Posters
Felix E. Laban, David Shabsovich, David Palencia , Joy King, David Trejo, Lorena Villalba
and Carlos A. Tirado (2020) An isochromosome 17q, a rare chromosomal abnormality in a female patient with leukocytosis. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Felix E. Laban, David Shabsovich, David Palencia , Joy King, David Trejo, Lorena Villalba
and Carlos A. Tirado (2020) An isochromosome 17q, a rare chromosomal abnormality in a female patient with leukocytosis. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Andrew Reyes, Félix Labán , David Shabsovich, John Reinartz, Kevin Stieglbauer and Carlos A. Tirado (2020) C-MYC amplification in a case of male patient diagnosed with B-CLL. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Leena Nabipur, Joy King, Anna Okabe, Felix Laban, William Koss2, Elaine Horton2, Maria T. Guardiola, Krystal Soyalp, and Carlos A. Tirado (2020) A t(9;11)(p22;q23) within the context of a complex karyotype is associated with a poor prognosis in a 19 year old patient with AML.Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Nguyen A, Tse V, Lapp K, Yang G, Peng E, Yun M, Cunnien K, Serk D, Wyatt B, Tirado CA. Molecular cytogenetic characterization of a complex karyotype of a pediatric male patient with B-acute lymphoblastic leukemia. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Okabe A, Nguyen A, Reyes A, Zhao D, Chung D, Laban F, Thompson L, Murphy M, Cunnien K, Wyatt B, Tirado CA Molecular cytogenetic characterization of a karyotype of a female patient with secondary amenorrhea. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Reyes A, Tse V, Yang G, Peng E, Yun M, Cunnien K, Lapp K, Wyatt B and Tirado CA A case of a lymphoblastic lymphoma with trisomy 12 in the lymphoid population and deletion 13q of myeloid origin. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Chung D, Reyes A, Nguyen A, Stieglbauer K. , Serk D , Ahmad J, Cunnien K, Bartholomaus L and Tirado, CA Molecular cytogenetic characterization of a case of a mixed myelodysplastic/myeloproliferative neoplasm: chronic myelomonocytic leukemia-1 (CMML-1) with an abnormal karyotype with an apparent monosomy 7 resulting in rearrangements involving chromosomes 7 and 21. Poster presented at the 2018 American Society of Human Genetics Annual Meeting (Oct 16th to 21st, 2018) in San Diego, CA.
Zhao D, Liu K, Reinartz J, Serk D , Ahmad J, Cunnien K, Bartholomaus L and Tirado CA Duplication of the band q21q27 on the long arm of chromosome 3 : A rare cytogenetic event in B- Chronic Lymphocytic Leukemia (B-CLL). Poster presented at the 2018 American Society of Human Genetics Annual Meeting (Oct 16th to 21st, 2018) in San Diego, CA.
Helmer J. and Tirado CA. A three way t(8;14;22)(q24;q24;q32;q11.2) characterized by molecular cytogenetics with involvement of MYC/ICH/IGL. Platform presentation at International Congress of Flow Cytometry, Chiclayo, Perú (6th to the 8th December 2018).
Nguyen A, Tirado CA . Cytogenetics of T-acute lymphoblastic leukemia . Platform presentation at
V Jornada Internacional de Genética & Biologia Molecular , Chiclayo, Perú (8th to the 10th August 2018).
Zhao D. and Tirado CA Transient Myeloproliferative Disorders in Down Syndrome. Platform presentation at V Jornada Internacional de Genética & Biologia Molecular , Chiclayo, Perú (8th to the 10th August 2018).
Tirado CA, Liu K, Dowiak AV, Wyatt W, Wheaton S, Peterson K., Serk D, Cunnien K & Reinartz JJ. A plasma cell myeloma case with an abnormal clone showing a t(8;22)(q24.1;q11.2) within the context of a hyperdiploid complex karyotype. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Crippen R, Salazar E, Liu K, Tirado CA Acute Myeloid Leukemia with t(3;8)(q26.2;q24) Involving
MECOM (EVI1) on Chromosome 3. Poster presented at UCLA Science Poster Day on May 22nd, 2018.
Zhao D, Nguyen A, Liu K and Tirado, CA A Rare Cytogenetic Abnormality in Chronic Lymphocytic Leukemia: t(18;22)(q21;q11) Involving IGL/BCL2. Poster presented at UCLA Science Poster Day on May 22nd, 2018.
Liu KQ, Tirado CA. The Cytogenetics of t(8;22)(q24.1;q11.2) in Plasma Cell Myeloma. Poster presented
at UCLA Science Poster Day on May 22nd, 2018.
