P. Lennon

发表

Sonic hedgehog signaling pathway is activated in ALK-positive anaplastic large cell lymphoma.

L. Medeiros, E. Drakos, R. Luthra, 2009, Cancer research.

Activity of tyrosine kinase inhibitors against human NUP214-ABL1-positive T cell malignancies

D. Gilliland, T. Manshouri, A. Quintás-Cardama, 2008, Leukemia.

Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

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 n

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

A National Multicenter Evaluation of the Clinical Utility of Optical Genome Mapping for Assessment of Genomic Aberrations in Acute Myeloid Leukemia

J. Broach, R. Kanagal-Shamanna, B. Levy, 2020, medRxiv.

B-cell lymphomas with MYC/8q24 rearrangements and IGH@BCL2/t(14;18)(q32;q21): an aggressive disease with heterogeneous histology, germinal center B-cell immunophenotype and poor outcome

L. Medeiros, Shaoying Li, C. Yin, 2012, Modern Pathology.

Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations.

S. Verstovsek, B. Barkoh, P. Lennon, 2010, Cancer genetics and cytogenetics.

Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia

L. Medeiros, P. Lin, S. Konoplev, 2007, Cancer.

Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation

Z. Ou, M. L. Cooper, S. Cheung, 2006, American journal of medical genetics. Part A.

Variations in MALT1 Gene Disruptions Detected by FISH in 109 MALT Lymphomas Occurring in Different Primary Sites.

J. Han, S. Konoplev, P. Lin, 2011, Journal of the Association of Genetic Technologists.

WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH

S. Cheung, D. Scott, S. Kirkpatrick, 2006, American journal of medical genetics. Part A.

Translocation (18;22)(q21;q11) in B-cell lymphomas: a report of 4 cases and review of the literature.

L. Medeiros, L. Abruzzo, P. Lin, 2008, Human pathology.

Aberrant EVI1 expression in acute myeloid leukemias associated with the t(3;8)(q26;q24).

S. Kornblau, L. Medeiros, L. Abruzzo, 2007, Cancer genetics and cytogenetics.

Ribosomal DNA internal transcribed spacer analysis supports synonomy of Scedosporium inflatum and Lomentospora prolificans

C. Cooper, P. Lennon, I. Salkin, 1994, Journal of clinical microbiology.

Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia

A. C. Chinault, Ankita Patel, C. Shaw, 2008, American journal of hematology.

Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors.

M. Correll, C. Coldren, M. Bouzyk, 2016, Cancer genetics.

Addition of chromosomal microarray and next generation sequencing to FISH and classical cytogenetics enhances genomic profiling of myeloid malignancies.

I. Flinn, M. Correll, C. Coldren, 2017, Cancer genetics.

Chronic myeloid leukemia in blast phase associated with t(3;8)(q26;q24).

L. Abruzzo, C. Yin, P. Lin, 2009, Cancer genetics and cytogenetics.

Prognostic value of MYC rearrangement in cases of B‐cell lymphoma, unclassifiable, with features intermediate between diffuse large B‐cell lymphoma and Burkitt lymphoma

M. Routbort, L. Medeiros, L. Fayad, 2012, Cancer.

Examining Hedgehog pathway genes GLI3, SHH, and PTCH1 and the p53 target GLIPR1/GLIPR1L1/GLIPR1L2 gene cluster using fluorescence in situ hybridization uncovers GLIPR1/GLIPR1L1/GLIPR1L2 deletion in 9% of patients with multiple myeloma.

P. Lin, P. Lennon, Peter Hu, 2010, Journal of the Association of Genetic Technologists.

Splenic marginal zone lymphomas are characterized by loss of interstitial regions of chromosome 7q, 7q31.32 and 7q36.2 that include the protection of telomere 1 (POT1) and sonic hedgehog (SHH) genes

R. Luthra, F. Vega, M. Luthra, 2008, British journal of haematology.

Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array‐based comparative genomic hybridization in a patient with mental retardation and dysmorphic features

Z. Ou, P. Stankiewicz, M. L. Cooper, 2005, American journal of medical genetics. Part A.

Immunohistochemical profile and fluorescence in situ hybridization analysis of diffuse large B-cell lymphoma in northern China.

L. Medeiros, J. Jorgensen, P. Lin, 2010, Archives of pathology & laboratory medicine.

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review

K. Gunderson, M. L. Cooper, S. Cheung, 2007, American journal of medical genetics. Part A.

Defining causative factors contributing in the activation of hedgehog signaling in diffuse large B-cell lymphoma.

A. Multani, J. Gu, Rajesh R. Singh, 2012, Leukemia research.

Prognostic value of MYC rearrangement in cases of B‐cell lymphoma, unclassifiable, with features intermediate between diffuse large B‐cell lymphoma and Burkitt lymphoma

M. Routbort, L. Medeiros, L. Fayad, 2012, Cancer.

Lack of correlation between HERV-K expression and HIV-1 viral load in plasma specimens.

Jianli Dong, Gengming Huang, P. Lennon, 2013, Annals of clinical and laboratory science.

Is monosomy 21 rare? Seven early miscarriages including one mosaic 45,XX,‐21/44,X,‐21 in a single study population

P. Lennon, P. Hardy, K. Hardy, 2012, American journal of medical genetics. Part A.

Optical genome mapping in acute myeloid leukemia: a multicenter evaluation

J. Broach, R. Kanagal-Shamanna, B. Levy, 2022, Blood advances.

Bacterial artificial chromosome array‐based comparative genomic hybridization using paired formalin‐fixed, paraffin‐embedded and fresh frozen tissue specimens in multiple myeloma

P. Lin, P. Lennon, Diane M Pierson, 2009, Cancer.

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.