Kristina M. Allen
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, RNA Research and Splicing, Wnt/β-catenin signaling in development and cancer, Ubiquitin and proteasome pathways, MicroRNA in disease regulation
Most-Cited Works
- → A Mutation in the LDL Receptor–Related Protein 5 Gene Results in the Autosomal Dominant High–Bone-Mass Trait(2002)1,291 cited
- → Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness(2002)1,098 cited
- → doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein(1998)1,083 cited
- → PAK3 mutation in nonsyndromic X-linked mental retardation(1998)469 cited
- → Characterization of mutations in the genedoublecortin in patients with double cortex syndrome(1999)166 cited
- → Bone biomechanical properties in LRP5 mutant mice(2004)160 cited
- → Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation(2000)138 cited
- → Structure-based mutation analysis shows the importance of LRP5 β-propeller 1 in modulating Dkk1-mediated inhibition of Wnt signaling(2006)48 cited
- → Genes that regulate neuronal migration in the cerebral cortex(1999)48 cited
- → Genomic Imprinting and Audiogenic Seizures in Mice(1997)24 cited