C. Tirado

发表

t(8;22)/BCR-FGFR1 myeloproliferative disorder presenting as B-acute lymphoblastic leukemia: report of a case treated with sorafenib and review of the literature.

R. Collins, Weina Chen, Jad J Wakim, 2011, Leukemia research.

Short communication Acute myeloid leukemia with inv(16) with CBFBeMYH11 ,3 0 CBFB deletion, variant t(9;22) with BCReABL1, and del(7)(q22q32) in a pediatric patient: case report and literature review

R. Collins, L. Klesse, A. Arbini, 2010 .

Novel JAK2 rearrangement resulting from a t(9;22)(p24;q11.2) in B-acute lymphoblastic leukemia.

P. Koduru, N. Winick, L. Huang, 2010, Leukemia research.

Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet‐derived growth factor receptor–alpha genes in a patient with atypical chronic myeloid leukemia

C. Tirado, A. Safley, S. Sebastian, 2004, Genes, chromosomes & cancer.

An unusual complex karyotype in myopericytoma.

S. Dry, Le Chang, A. James, 2015, Journal of orthopaedics.

A Comprehensive Update on Molecular and Cytogenetic Abnormalities in T-cell Prolymphocytic Leukemia (T-pll).

N. Rao, C. Tirado, Phillip Starshak, 2012, Journal of the Association of Genetic Technologists.

“T-cell prolymphocytic leukemia (T-PLL), a heterogeneous disease exemplified by two cases and the important role of cytogenetics: a multidisciplinary approach”

N. Rao, C. Tirado, Phillip Starshak, 2012, Experimental Hematology & Oncology.

Acute myeloid leukemia ( M 2 ) with a cryptic RUNX 1 / RUNX

C. Tirado, 2009 .

the nature of thevariant and to determine its role in the prog- nostic outcome of a particular hematological malignancy.

R. Collins, Weina Chen, C. Tirado, 2009 .

A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.

C. Tirado, J. Gong, B. Goodman, 2004, Cancer genetics and cytogenetics.

Short communication Unusual presentation of myeloid sarcoma in a case of acute promyelocytic leukemia with a cryptic PMLeRARA rearrangement involving multiple sites including the atrium

R. Collins, A. Arbini, N. Karandikar, 2010 .

Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies.

J. Butera, L. Glasser, A. Spira, 2006, Cancer Genetics and Cytogenetics.

A novel three-way rearrangement involving ETV6 (12p13) and ABL1 (9q34) with an unknown partner on 3p25 resulting in a possible ETV6-ABL1 fusion in a patient with acute myeloid leukemia: a case report and a review of the literature

G. Schiller, M. Sharifian, C. Tirado, 2016, Biomarker Research.

Abnormal karyotypes in osteochondroma: Case series and literature review.

S. Dry, A. James, C. Tirado, 2015, Journal of orthopaedics.

Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient

Stephanie Dallaire, P. Koduru, C. Tirado, 2012, American journal of medical genetics. Part A.

t(8;21)(q22;q22) Translocation involving AML1 and ETO in B lymphoblastic leukemia [corrected].

Huan-You Wang, C. Tirado, 2010, Human pathology.

Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.

J. Greenberg, A. Meloni-Ehrig, C. Tirado, 2007, Cancer genetics and cytogenetics.

Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.

N. Seibel, A. Meloni-Ehrig, H. Meany, 2005, Cancer genetics and cytogenetics.

Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.

A. Meloni-Ehrig, C. Tirado, P. Mowrey, 2005, Cancer genetics and cytogenetics.

Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion.

J. Moore, C. Tirado, S. Sebastian, 2005, Cancer genetics and cytogenetics.

Cytogenetics of melanoma: a review.

A. Cochran, Le Chang, A. James, 2014, Journal of the Association of Genetic Technologists.

Atypical rearrangement involving 3′-IGH@ and a breakpoint at least 400 Kb upstream of an intact MYC in a CLL patient with an apparently balanced t(8;14)(q24.1;q32) and negative MYC expression

N. Rao, S. Kantarci, Brit S Shackley, 2013, Molecular Cytogenetics.

Identification of a novel amplicon at 1q31 in pancreatic cancer cell lines.

C. Tirado, J. Stone, A. Sandberg, 1999, Cancer genetics and cytogenetics.

Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review

C. Tirado, S. Pullarkat, J. Ji, 2014, Experimental Hematology & Oncology.

The first case of Philadelphia chromosome-negative acute promyelocytic leukemia following imatinib for chronic myelogenous leukemia.

Weina Chen, J. Dowell, C. Tirado, 2012, Cancer genetics.

Epigenesis in acute myeloid leukemia: an update.

C. Tirado, John Boles, 2013, Journal of the Association of Genetic Technologists.

Childhood B-acute lymphoblastic leukemia: a genetic update

Jennifer S. Woo, C. Tirado, M. O. Alberti, 2014, Experimental Hematology & Oncology.

C-Terminal Regions of the Human Telomerase Catalytic Subunit Essential for In Vivo Enzyme Activity

Chuan-hai Guo, C. Counter, S. S. Margolis, 2002, Molecular and Cellular Biology.

