Florence H. J. van Tienen

Author

Also Known As

F H J van Tienen, F. H. J. van Tienen, F.H.J. van Tienen, F.H.J. van Tienen⁎, Florence H J van Tienen, Florence H. J. van Tienen, Florence H.J. van Tienen

Publications

689

Citations

H-Index

Concepts

All Affiliations

Maastricht University Maastricht University Medical Centre Radboud University Medical Center Radboud University Nijmegen Maastro Clinic

About

Florence H. J. van Tienen is an author at Maastricht University specializing in medicine, gene expression, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	238
2	Cell Biology	2	2	125
3	Molecular Genetics	2	2	44
4	Diabetes	1	1	92
5	Metabolism	1	1	102

Florence H. J. van Tienen

Publications

584

Citations

H-Index

Page 1

	Year	Citations
Physical Activity Is the Key Determinant of Skeletal Muscle Mitochondrial Function in Type 2 Diabetes Florence H. J. van Tienen, Stephan Praet, Henk M. De Feyter, The Journal of Clinical Endocrinology & Metabolism	2012	111
Wnt5b stimulates adipogenesis by activating PPARγ, and inhibiting the β-catenin dependent Wnt signaling pathway together with Wnt5a Florence H. J. van Tienen, Hilde Laeremans, Carla Kallen, Biochemical and Biophysical Research Communications Signal TransductionPhysiologyMetabolic SignalingMetabolic RegulationMetabolism	2009	102
Preadipocytes of type 2 diabetes subjects display an intrinsic gene expression profile of decreased differentiation capacity Florence H. J. van Tienen, Carla Kallen, Patrick Lindsey, International Journal of Obesity Metabolic SyndromeGenetic DeterminantDevelopmental BiologyDiabetesType 2	2011	92
Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success Suzanne C.E.H. Sallevelt, J. Dreesen, Marion Drüsedau, Journal of Medical Genetics	2013	91
Hypertrophic remodelling in cardiac regulatory myosin light chain (<i>MYL2</i>) founder mutation carriers Godelieve R.F. Claes, Florence H. J. van Tienen, Patrick Lindsey, European Heart Journal	2015	76
Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos Auke B.C. Otten, Rick Kamps, Patrick Lindsey, Frontiers in Cell and Developmental Biology	2020	48
Assessment of fibroblast nuclear morphology aids interpretation of LMNA variants Florence H. J. van Tienen, Patrick Lindsey, M. A. F. Kamps, European Journal of Human Genetics ChromatinLmna VariantsVariant InterpretationGenetic DisorderGenetics	2018	33
Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study Karlijn Bouman, Jan T. Groothuis, Jonne Doorduin, BMC Neurology	2021	20
Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency Le Guo, Bob P. H. Engelen, Irene M. G. M. Hemel, European Journal of Human Genetics Genetic DisorderNovel CauseGeneticsPathogenesisPathology	2021	11

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