Papenhausen PR - Search Results

1

B-lymphoblastic leukemia/lymphoma with MYC and BCL2 gene rearrangements shows evidence for clonal evolution and mitotic recombination.

Schichman SA, Penton AL, Ghanta SN, Konda M, Papenhausen PR. Schichman SA, et al. Among authors: papenhausen pr. J Hematop. 2023 Jun;16(2):111-117. doi: 10.1007/s12308-023-00541-y. Epub 2023 Apr 20. J Hematop. 2023. PMID: 38175445 Free PMC article.

2

Mitotic recombinatory evolution in acute leukemia.

Papenhausen P, Kelly CA, Zhang Z, Penton A. Papenhausen P, et al. Cancer Genet. 2023 Jun;274-275:33-40. doi: 10.1016/j.cancergen.2023.02.003. Epub 2023 Mar 11. Cancer Genet. 2023. PMID: 36966725

3

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes.

Johansen M, Haskell GT, Arreola A, Riordan C, Gadi IK, Penton A, Papenhausen PR, Schwartz S. Johansen M, et al. Among authors: papenhausen pr. Prenat Diagn. 2024 May;44(5):586-594. doi: 10.1002/pd.6554. Epub 2024 Apr 1. Prenat Diagn. 2024. PMID: 38558419

4

Clinical significance and mechanisms associated with segmental UPD.

Papenhausen PR, Kelly CA, Harris S, Caldwell S, Schwartz S, Penton A. Papenhausen PR, et al. Mol Cytogenet. 2021 Jul 20;14(1):38. doi: 10.1186/s13039-021-00555-0. Mol Cytogenet. 2021. PMID: 34284807 Free PMC article.

5

Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy.

Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Rudd MK, et al. Among authors: papenhausen pr. Prenat Diagn. 2018 Nov;38(12):920-923. doi: 10.1002/pd.5349. Epub 2018 Sep 24. Prenat Diagn. 2018. PMID: 30156302

6

Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms.

Cantú ES, Dong H, Forsyth DR, Espinoza FP, Papenhausen PR. Cantú ES, et al. Among authors: papenhausen pr. Ann Clin Lab Sci. 2018 May;48(3):264-272. Ann Clin Lab Sci. 2018. PMID: 29970427

7

Clinical experience of laboratory follow-up with noninvasive prenatal testing using cell-free DNA and positive microdeletion results in 349 cases.

Schwartz S, Kohan M, Pasion R, Papenhausen PR, Platt LD. Schwartz S, et al. Among authors: papenhausen pr. Prenat Diagn. 2018 Feb;38(3):210-218. doi: 10.1002/pd.5217. Epub 2018 Feb 26. Prenat Diagn. 2018. PMID: 29338128

8

Four-copy number intervals in SNP microarray analysis: unique patterns and positions.

Papenhausen PR, Kelly CA, Zvereff V, Schwartz S. Papenhausen PR, et al. Cytogenet Genome Res. 2014;144(2):92-103. doi: 10.1159/000368859. Epub 2014 Nov 15. Cytogenet Genome Res. 2014. PMID: 25401283

9

Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia.

Sweet K, Al Ali NH, Dalia SM, Komrokji RS, Crescentini RM, Tinsley S, Lancet JE, Papenhausen PR, Zhang L, Pinilla-Ibarz J. Sweet K, et al. Among authors: papenhausen pr. Int J Hematol. 2014 Dec;100(6):567-74. doi: 10.1007/s12185-014-1685-9. Epub 2014 Oct 4. Int J Hematol. 2014. PMID: 25281405

10

Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency.

Frank GR, Fox J, Candela N, Jovanovic Z, Bochukova E, Levine J, Papenhausen PR, O'Rahilly S, Farooqi IS. Frank GR, et al. Among authors: papenhausen pr. Mol Genet Metab. 2013 Sep-Oct;110(1-2):191-4. doi: 10.1016/j.ymgme.2013.04.005. Epub 2013 Apr 17. Mol Genet Metab. 2013. PMID: 23800642 Free PMC article.

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