Erratum to: A case of B-cell acute lymphoblastic leukemia in a child with Down syndrome bearing a t(2;12)(p12;p13) involving ETV6 and biallelic IGH@ rearrangements

C. Tirado, Nagesh Rao, S. Pullarkat, 2015, Biomarker Research.

A case of B-cell acute lymphoblastic leukemia in a child with Down syndrome bearing a t(2;12)(p12;p13) involving ETV6 and biallelic IGH@ rearrangements

C. Tirado, Nagesh Rao, S. Pullarkat, 2015, Biomarker Research.

Genomic profiling using array comparative genomic hybridization define distinct subtypes of diffuse large b-cell lymphoma: a review of the literature

N. Rao, Weina Chen, C. Tirado, 2012, Journal of hematology & oncology.

G. Schiller, M. Sharifian, C. Tirado, 2016, Biomarker Research.

Infantile mixed phenotype acute leukemia (bilineal and biphenotypic) with t(10;11)(p12;q23);MLL-MLLT10.

D. Oliver, C. Zhang, Junke Zheng, 2010, Leukemia research.

Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter

Stephanie Dallaire, R. Collins, C. Tirado, 2009, American journal of medical genetics. Part A.

Acute Promyelocytic Leukemia Lacking the Classic Translocation t(15;17)

C. Tirado, J. Wakim, 2012 .

Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).

J. Moore, P. Buckley, C. Tirado, 2003, Cancer genetics and cytogenetics.

B-lymphoblastic transformation of mantle cell lymphoma/leukemia with “double hit” changes

Jeffrey M. Miller, N. Rao, R. Ahmed, 2015, Journal of Hematopathology.

ATR functions as a gene dosage‐dependent tumor suppressor on a mismatch repair‐deficient background

Xiao-Fan Wang, R. Abraham, R. Furumai, 2004, The EMBO journal.

Pancreatic tumors: an overview

C. Tirado, J. Ji, D. Dawson, 2014 .

Atlas of Genetics and Cytogenetics in Oncology and Haematology Pancreatic tumors : an overview

C. Tirado, J. Ji, D. Shabsovich, 2014 .

A Cryptic t(11;14) Translocation in Mantle Cell Lymphoma Highlights the Importance of FISH.

N. Rao, C. Tirado, M. Kallen, 2015, Journal of the Association of Genetic Technologists.

Unusual presentation of myeloid sarcoma in a case of acute promyelocytic leukemia with a cryptic PML-RARA rearrangement involving multiple sites including the atrium.

R. Collins, A. Arbini, N. Karandikar, 2010, Cancer genetics and cytogenetics.

A t(3;8)(q26.2;q24) involving the EVI1 (MECOM) Gene.

C. Tirado, Kristie Liu, 2018, Journal of the Association of Genetic Technologists.

A t(16;21)(p11;q22) in Acute Myeloid Leukemia (AML) Resulting in Fusion of the FUS/TLS and ERG Genes: A Review of the Literature.

Justin Buchanan, C. Tirado, 2016, Journal of the Association of Genetic Technologists.

C-MYC Involvement in Chronic Lymphocytic Leukemia (CLL): A Molecular and Cytogenetic Update.

C. Tirado, Lakshan N Fonseka, 2015, Journal of the Association of Genetic Technologists.

Incontinentia pigmenti in a boy with XXY mosaicism detected by fluorescence in situ hybridization.

M. McDonald, M. Selim, J. Goldstein, 2006, Journal of American Academy of Dermatology.

MECOM: A Very Interesting Gene Involved also in Lymphoid Malignancies.

C. Tirado, Kristie Q. Liu, 2019, Journal of the Association of Genetic Technologists.

A (1;19) translocation involving TCF3-PBX1 fusion within the context of a hyperdiploid karyotype in adult B-ALL: a case report and review of the literature

N. Rao, C. Tirado, S. Pullarkat, 2015, Biomarker Research.

A Cryptic t(1;21;8)(p36;q22;q22) in a Case of Acute Myeloid Leukemia with Maturation.

R. Collins, C. Tirado, Federico J Valdez, 2009, Journal of the Association of Genetic Technologists.

The t(12;21)(p13;q22) in Pediatric B-Acute Lymphoblastic Leukemia: An Update.

C. Tirado, Kristie Q. Liu, Maximilian Becker, 2017, Journal of the Association of Genetic Technologists.

Hypodiploidy in AML.

C. Tirado, Wilson Yeh, 2021, Journal of the Association of Genetic Technologists.

Ring chromosome 7 in a child with T-cell acute lymphoblastic leukemia with myeloid markers

C. Tirado, W. Koss, A. Reyes, 2021, Proceedings.

Acute myeloid leukemia with inv(16) with CBFB-MYH11, 3'CBFB deletion, variant t(9;22) with BCR-ABL1, and del(7)(q22q32) in a pediatric patient: case report and literature review.

R. Collins, L. Klesse, A. Arbini, 2010, Cancer genetics and cytogenetics.

Testicular Germ Cell Tumors: A Cytogenomic Update.

C. Tirado, L. Blanco, 2018, Journal of the Association of Genetic Technologists.

A case of B-cell acute lymphoblastic leukemia in a child with Down syndrome bearing a t(2;12)(p12;p13) involving ETV6 and biallelic IGH@ rearrangements

N. Rao, C. Tirado, S. Pullarkat, 2015, Biomarker Research.

Erratum to: A case of B-cell acute lymphoblastic leukemia in a child with Down syndrome bearing a t(2;12)(p12;p13) involving ETV6 and biallelic IGH@ rearrangements

N. Rao, C. Tirado, S. Pullarkat, 2015, Biomarker Research.

Genes, chromosomes, and disorders of sex development: an update.

C. Tirado, D. Shabsovich, 2014, Journal of the Association of Genetic Technologists.

Short communication Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia

N. Seibel, A. Meloni-Ehrig, H. Meany, 2005 .