Liu K, Makar C, Bond A, Stieglbauer K, Wheaton S, Reinartz J, Cunnien K, Peterson K, Bartholomaus L, Serk D, Wyatt B, Khan S &Tirado CA. A t(3;8)(q26.2;q24) involving the EVI1 (MECOM) gene on 3q26.2 in a case of Acute Myeloid Leukemia preceded by Polycythemia vera. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Dowiak A, Ewing J, Khan S, Salazar E, Thompson L, Wyatt B, Peterson K, Bartholomaus L, Nguyen A, Crippen R, Reinartz J &Tirado CA. A t(18;22)(q21;q11) involving IGH/BCL2, a rare event in Chronic Lymphocytic leukemia. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Shabsovich, D, Rao N, Tirado, CA. Cytogenetic Analyis of Pancreatic Adenocarcinoma using Giemsa Banding and Fluorescence In Situ Hybridization. Eighteen Annual Science Poster Day May 12, 2015 Ackerman Grand Ballroom. University of California Los Angeles.
Chow R, Shabsovich D, Schiller G, Kallen M, Pullarkat ST, Rao N & , Tirado CA t(17;19)(q21;p13.3) involving TCF3; a t(1;19)(p13;p13) and a 5’IGH@ abnormality in a case of adult B-cell Acute Lymphoblastic Leukemia. Poster presented at the ASHG Meeting 2015, October 6th – 10th , 2015.
Shabsovich D and Tirado CA CML with cryptic BCR-ABL1 translocations. Platform presented at the XVI
Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Liu K and Tirado CA Gliomas: A genetic update. . Platform presented at the XVI Conebiol Meeting held in
Lambayeque, Peru on September 21-September 24th, 2015.
Shabsovich D and Tirado CA Molecular Cytogenetics of Pancreatic Cancer. Platform presented at the XVI
Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Chow R and Tirado CA A t(17;19) in B-ALL. Platform presented at the XVI Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Ji J, Loo E, Pullarkat S, Yang L &Tirado CA. 2014 Acute Myeloid Leukemia with t(7;21) and 5qLoss: a New Rare Entity of AML?. 2014 American Cytogenetics Conference, Asheville, NC, May 4-7, 2014.
Kallen ME, DeNicola MM, Pullarkat ST, Paquette R, Yang L, Rao NP, Tirado CA. 2014. Case Report:
BCR-ABL1 Amplification, a Unique Finding in B-Lymphoblastic Leukemia. 2014 American Cytogenetics Conference, Asheville, NC, May 4-7, 2014.
Kim Y, Yang L, Rao N,TiradoCA2014 Cytogenetics of Blastoid Crisis of Mantle Cell Lymphoma. III
International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Kim Y, Traum P, Pelkey J, Yang L, Rao N,Tirado CA2014 A t(2;12)(p12;p13) in a pediatric Down
Syndrome Patient with B-ALL. III International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Hasan A, Rao N, Tirado CANPM1 and FLT3 genes in acute myeloid leukemia. III International Workshop
in Henetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Ngo D, Das K, Tirado, CA Cytogenetics as a tool in non-small cell lung cancer. III International Workshop
in Henetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
18
Abusaba G, Yang L, Paquette R, Rao N, Tirado CABCR/ABL1 amplification a rare event in B-ALL. III
International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Allen D, Boles J, Rao N, Tirado CA Chronic Myelogenous Leukemia with a normal karyotype and
BCR/ABL1 fusion. BCR/ABL1 amplification a rare event in B-ALL. III International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Shabsovich D,Rao D, Ji J, Park K, Yang L &Tirado CA. Conventional Cytogenetic and Molecular Genetic Analysis of Pancreatic Cancer.American Society of Human Genetics Meeting , San Diego, CA, October 18- 22nd, 2014.
Lasky BJ, Yeh L, Kallen M, Pullarkat S, Yang L, Hasan A, Kim Y, Shabsovich D, Rao N, Tirado CA A
(1;19) translocation involving TCF3/PBX1 fusion within a context of a hyperdiploid karyotype.American Society of Human Genetics Meeting , San Diego, CA, October 18-22nd, 2014.
Kim Y, Traum P, Lasky B, Yang L, Ngo D, Pelkey J, Rao N, Tirado CAA (2;12)(p12;p13) translocation in
a Down Syndrome patient with B-ALL. American Society of Human Genetics Meeting, San Diego, CA, October 18-22nd, 2014.
Tirado CA, Kim Y, Yang L, Abusaba G, Lasky BJ, Rao N & Tirado CA A complex karyotype with a cryptic t(11;14)(q13;q32) in a Blastoid Crisis of Mantle Cell Lymphoma. American Society of Human Genetics Meeting , San Diego, CA, October 18-22nd, 2014.
DeNicola M, Pullakat S, Yea S, Delgado P, Yang L, Rao N, Tirado CA. 2013. A case of hyperdiploidy in
CLL/SLL: A Rare Cytogenetic Event Associated with Poor Prognosis. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Tirado CA,DeNicola M, Rao D, Delgado P, Jarrin A, Yang L, Rao N. 2013. A case of pediatric acute
lymphoblastic leukemia with a (9;12) translocation involving JAK2 and rearrangement of MLL at 11q23 with an apparent insertion at 6q27. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Delgado P, Iyer S, Jarrin A, Rao N, Tirado CA. 2013. Infertility related to a rearrangement of the Y
chromosome. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Bui PH, Amarillo I, Shackley BS, Rao N, Tirado CA. 2012. A t(8;14)(q24;q32) translocation resulting in an atypical IGH/MYC genomic fusion in clinically aggressive chronic lymphocytic leukemia. 2012 American Cytogenetics Conference, San Antonio, Texas, April 19-22, 2012.
