Findlay GM - Search Results

1

Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulation.

Birnbaum RY, Patwardhan RP, Kim MJ, Findlay GM, Martin B, Zhao J, Bell RJ, Smith RP, Ku AA, Shendure J, Ahituv N. Birnbaum RY, et al. Among authors: findlay gm. PLoS Genet. 2014 Oct 23;10(10):e1004592. doi: 10.1371/journal.pgen.1004592. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25340400 Free PMC article.

2

Saturation editing of genomic regions by multiplex homology-directed repair.

Findlay GM, Boyle EA, Hause RJ, Klein JC, Shendure J. Findlay GM, et al. Nature. 2014 Sep 4;513(7516):120-3. doi: 10.1038/nature13695. Nature. 2014. PMID: 25141179 Free PMC article.

3

Accurate classification of BRCA1 variants with saturation genome editing.

Findlay GM, Daza RM, Martin B, Zhang MD, Leith AP, Gasperini M, Janizek JD, Huang X, Starita LM, Shendure J. Findlay GM, et al. Nature. 2018 Oct;562(7726):217-222. doi: 10.1038/s41586-018-0461-z. Epub 2018 Sep 12. Nature. 2018. PMID: 30209399 Free PMC article.

4

Genomic Medicine-Progress, Pitfalls, and Promise.

Shendure J, Findlay GM, Snyder MW. Shendure J, et al. Among authors: findlay gm. Cell. 2019 Mar 21;177(1):45-57. doi: 10.1016/j.cell.2019.02.003. Cell. 2019. PMID: 30901547 Free PMC article. Review.

5

CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic Deletions.

Gasperini M, Findlay GM, McKenna A, Milbank JH, Lee C, Zhang MD, Cusanovich DA, Shendure J. Gasperini M, et al. Among authors: findlay gm. Am J Hum Genet. 2017 Aug 3;101(2):192-205. doi: 10.1016/j.ajhg.2017.06.010. Epub 2017 Jul 14. Am J Hum Genet. 2017. PMID: 28712454 Free PMC article.

6

Concurrent genome and epigenome editing by CRISPR-mediated sequence replacement.

Alexander J, Findlay GM, Kircher M, Shendure J. Alexander J, et al. Among authors: findlay gm. BMC Biol. 2019 Nov 18;17(1):90. doi: 10.1186/s12915-019-0711-z. BMC Biol. 2019. PMID: 31739790 Free PMC article.

7

Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy course.

Kumar A, Dougherty M, Findlay GM, Geisheker M, Klein J, Lazar J, Machkovech H, Resnick J, Resnick R, Salter AI, Talebi-Liasi F, Arakawa C, Baudin J, Bogaard A, Salesky R, Zhou Q, Smith K, Clark JI, Shendure J, Horwitz MS. Kumar A, et al. Among authors: findlay gm. PLoS One. 2014 Sep 5;9(9):e106744. doi: 10.1371/journal.pone.0106744. eCollection 2014. PLoS One. 2014. PMID: 25192356 Free PMC article.

8

Whole-organism lineage tracing by combinatorial and cumulative genome editing.

McKenna A, Findlay GM, Gagnon JA, Horwitz MS, Schier AF, Shendure J. McKenna A, et al. Among authors: findlay gm. Science. 2016 Jul 29;353(6298):aaf7907. doi: 10.1126/science.aaf7907. Epub 2016 May 26. Science. 2016. PMID: 27229144 Free PMC article.

9

Phosphoproteomics identifies a bimodal EPHA2 receptor switch that promotes embryonic stem cell differentiation.

Fernandez-Alonso R, Bustos F, Budzyk M, Kumar P, Helbig AO, Hukelmann J, Lamond AI, Lanner F, Zhou H, Petsalaki E, Findlay GM. Fernandez-Alonso R, et al. Among authors: findlay gm. Nat Commun. 2020 Mar 13;11(1):1357. doi: 10.1038/s41467-020-15173-4. Nat Commun. 2020. PMID: 32170114 Free PMC article.

10

Linking genome variants to disease: scalable approaches to test the functional impact of human mutations.

Findlay GM. Findlay GM. Hum Mol Genet. 2021 Oct 1;30(R2):R187-R197. doi: 10.1093/hmg/ddab219. Hum Mol Genet. 2021. PMID: 34338757 Free PMC article. Review.

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