Leena Peltonen - Concepedia

Author

Leena Peltonen

Institute for Molecular Medicine Finland

Also Known As

A Sajantila, Aarno Palotie, Kari Stefansson, L Peltonen, L. (a) Peltonen, L. PELTONEN, L. Peltonen, LEENA PELTONEN, Leena Peltonen, Luana Galver

174

Publications

12.2K

Citations

H-Index

175

Concepts

All Affiliations

Institute for Molecular Medicine Finland University of Helsinki Public Health Institute Helsinki University Hospital University of California, Los Angeles

About

Leena Peltonen is an author at Institute for Molecular Medicine Finland specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	57	5K
2	Natural Sciences	10	11	752
3	Public Health	9	9	343
4	Engineering	2	2	155
5	Health Sciences	1	1	42

Leena Peltonen

106

Publications

9.2K

Citations

H-Index

Page 1

	Year	Citations
Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance Jyrki Kaukonen, Jukka K. Juselius, Valeria Tiranti, Science	2000	630
Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin Peter Hackman, Anna Vihola, Henna Haravuori, The American Journal of Human Genetics Developmental BiologySkeletal MuscleGenetic DisorderMedicineGenetics	2002	479
Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts Juha Paloneva, Marjo Kestilä, Jun Wu, Nature Genetics Presenile DementiaBone CystsGeneticsPathologyDegenerative Disease	2000	467
Minisequencing: A Specific Tool for DNA Analysis and Diagnostics on Oligonucleotide Arrays Tomi Pastinen, Ants Kurg, Andres Metspalu, Genome Research Oligonucleotide Array FormatGeneticsDna MicroarraysDna AnalysisMolecular Biology	1997	347
Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory Tyrone D. Cannon, William Hennah, Theo G.M. van Erp, Archives of General Psychiatry	2005	341
Circadian Clock-Related Polymorphisms in Seasonal Affective Disorder and their Relevance to Diurnal Preference Carolina Johansson, Matthäus Willeit, Christina Smedh, Neuropsychopharmacology Diurnal PreferenceSocial SciencesPsychologyCircadian Clock-related PolymorphismsMood Symptom	2002	339
A population-specific HTR2B stop codon predisposes to severe impulsivity Laura Bevilacqua, Stéphane Doly, Jaakko Kaprio, Nature PharmacologyImpulsivityAddiction	2010	291
Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression Timo Partonen, Jens Treutlein, Asude Alpman, Annals of Medicine	2007	261
Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome Katariina Kainulainen, Leena Karttunen, Lea Puhakka, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesis	1994	260
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Yaoqin Gong, Miikka Vikkula, Laurence M. Boon, PubMed	1996	247

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