Concepedia

Author

Marit N. Nielsen

Aarhus University Hospital

Also Known As

M.N. Nielsen, Marit N. Nielsen, Marit Nyholm Nielsen

11

Publications

737

Citations

8

H-Index

13

Concepts

All Affiliations

Aarhus University HospitalAarhus UniversityInsermSorbonne UniversitéPitié-Salpêtrière Hospital
MN

About

Marit N. Nielsen is an author at Aarhus University Hospital specializing in genetics, mitochondrial function, and medicine.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

474

2

Natural Sciences

1

1

29

3

Biology

1

1

368

4

Cell Biology

1

1

77

5

Molecular Biology

1

1

29

Marit N. Nielsen

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8

Publications

726

Citations

8

H-Index

YearCitations

Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix,

The American Journal of Human Genetics

2002

368

Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice

Jane Christensen, Marit N. Nielsen, Jakob Hansen,

Cell Stress and Chaperones

2010

102

The Hsp60-(p.V98I) Mutation Associated with Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Both in Vitro and in Vivo

Peter Bross, Søren Naundrup, Jakob Hansen,

Journal of Biological Chemistry

2008

93

Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)

Jakob Hansen, Thomas J. Corydon, Johan Palmfeldt,

Neuroscience

2008

77

Exercise protects synaptic density in a rat model of Parkinson's disease

Karina Henrique Binda, Thea P. Lillethorup, Caroline Cristiano Real,

Experimental Neurology

2021

32

Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential

Peter Bross, Zhijie Li, Jakob Hansen,

Journal of Human Genetics

2006

29

Association analyses of depression and genes in the hypothalamus–pituitary–adrenal axis

Henriette N. Buttenschøn, Jesper Krogh, Marit N. Nielsen,

Acta Neuropsychiatrica

2016

14

Heterozygosity for an in‐frame deletion causes glutaryl‐CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allele

Peter Bross, Jane Hübertz Frederiksen, Anne Sigaard Bie,

Journal of Inherited Metabolic Disease

2012

11

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