Fowler DM[au] - Search Results

Year	Number of Results
2006	4
2007	3
2008	1
2009	2
2010	2
2011	4
2012	2
2013	3
2014	3
2015	2
2016	1
2017	13
2018	4
2019	11
2020	13
2021	7
2022	2
2023	12
2024	6

1

Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots".

Dines JN, Shirts BH, Slavin TP, Walsh T, King MC, Fowler DM, Pritchard CC. Dines JN, et al. Among authors: fowler dm. Genet Med. 2020 May;22(5):825-830. doi: 10.1038/s41436-019-0740-6. Epub 2020 Jan 8. Genet Med. 2020. PMID: 31911673 Free PMC article.

2

Will variants of uncertain significance still exist in 2030?

Fowler DM, Rehm HL. Fowler DM, et al. Am J Hum Genet. 2024 Jan 4;111(1):5-10. doi: 10.1016/j.ajhg.2023.11.005. Epub 2023 Dec 11. Am J Hum Genet. 2024. PMID: 38086381 Review.

3

Multiplex assessment of protein variant abundance by massively parallel sequencing.

Matreyek KA, Starita LM, Stephany JJ, Martin B, Chiasson MA, Gray VE, Kircher M, Khechaduri A, Dines JN, Hause RJ, Bhatia S, Evans WE, Relling MV, Yang W, Shendure J, Fowler DM. Matreyek KA, et al. Among authors: fowler dm. Nat Genet. 2018 Jun;50(6):874-882. doi: 10.1038/s41588-018-0122-z. Epub 2018 May 21. Nat Genet. 2018. PMID: 29785012 Free PMC article.

4

Massively Parallel Functional Analysis of BRCA1 RING Domain Variants.

Starita LM, Young DL, Islam M, Kitzman JO, Gullingsrud J, Hause RJ, Fowler DM, Parvin JD, Shendure J, Fields S. Starita LM, et al. Among authors: fowler dm. Genetics. 2015 Jun;200(2):413-22. doi: 10.1534/genetics.115.175802. Epub 2015 Mar 30. Genetics. 2015. PMID: 25823446 Free PMC article.

5

Deep mutational scanning: a new style of protein science.

Fowler DM, Fields S. Fowler DM, et al. Nat Methods. 2014 Aug;11(8):801-7. doi: 10.1038/nmeth.3027. Nat Methods. 2014. PMID: 25075907 Free PMC article.

6

An improved platform for functional assessment of large protein libraries in mammalian cells.

Matreyek KA, Stephany JJ, Chiasson MA, Hasle N, Fowler DM. Matreyek KA, et al. Among authors: fowler dm. Nucleic Acids Res. 2020 Jan 10;48(1):e1. doi: 10.1093/nar/gkz910. Nucleic Acids Res. 2020. PMID: 31612958 Free PMC article.

7

An Atlas of Variant Effects to understand the genome at nucleotide resolution.

Fowler DM, Adams DJ, Gloyn AL, Hahn WC, Marks DS, Muffley LA, Neal JT, Roth FP, Rubin AF, Starita LM, Hurles ME. Fowler DM, et al. Genome Biol. 2023 Jul 3;24(1):147. doi: 10.1186/s13059-023-02986-x. Genome Biol. 2023. PMID: 37394429 Free PMC article.

8

Keeping up with the genomes: scaling genomic variant interpretation.

Rehm HL, Fowler DM. Rehm HL, et al. Among authors: fowler dm. Genome Med. 2019 Dec 31;12(1):5. doi: 10.1186/s13073-019-0700-4. Genome Med. 2019. PMID: 31892366 Free PMC article. No abstract available.

9

Biophysical and Mechanistic Models for Disease-Causing Protein Variants.

Stein A, Fowler DM, Hartmann-Petersen R, Lindorff-Larsen K. Stein A, et al. Among authors: fowler dm. Trends Biochem Sci. 2019 Jul;44(7):575-588. doi: 10.1016/j.tibs.2019.01.003. Epub 2019 Jan 31. Trends Biochem Sci. 2019. PMID: 30712981 Free PMC article. Review.

10

A chemically controlled Cas9 switch enables temporal modulation of diverse effectors.

Wei CT, Popp NA, Peleg O, Powell RL, Borenstein E, Maly DJ, Fowler DM. Wei CT, et al. Among authors: fowler dm. Nat Chem Biol. 2023 Aug;19(8):981-991. doi: 10.1038/s41589-023-01278-6. Epub 2023 Mar 6. Nat Chem Biol. 2023. PMID: 36879061 Free PMC article.

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