Publications

A genetic analysis of neural progenitor differentiation

Geschwind DH, Ou J, Easterday MC, Dougherty JD, Jackson RJ, Chen Z, Antoine H, Terskikh A, Weissman IL, Nelson SF, Kornblum HI (2001). A genetic analysis of neural progenitor differentiation. Neuron. 29(2): 325-39.

Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease)

Geschwind DH, Loginov M, Stern JM (1999). Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). American Journal of Human Genetics. 65: 764- 772.

The inheritance of frontotemporal dementia

Chow T, Miller BL, Hayashi V, Geschwind DH (1999). The inheritance of frontotemporal dementia. Archives of Neurology. 56: 817-822.

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

Nasreddine ZS, Loginov M, Clark L, Lamarche J, Miller BL, Lamontagne A, Zhukareva V, Lee VM-Y, Wilhelmsen K, Geschwind DH (1999). From genotype to phenotype: A clinical, pathological and biochemical investigation of frontotemporal dementia and Parkinsonism (FTDP-17) caused by the P301L tau mutation. Annals of Neurology. 45: 704-715.

Klinefelter’s syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray

Geschwind DH, Gregg J, Boone K, Karrim J, Pawlikowska-Haddal A, Rao E, Ellison J, Ciccodicola A, D’Urso M, Woods R, Rappold GA, Swerdloff R, Nelson SF (1998). Klinefelter’s syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray. Developmental Genetics. 23(3): 215-29.

Mutation-specific functional impairments in distinct tau isoforms in hereditary FTDP-17

Hong M, Zhukareva V, Vogelsberg-Ragaglia V, Wszolek Z, Reed L, Miller B, Geschwind DH, Bird TD, McKeel D, Goate A, Morris JC, Wilhelmsen KC, Schellenberg GD, Trojanowski JQ, Lee VM-Y (1998). Mutation-specific functional impairments in distinct tau isoforms in hereditary FTDP-17. Science. 282(5395): 1914-1917.

Oculomotor phenotypes in autosomal dominant ataxias

Buttner N, Geschwind DH, Jen JC, Perlman S, Pulst S-M, Baloh RW (1998). Oculomotor phenotypes in autosomal dominant ataxias. Archives of Neurology. 55(10): 1353-7.

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 1

Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller BL, Li D, Payami H, Arwert F, Markopoulou K, Andreadis A, D’Souza I, Lee VM-Y, Reed L, Trojanowski JQ, Zhukareva V, Bird T, Schellenberg G, Wilhelmsen KC (1998). Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 1. Proceedings of the National Academy of Sciences USA. 95(22): 13103-7.

The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia

Geschwind DH, Karrim J, Nelson SF, Miller B (1998). The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia. Annals of Neurology. 44(1): 134-138.

Genomic organization, 5′ flanking enhancer region, and chromosomal assignment of the cell cycle gene, p55Cdc

Weinstein J, Karrim J, Geschwind DH, Nelson SF, J Krumm, Sakamoto KM (1998). Genomic organization, 5′ flanking enhancer region, and chromosomal assignment of the cell cycle gene, p55Cdc. Molecular Genetics and Metabolism. 64: 52-7.