Tuula Manninen
University of Helsinki(FI)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Lysosomal Storage Disorders Research, Glycosylation and Glycoproteins Research, Cellular transport and secretion, ATP Synthase and ATPases Research
Most-Cited Works
- → Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype(2002)691 cited
- → Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model(2013)204 cited
- → Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: Application to aspartylglucosaminuria in Finland(1992)137 cited
- → Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1(1991)133 cited
- → TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes(2019)108 cited
- → New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies(2012)97 cited
- → Mice with Ppt1Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons(2004)90 cited
- → A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging(2004)86 cited
- → USF1 deficiency activates brown adipose tissue and improves cardiometabolic health(2016)74 cited
- → Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation(2010)59 cited