261
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders Jenni M. Lehtonen, Saara Forsström, Emanuela Bottani, Neurology	2016	216
Concentrations and Effects of Oral Midazolam are Greatly Reduced in Patients Treated with Carbamazepine or Phenytoin Janne T. Backman, Klaus T. Olkkola, Mikael Ojala, Epilepsia Peak Midazolam ConcentrationPsychoactive DrugPatients TreatedGreatly ReducedMedicine	1996	147
Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis Janel O. Johnson, Ruth Chia, Danny E. Miller, JAMA Neurology	2021	78
Magnetoencephalographic evidence of abnormal auditory processing in amyotrophic lateral sclerosis with bulbar signs Eero Pekkonen, Daria Osipova, Hannu Laaksovirta Clinical Neurophysiology Abnormal Auditory ProcessingAuditory ProcessingAmyotrophic Lateral SclerosisBulbar SignsNeurophysiology	2003	29
Serum level of CNTF is elevated in patients with amyotrophic lateral sclerosis and correlates with site of disease onset Hannu Laaksovirta, Seppo Soinila, Veijo Hukkanen, European Journal of Neurology	2008	28
Increased occurrence of free immunoglobulin light chains in cerebrospinal fluid and serum in human immunodeficiency virus-1 infection Irina Elovaara, Ilkka Seppälä, E. Kinnunen, Journal of Neuroimmunology Primary ImmunodeficiencyMedicineCerebrospinal FluidHuman RetrovirusImmunology	1991	27
Intrafamilial clinical variability in individuals carrying the<i>CHCHD10</i>mutation Gly66Val Petra Pasanen, Liisa Myllykangas, Minna Pöyhönen, Acta Neurologica Scandinavica	2015	24

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