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Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82.
Erjavec SO, Gelfman S, Abdelaziz AR, Lee EY, Monga I, Alkelai A, Ionita-Laza I, Petukhova L, Christiano AM. Erjavec SO, et al. Among authors: christiano am. Nat Commun. 2022 Feb 10;13(1):800. doi: 10.1038/s41467-022-28343-3. Nat Commun. 2022. PMID: 35145093 Free PMC article.
Genetic linkage studies in alopecia areata.
Martinez-Mir A, Zlotogorski A, Ott J, Gordon D, Christiano AM. Martinez-Mir A, et al. Among authors: christiano am. J Investig Dermatol Symp Proc. 2003 Oct;8(2):199-203. doi: 10.1046/j.1087-0024.2003.00809.x. J Investig Dermatol Symp Proc. 2003. PMID: 14582673 Free article. Review.
Search for susceptibility genes in alopecia areata.
Martinez-Mir A, Zlotogorski A, Christiano AM. Martinez-Mir A, et al. Among authors: christiano am. J Investig Dermatol Symp Proc. 2005 Dec;10(3):281-2. doi: 10.1111/j.0022-202X.2005.10130_3.x. J Investig Dermatol Symp Proc. 2005. PMID: 16402481 Free article. No abstract available.
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.
Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, Londono D, Haynes C, Ott J, Hordinsky M, Nanova K, Norris D, Price V, Duvic M, Christiano AM. Martinez-Mir A, et al. Among authors: christiano am. Am J Hum Genet. 2007 Feb;80(2):316-28. doi: 10.1086/511442. Epub 2007 Jan 5. Am J Hum Genet. 2007. PMID: 17236136 Free PMC article.
APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.
Shimomura Y, Agalliu D, Vonica A, Luria V, Wajid M, Baumer A, Belli S, Petukhova L, Schinzel A, Brivanlou AH, Barres BA, Christiano AM. Shimomura Y, et al. Among authors: christiano am. Nature. 2010 Apr 15;464(7291):1043-7. doi: 10.1038/nature08875. Nature. 2010. PMID: 20393562 Free PMC article.
436 results