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31 results
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Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.
Bossler AD, Richards J, George C, Godmilow L, Ganguly A. Bossler AD, et al. Hum Mutat. 2006 Jul;27(7):667-75. doi: 10.1002/humu.20342. Hum Mutat. 2006. PMID: 16752392
A novel t(3;8)(q27;q24.1) simultaneously involving both the BCL6 and MYC genes in a diffuse large B-cell lymphoma.
Wang HY, Bossler AD, Schaffer A, Tomczak E, DiPatri D, Frank DM, Nowell PC, Bagg A. Wang HY, et al. Among authors: bossler ad. Cancer Genet Cytogenet. 2007 Jan 1;172(1):45-53. doi: 10.1016/j.cancergencyto.2006.07.016. Cancer Genet Cytogenet. 2007. PMID: 17175379
The NAB2-STAT6 gene fusion in solitary fibrous tumor can be reliably detected by anchored multiplexed PCR for targeted next-generation sequencing.
Guseva NV, Tanas MR, Stence AA, Sompallae R, Schade JC, Bossler AD, Bellizzi AM, Ma D. Guseva NV, et al. Among authors: bossler ad. Cancer Genet. 2016 Jul-Aug;209(7-8):303-12. doi: 10.1016/j.cancergen.2016.05.071. Epub 2016 May 24. Cancer Genet. 2016. PMID: 27292373
Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.
Brogden KA, Parashar D, Hallier AR, Braun T, Qian F, Rizvi NA, Bossler AD, Milhem MM, Chan TA, Abbasi T, Vali S. Brogden KA, et al. Among authors: bossler ad. BMC Cancer. 2018 Feb 27;18(1):225. doi: 10.1186/s12885-018-4134-y. BMC Cancer. 2018. PMID: 29486723 Free PMC article.
Correction to: Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.
Brogden KA, Parashar D, Hallier AR, Braun T, Qian F, Rizvi NA, Bossler AD, Milhem MM, Chan TA, Abbasi T, Vali S. Brogden KA, et al. Among authors: bossler ad. BMC Cancer. 2018 Apr 12;18(1):413. doi: 10.1186/s12885-018-4200-5. BMC Cancer. 2018. PMID: 29649990 Free PMC article.
Simultaneous detection of single-nucleotide variant, deletion/insertion, and fusion in lung and thyroid carcinoma using cytology specimen and an RNA-based next-generation sequencing assay.
Guseva NV, Jaber O, Stence AA, Sompallae K, Bashir A, Sompallae R, Bossler AD, Jensen CS, Ma D. Guseva NV, et al. Among authors: bossler ad. Cancer Cytopathol. 2018 Mar;126(3):158-169. doi: 10.1002/cncy.21963. Epub 2018 Jan 24. Cancer Cytopathol. 2018. PMID: 29364576
Genomic Sequencing Procedure Microcosting Analysis and Health Economic Cost-Impact Analysis: A Report of the Association for Molecular Pathology.
Sabatini LM, Mathews C, Ptak D, Doshi S, Tynan K, Hegde MR, Burke TL, Bossler AD. Sabatini LM, et al. Among authors: bossler ad. J Mol Diagn. 2016 May;18(3):319-328. doi: 10.1016/j.jmoldx.2015.11.010. Epub 2016 Apr 13. J Mol Diagn. 2016. PMID: 27080370 Free PMC article. Review.
Biallelic TP53 gain of function mutations in rapidly progressing solid tumors.
Sande CM, Chang B, Monga V, Bossler AD, Ma D. Sande CM, et al. Among authors: bossler ad. Cancer Genet. 2018 Apr;222-223:20-24. doi: 10.1016/j.cancergen.2018.02.001. Epub 2018 Feb 24. Cancer Genet. 2018. PMID: 29666004
Anchored multiplex PCR for targeted next-generation sequencing reveals recurrent and novel USP6 fusions and upregulation of USP6 expression in aneurysmal bone cyst.
Guseva NV, Jaber O, Tanas MR, Stence AA, Sompallae R, Schade J, Fillman AN, Miller BJ, Bossler AD, Ma D. Guseva NV, et al. Among authors: bossler ad. Genes Chromosomes Cancer. 2017 Apr;56(4):266-277. doi: 10.1002/gcc.22432. Epub 2016 Dec 2. Genes Chromosomes Cancer. 2017. PMID: 27910166
Targeting epigenetics for treatment of BRAF mutated metastatic melanoma with decitabine in combination with vemurafenib: A phase lb study.
Zakharia Y, Monga V, Swami U, Bossler AD, Freesmeier M, Frees M, Khan M, Frydenlund N, Srikantha R, Vanneste M, Henry M, Milhem M. Zakharia Y, et al. Among authors: bossler ad. Oncotarget. 2017 Sep 26;8(51):89182-89193. doi: 10.18632/oncotarget.21269. eCollection 2017 Oct 24. Oncotarget. 2017. PMID: 29179510 Free PMC article.
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