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Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82.
Nat Commun. 2022 Feb 10;13(1):800. doi: 10.1038/s41467-022-28343-3.
Nat Commun. 2022.
PMID: 35145093
Free PMC article.
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy.
Petukhova L, Patel AV, Rigo RK, Bian L, Verbitsky M, Sanna-Cherchi S, Erjavec SO, Abdelaziz AR, Cerise JE, Jabbari A, Christiano AM.
Petukhova L, et al. Among authors: erjavec so.
Exp Dermatol. 2020 Mar;29(3):243-253. doi: 10.1111/exd.13986. Epub 2019 Jul 9.
Exp Dermatol. 2020.
PMID: 31169925
Free PMC article.
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A semi-supervised model to predict regulatory effects of genetic variants at single nucleotide resolution using massively parallel reporter assays.
Yang Z, Wang C, Erjavec S, Petukhova L, Christiano A, Ionita-Laza I.
Yang Z, et al.
Bioinformatics. 2021 Jan 30;37(14):1953-62. doi: 10.1093/bioinformatics/btab040. Online ahead of print.
Bioinformatics. 2021.
PMID: 33515242
Free PMC article.
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Improved therapeutic efficacy of unmodified anti-tumor antibodies by immune checkpoint blockade and kinase targeted therapy in mouse models of melanoma.
Pérez-Lorenzo R, Erjavec SO, Christiano AM, Clynes R.
Pérez-Lorenzo R, et al. Among authors: erjavec so.
Oncotarget. 2021 Jan 19;12(2):66-80. doi: 10.18632/oncotarget.27868. eCollection 2021 Jan 19.
Oncotarget. 2021.
PMID: 33520112
Free PMC article.
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