Starshak P, Linhares Y, Delgado P, Rao PN, Tirado CA. 2012. T-cell prolymphoytic Leukemia (T-PLL), a heterogeneous disease exemplified by two cases and the important role of cytogenetics. American Cytogenetics Conference 2012, San Antonio, Texas, April 19-22, 2012.
Tirado CA, Boles JW, Quintero-Rivera F. 2012. An unbalanced rearrangement involving a translocation (6;8) in a case of diffuse large B-cell lymphoma. American Cytogenetics Conference 2012, San Antonio, Texas, April 19-22, 2012.
Delgado PA, Rao N, Tirado CA. Cytogenetics and Molecular findings in T-PLL. 2012. International
Workshop of Human Genetics. Chiclayo, Peru. October 17-19, 2012.
Boles J, Tirado CA. Epigenetic events in leukemia. 2012. International Workshop of Human Genetics.
Chiclayo, Peru. October 17-19, 2012.
Marinoni M, Tirado CA. 2012. Cytogenetic and Molecular cytogenetic findings in Pancreatic Cancer.
International Workshop of Human Genetics, Universidad Nacional Pedro Ruiz Gallo. Lambayeque, Peru, October 17-19, 2012.
Garcia L, Marinoni M, Meisner L, Tirado CA. 2012. Update in Stem Cell Research. International Workshop
of Human Genetics, Circle of Genetic Studies Francis Collins. Universidad Nacional Pedro Ruiz Gallo, Lambayeque, Peru October 17-19, 2012.
Marinoni M, Tirado CA. 2012. Hermaphroditism and Intersex: An Update. International Workshop of
Human Genetics, Circle of Genetic Studies Francis Collins. Universidad Nacional Pedro Ruiz Gallo, Lambayeque, Peru. October 17-19, 2012.
Delgado P, Crandall B, Rao N, Bui P, Tirado CA. 2012 Low Klinefelter mosaicism in a male with azoospermia detected by FISH. 2012 American Society of Human Genetics Meeting, San Francisco, CA. November 6-10, 2012.
DeNicola M, Boles J, Collins R, Garcia R, Tirado CA. 2012 A CML case with normal karyotype and positive BCR/ABL1 fusion. 2012 American Society of Human Genetics Meeting in San Francisco, CA, November 6-10, 2012.
Martinez D, Garcia R, Koduru P, Tirado CA. 2011. Recurrent Cytogenetic aberrations predict MYC breakpoints in diffuse large B-cell lymphoma and help define Burkitt lymphoma versus diffuse large B-cell lymphoma with MyC rearrangaements. 12th International Congress of Human Genetics , Montreal Oct 11- 15, 2011.
Wakim JJ, Tirado CA, Chen WC. 2011. The first case of a Ph-negative acute promyelocytic leukemia following imatinib for chronic myeloid leukemia. 12th International Congress of Human Genetics , Montreal Oct 11-15, 2011.
Hiemenz M, Chen W, Winick N, Tirado CA. 2011. Coexistence of t(12;21)(p13;q22)/ETV6-RUNX1 and MLL rearrangement in a pediatric patient with B-lymphoblastic leukemia. 12th International Congress of Human Genetics , Montreal Oct 11-15, 2011
Garcia R, Seegmiller A, Maleki A, Tirado CA, Chen W. 2010. Recurrent Aberrations in High Grade B-Cell Lymphomas with IG-MYC Rearrangement and their Impact on Survival. Presented at the 2010 US & Canadian Academy of Pathology Meeting. Washington D.C., March 20-26, 2010
Lou Z, Zhang J, Tirado CA, Slone T, Zaremba CM, Oliver D, Chen W. 2010 Infantile Mixed Phenotype Acute Leukemia (Bilineal and Biphenotypic) with t(10;11)(p12;q23); MLL-MLLT10. 2010 American Cytogenetics Conference Meeting, Ontario, Canada, May 13-16, 2010.
Hiemenz M, Chen W, Huang LJ, Laborde C, Lou Z, Valdez F, Winick N, Ho K, Koduru P, Tirado CA. 2010. Novel JAK2 rearrangement resulting from a t(9;22)(p24;p11.2) in B lymphoblastic leukemia. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Torgbe E, Tirado CA, Gotway G, Valdez F, Suterwala M, Iyer S, Garcia R, Shah N, Dallaire S, Appleberry T, Pichurin P, Koduru P. 2010. Recombinant chromosome 7 in a mosaic triple X/Turner patient. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Davila O, Garcia R, Garay N, Koller M, Liu YH, Koduru P, Tirado CA. 2010. Secondary Chromosome Aberrations in Non-Hodgkin Lymphoma with IG/MYC Rearrangement defined Burkitt Lymphoma from Diffuse Large B-cell Lymphoma: A meta-analysis of Cytogenetic Data. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Garay N, Garcia R, Tirado CA. 2010. Comparison of Secondary Chromosome Aberrations between Follicular Lymphoma and Diffuse Large B-Cell Lymphoma with t(14;18): Review from the Mitelman Data Base. American Society of Human Genetics Meeting, Washington DC, November 2-6, 2010.
