Weber J - Search Results

1

Heutink P, Sandkuyl LA, van de Wetering BJ, Oostra BA, Weber J, Wilkie P, Devor EJ, Pakstis AJ, Pauls D, Kidd KK. Heutink P, et al. Among authors: weber j. Lancet. 1991 Jan 12;337(8733):122-3. doi: 10.1016/0140-6736(91)90788-q. Lancet. 1991. PMID: 1670715 No abstract available.

2

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.

3

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

4

Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population.

Simonic I, Gericke GS, Ott J, Weber JL. Simonic I, et al. Among authors: weber jl. Am J Hum Genet. 1998 Sep;63(3):839-46. doi: 10.1086/302002. Am J Hum Genet. 1998. PMID: 9718333 Free PMC article.

5

Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p.

Vitale E, Brancolini V, De Rienzo A, Bird L, Allada V, Sklansky M, Chae CU, Ferrero GB, Weber J, Devoto M, Casey B. Vitale E, et al. Among authors: weber j. J Med Genet. 2001 Mar;38(3):182-5. doi: 10.1136/jmg.38.3.182. J Med Genet. 2001. PMID: 11303511 Free PMC article. No abstract available.

6

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.

7

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

8

North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.

Small KW, Weber J, Roses A, Pericak-Vance P. Small KW, et al. Among authors: weber j. Ophthalmic Paediatr Genet. 1993 Dec;14(4):143-50. doi: 10.3109/13816819309042913. Ophthalmic Paediatr Genet. 1993. PMID: 8015785 Review.

9

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

10

Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

Kissebah AH, Sonnenberg GE, Myklebust J, Goldstein M, Broman K, James RG, Marks JA, Krakower GR, Jacob HJ, Weber J, Martin L, Blangero J, Comuzzie AG. Kissebah AH, et al. Among authors: weber j. Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14478-83. doi: 10.1073/pnas.97.26.14478. Proc Natl Acad Sci U S A. 2000. PMID: 11121050 Free PMC article.

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