Zhou AY - Search Results

1

Identification of a novel GREM1 duplication in a patient with multiple colon polyps.

McKenna DB, Van Den Akker J, Zhou AY, Ryan L, Leon A, O'Connor R, Shah PD, Rustgi AK, Katona BW. McKenna DB, et al. Among authors: zhou ay. Fam Cancer. 2019 Jan;18(1):63-66. doi: 10.1007/s10689-018-0090-6. Fam Cancer. 2019. PMID: 29804199 Free PMC article.

2

Inherited predisposition to breast and ovarian cancer in non-Jewish populations in Israel.

Zidan J, Zhou AY, van den Akker J, Laitman Y, Schayek H, Schnaider J, Friedman E. Zidan J, et al. Among authors: zhou ay. Breast Cancer Res Treat. 2017 Dec;166(3):881-885. doi: 10.1007/s10549-017-4474-3. Epub 2017 Aug 21. Breast Cancer Res Treat. 2017. PMID: 28828701

3

A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencing.

van den Akker J, Mishne G, Zimmer AD, Zhou AY. van den Akker J, et al. Among authors: zhou ay. BMC Genomics. 2018 Apr 17;19(1):263. doi: 10.1186/s12864-018-4659-0. BMC Genomics. 2018. PMID: 29665779 Free PMC article.

4

Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines.

Neben CL, Zimmer AD, Stedden W, van den Akker J, O'Connor R, Chan RC, Chen E, Tan Z, Leon A, Ji J, Topper S, Zhou AY. Neben CL, et al. Among authors: zhou ay. J Mol Diagn. 2019 Jul;21(4):646-657. doi: 10.1016/j.jmoldx.2019.03.001. Epub 2019 Jun 11. J Mol Diagn. 2019. PMID: 31201024 Free article.

5

LEAP: Using machine learning to support variant classification in a clinical setting.

Lai C, Zimmer AD, O'Connor R, Kim S, Chan R, van den Akker J, Zhou AY, Topper S, Mishne G. Lai C, et al. Among authors: zhou ay. Hum Mutat. 2020 Jun;41(6):1079-1090. doi: 10.1002/humu.24011. Epub 2020 Apr 1. Hum Mutat. 2020. PMID: 32176384 Free PMC article.

6

Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.

Caswell-Jin JL, Zimmer AD, Stedden W, Kingham KE, Zhou AY, Kurian AW. Caswell-Jin JL, et al. Among authors: zhou ay. J Natl Cancer Inst. 2019 Jan 1;111(1):95-98. doi: 10.1093/jnci/djy147. J Natl Cancer Inst. 2019. PMID: 30239769 Free PMC article.

7

A scalable, aggregated genotypic-phenotypic database for human disease variation.

Barrett R, Neben CL, Zimmer AD, Mishne G, McKennon W, Zhou AY, Ginsberg J. Barrett R, et al. Among authors: zhou ay. Database (Oxford). 2019 Jan 1;2019:baz013. doi: 10.1093/database/baz013. Database (Oxford). 2019. PMID: 30759220 Free PMC article.

8

Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening.

Cremin C, Lee MK, Hong Q, Hoeschen C, Mackenzie A, Dixon K, McCullum M, Nuk J, Kalloger S, Karasinska J, Scudamore C, Kim PTW, Donnellan F, Lam ECS, Lim HJ, Neben CL, Stedden W, Zhou AY, Schaeffer DF, Sun S, Renouf DJ, Schrader KA. Cremin C, et al. Among authors: zhou ay. Cancer Med. 2020 Jun;9(11):4004-4013. doi: 10.1002/cam4.2973. Epub 2020 Apr 7. Cancer Med. 2020. PMID: 32255556 Free PMC article.

9

Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets.

Berger MJ, Williams HE, Barrett R, Zimmer AD, McKennon W, Hong H, Ginsberg J, Zhou AY, Neben CL. Berger MJ, et al. Among authors: zhou ay. Database (Oxford). 2020 Jan 1;2020:baaa083. doi: 10.1093/database/baaa083. Database (Oxford). 2020. PMID: 33181822 Free PMC article.

10

Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel.

AlHarbi M, Mobark NA, AlJabarat WAR, ElBardis H, AlSolme E, Hamdan AB, AlFakeeh AH, AlMushawah F, AlHarthi F, AlSharm AA, Balbaid AAO, AlJohani N, Zhou AY, Robinson HA, Alqahtani SA, Abedalthagafi M. AlHarbi M, et al. Among authors: zhou ay. Oncotarget. 2023 Jun 12;14:580-594. doi: 10.18632/oncotarget.28457. Oncotarget. 2023. PMID: 37306523 Free PMC article.

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