Riikka H. Hämäläinen

Author

Also Known As

R. Hämäläinen, R.H. Hämäläinen, Riikka H Hämäläinen, Riikka H. Hämäläinen, Riikka Hamalainen, Riikka Hämäläinen, Riikka H. Hämäläinen

381

Publications

5.9K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki University of Eastern Finland Helsinki University Hospital Institute for Molecular Medicine Finland Karolinska Institutet

About

Riikka H. Hämäläinen is an author at University of Helsinki specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	3.2K
2	Natural Sciences	4	4	260
3	Engineering	3	3	1.1K
4	Biology	1	1	81
5	Biomedical Engineering	1	1	41

Riikka H. Hämäläinen

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells Knut Woltjen, Iacovos P. Michael, Paria Mohseni, Nature Induced Pluripotent Stem CellMedicinePiggybac Transposition ReprogramsStem Cell ResearchStem-cell Therapy	2009	1.8K
Copy number variation and selection during reprogramming to pluripotency Samer M. I. Hussein, Nizar N. Batada, Sanna Vuoristo, Nature EngineeringProgram AnalysisCopy Number VariationData DeduplicationComputer Science	2011	938
PSEN1 Mutant iPSC-Derived Model Reveals Severe Astrocyte Pathology in Alzheimer's Disease Minna Oksanen, Andrew J. Petersen, Nikolay Naumenko, Stem Cell Reports	2017	327
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
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone Anna‐Kaisa Anttonen, I. Mahjneh, Riikka H. Hämäläinen, Nature Genetics Autoimmune DiseaseGenetic DisorderGeneticsPathologyHspa5 Cochaperone	2005	241
Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice Kati J. Ahlqvist, Riikka H. Hämäläinen, Shuichi Yatsuga, Cell Metabolism Mitochondrial FunctionSomatic Cell GeneticsGeneticsDna ReplicationCell Death	2012	238
Mutations in a Novel Gene with Transmembrane Domains Underlie Usher Syndrome Type 3 Tarja Joensuu, Riikka H. Hämäläinen, Bo Yuan, The American Journal of Human Genetics Molecular PhysiologyDevelopmental BiologyNovel GeneGenetic DisorderMendelian Disorder	2001	215
Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model Riikka H. Hämäläinen, Tuula Manninen, Hanna Koivumäki, Proceedings of the National Academy of Sciences	2013	204
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses Avital Adato, Sarah Vreugde, Tarja Joensuu, European Journal of Human Genetics	2002	172
Metabolic alterations in Parkinson’s disease astrocytes Tuuli-Maria Sonninen, Riikka H. Hämäläinen, Marja Koskuvi, Scientific Reports	2020	167

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