Weber J - Search Results

1

Evidence that a locus for familial psoriasis maps to chromosome 4q.

Matthews D, Fry L, Powles A, Weber J, McCarthy M, Fisher E, Davies K, Williamson R. Matthews D, et al. Among authors: weber j. Nat Genet. 1996 Oct;14(2):231-3. doi: 10.1038/ng1096-231. Nat Genet. 1996. PMID: 8841203

2

Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.

Twells R, Yenchitsomanus PT, Sirinavin C, Allotey R, Poungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P, et al. Twells R, et al. Among authors: weber j. Hum Mol Genet. 1994 Jan;3(1):177-80. doi: 10.1093/hmg/3.1.177. Hum Mol Genet. 1994. PMID: 8162021

3

Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q.

Fenske CD, Jeffery S, Weber JL, Houlston RS, Leonard JV, Lee PJ. Fenske CD, et al. Among authors: weber jl. J Med Genet. 1998 Apr;35(4):269-72. doi: 10.1136/jmg.35.4.269. J Med Genet. 1998. PMID: 9598717 Free PMC article.

4

Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.

Ocaka L, Zhao C, Reed JA, Ebenezer ND, Brice G, Morley T, Mehta M, O'Dowd J, Weber JL, Hardcastle AJ, Child AH. Ocaka L, et al. Among authors: weber jl. J Med Genet. 2008 Feb;45(2):87-92. doi: 10.1136/jmg.2007.051896. Epub 2007 Oct 11. J Med Genet. 2008. PMID: 17932119

5

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.

Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C, et al. Gispert S, et al. Among authors: weber j. Nat Genet. 1993 Jul;4(3):295-9. doi: 10.1038/ng0793-295. Nat Genet. 1993. PMID: 8358438

6

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. Heutink P, et al. Among authors: weber j. J Med Genet. 1990 Jul;27(7):433-6. doi: 10.1136/jmg.27.7.433. J Med Genet. 1990. PMID: 2395161 Free PMC article.

7

Genetic linkage of Werner's syndrome to five markers on chromosome 8.

Goto M, Rubenstein M, Weber J, Woods K, Drayna D. Goto M, et al. Among authors: weber j. Nature. 1992 Feb 20;355(6362):735-8. doi: 10.1038/355735a0. Nature. 1992. PMID: 1741060

8

The Iceland map.

Weber JL. Weber JL. Nat Genet. 2002 Jul;31(3):225-6. doi: 10.1038/ng920. Epub 2002 Jun 10. Nat Genet. 2002. PMID: 12053179 No abstract available.

9

Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.

Cho JH, Nicolae DL, Gold LH, Fields CT, LaBuda MC, Rohal PM, Pickles MR, Qin L, Fu Y, Mann JS, Kirschner BS, Jabs EW, Weber J, Hanauer SB, Bayless TM, Brant SR. Cho JH, et al. Among authors: weber j. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7502-7. doi: 10.1073/pnas.95.13.7502. Proc Natl Acad Sci U S A. 1998. PMID: 9636179 Free PMC article.

10

Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.

Niemann S, Zhao C, Pascu F, Stahl U, Aulepp U, Niswander L, Weber JL, Müller U. Niemann S, et al. Am J Hum Genet. 2004 Mar;74(3):558-63. doi: 10.1086/382196. Epub 2004 Feb 5. Am J Hum Genet. 2004. PMID: 14872406 Free PMC article.

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