Anna Majander - Concepedia

Author

Anna Majander

University of Helsinki ORCID

Also Known As

A MAJANDER, A Majander, A. Majander, A. S. Maj, A.S. Majander, Anna Majander, Anna S. Majander

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Helsinki University Hospital University College London Moorfields Eye Hospital MRC Mitochondrial Biology Unit

About

Anna Majander is an author at University of Helsinki specializing in medicine, ophthalmology, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	15	982
2	Health Sciences	1	1	24
3	Natural Sciences	1	1	66
4	Anesthesia	1	1	53
5	Applied Physiology	1	1	24

Anna Majander

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
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
Diphenyleneiodonium inhibits reduction of iron-sulfur clusters in the mitochondrial NADH-ubiquinone oxidoreductase (Complex I). Anna Majander, Moshe Finel, Mårten Wikström Journal of Biological Chemistry	1994	201
Neuroradiologic findings in children with mitochondrial disorders. Leena Valanne, Leena Ketonen, Anna Majander, PubMed	1998	196
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
Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA Anu Suomalainen, Laura‐Maria Peltonen, Anders Paetau, The Lancet CardiomyopathyHeart FailureMitochondrial FunctionGeneticsDna Replication	1992	152
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA Anu Suomalainen, Anna Majander, Mitchell T. Wallin, Neurology	1997	139
Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome Päivi Mäkelä‐Bengs, Anu Suomalainen, Anna Majander, Pediatric Research Narp SyndromeClinical SymptomsMendelian DisorderGenetic DisorderGenetics	1995	100
Congenital Hypoplastic Anemia, Diabetes, and Severe Renal Tubular Dysfunction Associated with a Mitochondrial DNA Deletion Anna Majander, Anu Suomalainen, Kim Vettenranta, Pediatric Research UrologyMendelian DisorderMitochondrial FunctionGenetic DisorderMedicine	1991	79
Childhood-onset Leber hereditary optic neuropathy Anna Majander, Richard Bowman, Joanna Poulton, British Journal of Ophthalmology	2017	76
Catalytic Activity of Complex I in Cell Lines that Possess Replacement Mutations in the ND Genes in Leber's Hereditary Optic Neuropathy Anna Majander, Moshe Finel, Marja‐Liisa Savontaus, European Journal of Biochemistry	1996	72

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