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Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.Science (New York, N.Y.)|December 4, 1998
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17M Hong, V Zhukareva, V Vogelsberg-Ragaglia, et al.Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.Proceedings of the National Academy of Sciences of the United States of America|November 9, 2006
Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular targetS Horvath, B Zhang, M Carlson, et al.Molecular Psychiatry|September 10, 2014
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneityJ Ellegood, E Anagnostou, B A Babineau, et al.Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.Pageof 13