M L Savontaus - Concepedia

Author

M L Savontaus

University of Turku

Also Known As

M L Savontaus, M. -L. Savontaus, M.-L. Savontaus, M.‐L. Savontaus

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

University of Turku University of Helsinki Institute for Molecular Medicine Finland Umeå University Karolinska University Hospital

About

M L Savontaus is an author at University of Turku specializing in genetics, medicine, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	347
2	Neurology	2	2	276
3	Pathology	2	2	265
4	Public Health	1	1	48
5	Molecular Genetics	1	1	34

M L Savontaus

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Alan H. Beggs, Mary B. Moyer, S. Scherpf, PubMed	1989	961
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy. Kirsi Huoponen, Johanna Vilkki, P Aula, PubMed	1991	393
Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy. Eeva Nikoskelainen, R. J. Marttila, Kirsi Huoponen, Journal of Neurology Neurosurgery & Psychiatry	1995	265
Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. Anu Suomalainen, Anna Majander, Matti Haltia, Journal of Clinical Investigation Mitochondrial MyopathyNeurodegenerative DiseasesMendelian DisorderPsychiatryOphthalmology	1992	242
Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON) Anna Majander, Kirsi Huoponen, M L Savontaus, FEBS Letters	1991	166
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7. Johanna Vilkki, J. Ott, M L Savontaus, PubMed	1991	124
An expanded CAG repeat sequence in spinocerebellar ataxia type 7. K Lindblad, M L Savontaus, Giovanni Stévanin, Genome Research	1996	106
Migration Waves to the Baltic Sea Region Tuuli Lappalainen, Virpi H. Laitinen, Elina Salmela, Annals of Human Genetics	2008	96
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism. Johanna Vilkki, M L Savontaus, Eeva Nikoskelainen PubMed	1989	75
Gene deletions in X-linked muscular dystrophy. Mikael Lindlöf, A Kiuru, H Kääriäinen, PubMed	1989	74

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