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Leena Peltonen | Researchclopedia

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Leena Peltonen

University of Helsinki

172

Works

12,135

Citations

56

h-index

121

i10-index

Research Topics

Connective tissue disorders research Genetic Associations and Epidemiology Mitochondrial Function and Pathology

Affiliations

Rutgers, The State University of New Jersey1980–1980

Broad Institute2005–2008

Research Council of Finland2005–2005

Yrjö Jahnsson Foundation2005–2005

Oslo University Hospital2008–2008

Top Works

Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

Jyrki Kaukonen,Jukka K. Juselius,et al.

2000632 citations

Genetic Neurodegenerative Diseases

Genetics and Neurodevelopmental Disorders

Disruption of the neurexin 1 gene is associated with schizophrenia

Dan Rujescu,Andrés Ingason,et al.

2008485 citations

Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin

Peter Hackman,Anna Vihola,et al.

2002482 citations

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts

Juha Paloneva,Marjo Kestilä,et al.

2000467 citations

Minisequencing: A Specific Tool for DNA Analysis and Diagnostics on Oligonucleotide Arrays

Tomi Pastinen,Ants Kurg,et al.

1997347 citations

Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory

Tyrone D. Cannon,William Hennah,et al.

2005341 citations

Circadian Clock-Related Polymorphisms in Seasonal Affective Disorder and their Relevance to Diurnal Preference

Carolina Johansson,Matthäus Willeit,et al.

2002340 citations

Update of the UMD-<i>FBN1</i>mutation database and creation of an<i>FBN1</i>polymorphism database

Gwenaëlle Collod‐Béroud,Saga Le Bourdelles,et al.

2003330 citations

A population-specific HTR2B stop codon predisposes to severe impulsivity

Laura Bevilacqua,Stéphane Doly,et al.

2010294 citations