Amanda Figueiredo

All papers authored by Amanda Figueiredo

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2020 Amanda F. de Figueiredo

, Marcelo G. P. Land, Gerson M. Ferreira

, Andre Mencalha, Renata Binato, Roberto R. Capela de Matos, Thomas Liehr, Maria Luiza M. Silva, Eliana Abdelhay

Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia

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2017 Daiane Correa de Souza, Amanda Faria de Figueiredo

, Daniela R. Ney Garcia, Elaine Sobral da Costa, Moneeb A. K. Othman, Thomas Liehr, Eliana Abdelhay, Maria Luiza Macedo Silva, Teresa de Souza Fernandez

A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome

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2016 Daniela R. Ney Garcia, Mariana T. de Souza, Amanda F. de Figueiredo

, Moneeb A. K. Othman, Katharina Rittscher, Eliana Abdelhay, Roberto R. Capela de Matos, Claus Meyer, Rolf Marschalek, Marcelo G. P. Land, Thomas Liehr, Raul C. Ribeiro, Maria Luiza Macedo Silva

Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes

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2015 Amanda Faria de Figueiredo

, Roberto Rodrigues Capela de Matos, Roberto Rodrigues Capela de Matos, Moneeb A. K. Othman, Thomas Liehr, Elaine Sobral da Costa, Marcelo Geradin Poirot Land, Raul C. Ribeiro, Eliana Abdelhay, Maria Luiza Macedo Silva

Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia

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Roberto R. Capela de Matos, Amanda F. De Figueiredo

, Thomas Liehr, Eyad Alhourani, Mariana T. De Souza, Renata Binato, Raul C. Ribeiro, Maria Luiza Macedo Silva

A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with <b><i>RUNX1/RUNX1T1</i></b>: The Contribution of Molecular Approaches for Revealing t(8;21) Variants

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2014 Daniela Ribeiro Ney Garcia, Amanda Faria de Figueiredo

, André Luiz Mencalha, Roberto Rodrigues Capela de Matos, Fábia Neves, Raul Correa Ribeiro, Marcelo Gerardin Poirot Land, Maria Luiza Macedo Silva

Overexpression of the MLL Gene Combined With 11q Trisomy in a Child With Acute Lymphoblastic Leukemia

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Daiane Correa de Souza, Amanda Faria de Figueiredo

, Hasmik Mkrtchyan, Moneeb A. K. Othman, Thomas Liehr, Jane Dobbin, Maria Luiza Macedo Silva, Maria Luiza Macedo Silva, Eliana Abdelhay, Teresa de Souza Fernandez

A yet unreported der(11)t(6;11)(p21;q21) included in a complex Karyotype of a refractory anemia with ring sideroblasts and poor prognosis

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2013 Renata Binato, Claus Meyer, Maria Luiza Macedo-Silva, Daniela Garcia, Amanda Figueiredo

, Julia Hofmann, Tarsis Paiva Vieira, Eliana Abdelhay, Rolf Marschalek

Analyzing acute leukemia patients with complex MLL rearrangements by a sequential LDI-PCR approach

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R. R. C. Matos, H. Mkrtchyan, B. A. S. Amaral, T. Liehr, M. T. de Souza, D. R. Ney Garcia, N. Santos, T. J. Marques Salles, R. C. Ribeiro, A. F. Figueiredo

, Maria Luiza Macedo Silva

An Unusual Cytogenetic Rearrangement Originating from Two Different Abnormalities in Chromosome 6 in a Child with Acute Promyelocytic Leukemia

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2012 Daniela Ribeiro Ney-Garcia, Társis Paiva Vieira, Thomas Liehr, Samarth Bhatt, Mariana Tavares de Souza, Amanda Faria de Figueiredo

, Raul Correa Ribeiro, Maria Luiza Macedo Silva

A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone

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Amanda Faria de Figueiredo

, Mariana Tavares de Souza, Tarsis Paiva Vieira, Thomas Liehr, Samarth Bhatt, Renata Binato, Terezinha de Jesus Marques-Salles, Terezinha de Jesus Marques-Salles, Edna Carboni, Raul C. Ribeiro, Maria Luiza Macedo Silva, Eliana Abdelhay

A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5)

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2011 Amanda Faria De Figueiredo

, Thomas Liehr, Samarth Bhatt, Renata Binato, Mariana Tavares De Souza, Roberto Rodrigues Capela De Matos, Terezinha De Jesus Marques Salles, Fernanda C. Jordy, Raul C. Ribeiro, Eliana Abdelhay, Maria Luiza Macedo Silva

A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia

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Mariana Tavares de Souza, Hasmik Mkrtchyan, Rocio Hassan, Daniela Ribeiro Ney-Garcia, Alice Maria Boulhosa de Azevedo, Elaine Sobral da Costa, Amanda Faria de Figueiredo

, Thomas Liehr, Eliana Abdelhay, Maria Luiza Macedo Silva

Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis

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2010 Amanda Faria de Figueiredo

, Thomas Liehr, Samarth Bath, Renata Binato, Eliane Maria Soares Ventura, Mariana Tavares de Souza, Roberto Rodrigues Capela de Matos, Raul Correa Ribeiro, Eliana Abdelhay, Maria Luiza Macedo Silva

A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5

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2009 Amanda Faria de Figueiredo

, Hasmik Mkrtchyan, Thomas Liehr, Eliane Maria Soares Ventura, Terezinha de Jesus Marques-Salles, Neide Santos, Raul Corrêa Ribeiro, Eliana Abdelhay, Maria Luiza Macedo Silva, Maria Luiza Macedo Silva

A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter→q23∼24::q23∼24→q43→neo→q43→qter) and tetrasomy of chromosomes 8 and 21

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Terezinha de Jesus Marques-Salles, Mariana Tavares de Souza, Thomas Liehr, Hasmik Mkrtchyan, Susana C. Raimondi, Mariana Tavares de Souza, Amanda Faria de Figueiredo

, Amanda Faria de Figueiredo, Soraia Rouxinol, Fernanda C. Jordy Macedo, Eliana Abdelhay, Neide Santos, Maria Luiza Macedo Silva, Maria Luiza Macedo Silva

A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia

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Maria Luiza Macedo Silva, Maria do Socorro Pombo-De-Oliveira

, Susana C. Raimondi, Hasmik Mkrtchyan, Eliana Abdelhay, Amanda Faria de Figueiredo

, Mariana Tavares de Souza, Daniela Ribeiro Ney Garcia, Eliane Maria Soares de Ventura, Adriana Martins de Sousa, Thomas Liehr

Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia

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2008 Maria Luiza Macedo Silva, Susana C. Raimondi, Eliana Abdelhay, Madeleine Gross, Hasmik Mkrtchyan, Amanda Faria de Figueiredo

, Raul C. Ribeiro, Terezinha de Jesus Marques-Salles, Elaine S. Sobral, Marcelo Poirot Gerardin Land, Thomas Liehr

Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo

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All papers authored by Amanda Figueiredo