Lander ES - Search Results

1

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.

Bulman MP, Kusumi K, Frayling TM, McKeown C, Garrett C, Lander ES, Krumlauf R, Hattersley AT, Ellard S, Turnpenny PD. Bulman MP, et al. Among authors: lander es. Nat Genet. 2000 Apr;24(4):438-41. doi: 10.1038/74307. Nat Genet. 2000. PMID: 10742114

2

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

Kusumi K, Sun ES, Kerrebrock AW, Bronson RT, Chi DC, Bulotsky MS, Spencer JB, Birren BW, Frankel WN, Lander ES. Kusumi K, et al. Among authors: lander es. Nat Genet. 1998 Jul;19(3):274-8. doi: 10.1038/961. Nat Genet. 1998. PMID: 9662403

3

Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis.

Lisitsyn NA, Segre JA, Kusumi K, Lisitsyn NM, Nadeau JH, Frankel WN, Wigler MH, Lander ES. Lisitsyn NA, et al. Among authors: lander es. Nat Genet. 1994 Jan;6(1):57-63. doi: 10.1038/ng0194-57. Nat Genet. 1994. PMID: 8136836

4

Disruption of the nuclear hormone receptor RORalpha in staggerer mice.

Hamilton BA, Frankel WN, Kerrebrock AW, Hawkins TL, FitzHugh W, Kusumi K, Russell LB, Mueller KL, van Berkel V, Birren BW, Kruglyak L, Lander ES. Hamilton BA, et al. Among authors: lander es. Nature. 1996 Feb 22;379(6567):736-9. doi: 10.1038/379736a0. Nature. 1996. PMID: 8602221

5

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.

Savukoski M, Klockars T, Holmberg V, Santavuori P, Lander ES, Peltonen L. Savukoski M, et al. Among authors: lander es. Nat Genet. 1998 Jul;19(3):286-8. doi: 10.1038/975. Nat Genet. 1998. PMID: 9662406

6

Construction of a large-insert yeast artificial chromosome library of the mouse genome.

Kusumi K, Smith JS, Segre JA, Koos DS, Lander ES. Kusumi K, et al. Among authors: lander es. Mamm Genome. 1993;4(7):391-2. doi: 10.1007/BF00360591. Mamm Genome. 1993. PMID: 8358173 No abstract available.

7

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.

Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E. Hästbacka J, et al. Nat Genet. 1992 Nov;2(3):204-11. doi: 10.1038/ng1192-204. Nat Genet. 1992. PMID: 1345170

8

Variation in genome-wide mutation rates within and between human families.

Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P; 1000 Genomes Project. Conrad DF, et al. Nat Genet. 2011 Jun 12;43(7):712-4. doi: 10.1038/ng.862. Nat Genet. 2011. PMID: 21666693 Free PMC article.

9

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

Laitinen T, Daly MJ, Rioux JD, Kauppi P, Laprise C, Petäys T, Green T, Cargill M, Haahtela T, Lander ES, Laitinen LA, Hudson TJ, Kere J. Laitinen T, et al. Among authors: lander es. Nat Genet. 2001 May;28(1):87-91. doi: 10.1038/ng0501-87. Nat Genet. 2001. PMID: 11326283

10

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.

Sidow A, Bulotsky MS, Kerrebrock AW, Birren BW, Altshuler D, Jaenisch R, Johnson KR, Lander ES. Sidow A, et al. Among authors: lander es. Nat Genet. 1999 Sep;23(1):104-7. doi: 10.1038/12709. Nat Genet. 1999. PMID: 10471509

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