McInnes G - Search Results

1

Cloud-based interactive analytics for terabytes of genomic variants data.

Pan C, McInnes G, Deflaux N, Snyder M, Bingham J, Datta S, Tsao PS. Pan C, et al. Among authors: mcinnes g. Bioinformatics. 2017 Dec 1;33(23):3709-3715. doi: 10.1093/bioinformatics/btx468. Bioinformatics. 2017. PMID: 28961771 Free PMC article.

2

Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.

McInnes G, Tanigawa Y, DeBoever C, Lavertu A, Olivieri JE, Aguirre M, Rivas MA. McInnes G, et al. Bioinformatics. 2019 Jul 15;35(14):2495-2497. doi: 10.1093/bioinformatics/bty999. Bioinformatics. 2019. PMID: 30520965 Free PMC article.

3

Transfer learning enables prediction of CYP2D6 haplotype function.

McInnes G, Dalton R, Sangkuhl K, Whirl-Carrillo M, Lee SB, Tsao PS, Gaedigk A, Altman RB, Woodahl EL. McInnes G, et al. PLoS Comput Biol. 2020 Nov 2;16(11):e1008399. doi: 10.1371/journal.pcbi.1008399. eCollection 2020 Nov. PLoS Comput Biol. 2020. PMID: 33137098 Free PMC article.

4

Pharmacogenomics and big genomic data: from lab to clinic and back again.

Lavertu A, McInnes G, Daneshjou R, Whirl-Carrillo M, Klein TE, Altman RB. Lavertu A, et al. Among authors: mcinnes g. Hum Mol Genet. 2018 May 1;27(R1):R72-R78. doi: 10.1093/hmg/ddy116. Hum Mol Genet. 2018. PMID: 29635477 Free PMC article. Review.

5

Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study.

DeBoever C, Tanigawa Y, Lindholm ME, McInnes G, Lavertu A, Ingelsson E, Chang C, Ashley EA, Bustamante CD, Daly MJ, Rivas MA. DeBoever C, et al. Among authors: mcinnes g. Nat Commun. 2018 Apr 24;9(1):1612. doi: 10.1038/s41467-018-03910-9. Nat Commun. 2018. PMID: 29691392 Free PMC article.

6

Genetic Variation among Pharmacogenes in the Sardinian Population.

Idda ML, Zoledziewska M, Urru SAM, McInnes G, Bilotta A, Nuvoli V, Lodde V, Orrù S, Schlessinger D, Cucca F, Floris M. Idda ML, et al. Among authors: mcinnes g. Int J Mol Sci. 2022 Sep 2;23(17):10058. doi: 10.3390/ijms231710058. Int J Mol Sci. 2022. PMID: 36077453 Free PMC article.

7

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods.

Critical Assessment of Genome Interpretation Consortium. Critical Assessment of Genome Interpretation Consortium. Genome Biol. 2024 Feb 22;25(1):53. doi: 10.1186/s13059-023-03113-6. Genome Biol. 2024. PMID: 38389099 Free PMC article.

8

Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.

DeBoever C, Tanigawa Y, Aguirre M, McInnes G, Lavertu A, Rivas MA. DeBoever C, et al. Among authors: mcinnes g. Am J Hum Genet. 2020 May 7;106(5):611-622. doi: 10.1016/j.ajhg.2020.03.007. Epub 2020 Apr 9. Am J Hum Genet. 2020. PMID: 32275883 Free PMC article.

9

Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.

McInnes G, Daneshjou R, Katsonis P, Lichtarge O, Srinivasan R, Rana S, Radivojac P, Mooney SD, Pagel KA, Stamboulian M, Jiang Y, Capriotti E, Wang Y, Bromberg Y, Bovo S, Savojardo C, Martelli PL, Casadio R, Pal LR, Moult J, Brenner SE, Altman R. McInnes G, et al. Hum Mutat. 2019 Sep;40(9):1314-1320. doi: 10.1002/humu.23825. Epub 2019 Jun 24. Hum Mutat. 2019. PMID: 31140652 Free PMC article.

10

Homology modeling of TMPRSS2 yields candidate drugs that may inhibit entry of SARS-CoV-2 into human cells.

Rensi S, Keys A, Lo YC, Derry A, McInnes G, Liu T, Altman R. Rensi S, et al. Among authors: mcinnes g. ChemRxiv [Preprint]. 2020 Mar 20. doi: 10.26434/chemrxiv.12009582. ChemRxiv. 2020. PMID: 32511288 Free PMC article. Preprint.

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