Lathrop GM - Search Results

1

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q.

Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann JS, Velho G, Lathrop GM, Froguel P. Vaxillaire M, et al. Among authors: lathrop gm. Nat Genet. 1995 Apr;9(4):418-23. doi: 10.1038/ng0495-418. Nat Genet. 1995. PMID: 7795649

2

Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).

Vaxillaire M, Rouard M, Yamagata K, Oda N, Kaisaki PJ, Boriraj VV, Chevre JC, Boccio V, Cox RD, Lathrop GM, Dussoix P, Philippe J, Timsit J, Charpentier G, Velho G, Bell GI, Froguel P. Vaxillaire M, et al. Among authors: lathrop gm. Hum Mol Genet. 1997 Apr;6(4):583-6. doi: 10.1093/hmg/6.4.583. Hum Mol Genet. 1997. PMID: 9097962

3

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

Julier C, Delépine M, Keavney B, Terwilliger J, Davis S, Weeks DE, Bui T, Jeunemaître X, Velho G, Froguel P, Ratcliffe P, Corvol P, Soubrier F, Lathrop GM. Julier C, et al. Among authors: lathrop gm. Hum Mol Genet. 1997 Nov;6(12):2077-85. doi: 10.1093/hmg/6.12.2077. Hum Mol Genet. 1997. PMID: 9328471

4

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3).

Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Bell GI, et al. Yamagata K, et al. Among authors: lathrop gm. Nature. 1996 Dec 5;384(6608):455-8. doi: 10.1038/384455a0. Nature. 1996. PMID: 8945470 Free article.

5

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12.

Satsangi J, Parkes M, Louis E, Hashimoto L, Kato N, Welsh K, Terwilliger JD, Lathrop GM, Bell JI, Jewell DP. Satsangi J, et al. Among authors: lathrop gm. Nat Genet. 1996 Oct;14(2):199-202. doi: 10.1038/ng1096-199. Nat Genet. 1996. PMID: 8841195

6

Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish population.

Peral B, San Millán JL, Hernández C, Valero A, Lathrop GM, Beckmann JS, Moreno F. Peral B, et al. Among authors: lathrop gm. J Med Genet. 1993 Nov;30(11):910-3. doi: 10.1136/jmg.30.11.910. J Med Genet. 1993. PMID: 7905535 Free PMC article.

7

Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis.

Trembath RC, Clough RL, Rosbotham JL, Jones AB, Camp RD, Frodsham A, Browne J, Barber R, Terwilliger J, Lathrop GM, Barker JN. Trembath RC, et al. Among authors: lathrop gm. Hum Mol Genet. 1997 May;6(5):813-20. doi: 10.1093/hmg/6.5.813. Hum Mol Genet. 1997. PMID: 9158158

8

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.

Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, et al. Tournier-Lasserve E, et al. Among authors: lathrop gm. Nat Genet. 1993 Mar;3(3):256-9. doi: 10.1038/ng0393-256. Nat Genet. 1993. PMID: 8485581

9

True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping.

Terwilliger JD, Shannon WD, Lathrop GM, Nolan JP, Goldin LR, Chase GA, Weeks DE. Terwilliger JD, et al. Among authors: lathrop gm. Am J Hum Genet. 1997 Aug;61(2):430-8. doi: 10.1086/514855. Am J Hum Genet. 1997. PMID: 9311749 Free PMC article.

10

A first high-density map of 981 biallelic markers on human chromosome 14.

Escary JL, Bottius E, Prince N, Reyes C, Fiawoumo Y, Caloustian C, Bruls T, Fujiyama A, Cooper RS, Adeyemo AA, Lathrop GM, Weissenbach J, Gyapay G, Foglio M, Beckmann JS. Escary JL, et al. Among authors: lathrop gm. Genomics. 2000 Dec 1;70(2):153-64. doi: 10.1006/geno.2000.6369. Genomics. 2000. PMID: 11112343

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