Nandita Quaderi
Publications by Year
Research Areas
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Genetics and Neurodevelopmental Disorders, RNA modifications and cancer, Hedgehog Signaling Pathway Studies, Developmental Biology and Gene Regulation
Most-Cited Works
- → Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22(1997)368 cited
- → Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development(1999)154 cited
- → Isolation, physical mapping, and Northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2(1996)139 cited
- → Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain(1998)69 cited
- → MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development(1999)60 cited
- → Genetic and Physical Mapping of a Gene Encoding a Methyl CpG Binding Protein, Mecp2, to the Mouse X Chromosome(1994)58 cited
- → The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen’s node(2003)48 cited
- → The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse(1995)42 cited
- → Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome(2004)32 cited
- → Identification of a New EGF-Repeat-Containing Gene from Human Xp22: A Candidate for Developmental Disorders(2000)31 cited