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Page 1
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.
Mahtani MM, Widén E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. Mahtani MM, et al. Among authors: lander es. Nat Genet. 1996 Sep;14(1):90-4. doi: 10.1038/ng0996-90. Nat Genet. 1996. PMID: 8782826
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.
Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström M, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen MR, Groop L. Lehto M, et al. J Clin Invest. 1997 Feb 15;99(4):582-91. doi: 10.1172/JCI119199. J Clin Invest. 1997. PMID: 9045858 Free PMC article.
The mosaic structure of variation in the laboratory mouse genome.
Wade CM, Kulbokas EJ 3rd, Kirby AW, Zody MC, Mullikin JC, Lander ES, Lindblad-Toh K, Daly MJ. Wade CM, et al. Among authors: lander es. Nature. 2002 Dec 5;420(6915):574-8. doi: 10.1038/nature01252. Nature. 2002. PMID: 12466852
Limits on fine mapping of complex traits.
Kruglyak L, Lander ES. Kruglyak L, et al. Among authors: lander es. Am J Hum Genet. 1996 May;58(5):1092-3. Am J Hum Genet. 1996. PMID: 8651271 Free PMC article. No abstract available.
554 results