Jan Osinga
Publications by Year
Research Areas
Epigenetics and DNA Methylation, Renal cell carcinoma treatment, Renal and related cancers, Congenital gastrointestinal and neural anomalies, RNA Research and Splicing
Most-Cited Works
- → Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer(1987)394 cited
- → Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems(2005)148 cited
- → A Loss-of-Function Mutation in the Endothelin-Converting Enzyme 1 (ECE-1) Associated with Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction(1999)142 cited
- → MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis(1997)120 cited
- → Abundance of protein-bound sulfhydryl and bisulfide groups at chromosomal nucleolus organizing regions(1980)106 cited
- → Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene(2007)96 cited
- → RET-Familial Medullary Thyroid Carcinoma Mutants Y791F and S891A Activate a Src/JAK/STAT3 Pathway, Independent of Glial Cell Line–Derived Neurotrophic Factor(2005)93 cited
- → The Effects of Four Different Tyrosine Kinase Inhibitors on Medullary and Papillary Thyroid Cancer Cells(2011)81 cited
- → Mutations in Hirschsprung Disease: When Does a Mutation Contribute to the Phenotype(1997)78 cited
- → Selective staining of the same set of nucleolar phosphoproteins by silver and Giemsa(1984)64 cited