R01 CA138836/CA/NCI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2010	1
2011	5
2012	4
2013	4
2014	1
2015	3
2016	3
2018	1
2019	1
2024	0

1

Phenotypic manifestations of copy number variation in chromosome 16p13.11.

Nagamani SC, Erez A, Bader P, Lalani SR, Scott DA, Scaglia F, Plon SE, Tsai CH, Reimschisel T, Roeder E, Malphrus AD, Eng PA, Hixson PM, Kang SH, Stankiewicz P, Patel A, Cheung SW. Nagamani SC, et al. Eur J Hum Genet. 2011 Mar;19(3):280-6. doi: 10.1038/ejhg.2010.184. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150890 Free PMC article.

2

Unifying cancer genetics.

Plon SE. Plon SE. Genet Med. 2011 Mar;13(3):203-4. doi: 10.1097/GIM.0b013e31820d5e87. Genet Med. 2011. PMID: 21311342 Free PMC article. No abstract available.

3

Insights into the pathogenesis and treatment of cancer from inborn errors of metabolism.

Erez A, Shchelochkov OA, Plon SE, Scaglia F, Lee B. Erez A, et al. Am J Hum Genet. 2011 Apr 8;88(4):402-21. doi: 10.1016/j.ajhg.2011.03.005. Am J Hum Genet. 2011. PMID: 21473982 Free PMC article. Review.

4

SV-STAT accurately detects structural variation via alignment to reference-based assemblies.

Davis CF, Ritter DI, Wheeler DA, Wang H, Ding Y, Dugan SP, Bainbridge MN, Muzny DM, Rao PH, Man TK, Plon SE, Gibbs RA, Lau CC. Davis CF, et al. Source Code Biol Med. 2016 Jun 18;11:8. doi: 10.1186/s13029-016-0051-0. eCollection 2016. Source Code Biol Med. 2016. PMID: 27330550 Free PMC article.

5

Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs.

Saliba J, Zabriskie R, Ghosh R, Powell BC, Hicks S, Kimmel M, Meng Q, Ritter DI, Wheeler DA, Gibbs RA, Tsai FT, Plon SE. Saliba J, et al. Pharmacogenet Genomics. 2016 Jun;26(6):271-9. doi: 10.1097/FPC.0000000000000208. Pharmacogenet Genomics. 2016. PMID: 26906009 Free PMC article.

6

Framework for microRNA variant annotation and prioritization using human population and disease datasets.

Oak N, Ghosh R, Huang KL, Wheeler DA, Ding L, Plon SE. Oak N, et al. Hum Mutat. 2019 Jan;40(1):73-89. doi: 10.1002/humu.23668. Epub 2018 Nov 8. Hum Mutat. 2019. PMID: 30302893 Free PMC article.

7

Exploring concordance and discordance for return of incidental findings from clinical sequencing.

Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock DP, Evans JP, Grody WW, Hegde MR, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum RL, Plon SE, Rehm HL, Jacob HJ. Green RC, et al. Genet Med. 2012 Apr;14(4):405-10. doi: 10.1038/gim.2012.21. Epub 2012 Mar 15. Genet Med. 2012. PMID: 22422049 Free PMC article.

8

Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing.

Ritter DI, Haines K, Cheung H, Davis CF, Lau CC, Berg JS, Brown CW, Thompson PA, Gibbs R, Wheeler DA, Plon SE. Ritter DI, et al. Genet Med. 2015 Oct;17(10):831-5. doi: 10.1038/gim.2014.189. Epub 2015 Jan 8. Genet Med. 2015. PMID: 25569436 Free PMC article.

9

Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium.

Jalali A, Amirian ES, Bainbridge MN, Armstrong GN, Liu Y, Tsavachidis S, Jhangiani SN, Plon SE, Lau CC, Claus EB, Barnholtz-Sloan JS, Il'yasova D, Schildkraut J, Ali-Osman F, Sadetzki S, Johansen C, Houlston RS, Jenkins RB, Lachance D, Olson SH, Bernstein JL, Merrell RT, Wrensch MR, Davis FG, Lai R, Shete S, Aldape K, Amos CI, Muzny DM, Gibbs RA, Melin BS, Bondy ML. Jalali A, et al. Sci Rep. 2015 Feb 5;5:8278. doi: 10.1038/srep08278. Sci Rep. 2015. PMID: 25652157 Free PMC article.

10

Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel.

Plon SE, Wheeler DA, Strong LC, Tomlinson GE, Pirics M, Meng Q, Cheung HC, Begin PR, Muzny DM, Lewis L, Biegel JA, Gibbs RA. Plon SE, et al. Cancer Genet. 2011 Jan;204(1):19-25. doi: 10.1016/j.cancergencyto.2010.11.001. Cancer Genet. 2011. PMID: 21356188 Free PMC article.

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