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Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genome.
Cell Rep. 2021 Aug 31;36(9):109597. doi: 10.1016/j.celrep.2021.109597.
Cell Rep. 2021.
PMID: 34469736
Free PMC article.
CRISPR base editor screens identify variant function at scale.
Parrish PCR, Berger AH.
Parrish PCR, et al.
Mol Cell. 2021 Feb 18;81(4):647-648. doi: 10.1016/j.molcel.2021.01.036.
Mol Cell. 2021.
PMID: 33606973
Free PMC article.
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Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer.
Vichas A, Riley AK, Nkinsi NT, Kamlapurkar S, Parrish PCR, Lo A, Duke F, Chen J, Fung I, Watson J, Rees M, Gabel AM, Thomas JD, Bradley RK, Lee JK, Hatch EM, Baine MK, Rekhtman N, Ladanyi M, Piccioni F, Berger AH.
Vichas A, et al. Among authors: parrish pcr.
Nat Commun. 2021 Aug 9;12(1):4789. doi: 10.1038/s41467-021-24841-y.
Nat Commun. 2021.
PMID: 34373451
Free PMC article.
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Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk.
Parrish PCR, Liu D, Knutsen RH, Billington CJ, Mecham RP, Fu YP, Kozel BA.
Parrish PCR, et al.
Hum Mol Genet. 2020 Jul 29;29(12):2035-2050. doi: 10.1093/hmg/ddaa093.
Hum Mol Genet. 2020.
PMID: 32412588
Free PMC article.
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Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
Kopp ND, Parrish PCR, Lugo M, Dougherty JD, Kozel BA.
Kopp ND, et al. Among authors: parrish pcr.
Mol Genet Genomic Med. 2018 Sep;6(5):749-765. doi: 10.1002/mgg3.429. Epub 2018 Jul 15.
Mol Genet Genomic Med. 2018.
PMID: 30008175
Free PMC article.
Clinical Trial.
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Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.
Lugo M, Wong ZC, Billington CJ Jr, Parrish PCR, Muldoon G, Liu D, Pober BR, Kozel BA.
Lugo M, et al. Among authors: parrish pcr.
Am J Med Genet A. 2020 May;182(5):1008-1020. doi: 10.1002/ajmg.a.61522. Epub 2020 Feb 20.
Am J Med Genet A. 2020.
PMID: 32077592
Free PMC article.
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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.
Liu D, Billington CJ Jr, Raja N, Wong ZC, Levin MD, Resch W, Alba C, Hupalo DN, Biamino E, Bedeschi MF, Digilio MC, Squeo GM, Villa R, Parrish PCR, Knutsen RH, Osgood S, Freeman JA, Dalgard CL, Merla G, Pober BR, Mervis CB, Roberts AE, Morris CA, Osborne LR, Kozel BA.
Liu D, et al. Among authors: parrish pcr.
J Am Heart Assoc. 2024 Feb 6;13(3):e031377. doi: 10.1161/JAHA.123.031377. Epub 2024 Jan 31.
J Am Heart Assoc. 2024.
PMID: 38293922
Free PMC article.
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pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screens.
Parrish PCR, Groso DJ, Thomas JD, Bradley RK, Berger AH.
Parrish PCR, et al.
ArXiv [Preprint]. 2023 Jun 1:arXiv:2306.00944v1.
ArXiv. 2023.
PMID: 37396617
Free PMC article.
Preprint.
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