Lou Z, Tirado CA, Chen W, Garcia R, S. Iyer, J Doolittle, P. Koduru. 2010. Interphase FISH and chromosome Analysis on ETV6/RUNX1-positive childhood acute lymphoblastic leukemia reveal an increased risk in a patient with additional copies of both normal and derivative chromosome 21. 2010 American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Valdez FJ, Tirado CA, Henderson S, Horna P, Doolittle J, Garcia R, Auchus M, Collins RH. 2009. A cryptic t(1;21;8)(p36.1;q22;q22): A variant involving a single RUNX1/CBFA2T1fusion in a patient with acute myeloid leukemia (AML-M2). American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Uddin N, Chen W, Arbini A, Klesse L, Karandikar N, Fustino N, Almiski M, Holdridge S, Doolittle J, Villalobos I, Tirado CA. 2009. Acute myeloid leukemia with inv(16), 3’CBFB deletion, variant t(9;22) & del(7)(q) in a pediatric patient, a case report. American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Garcia R, Uddin N, Villalobos I, Holdridge S, Chastain C, Doolittle J, Tirado CA. 2009. Recurrent aberrations in High Grade B-Cell Lymphomas with concurrent 8q24/MYC Rearrangements and t(14;18). American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Henderson S, Uddin N, Stewart E, Iyer S, Ratner IM, Matthews E, Doolittle J, Garcia R, Valdez F, Dallaire S, Payne D, Collins R, Tirado CA. 2009. Cytogenetic and Molecular Characterization of a Partial Trisomy 2p Arising from Inverted Duplication of 2p with Terminal Deletion of 2pter. American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Tirado CA, Meloni-Ehrig AM, Edwards T, Scheerle J, Burks K, Repetti C, Christacos NC, Kelly JC, Greenberg J, Murphy C, Croft CD, Heritage D, Mowrey PN. 2006. Cryptic ins(4;11)(q21;q23q23): a Variant of t(4;11)(q21;q23) in an Infant with a Precursor B-cell Acute Lymphoblastic Leukemia. American Society of Human Genetics Meeting, New Orleans, Lousiana. October 9-13, 2006.
Tirado CA, Meloni-Ehrig AM, Burks K, Wallenhorst E, Scheerle J, Kelly JC, Heritage D, Spira A, Glasser L, Mowrey P. 2005. Two cases of dic(17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality associated with poor prognosis . American Society of Human Genetics Meeting, Salt Lake City, Utah. October 25-29, 2005.
Meloni-Ehrig AM, Tirado CA, Scheerle J, Beveridge R, Ueno WM, Francis P, Croft CD, Mowrey P. 2005. Complex translocation (8;14;18)(q24;q32;q21) in an aggressive follicular lymphoma. American Society of Human Genetics Meeting, Salt Lake City, Utah. October 25-29, 2005.
Meloni-Ehrig AM, Tirado CA, Chen K, Jahn J, Suchan S, Scheerle J, Crosby MG, Seibel N, Leitenberg D, Mowrey P. 2004. Deletion (14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia. Quest Diagnostics Nichols Institute Symposium. September 2004.
Tirado CA, Jahn JA, Scheerle J, Eid M, Meister RJ, Christie RJ, Croft CD, Wallingford S, Heritage DW, Mowrey PN, Aurelia M. Meloni-Ehrig.2004. Variant APL t(15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion. American Society of Human Genetics Meeting, Toronto, Canada, October 26-30, 2004.
Tirado CA, Lager J, Golembiewski-Ruiz V, Rosoff P, Gong J, Goodman B. 2003. A case of infantile ALL presenting with rearrangement of MLL at 11q23 and apparent insertion/translocation at 10p12. American Journal of Human Genetics 73(A)752:298.
Sebastian S, Tirado CA, Moore JO, Goodman BK. 2003. Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12 and 17 resulting in ETV6(TEL) and ABL fusion in a patient with BCR/ABL-negative Chronic myeloid leukemia. American College of Molecular Pathology Meeting 2003.
Coleman LW, Herman CM, Goodman BK, Madden JF, Golembiewski-Ruiz VA, Molino AC, Tirado CA, Grichnik JM, Selim MA. 2002. Abnormalities of chromosome 7 in Thin Lethal Melanomas by Fluorescence In Situ Hybridization on Paraffin-embedded material. 39th Annual Meeting of the American Society of Dermatopathology. Phoenix, Arizona (10/10/2002-10/13/2002)
and Carlos A. Tirado (2020) An isochromosome 17q, a rare chromosomal abnormality in a female patient with leukocytosis. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Felix E. Laban, David Shabsovich, David Palencia , Joy King, David Trejo, Lorena Villalba
and Carlos A. Tirado (2020) An isochromosome 17q, a rare chromosomal abnormality in a female patient with leukocytosis. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Andrew Reyes, Félix Labán , David Shabsovich, John Reinartz, Kevin Stieglbauer and Carlos A. Tirado (2020) C-MYC amplification in a case of male patient diagnosed with B-CLL. Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Leena Nabipur, Joy King, Anna Okabe, Felix Laban, William Koss2, Elaine Horton2, Maria T. Guardiola, Krystal Soyalp, and Carlos A. Tirado (2020) A t(9;11)(p22;q23) within the context of a complex karyotype is associated with a poor prognosis in a 19 year old patient with AML.Poster presented at the ASHG 2020 Annual Meeting in San Diego.
