Tiina Tyni - Concepedia

Author

Tiina Tyni

Helsinki University Hospital

Also Known As

T TYNI, T Tyni, T. Tyni, Tiina A. Tyni, Tiina Tyni

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Helsinki University Hospital University of Helsinki University of Gothenburg Turku University Hospital

About

Tiina Tyni is an author at Helsinki University Hospital specializing in medicine, genetics, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	1.8K
2	Biochemistry	6	6	480
3	Public Health	3	3	195
4	Health Sciences	2	2	116
5	Natural Sciences	1	1	16

Tiina Tyni

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study Anu Suomalainen, Jenni M. Elo, Kirsi H. Pietiläinen, The Lancet Neurology Diagnostic StudyFibrosisMitochondrial FunctionPhysiologyMedicine	2011	414
Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy Alexandra Götz, Henna Tyynismaa, Liliya Euro, The American Journal of Human Genetics CardiomyopathyMendelian DisorderMitochondrial FunctionGeneticsMolecular Biology	2011	252
Genetic Basis of Severe Childhood-Onset Cardiomyopathies Catalina Vasilescu, Tiina Ojala, Virginia Brilhante, Journal of the American College of Cardiology CardiomyopathyHeart FailureGeneticsPediatricsMedicine	2018	156
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency Rikke Katrine Jentoft Olsen, Eliška Koňaříková, Teresa Anna Giancaspero, The American Journal of Human Genetics	2016	146
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Tiina Tyni, Eeva Ekholm, Helena Pihko American Journal of Obstetrics and Gynecology InfertilityGeneticsReproductive HealthPregnancy ComplicationsGynecology	1998	141
Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients Tiina Tyni, Aarno Palotie, Lasse Viinikka, The Journal of Pediatrics Mendelian DisorderBiochemistryGenetic DisorderMedicineGenetics	1997	132
Ophthalmologic findings in long-chain 3-hydroxyacyl-Coa dehydrogenase deficiency caused by the G1528C mutation Tiina Tyni, Tero Kivelä, Marjatta Lappi, Ophthalmology Mendelian DisorderAldehyde DehydrogenaseBiochemistryGenetic DisorderGenetics	1998	105
New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies Tiina Ojala, Padmini P. Polinati, Tuula Manninen, Pediatric Research New MutationMendelian DisorderMitochondrial FunctionGenetic DisorderMedicine	2012	97
Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency Tiina Tyni, Helena Pihko Acta Paediatrica Metabolic DisorderGeneticsDehydrogenase DeficiencyOxidative StressMetabolic Syndrome	1999	96
Mitochondrial Fatty Acid β-Oxidation in the Human Eye and Brain: Implications for the Retinopathy of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Tiina Tyni, Anders Paetau, Arnold W. Strauss, Pediatric Research Ocular DiseaseMitochondrial FunctionOphthalmologyBiochemistryHuman Eye	2004	79

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