Rogers HJ - Search Results

1

Concurrent juvenile myelomonocytic leukemia and T-lymphoblastic lymphoma with a shared missense mutation in NRAS.

Ly B, Modi A, Rogers HJ, Makishima H, Hanna R, Cook JR, Theil KS, Maciejewski JP. Ly B, et al. Among authors: rogers hj. Pediatr Blood Cancer. 2014 May;61(5):946-8. doi: 10.1002/pbc.24797. Epub 2013 Oct 8. Pediatr Blood Cancer. 2014. PMID: 24610751

2

SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts.

Visconte V, Makishima H, Jankowska A, Szpurka H, Traina F, Jerez A, O'Keefe C, Rogers HJ, Sekeres MA, Maciejewski JP, Tiu RV. Visconte V, et al. Among authors: rogers hj. Leukemia. 2012 Mar;26(3):542-5. doi: 10.1038/leu.2011.232. Epub 2011 Sep 2. Leukemia. 2012. PMID: 21886174 No abstract available.

3

SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes.

Visconte V, Rogers HJ, Singh J, Barnard J, Bupathi M, Traina F, McMahon J, Makishima H, Szpurka H, Jankowska A, Jerez A, Sekeres MA, Saunthararajah Y, Advani AS, Copelan E, Koseki H, Isono K, Padgett RA, Osman S, Koide K, O'Keefe C, Maciejewski JP, Tiu RV. Visconte V, et al. Among authors: rogers hj. Blood. 2012 Oct 18;120(16):3173-86. doi: 10.1182/blood-2012-05-430876. Epub 2012 Jul 23. Blood. 2012. PMID: 22826563 Free PMC article.

4

Modified array-based comparative genomic hybridization detects cryptic and variant PML-RARA rearrangements in acute promyelocytic leukemia lacking classic translocations.

Gruver AM, Rogers HJ, Cook JR, Ballif BC, Schultz RA, Batanian JR, Fesler MJ, Tubbs RR. Gruver AM, et al. Among authors: rogers hj. Diagn Mol Pathol. 2013 Mar;22(1):10-21. doi: 10.1097/PDM.0b013e31825b8326. Diagn Mol Pathol. 2013. PMID: 23370423

5

Frequency, interobserver reproducibility and clinical significance of equivocal peaks in PCR clonality testing using Euroclonality/BIOMED-2 primers.

Park IJ, Bena J, Cotta CV, Hsi ED, Jegalian AG, Rogers HJ, Tubbs RR, Wang L, Cook JR. Park IJ, et al. Among authors: rogers hj. J Clin Pathol. 2014 Dec;67(12):1093-8. doi: 10.1136/jclinpath-2014-202454. Epub 2014 Sep 22. J Clin Pathol. 2014. PMID: 25244911

6

Molecular and phenotypic heterogeneity of refractory anemia with ring sideroblasts associated with marked thrombocytosis.

Visconte V, Tabarroki A, Hasrouni E, Maciejewski JP, Hsi ED, Tiu RV, Rogers HJ. Visconte V, et al. Among authors: rogers hj. Leuk Lymphoma. 2016;57(1):212-5. doi: 10.3109/10428194.2015.1045895. Epub 2015 Jun 25. Leuk Lymphoma. 2016. PMID: 25926061 No abstract available.

7

A case of mistaken identity: When lupus masquerades as primary myelofibrosis.

Hasrouni E, Rogers HJ, Tabarroki A, Visconte V, Traina F, Afable M, Sekeres MA, Maciejewski JP, Tiu RV. Hasrouni E, et al. Among authors: rogers hj. SAGE Open Med Case Rep. 2013 Aug 20;1:2050313X13498709. doi: 10.1177/2050313X13498709. eCollection 2013. SAGE Open Med Case Rep. 2013. PMID: 27489629 Free PMC article.

8

Clinicopathologic and molecular characterization of myeloid neoplasms with isolated t(6;9)(p23;q34).

Visconte V, Shetty S, Przychodzen B, Hirsch C, Bodo J, Maciejewski JP, Hsi ED, Rogers HJ. Visconte V, et al. Among authors: rogers hj. Int J Lab Hematol. 2017 Aug;39(4):409-417. doi: 10.1111/ijlh.12641. Epub 2017 Mar 20. Int J Lab Hematol. 2017. PMID: 28318095 Free PMC article.

9

What Is the Clinical Utility of Repeat SNP Array Testing in the Follow-up of Myeloid Neoplasms?: A Retrospective Analysis of 44 Patients With Serial SNP Arrays.

Basha B, Smith J, Rogers HJ, Cook JR. Basha B, et al. Among authors: rogers hj. Am J Clin Pathol. 2017 Mar 1;147(3):278-284. doi: 10.1093/ajcp/aqx003. Am J Clin Pathol. 2017. PMID: 28395056

10

Very rare lineage switch from acute myeloid leukemia to mixed phenotype acute leukemia, B/Myeloid, during chemotherapy with no clonal evolution.

Nomani L, Cook JR, Rogers HJ. Nomani L, et al. Among authors: rogers hj. Int J Lab Hematol. 2019 Aug;41(4):e86-e88. doi: 10.1111/ijlh.12977. Epub 2019 Feb 1. Int J Lab Hematol. 2019. PMID: 30707502 No abstract available.

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