Nguyen A, Tse V, Lapp K, Yang G, Peng E, Yun M, Cunnien K, Serk D, Wyatt B, Tirado CA. Molecular cytogenetic characterization of a complex karyotype of a pediatric male patient with B-acute lymphoblastic leukemia. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Okabe A, Nguyen A, Reyes A, Zhao D, Chung D, Laban F, Thompson L, Murphy M, Cunnien K, Wyatt B, Tirado CA Molecular cytogenetic characterization of a karyotype of a female patient with secondary amenorrhea. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Reyes A, Tse V, Yang G, Peng E, Yun M, Cunnien K, Lapp K, Wyatt B and Tirado CA A case of a lymphoblastic lymphoma with trisomy 12 in the lymphoid population and deletion 13q of myeloid origin. Poster presented at the 2019 American Society of Human Genetics Annual Meeting (Oct 15th to 21st, 2019) in Houston, TX.
Chung D, Reyes A, Nguyen A, Stieglbauer K. , Serk D , Ahmad J, Cunnien K, Bartholomaus L and Tirado, CA Molecular cytogenetic characterization of a case of a mixed myelodysplastic/myeloproliferative neoplasm: chronic myelomonocytic leukemia-1 (CMML-1) with an abnormal karyotype with an apparent monosomy 7 resulting in rearrangements involving chromosomes 7 and 21. Poster presented at the 2018 American Society of Human Genetics Annual Meeting (Oct 16th to 21st, 2018) in San Diego, CA.
Zhao D, Liu K, Reinartz J, Serk D , Ahmad J, Cunnien K, Bartholomaus L and Tirado CA Duplication of the band q21q27 on the long arm of chromosome 3 : A rare cytogenetic event in B- Chronic Lymphocytic Leukemia (B-CLL). Poster presented at the 2018 American Society of Human Genetics Annual Meeting (Oct 16th to 21st, 2018) in San Diego, CA.
Helmer J. and Tirado CA. A three way t(8;14;22)(q24;q24;q32;q11.2) characterized by molecular cytogenetics with involvement of MYC/ICH/IGL. Platform presentation at International Congress of Flow Cytometry, Chiclayo, Perú (6th to the 8th December 2018).
Nguyen A, Tirado CA . Cytogenetics of T-acute lymphoblastic leukemia . Platform presentation at
V Jornada Internacional de Genética & Biologia Molecular , Chiclayo, Perú (8th to the 10th August 2018).
Zhao D. and Tirado CA Transient Myeloproliferative Disorders in Down Syndrome. Platform presentation at V Jornada Internacional de Genética & Biologia Molecular , Chiclayo, Perú (8th to the 10th August 2018).
Tirado CA, Liu K, Dowiak AV, Wyatt W, Wheaton S, Peterson K., Serk D, Cunnien K & Reinartz JJ. A plasma cell myeloma case with an abnormal clone showing a t(8;22)(q24.1;q11.2) within the context of a hyperdiploid complex karyotype. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Crippen R, Salazar E, Liu K, Tirado CA Acute Myeloid Leukemia with t(3;8)(q26.2;q24) Involving
MECOM (EVI1) on Chromosome 3. Poster presented at UCLA Science Poster Day on May 22nd, 2018.
Zhao D, Nguyen A, Liu K and Tirado, CA A Rare Cytogenetic Abnormality in Chronic Lymphocytic Leukemia: t(18;22)(q21;q11) Involving IGL/BCL2. Poster presented at UCLA Science Poster Day on May 22nd, 2018.
Liu KQ, Tirado CA. The Cytogenetics of t(8;22)(q24.1;q11.2) in Plasma Cell Myeloma. Poster presented
at UCLA Science Poster Day on May 22nd, 2018.
Liu K, Makar C, Bond A, Stieglbauer K, Wheaton S, Reinartz J, Cunnien K, Peterson K, Bartholomaus L, Serk D, Wyatt B, Khan S &Tirado CA. A t(3;8)(q26.2;q24) involving the EVI1 (MECOM) gene on 3q26.2 in a case of Acute Myeloid Leukemia preceded by Polycythemia vera. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Dowiak A, Ewing J, Khan S, Salazar E, Thompson L, Wyatt B, Peterson K, Bartholomaus L, Nguyen A, Crippen R, Reinartz J &Tirado CA. A t(18;22)(q21;q11) involving IGH/BCL2, a rare event in Chronic Lymphocytic leukemia. Poster presented at the ASHG Meeting 2017, October 17th – 20th , 2017.
