Nurten Akarsu
Institute of Child Health(IN)
Publications by Year
Research Areas
Congenital limb and hand anomalies, Hedgehog Signaling Pathway Studies, Craniofacial Disorders and Treatments, Connective tissue disorders research, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder(2003)571 cited
- → Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly(2002)456 cited
- → Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1(1998)392 cited
- → Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta(2010)314 cited
- → Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome(2000)270 cited
- → Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)(2003)262 cited