Jaakko Leisti - Concepedia

Author

Jaakko Leisti

Oulu University Hospital

Also Known As

J Leisti, J T Leisti, J. LEISTI, J. Leisti, J. T. LEISTI, JAAKKO LEISTI, JAAKKO T. LEISTI, Jaakko Leisti

103

Publications

3.9K

Citations

H-Index

116

Concepts

All Affiliations

Oulu University Hospital University of Oulu University of Helsinki Karolinska University Hospital Kajaani University of Applied Sciences

About

Jaakko Leisti is an author at Oulu University Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	44	2.7K
2	Public Health	5	5	160
3	Health Sciences	2	2	148
4	Education	1	1	25
5	Engineering	1	1	160

Jaakko Leisti

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Identification of the familial cylindromatosis tumour-suppressor gene Graham R. Bignell, William Warren, Sheila Seal, Nature Genetics Tumor BiologyGeneticsPathologyMolecular PathologyCancer Genetics	2000	667
Muscle-eye-brain disease (MEB) Pirkko Santavuori, Hannu Somer, Kimmo Sainio, Brain and Development OphthalmologyCorticobasal DegenerationNeurological DisorderNeurologyCommon Diseases	1989	235
Characterization of the full fragile X syndrome mutation in fetal gametes Henry Malter, Jane Iber, Rob Willemsen, Nature Genetics Developmental AnomalyDevelopmental BiologyCytogeneticsGenetic DisorderGenetics	1997	196
Mutation Analysis of the<i>MEN1</i>Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism<sup>1</sup> Bin Tean Teh, Soili Kytölä, Filip Farnebo, The Journal of Clinical Endocrinology & Metabolism EngineeringGeneticsParathyroid DiseasePathologyDisease Gene Identification	1998	160
Muscle, Eye and Brain Disease: A New Syndrome Pirkko Santavuori, Jaakko Leisti, S. Kruus Neuropediatrics OphthalmologyNeurological DisorderBrain DiseaseMotor DisorderNeurology	1977	130
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype Peggy Shelbourne, Robert Winqvist, E. Kunert, Human Molecular Genetics	1992	116
A lethal autosomal recessive syndrome of multiple congenital contractures Riitta Herva, Jaakko Leisti, Pertti Kirkinen, American Journal of Medical Genetics	1985	106
Chromosome aberrations in lymphocytes of nurses handling cytostatic agents. E. Nikula, K Kiviniitty, Jaakko Leisti, Scandinavian Journal of Work Environment & Health Occupational ToxicologyChromatinChromosome DynamicsPossible Chromosome DamageChromosome-type Breaks	1984	94
Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration. Aune Hirvasniemi, Huynh Ngoc Lang, A E Lehesjoki, Journal of Medical Genetics NeuropsychologyNeurological DisorderNeuropsychiatryAssociated Mental DeteriorationSocial Sciences	1994	88
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8. Esa Tahvanainen, Susanna Ranta, Aune Hirvasniemi, Proceedings of the National Academy of Sciences Gene LocusCytogeneticsChildhood EpilepsyGeneticsEvolutionary Biology	1994	82

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