Shabsovich, D, Rao N, Tirado, CA. Cytogenetic Analyis of Pancreatic Adenocarcinoma using Giemsa Banding and Fluorescence In Situ Hybridization. Eighteen Annual Science Poster Day May 12, 2015 Ackerman Grand Ballroom. University of California Los Angeles.
Chow R, Shabsovich D, Schiller G, Kallen M, Pullarkat ST, Rao N & , Tirado CA t(17;19)(q21;p13.3) involving TCF3; a t(1;19)(p13;p13) and a 5’IGH@ abnormality in a case of adult B-cell Acute Lymphoblastic Leukemia. Poster presented at the ASHG Meeting 2015, October 6th – 10th , 2015.
Shabsovich D and Tirado CA CML with cryptic BCR-ABL1 translocations. Platform presented at the XVI
Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Liu K and Tirado CA Gliomas: A genetic update. . Platform presented at the XVI Conebiol Meeting held in
Lambayeque, Peru on September 21-September 24th, 2015.
Shabsovich D and Tirado CA Molecular Cytogenetics of Pancreatic Cancer. Platform presented at the XVI
Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Chow R and Tirado CA A t(17;19) in B-ALL. Platform presented at the XVI Conebiol Meeting held in Lambayeque, Peru on September 21-September 24th, 2015.
Ji J, Loo E, Pullarkat S, Yang L &Tirado CA. 2014 Acute Myeloid Leukemia with t(7;21) and 5qLoss: a New Rare Entity of AML?. 2014 American Cytogenetics Conference, Asheville, NC, May 4-7, 2014.
Kallen ME, DeNicola MM, Pullarkat ST, Paquette R, Yang L, Rao NP, Tirado CA. 2014. Case Report:
BCR-ABL1 Amplification, a Unique Finding in B-Lymphoblastic Leukemia. 2014 American Cytogenetics Conference, Asheville, NC, May 4-7, 2014.
Kim Y, Yang L, Rao N,TiradoCA2014 Cytogenetics of Blastoid Crisis of Mantle Cell Lymphoma. III
International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Kim Y, Traum P, Pelkey J, Yang L, Rao N,Tirado CA2014 A t(2;12)(p12;p13) in a pediatric Down
Syndrome Patient with B-ALL. III International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Hasan A, Rao N, Tirado CANPM1 and FLT3 genes in acute myeloid leukemia. III International Workshop
in Henetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Ngo D, Das K, Tirado, CA Cytogenetics as a tool in non-small cell lung cancer. III International Workshop
in Henetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
18
Abusaba G, Yang L, Paquette R, Rao N, Tirado CABCR/ABL1 amplification a rare event in B-ALL. III
International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Allen D, Boles J, Rao N, Tirado CA Chronic Myelogenous Leukemia with a normal karyotype and
BCR/ABL1 fusion. BCR/ABL1 amplification a rare event in B-ALL. III International Workshop in Genetics “58 years of 46 human chromosomes”, Chiclayo, Peru. August 11-13th, 2014.
Shabsovich D,Rao D, Ji J, Park K, Yang L &Tirado CA. Conventional Cytogenetic and Molecular Genetic Analysis of Pancreatic Cancer.American Society of Human Genetics Meeting , San Diego, CA, October 18- 22nd, 2014.
Lasky BJ, Yeh L, Kallen M, Pullarkat S, Yang L, Hasan A, Kim Y, Shabsovich D, Rao N, Tirado CA A
(1;19) translocation involving TCF3/PBX1 fusion within a context of a hyperdiploid karyotype.American Society of Human Genetics Meeting , San Diego, CA, October 18-22nd, 2014.
Kim Y, Traum P, Lasky B, Yang L, Ngo D, Pelkey J, Rao N, Tirado CAA (2;12)(p12;p13) translocation in
a Down Syndrome patient with B-ALL. American Society of Human Genetics Meeting, San Diego, CA, October 18-22nd, 2014.
Tirado CA, Kim Y, Yang L, Abusaba G, Lasky BJ, Rao N & Tirado CA A complex karyotype with a cryptic t(11;14)(q13;q32) in a Blastoid Crisis of Mantle Cell Lymphoma. American Society of Human Genetics Meeting , San Diego, CA, October 18-22nd, 2014.
DeNicola M, Pullakat S, Yea S, Delgado P, Yang L, Rao N, Tirado CA. 2013. A case of hyperdiploidy in
CLL/SLL: A Rare Cytogenetic Event Associated with Poor Prognosis. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Tirado CA,DeNicola M, Rao D, Delgado P, Jarrin A, Yang L, Rao N. 2013. A case of pediatric acute
lymphoblastic leukemia with a (9;12) translocation involving JAK2 and rearrangement of MLL at 11q23 with an apparent insertion at 6q27. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Delgado P, Iyer S, Jarrin A, Rao N, Tirado CA. 2013. Infertility related to a rearrangement of the Y
chromosome. American Society of Human Genetics Meeting, Boston, MA, October 22-26, 2013.
