The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. 1.Hamilton BA, Smith DJ, Mueller KL, et al. The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron. 1997;18(5):711-22. Read more
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect. 1.Lehto M, Tuomi T, Mahtani MM, et al. Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect. J Clin Invest. 1997;99(4):582-91. doi:10.1172/JCI119199. Read more
Genetic evaluation of candidate genes for the Mom1 modifier of intestinal neoplasia in mice. 1.Gould KA, Luongo C, Moser AR, et al. Genetic evaluation of candidate genes for the Mom1 modifier of intestinal neoplasia in mice. Genetics. 1996;144(4):1777-85. Read more
Mom1 is a semi-dominant modifier of intestinal adenoma size and multiplicity in Min/+ mice. 1.Gould KA, Dietrich WF, Borenstein N, Lander ES, Dove WF. Mom1 is a semi-dominant modifier of intestinal adenoma size and multiplicity in Min/+ mice. Genetics. 1996;144(4):1769-76. Read more
The new genomics: global views of biology. 1.Lander ES. The new genomics: global views of biology. Science. 1996;274(5287):536-9. Read more
The importance of being independent: sib pair analysis in diabetes. 1.Daly MJ, Lander ES. The importance of being independent: sib pair analysis in diabetes. Nat Genet. 1996;14(2):131-2. doi:10.1038/ng1096-131. Read more
A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome. 1.Haldi ML, Strickland C, Lim P, et al. A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome. Mamm Genome. 1996;7(10):767-9. Read more
Mouse Y-specific repeats isolated by whole chromosome representational difference analysis. 1.Navin A, Prekeris R, Lisitsyn NA, et al. Mouse Y-specific repeats isolated by whole chromosome representational difference analysis. Genomics. 1996;36(2):349-53. doi:10.1006/geno.1996.0473. Read more
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. 1.Mahtani MM, Widen E, Lehto M, et al. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nat Genet. 1996;14(1):90-4. doi:10.1038/ng0996-90. Read more
A locus for Fanconi anemia on 16q determined by homozygosity mapping. 1.Gschwend M, Levran O, Kruglyak L, et al. A locus for Fanconi anemia on 16q determined by homozygosity mapping. Am J Hum Genet. 1996;59(2):377-84. Read more