Jarmo Körkkö

Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen

Gloria A. Di Lullo, Shawn M. Sweeney, Jarmo Körkkö et al. · Journal of Biological Chemistry · 2002 · 890 citations · Full text

MicroSAGE Analysis of 2,353 Expressed Genes in a Single Cell‐Derived Colony of Undifferentiated Human Mesenchymal Stem Cells Reveals mRNAs of Multiple Cell Lineages

Nicola Tremain, Jarmo Körkkö, David Ibberson et al. · Stem Cells · 2001 · 271 citations · Full text

Microsage Analysis, Adult Stem Cell, Stem Cell Biology +18

Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes

Susanna Annunen, Jarmo Körkkö, Malwina Czarny‐Ratajczak et al. · The American Journal of Human Genetics · 1999 · 258 citations · Full text

Systems Biology, Mendelian Disorder, Genetic Disorder +8

Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

Murat Bastepe, Leopold F. Fröhlich, Geoffrey N. Hendy et al. · Journal of Clinical Investigation · 2003 · 256 citations · Full text

Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: Comparison with denaturing gradient gel electrophoresis and nucleotide sequencing

Jarmo Körkkö, Susanna Annunen, Tero Pihlajamaa et al. · Proceedings of the National Academy of Sciences · 1998 · 236 citations · Full text

Genetics, Dna Analysis, Molecular Biology +21