Bui PH, Amarillo I, Shackley BS, Rao N, Tirado CA. 2012. A t(8;14)(q24;q32) translocation resulting in an atypical IGH/MYC genomic fusion in clinically aggressive chronic lymphocytic leukemia. 2012 American Cytogenetics Conference, San Antonio, Texas, April 19-22, 2012.
Starshak P, Linhares Y, Delgado P, Rao PN, Tirado CA. 2012. T-cell prolymphoytic Leukemia (T-PLL), a heterogeneous disease exemplified by two cases and the important role of cytogenetics. American Cytogenetics Conference 2012, San Antonio, Texas, April 19-22, 2012.
Tirado CA, Boles JW, Quintero-Rivera F. 2012. An unbalanced rearrangement involving a translocation (6;8) in a case of diffuse large B-cell lymphoma. American Cytogenetics Conference 2012, San Antonio, Texas, April 19-22, 2012.
Delgado PA, Rao N, Tirado CA. Cytogenetics and Molecular findings in T-PLL. 2012. International
Workshop of Human Genetics. Chiclayo, Peru. October 17-19, 2012.
Boles J, Tirado CA. Epigenetic events in leukemia. 2012. International Workshop of Human Genetics.
Chiclayo, Peru. October 17-19, 2012.
Marinoni M, Tirado CA. 2012. Cytogenetic and Molecular cytogenetic findings in Pancreatic Cancer.
International Workshop of Human Genetics, Universidad Nacional Pedro Ruiz Gallo. Lambayeque, Peru, October 17-19, 2012.
Garcia L, Marinoni M, Meisner L, Tirado CA. 2012. Update in Stem Cell Research. International Workshop
of Human Genetics, Circle of Genetic Studies Francis Collins. Universidad Nacional Pedro Ruiz Gallo, Lambayeque, Peru October 17-19, 2012.
Marinoni M, Tirado CA. 2012. Hermaphroditism and Intersex: An Update. International Workshop of
Human Genetics, Circle of Genetic Studies Francis Collins. Universidad Nacional Pedro Ruiz Gallo, Lambayeque, Peru. October 17-19, 2012.
Delgado P, Crandall B, Rao N, Bui P, Tirado CA. 2012 Low Klinefelter mosaicism in a male with azoospermia detected by FISH. 2012 American Society of Human Genetics Meeting, San Francisco, CA. November 6-10, 2012.
DeNicola M, Boles J, Collins R, Garcia R, Tirado CA. 2012 A CML case with normal karyotype and positive BCR/ABL1 fusion. 2012 American Society of Human Genetics Meeting in San Francisco, CA, November 6-10, 2012.
Martinez D, Garcia R, Koduru P, Tirado CA. 2011. Recurrent Cytogenetic aberrations predict MYC breakpoints in diffuse large B-cell lymphoma and help define Burkitt lymphoma versus diffuse large B-cell lymphoma with MyC rearrangaements. 12th International Congress of Human Genetics , Montreal Oct 11- 15, 2011.
Wakim JJ, Tirado CA, Chen WC. 2011. The first case of a Ph-negative acute promyelocytic leukemia following imatinib for chronic myeloid leukemia. 12th International Congress of Human Genetics , Montreal Oct 11-15, 2011.
Hiemenz M, Chen W, Winick N, Tirado CA. 2011. Coexistence of t(12;21)(p13;q22)/ETV6-RUNX1 and MLL rearrangement in a pediatric patient with B-lymphoblastic leukemia. 12th International Congress of Human Genetics , Montreal Oct 11-15, 2011
Garcia R, Seegmiller A, Maleki A, Tirado CA, Chen W. 2010. Recurrent Aberrations in High Grade B-Cell Lymphomas with IG-MYC Rearrangement and their Impact on Survival. Presented at the 2010 US & Canadian Academy of Pathology Meeting. Washington D.C., March 20-26, 2010
Lou Z, Zhang J, Tirado CA, Slone T, Zaremba CM, Oliver D, Chen W. 2010 Infantile Mixed Phenotype Acute Leukemia (Bilineal and Biphenotypic) with t(10;11)(p12;q23); MLL-MLLT10. 2010 American Cytogenetics Conference Meeting, Ontario, Canada, May 13-16, 2010.
Hiemenz M, Chen W, Huang LJ, Laborde C, Lou Z, Valdez F, Winick N, Ho K, Koduru P, Tirado CA. 2010. Novel JAK2 rearrangement resulting from a t(9;22)(p24;p11.2) in B lymphoblastic leukemia. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Torgbe E, Tirado CA, Gotway G, Valdez F, Suterwala M, Iyer S, Garcia R, Shah N, Dallaire S, Appleberry T, Pichurin P, Koduru P. 2010. Recombinant chromosome 7 in a mosaic triple X/Turner patient. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Davila O, Garcia R, Garay N, Koller M, Liu YH, Koduru P, Tirado CA. 2010. Secondary Chromosome Aberrations in Non-Hodgkin Lymphoma with IG/MYC Rearrangement defined Burkitt Lymphoma from Diffuse Large B-cell Lymphoma: A meta-analysis of Cytogenetic Data. American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Garay N, Garcia R, Tirado CA. 2010. Comparison of Secondary Chromosome Aberrations between Follicular Lymphoma and Diffuse Large B-Cell Lymphoma with t(14;18): Review from the Mitelman Data Base. American Society of Human Genetics Meeting, Washington DC, November 2-6, 2010.
