Moult J - Search Results

1

Lessons from the CAGI-4 Hopkins clinical panel challenge.

Chandonia JM, Adhikari A, Carraro M, Chhibber A, Cutting GR, Fu Y, Gasparini A, Jones DT, Kramer A, Kundu K, Lam HYK, Leonardi E, Moult J, Pal LR, Searls DB, Shah S, Sunyaev S, Tosatto SCE, Yin Y, Buckley BA. Chandonia JM, et al. Among authors: moult j. Hum Mutat. 2017 Sep;38(9):1155-1168. doi: 10.1002/humu.23225. Epub 2017 Jun 12. Hum Mutat. 2017. PMID: 28397312 Free PMC article.

2

SNPs, protein structure, and disease.

Wang Z, Moult J. Wang Z, et al. Among authors: moult j. Hum Mutat. 2001 Apr;17(4):263-70. doi: 10.1002/humu.22. Hum Mutat. 2001. PMID: 11295823

3

Protein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitution.

Gorlatova N, Chao K, Pal LR, Araj RH, Galkin A, Turko I, Moult J, Herzberg O. Gorlatova N, et al. Among authors: moult j. PLoS One. 2011;6(11):e27269. doi: 10.1371/journal.pone.0027269. Epub 2011 Nov 7. PLoS One. 2011. PMID: 22087277 Free PMC article.

4

Increasing the stability of the bacteriophage endolysin PlyC using rationale-based FoldX computational modeling.

Heselpoth RD, Yin Y, Moult J, Nelson DC. Heselpoth RD, et al. Among authors: moult j. Protein Eng Des Sel. 2015 Apr;28(4):85-92. doi: 10.1093/protein/gzv004. Epub 2015 Mar 3. Protein Eng Des Sel. 2015. PMID: 25740429

5

Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.

Pal LR, Moult J. Pal LR, et al. Among authors: moult j. J Mol Biol. 2015 Jul 3;427(13):2271-89. doi: 10.1016/j.jmb.2015.04.014. Epub 2015 May 1. J Mol Biol. 2015. PMID: 25937569 Free PMC article.

6

Insights from GWAS: emerging landscape of mechanisms underlying complex trait disease.

Pal LR, Yu CH, Mount SM, Moult J. Pal LR, et al. Among authors: moult j. BMC Genomics. 2015;16 Suppl 8(Suppl 8):S4. doi: 10.1186/1471-2164-16-S8-S4. Epub 2015 Jun 18. BMC Genomics. 2015. PMID: 26110739 Free PMC article.

7

Consensus Genome-Wide Expression Quantitative Trait Loci and Their Relationship with Human Complex Trait Disease.

Yu CH, Pal LR, Moult J. Yu CH, et al. Among authors: moult j. OMICS. 2016 Jul;20(7):400-14. doi: 10.1089/omi.2016.0063. OMICS. 2016. PMID: 27428252 Free PMC article.

8

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.

Carraro M, Minervini G, Giollo M, Bromberg Y, Capriotti E, Casadio R, Dunbrack R, Elefanti L, Fariselli P, Ferrari C, Gough J, Katsonis P, Leonardi E, Lichtarge O, Menin C, Martelli PL, Niroula A, Pal LR, Repo S, Scaini MC, Vihinen M, Wei Q, Xu Q, Yang Y, Yin Y, Zaucha J, Zhao H, Zhou Y, Brenner SE, Moult J, Tosatto SCE. Carraro M, et al. Among authors: moult j. Hum Mutat. 2017 Sep;38(9):1042-1050. doi: 10.1002/humu.23235. Epub 2017 May 16. Hum Mutat. 2017. PMID: 28440912 Free PMC article.

9

Determination of disease phenotypes and pathogenic variants from exome sequence data in the CAGI 4 gene panel challenge.

Kundu K, Pal LR, Yin Y, Moult J. Kundu K, et al. Among authors: moult j. Hum Mutat. 2017 Sep;38(9):1201-1216. doi: 10.1002/humu.23249. Epub 2017 Jun 27. Hum Mutat. 2017. PMID: 28497567 Free PMC article.

10

CAGI4 SickKids clinical genomes challenge: A pipeline for identifying pathogenic variants.

Pal LR, Kundu K, Yin Y, Moult J. Pal LR, et al. Among authors: moult j. Hum Mutat. 2017 Sep;38(9):1169-1181. doi: 10.1002/humu.23257. Epub 2017 Jun 27. Hum Mutat. 2017. PMID: 28512736 Free PMC article.

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