Publications

2000-2005

Gene structure and alternative splicing of glycogen synthase kinase-3 beta (GSK-3ß) in neural and non-neural tissues

Schaffer BAJ, Wiedau-Pazos M, Geschwind DH (2003). Gene structure and alternative splicing of glycogen synthase kinase-3 beta (GSK-3ß) in neural and non-neural tissues. Gene. 302: 73-81.

Human ARX gene: Genomic characterization and expression

Ohira R, Zhang Y-H, Guo W, Dipple K, Shih SL, Doerr J, Huang B-L, Fu L, Abu-Khalil A, Geschwind DH, McCabe ERB (2002). Human ARX gene: Genomic characterization and expression. Molecular Genetics and Metabolism. 77: 179-188.

Human wild type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila

Jackson GR, Wiedau-Pazos M, Sang T-K, Wagle N, Brown CA, Massachi S, Geschwind DH (2002). Human wild type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila. Neuron. 34: 1-20.

Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness

Geschwind DH, Miller BL, DeCarli C, Carmelli D (2002). Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness. Proceedings of the National Academy of Sciences USA. 99: 3176-3181.

Threshholding rules for recovering a sparse signal from microarray experiments

Sabatti C, Karsten SL, Geschwind DH (2002). Threshholding rules for recovering a sparse signal from microarray experiments. Mathematical Biosciences. 176: 17-34.

An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis

Karsten SL, Van Deerlin VMD, Sabatti C, Gill L, Geschwind DH (2002). An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis. Nucleic Acids Research. 30(2): E4.

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

Alarcón M, Cantor RM, Liu J, Gilliam TC, The Autism Genetic Resource Exchange Consortium, Geschwind DH (2002). Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. American Journal of Human Genetics. 70: 60-71.

Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia

Geschwind DH, Robidoux J, Alarcón M, Miller BL, Wilhelmsen KC, Cummings JL, Nasreddine ZS (2001). Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia. Annals of Neurology. 50: 741-746.

The SCA12 mutation as a rare cause of spinocerebellar ataxia

Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH (2001). The SCA12 mutation as a rare cause of spinocerebellar ataxia. Archives of Neurology. 58: 1833-1835.

Report of the Work Group* on frontotemporal dementia and Pick’s disease

McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ (2001). Report of the Work Group* on frontotemporal dementia and Pick’s disease. Archives of Neurology. 58: 1803-1809. (*DH Geschwind, Work Group member and contributor to the Summary.)