Lou Z, Tirado CA, Chen W, Garcia R, S. Iyer, J Doolittle, P. Koduru. 2010. Interphase FISH and chromosome Analysis on ETV6/RUNX1-positive childhood acute lymphoblastic leukemia reveal an increased risk in a patient with additional copies of both normal and derivative chromosome 21. 2010 American Society of Human Genetics Meeting. Washington DC, November 2-6, 2010.
Valdez FJ, Tirado CA, Henderson S, Horna P, Doolittle J, Garcia R, Auchus M, Collins RH. 2009. A cryptic t(1;21;8)(p36.1;q22;q22): A variant involving a single RUNX1/CBFA2T1fusion in a patient with acute myeloid leukemia (AML-M2). American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Uddin N, Chen W, Arbini A, Klesse L, Karandikar N, Fustino N, Almiski M, Holdridge S, Doolittle J, Villalobos I, Tirado CA. 2009. Acute myeloid leukemia with inv(16), 3’CBFB deletion, variant t(9;22) & del(7)(q) in a pediatric patient, a case report. American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Garcia R, Uddin N, Villalobos I, Holdridge S, Chastain C, Doolittle J, Tirado CA. 2009. Recurrent aberrations in High Grade B-Cell Lymphomas with concurrent 8q24/MYC Rearrangements and t(14;18). American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Henderson S, Uddin N, Stewart E, Iyer S, Ratner IM, Matthews E, Doolittle J, Garcia R, Valdez F, Dallaire S, Payne D, Collins R, Tirado CA. 2009. Cytogenetic and Molecular Characterization of a Partial Trisomy 2p Arising from Inverted Duplication of 2p with Terminal Deletion of 2pter. American Society of Human Genetics Meeting, Honolulu, Hawaii, October 20-24, 2009.
Tirado CA, Meloni-Ehrig AM, Edwards T, Scheerle J, Burks K, Repetti C, Christacos NC, Kelly JC, Greenberg J, Murphy C, Croft CD, Heritage D, Mowrey PN. 2006. Cryptic ins(4;11)(q21;q23q23): a Variant of t(4;11)(q21;q23) in an Infant with a Precursor B-cell Acute Lymphoblastic Leukemia. American Society of Human Genetics Meeting, New Orleans, Lousiana. October 9-13, 2006.
Tirado CA, Meloni-Ehrig AM, Burks K, Wallenhorst E, Scheerle J, Kelly JC, Heritage D, Spira A, Glasser L, Mowrey P. 2005. Two cases of dic(17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality associated with poor prognosis . American Society of Human Genetics Meeting, Salt Lake City, Utah. October 25-29, 2005.
Meloni-Ehrig AM, Tirado CA, Scheerle J, Beveridge R, Ueno WM, Francis P, Croft CD, Mowrey P. 2005. Complex translocation (8;14;18)(q24;q32;q21) in an aggressive follicular lymphoma. American Society of Human Genetics Meeting, Salt Lake City, Utah. October 25-29, 2005.
Meloni-Ehrig AM, Tirado CA, Chen K, Jahn J, Suchan S, Scheerle J, Crosby MG, Seibel N, Leitenberg D, Mowrey P. 2004. Deletion (14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia. Quest Diagnostics Nichols Institute Symposium. September 2004.
Tirado CA, Jahn JA, Scheerle J, Eid M, Meister RJ, Christie RJ, Croft CD, Wallingford S, Heritage DW, Mowrey PN, Aurelia M. Meloni-Ehrig.2004. Variant APL t(15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion. American Society of Human Genetics Meeting, Toronto, Canada, October 26-30, 2004.
Tirado CA, Lager J, Golembiewski-Ruiz V, Rosoff P, Gong J, Goodman B. 2003. A case of infantile ALL presenting with rearrangement of MLL at 11q23 and apparent insertion/translocation at 10p12. American Journal of Human Genetics 73(A)752:298.
Sebastian S, Tirado CA, Moore JO, Goodman BK. 2003. Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12 and 17 resulting in ETV6(TEL) and ABL fusion in a patient with BCR/ABL-negative Chronic myeloid leukemia. American College of Molecular Pathology Meeting 2003.
Coleman LW, Herman CM, Goodman BK, Madden JF, Golembiewski-Ruiz VA, Molino AC, Tirado CA, Grichnik JM, Selim MA. 2002. Abnormalities of chromosome 7 in Thin Lethal Melanomas by Fluorescence In Situ Hybridization on Paraffin-embedded material. 39th Annual Meeting of the American Society of Dermatopathology. Phoenix, Arizona (10/10/2002-10/13/2002)