Alkhateeb A - Search Results

1

Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2.

Alkhateeb A, Stetler GL, Old W, Talbert J, Uhlhorn C, Taylor M, Fox A, Miller C, Dills DG, Ridgway EC, Bennett DC, Fain PR, Spritz RA. Alkhateeb A, et al. Hum Mol Genet. 2002 Mar 15;11(6):661-7. doi: 10.1093/hmg/11.6.661. Hum Mol Genet. 2002. PMID: 11912181

2

A genomewide screen for generalized vitiligo: confirmation of AIS1 on chromosome 1p31 and evidence for additional susceptibility loci.

Fain PR, Gowan K, LaBerge GS, Alkhateeb A, Stetler GL, Talbert J, Bennett DC, Spritz RA. Fain PR, et al. Among authors: alkhateeb a. Am J Hum Genet. 2003 Jun;72(6):1560-4. doi: 10.1086/375451. Epub 2003 Apr 18. Am J Hum Genet. 2003. PMID: 12707860 Free PMC article.

3

Epidemiology of vitiligo and associated autoimmune diseases in Caucasian probands and their families.

Alkhateeb A, Fain PR, Thody A, Bennett DC, Spritz RA. Alkhateeb A, et al. Pigment Cell Res. 2003 Jun;16(3):208-14. doi: 10.1034/j.1600-0749.2003.00032.x. Pigment Cell Res. 2003. PMID: 12753387

4

Human and mouse disorders of pigmentation.

Spritz RA, Chiang PW, Oiso N, Alkhateeb A. Spritz RA, et al. Among authors: alkhateeb a. Curr Opin Genet Dev. 2003 Jun;13(3):284-9. doi: 10.1016/s0959-437x(03)00059-5. Curr Opin Genet Dev. 2003. PMID: 12787791 Review.

5

Candidate functional promoter variant in the FOXD3 melanoblast developmental regulator gene in autosomal dominant vitiligo.

Alkhateeb A, Fain PR, Spritz RA. Alkhateeb A, et al. J Invest Dermatol. 2005 Aug;125(2):388-91. doi: 10.1111/j.0022-202X.2005.23822.x. J Invest Dermatol. 2005. PMID: 16098053 Free article. No abstract available.

6

Fine mapping of progressive pseudorheumatoid dysplasia: a tool for heterozygote identification.

Alkhateeb A, al-Alami J, Leal SM, el-Shanti H. Alkhateeb A, et al. Genet Test. 1999;3(4):329-33. doi: 10.1089/gte.1999.3.329. Genet Test. 1999. PMID: 10627939 Free PMC article.

7

Propionic acidemia: analysis of mutant propionyl-CoA carboxylase enzymes expressed in Escherichia coli.

Chloupkova M, Maclean KN, Alkhateeb A, Kraus JP. Chloupkova M, et al. Among authors: alkhateeb a. Hum Mutat. 2002 Jun;19(6):629-40. doi: 10.1002/humu.10085. Hum Mutat. 2002. PMID: 12007220

8

NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.

Waggoner DJ, Raca G, Welch K, Dempsey M, Anderes E, Ostrovnaya I, Alkhateeb A, Kamimura J, Matsumoto N, Schaeffer GB, Martin CL, Das S. Waggoner DJ, et al. Among authors: alkhateeb a. Genet Med. 2005 Oct;7(8):524-33. doi: 10.1097/01.GIM.0000178503.15559.d3. Genet Med. 2005. PMID: 16247291 Free article.

9

Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population.

Alkhateeb A, Marzouka NA, Tashtoush R. Alkhateeb A, et al. Endocrine. 2013 Dec;44(3):702-9. doi: 10.1007/s12020-013-9908-z. Epub 2013 Mar 6. Endocrine. 2013. PMID: 23463390

10

Genetic association of NALP1 with generalized vitiligo in Jordanian Arabs.

Alkhateeb A, Qarqaz F. Alkhateeb A, et al. Arch Dermatol Res. 2010 Oct;302(8):631-4. doi: 10.1007/s00403-010-1064-1. Epub 2010 Jun 24. Arch Dermatol Res. 2010. PMID: 20574744

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