Swisshelm K - Search Results

1

Clinicopathologic and genetic spectrum of infantile B-lymphoblastic leukemia: a multi-institutional study.

Knez V, Liu X, Schowinsky J, Pan Z, Wang D, Lorsbach R, Lu C, Luedke C, Haag M, Carstens B, Swisshelm K, Yang LH, Jug R, Wang E, Liang X. Knez V, et al. Among authors: swisshelm k. Leuk Lymphoma. 2019 Apr;60(4):1006-1013. doi: 10.1080/10428194.2018.1508667. Epub 2018 Sep 6. Leuk Lymphoma. 2019. PMID: 30188223

2

Heterogeneity of Abnormal RUNX1 Leading to Clinicopathologic Variations in Childhood B-Lymphoblastic Leukemia.

Knez VM, Carstens BJ, Swisshelm KL, McGranahan AN, Liang X. Knez VM, et al. Among authors: swisshelm kl. Am J Clin Pathol. 2015 Aug;144(2):305-14. doi: 10.1309/AJCPVY5E5OMMYBFJ. Am J Clin Pathol. 2015. PMID: 26185316

3

Clonality of neutrophilia associated with plasma cell neoplasms: report of a SETBP1 mutation and analysis of a single institution series.

Stevens B, Maxson J, Tyner J, Smith CA, Gutman JA, Robinson W, Jordan CT, Lee CK, Swisshelm K, Tobin J, Wei Q, Schowinsky J, Rinella S, Lee HG, Pollyea DA. Stevens B, et al. Among authors: swisshelm k. Leuk Lymphoma. 2016;57(4):927-34. doi: 10.3109/10428194.2015.1094697. Epub 2015 Oct 27. Leuk Lymphoma. 2016. PMID: 26389776 Free PMC article.

4

Primary high-grade B-cell lymphoma of the breast with concurrent IGH-BCL2 and MYC-IGL translocations in an adolescent patient.

Liang X, Jones A, Giller RH, Swisshelm K, McGavran L, Meltesen L, Carstens B, McGranahan AN, Albano EA. Liang X, et al. Among authors: swisshelm k. Pediatr Dev Pathol. 2011 Sep-Oct;14(5):402-6. doi: 10.2350/10-10-0927-CR.1. Epub 2011 Apr 14. Pediatr Dev Pathol. 2011. PMID: 21491965

5

21q22 amplification detection in three patients with acute myeloid leukemia: cytogenomic profiling and literature review.

Kudalkar EM, Pang C, Haag MM, Pollyea DA, Kamdar M, Xu G, Su M, Carstens B, Swisshelm K, Bao L. Kudalkar EM, et al. Among authors: swisshelm k. Mol Cytogenet. 2022 Jul 7;15(1):30. doi: 10.1186/s13039-022-00606-0. Mol Cytogenet. 2022. PMID: 35799207 Free PMC article.

6

Clinical utility and cost-effectiveness analysis of chromosome testing concomitant with chromosomal microarray of patients with constitutional disorders in a U.S. academic medical center.

Su M, Page S, Haag M, Swisshelm K, Hennerich D, Graw S, LeRoux J, Brzeskiewicz P, Svihovec S, Bao L. Su M, et al. Among authors: swisshelm k. J Genet Couns. 2022 Apr;31(2):364-374. doi: 10.1002/jgc4.1496. Epub 2021 Aug 16. J Genet Couns. 2022. PMID: 34397147

7

Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder.

Graw SL, Swisshelm K, Floyd K, Carstens BJ, Wamboldt MZ, Ross RG, Leonard S. Graw SL, et al. Among authors: swisshelm k. Mol Cytogenet. 2012 Jan 3;5(1):2. doi: 10.1186/1755-8166-5-2. Mol Cytogenet. 2012. PMID: 22214315 Free PMC article.

8

Rare double-hit with two translocations involving IGH both, with BCL2 and BCL3, in a monoclonal B-cell lymphoma/leukemia.

Alpatov R, Carstens B, Harding K, Jarrett C, Balakhani S, Lincoln J, Brzeskiewicz P, Guo Y, Ohene-Mobley A, LeRoux J, McDaniel V, Meltesen L, Minka D, Patel M, Manavi C, Swisshelm K. Alpatov R, et al. Among authors: swisshelm k. Mol Cytogenet. 2015 Dec 30;8:101. doi: 10.1186/s13039-015-0203-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26719766 Free PMC article.

9

High prevalence of array comparative genomic hybridization abnormalities in adults with unexplained intellectual disability.

Taylor MR, Jirikowic J, Wells C, Springer M, McGavran L, Lunt B, Swisshelm K. Taylor MR, et al. Among authors: swisshelm k. Genet Med. 2010 Jan;12(1):32-8. doi: 10.1097/GIM.0b013e3181c83de0. Genet Med. 2010. PMID: 20009761 Free article.

10

Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.

Baker PR, Tsai AC, Springer M, Swisshelm K, March J, Brown K, Bellus G. Baker PR, et al. Among authors: swisshelm k. J Craniofac Surg. 2010 Sep;21(5):1369-75. doi: 10.1097/SCS.0b013e3181ec6ac0. J Craniofac Surg. 2010. PMID: 20856023

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