Weber JL - Search Results

1

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.

Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, Morrison LA, Green ED, Weber JL. Johnson EW, et al. Among authors: weber jl. Genome Res. 1995 Nov;5(4):368-80. doi: 10.1101/gr.5.4.368. Genome Res. 1995. PMID: 8750196 Free article.

2

A gene responsible for cavernous malformations of the brain maps to chromosome 7q.

Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL. Dubovsky J, et al. Among authors: weber jl. Hum Mol Genet. 1995 Mar;4(3):453-8. doi: 10.1093/hmg/4.3.453. Hum Mol Genet. 1995. PMID: 7795602

3

Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.

Johnson EW, Dubovsky J, Rich SS, O'Donovan CA, Orr HT, Anderson VE, Gil-Nagel A, Ahmann P, Dokken CG, Schneider DT, Weber JL. Johnson EW, et al. Among authors: weber jl. Hum Mol Genet. 1998 Jan;7(1):63-7. doi: 10.1093/hmg/7.1.63. Hum Mol Genet. 1998. PMID: 9384604

4

Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q.

Gil-Nagel A, Dubovsky J, Wilcox KJ, Stewart JM, Anderson VE, Leppik IE, Orr HT, Johnson EW, Weber JL, Rich SS. Gil-Nagel A, et al. Among authors: weber jl. Ann Neurol. 1996 Jun;39(6):807-10. doi: 10.1002/ana.410390619. Ann Neurol. 1996. PMID: 8651655

5

Absence of linkage between 5q markers and serum IgE levels in four large atopic families.

Blumenthal MN, Wang Z, Weber JL, Rich SS. Blumenthal MN, et al. Among authors: weber jl. Clin Exp Allergy. 1996 Aug;26(8):892-6. Clin Exp Allergy. 1996. PMID: 8877153

6

Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.

Matsumoto N, David DE, Johnson EW, Konecki D, Burmester JK, Ledbetter DH, Weber JL. Matsumoto N, et al. Among authors: weber jl. Eur J Hum Genet. 2000 Nov;8(11):875-83. doi: 10.1038/sj.ejhg.5200549. Eur J Hum Genet. 2000. PMID: 11093278

7

Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.

Schellenberg GD, Bird TD, Wijsman EM, Orr HT, Anderson L, Nemens E, White JA, Bonnycastle L, Weber JL, Alonso ME, et al. Schellenberg GD, et al. Among authors: weber jl. Science. 1992 Oct 23;258(5082):668-71. doi: 10.1126/science.1411576. Science. 1992. PMID: 1411576

8

A continuous linkage map of 22 short tandem repeat polymorphisms on human chromosome 12.

Dawson E, Shaikh S, Weber JL, Wang Z, Weissenbach J, Powell JF, Gill M. Dawson E, et al. Among authors: weber jl. Genomics. 1993 Jul;17(1):245-8. doi: 10.1006/geno.1993.1314. Genomics. 1993. PMID: 8406462

9

Mapping of short tandem repeat polymorphisms on human chromosome 3.

Wilkie PJ, Weber JL. Wilkie PJ, et al. Among authors: weber jl. Genomics. 1994 Jan 1;19(1):167-9. doi: 10.1006/geno.1994.1030. Genomics. 1994. PMID: 8188221

10

Continuous linkage map of human chromosome 14 short tandem repeat polymorphisms.

Wang Z, Weber JL. Wang Z, et al. Among authors: weber jl. Genomics. 1992 Jul;13(3):532-6. doi: 10.1016/0888-7543(92)90121-8. Genomics. 1992. PMID: 1639382

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