Patricia T Greipp, DO

Assistant Professor

  • 480 Citations
  • 10 h-Index
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Carcinoma Medicine & Life Sciences
Acute Myeloid Leukemia Medicine & Life Sciences

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Research Output 2004 2019

  • 480 Citations
  • 10 h-Index
  • 46 Article
  • 2 Letter

Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia

Aypar, U., Smoley, S. A., Pitel, B. A., Pearce, K. E., Zenka, R. M., Vasmatzis, G., Johnson, S. H., Smadbeck, J. B., Peterson, J. F., Geiersbach, K. B., Van Dyke, D. L., Thorland, E. C., Jenkins, R. B., Ketterling, R. P., Greipp, P. T., Kearney, H. M., Hoppman, N. L. & Baughn, L., Jan 1 2019, In : European Journal of Haematology. 102, 1, p. 87-96 10 p.

Research output: Contribution to journalArticle

Acute Myeloid Leukemia
Hematologic Neoplasms
Fluorescence In Situ Hybridization
Molecular Biology

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms

Kanagal-Shamanna, R., Hodge, J. C., Tucker, T., Shetty, S., Yenamandra, A., Dixon-McIver, A., Bryke, C., Huxley, E., Lennon, P. A., Raca, G., Xu, X., Jeffries, S., Quintero-Rivera, F., Greipp, P. T., Slovak, M. L., Iqbal, M. A. & Fang, M., Jan 1 2018, (Accepted/In press) In : Cancer Genetics.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Myelodysplastic Syndromes
Practice Guidelines

A test utilization approach to the diagnostic workup of isolated eosinophilia in otherwise morphologically unremarkable bone marrow: A single institutional experience

Fang, H., Ketterling, R. P., Hanson, C. A., Pardanani, A. D., Kurtin, P. J., Chen, D., Greipp, P. T., Howard, M. T., King, R. L., Van Dyke, D. L. & Reichard, K. K., Oct 1 2018, In : American journal of clinical pathology. 150, 5, p. 421-431 11 p.

Research output: Contribution to journalArticle

Bone Marrow
Platelet-Derived Growth Factor beta Receptor
Systemic Mastocytosis
Hypereosinophilic Syndrome

Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature

Peterson, J. F., Pitel, B. A., Smoley, S. A., Smadbeck, J. B., Johnson, S. H., Vasmatzis, G., Pearce, K. E., He, R., Kelemen, K., Al-Mondhiry, H. A. B., Lamparella, N. E., Hoppman, N. L., Kearney, H. M., Baughn, L., Ketterling, R. P. & Greipp, P. T., Jan 1 2018, (Accepted/In press) In : Cancer Genetics.

Research output: Contribution to journalArticle

Acute Myeloid Leukemia
Bone Marrow
Primary Ovarian Insufficiency
Hematologic Neoplasms

Defining lymphoplasmacytic lymphoma: Does MYD88L265P define a pathologically distinct entity among patients with an IgM paraprotein and bone marrow-based low-grade b-cell lymphomas with plasmacytic differentiation?

Fang, H., Kapoor, P., Gonsalves, W., Frederick, L. A., Viswanatha, D., Howard, M. T., He, R., Morice, W. G., McPhail, E., Greipp, P. T., Ansell, S. M., Kyle, R. A., Gertz, M., Paludo, J., Abeykoon, J. & King, R. L., Jul 3 2018, In : American Journal of Clinical Pathology. 150, 2, p. 168-176 9 p.

Research output: Contribution to journalArticle

Immunoglobulin M
Bone Marrow
Waldenstrom Macroglobulinemia