Bhidayasiri R, Perlman SL, Pulst SM, Geschwind DH (2005). Late-onset Friedreich ataxia: Phenotypic analysis, magnetic resonance imaging findings, and review of the literature. Archives of Neurology. 62(12): 1865-1869.
Publications
2000-2005
Jarvik LF, LaRue A, Gokhman I, Harrison T, Holt L, Steh B, Harker J, Larson S, Yaralian P, Matsuyama S, Ragson N, Geschwind DH, Freimer N, Jiminez E, Schaeffer J (2005). Middle-aged children of Alzheimer parents, a pilot study: stable neurocognitive performance at 20-year follow-up. Journal of Geriatric Psychiatry and Neurology. 18:187-191.
Dougherty JD, Garcia ADR, Nakano I, Livingstone M, Norris B, Polakiewicz R, Wexler EM, Sofroniew MV, Kornblum HI, Geschwind DH (2005). PBK/TopK, a proliferating neural progenitor-specific mitogen-activated protein kinase kinase. Journal of Neuroscience. 25:10773-10785.
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
Alarcón M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH (2005). Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Molecular Psychiatry. 10:747-757.
Nakano I, Paucar AA, Bajpai R, Dougherty JD, Zewail A, Kelly TK, Kim KJ, Ou J, Grozer M, Imura T, Freije WA, Nelson SF, Sofroniew MV, Wu H, Liu X, Terskikh AV, Geschwind DH, Kornblum HI (2005). Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation. Journal of Cell Biology. 170(3): 413-427.
Bartzokis G, Lu PH, Geschwind DH, Edwards N, Mintz J, Cummings JL (2005). Impact of APOE alleles on age-related myelin breakdown. Journal of Alzheimer’s and Dementia. 1: 28.
Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcón M, Nelson SF, Geschwind DH (2005). Replication of autism linkage: Fine-mapping peak at 17q21. American Journal of Human Genetics. 76:1050-1056.
Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry JT, Orkin SH, Geschwind DH, Walsh CA (2005). Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Science. 308(5729): 1794-1798.
Oliveira JRM. Spiteri E, Sobrido MJ, Hopfer S, Klepper J, Voit T, Gilbert J, Wszolek ZK, Calne DB, Stoessl AJ, Hutton M, Manyam BV, Boller F, Baquero M, Geschwind DH (2004). Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease). Neurology. 63: 2165-7.
Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF (2004). Evidence for sex-specific risk alleles in autism spectrum disorder. American Journal of Human Genetics. 75:1117-1123.
