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Eric Lander

A radiation hybrid map of mouse genes.

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Hudson TJ, Church DM, Greenaway S, et al. A radiation hybrid map of mouse genes. Nat Genet. 2001;29(2):201-5. doi:10.1038/ng1001-201.

On the allelic spectrum of human disease.

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Reich DE, Lander ES. On the allelic spectrum of human disease. Trends Genet. 2001;17(9):502-10.

Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.

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Ardlie K, Liu-Cordero SN, Eberle MA, et al. Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion. Am J Hum Genet. 2001;69(3):582-9. doi:10.1086/323251.

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells.

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Barclay J, Balaguero N, Mione M, et al. Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells. J Neurosci. 2001;21(16):6095-104.

Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.

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Hirschhorn JN, Lindgren CM, Daly MJ, et al. Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet. 2001;69(1):106-16. doi:10.1086/321287.

Growth factor-specific signaling pathway stimulation and gene expression mediated by ErbB receptors.

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Sweeney C, Fambrough D, Huard C, et al. Growth factor-specific signaling pathway stimulation and gene expression mediated by ErbB receptors. J Biol Chem. 2001;276(25):22685-98. doi:10.1074/jbc.M100602200.

Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.

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Sklar P, Schwab SG, Williams NM, et al. Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nat Genet. 2001;28(2):126-8. doi:10.1038/88836.

The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.

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Inoue K, Dewar K, Katsanis N, et al. The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes. Genome Res. 2001;11(6):1018-33. doi:10.1101/gr.180401.

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

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Cavanaugh J, IBD International Genetics Consortium. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am J Hum Genet. 2001;68(5):1165-71. doi:10.1086/320119.

A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.

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Laitinen T, Daly MJ, Rioux JD, et al. A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population. Nat Genet. 2001;28(1):87-91. doi:10.1038/88319.