Evans P - Search Results

1

Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach.

Wu C, Devkota B, Evans P, Zhao X, Baker SW, Niazi R, Cao K, Gonzalez MA, Jayaraman P, Conlin LK, Krock BL, Deardorff MA, Spinner NB, Krantz ID, Santani AB, Tayoun ANA, Sarmady M. Wu C, et al. Among authors: evans p. Eur J Hum Genet. 2019 Apr;27(4):612-620. doi: 10.1038/s41431-018-0328-7. Epub 2019 Jan 9. Eur J Hum Genet. 2019. PMID: 30626929 Free PMC article.

2

The Development and Validation of Clinical Exome-Based Panels Using ExomeSlicer: Considerations and Proof of Concept Using an Epilepsy Panel.

Niazi R, Gonzalez MA, Balciuniene J, Evans P, Sarmady M, Abou Tayoun AN. Niazi R, et al. Among authors: evans p. J Mol Diagn. 2018 Sep;20(5):643-652. doi: 10.1016/j.jmoldx.2018.05.003. Epub 2018 Jun 22. J Mol Diagn. 2018. PMID: 29936260 Free article.

3

Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets.

Evans P, Wu C, Lindy A, McKnight DA, Lebo M, Sarmady M, Abou Tayoun AN. Evans P, et al. Genome Res. 2019 Jul;29(7):1144-1151. doi: 10.1101/gr.240994.118. Epub 2019 Jun 24. Genome Res. 2019. PMID: 31235655 Free PMC article.

4

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

Chang X, Zhao Y, Hou C, Glessner J, McDaniel L, Diamond MA, Thomas K, Li J, Wei Z, Liu Y, Guo Y, Mentch FD, Qiu H, Kim C, Evans P, Vaksman Z, Diskin SJ, Attiyeh EF, Sleiman P, Maris JM, Hakonarson H. Chang X, et al. Among authors: evans p. Nat Commun. 2017 Sep 18;8(1):569. doi: 10.1038/s41467-017-00408-8. Nat Commun. 2017. PMID: 28924153 Free PMC article.

5

Exploiting genetic variation to uncover rules of transcription factor binding and chromatin accessibility.

Behera V, Evans P, Face CJ, Hamagami N, Sankaranarayanan L, Keller CA, Giardine B, Tan K, Hardison RC, Shi J, Blobel GA. Behera V, et al. Among authors: evans p. Nat Commun. 2018 Feb 22;9(1):782. doi: 10.1038/s41467-018-03082-6. Nat Commun. 2018. PMID: 29472540 Free PMC article.

6

Red blood cell alloimmunization in transfused patients with bone marrow failure syndromes.

Cohen D, Hartung H, Evans P, Friedman DF, Chou ST. Cohen D, et al. Among authors: evans p. Transfusion. 2016 Jun;56(6):1314-9. doi: 10.1111/trf.13608. Epub 2016 Apr 15. Transfusion. 2016. PMID: 27080340

7

Functions of BET proteins in erythroid gene expression.

Stonestrom AJ, Hsu SC, Jahn KS, Huang P, Keller CA, Giardine BM, Kadauke S, Campbell AE, Evans P, Hardison RC, Blobel GA. Stonestrom AJ, et al. Among authors: evans p. Blood. 2015 Apr 30;125(18):2825-34. doi: 10.1182/blood-2014-10-607309. Epub 2015 Feb 18. Blood. 2015. PMID: 25696920 Free PMC article.

8

The BET Protein BRD2 Cooperates with CTCF to Enforce Transcriptional and Architectural Boundaries.

Hsu SC, Gilgenast TG, Bartman CR, Edwards CR, Stonestrom AJ, Huang P, Emerson DJ, Evans P, Werner MT, Keller CA, Giardine B, Hardison RC, Raj A, Phillips-Cremins JE, Blobel GA. Hsu SC, et al. Among authors: evans p. Mol Cell. 2017 Apr 6;66(1):102-116.e7. doi: 10.1016/j.molcel.2017.02.027. Mol Cell. 2017. PMID: 28388437 Free PMC article.

9

A hyperactive transcriptional state marks genome reactivation at the mitosis-G1 transition.

Hsiung CC, Bartman CR, Huang P, Ginart P, Stonestrom AJ, Keller CA, Face C, Jahn KS, Evans P, Sankaranarayanan L, Giardine B, Hardison RC, Raj A, Blobel GA. Hsiung CC, et al. Among authors: evans p. Genes Dev. 2016 Jun 15;30(12):1423-39. doi: 10.1101/gad.280859.116. Genes Dev. 2016. PMID: 27340175 Free PMC article.

10

Induction of the Immunoproteasome Subunit Lmp7 Links Proteostasis and Immunity in α-Synuclein Aggregation Disorders.

Ugras S, Daniels MJ, Fazelinia H, Gould NS, Yocum AK, Luk KC, Luna E, Ding H, McKennan C, Seeholzer S, Martinez D, Evans P, Brown D, Duda JE, Ischiropoulos H. Ugras S, et al. Among authors: evans p. EBioMedicine. 2018 May;31:307-319. doi: 10.1016/j.ebiom.2018.05.007. EBioMedicine. 2018. PMID: 29759483 Free PMC article.

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