Juha Kolehmainen
Finnish Medicines Agency Fimea(FI)
Publications by Year
Research Areas
Immunodeficiency and Autoimmune Disorders, Blood disorders and treatments, Corneal surgery and disorders, Retinal Development and Disorders, Blood groups and transfusion
Most-Cited Works
- → Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport(2003)374 cited
- → Modulatory Neurotransmitter Systems and Behavior: Towards Zebrafish Models of Neurodegenerative Diseases(2006)294 cited
- → Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen(2004)124 cited
- → Dopaminergic cell damage and vulnerability to MPTP in Pink1 knockdown zebrafish(2010)87 cited
- → Evaluation of immunofluorescence microscopy and enzyme-linked immunosorbent assay in detection of Cryptosporidium and Giardia infections in asymptomatic dogs(2007)77 cited
- → The First Sex-Specific Molecular Marker Discovered in the Moss Pseudocalliergon trifarium(2008)60 cited
- → Cohen syndrome in the Ohio Amish(2004)51 cited
- → A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis(1995)49 cited
- → Refined Mapping of the Cohen Syndrome Gene by Linkage Disequilibrium(1997)36 cited
- Refined mapping of the Cohen syndrome gene by linkage disequilibrium.(1998)