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Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway.
Andreoletti G, Shakhnovich V, Christenson K, Coelho T, Haggarty R, Afzal NA, Batra A, Petersen BS, Mort M, Beattie RM, Ennis S. Andreoletti G, et al. Among authors: mort m. Sci Rep. 2017 Apr 19;7:46454. doi: 10.1038/srep46454. Sci Rep. 2017. PMID: 28422189 Free PMC article.
Genetic Sequencing of Pediatric Patients Identifies Mutations in Monogenic Inflammatory Bowel Disease Genes that Translate to Distinct Clinical Phenotypes.
Ashton JJ, Mossotto E, Stafford IS, Haggarty R, Coelho TAF, Batra A, Afzal NA, Mort M, Bunyan D, Beattie RM, Ennis S. Ashton JJ, et al. Among authors: mort m. Clin Transl Gastroenterol. 2020 Feb;11(2):e00129. doi: 10.14309/ctg.0000000000000129. Clin Transl Gastroenterol. 2020. PMID: 32463623 Free PMC article.
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
Fragoza R, Das J, Wierbowski SD, Liang J, Tran TN, Liang S, Beltran JF, Rivera-Erick CA, Ye K, Wang TY, Yao L, Mort M, Stenson PD, Cooper DN, Wei X, Keinan A, Schimenti JC, Clark AG, Yu H. Fragoza R, et al. Among authors: mort m. Nat Commun. 2019 Sep 12;10(1):4141. doi: 10.1038/s41467-019-11959-3. Nat Commun. 2019. PMID: 31515488 Free PMC article.
Demographic history and rare allele sharing among human populations.
Gravel S, Henn BM, Gutenkunst RN, Indap AR, Marth GT, Clark AG, Yu F, Gibbs RA; 1000 Genomes Project; Bustamante CD. Gravel S, et al. Proc Natl Acad Sci U S A. 2011 Jul 19;108(29):11983-8. doi: 10.1073/pnas.1019276108. Epub 2011 Jul 5. Proc Natl Acad Sci U S A. 2011. PMID: 21730125 Free PMC article.
168 results