Amanda Faria de Figueiredo

Instituição:

Universidade Federal do Rio de Janeiro

Centro:

Centro de Ciências da Saúde

Unidade:

Instituto de Puericultura e Pediatria

Departamento:

Serviço de Apoio e Diagnóstico IPPMG

ORCID:

https://orcid.org/0000-0002-2982-0745


Formação:

  • Instituto Nacional de Câncer

    | Pós-Doutorado | 2014 - 2017

  • Friedrich-Schiller-Universität Jena

    | Pós-Doutorado | 2014 - 2014

  • Instituto Nacional de Câncer

    Oncologia | Doutorado | 2010 - 2014

  • Universidade Federal do Rio de Janeiro

    Instituto de Biofisíca Carlos Chagas Filho | Mestrado | 2007 - 2009

  • Universidade Federal Rural do Rio de Janeiro

    Ciências Biológicas | Graduação | 2000 - 2004

  • Universidade Federal Rural do Rio de Janeiro

    Licenciatura em Ciencias Biológicas | Graduação | 2000 - 2004
Laboratórios:
Nenhum laboratório cadastrado
Nuvens de Palavras:
Artigos:

(100.00% artigos com DOI)

Titulo DOI Ano
Cellular consequences of small supernumerary marker chromosome derived from chromosome 12: mosaicism in daughter and father 10.1590/1414-431x2022e12072 2022
CARDIAC DIFFERENTIATION OF INDUCED PLURIPOTENT STEM CELLS DERIVED FROM PATIENTS WITH HUTCHINSON-GILFORD PROGERIA SYNDROME 10.1016/j.jcyt.2021.02.022 2021
IS IT POSSIBLE TO MODEL JERVELL AND LANGE-NIELSEN SYNDROME (JLNS) USING PATIENT-SPECIFIC INDUCED PLURIPOTENT STEM CELLS (IPSC)? 10.1016/j.jcyt.2021.02.063 2021
EFFECTS OF DOXORUBICIN ON HUMAN INDUCED PLURIPOTENT STEM CELL-DERIVED CARDIOMYOCYTES OBTAINED FROM PATIENTS SENSITIVE AND RESISTANT TO ANTHRACYCLINE-INDUCED CARDIOTOXICITY 10.1016/j.jcyt.2021.02.041 2021
Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia 10.1111/bjh.16675 2020
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome 10.1186/s13039-017-0335-3 2017
Molecular characterization of fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes 10.1002/hon.2299 2016
A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1: The Contribution of Molecular Approaches for Revealing t(8;21) Variants 10.1159/000431073 2015
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia 10.1186/s13039-015-0167-y 2015
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 10.1016/j.bcmd.2013.12.006 2014
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 10.1016/j.bcmd.2012.09.005 2013
An Unusual Cytogenetic Rearrangement Originating from Two Different Abnormalities in Chromosome 6 in a Child with Acute Promyelocytic Leukemia 10.1159/000345828 2013
Analyzing acute leukemia patients with complex MLL rearrangements by a sequential LDI-PCR approach 10.1016/j.canlet.2013.03.029 2013
Overexpression of the MLL gene combined with 11q trisomy in a child with acute lymphoblastic leukemia 10.1016/j.clml.2013.10.008 2013
Expression Profiling Of Selected Polycomb Complex Genes In Childhood Acute Myeloid Leukemia Revealed An Overexpression Of EZH2 In Acute Promyelocytic Leukemia 10.1182/blood.v122.21.4895.4895 2013
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) 10.1016/j.leukres.2011.12.009 2012
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis 10.1007/s12185-010-0757-8 2011
A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia 10.3109/10428194.2011.576286 2011
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 10.1016/j.bcmd.2010.07.001 2010
Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia 10.1186/1755-8166-2-7 2009
A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia 10.1016/j.cancergencyto.2008.10.009 2009
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 10.1016/j.cancergencyto.2009.05.001 2009
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 10.1016/j.cancergencyto.2007.12.014 2008
Eventos:

(0.00% eventos com DOI)

Titulo DOI Ano
A importancia da investigação familiar nos casos de translocação aparentemente balanceada 2019
Herdabilidade e repercurssão fenotípica de cromossomo marcador familiar 2019
CLINICAL AND BIOLOGICAL CORRELATES OF SELECTED POLYCOMB COMPLEX GENES EXPRESSION IN BRAZILIAN CHILDREN WITH ACUTE PROMYELOCYTIC LEUKEMIA 2016
CARACTERIZAÇÃO MOLECULAR DOS GENES PARCEIROS DE FUSÃO DO KMT2A EM 6 CASOS DE LEUCEMIA AGUDA DO LACTENTE > 12 MESES DE IDADE COM CARÍTIPOS COMPLEXOS OU CRÍPTICOS 2016
PERFIL CITOGENÉTICO E MUTACIONAL DO GENE FLT3 EM 70 CASOS DE LEUCEMIA MIELÓIDE AGUDA DA INFÂNCIA 2016
HIPERDIPLOIDIA, UM CASO RARO DE LEUCEMIA MIELÓIDE AGUDA PEDIÁTRICA ENVOLVENDO A DUPLICAÇÃO DA FUSÃO REVERSA MLLT3-KMT2A E DO GENE GAS6, REVELADO POR ABORDAGENS CITOGENÉTICAS MOLECULARES MODERNAS 2016
CONVENTIONAL AND MOLECULAR CYTOGENETIC STUDIES REVEALING AN ORIGINAL KARYOTYPE, 46,XX,DER(3)T(3;7)(Q26;Q21.1̃21.2),DEL(7)(Q21.1̃21.2), ASSOCIATED WITH A DISMAL OUTCOME IN A PEDIATRIC ACUTE MYELOID LEUKEMIA PATIENT 2015
MLL/MLLT4 AND MLL/MLLT10 FUSION GENES WITHIN COMPLEX KARYOTYPES: MOLECULAR CYTOGENETICS AND LDI-PCR CHARACTERIZATION OF 2 CHILDHOOD CASES WITH ACUTE MYELOID LEUKEMIA 2015
MOLECULAR CYTOGENETIC STUDIES CHARACTERIZING A NOVEL COMPLEX KARYOTYPE WITH AN UNCOMMON 5Q22 DELETION IN CHILDHOOD ACUTE MYELOID LEUKEMIA 2015
CYTOGENETICS AND MOLECULAR CHARACTERIZATION OF MIXED LINEAGE LEUKEMIA GENE REARRANGEMENTS IN CHILDHOOD ACUTE LEUKEMIA WITH COMPLEX KARYOTYPES 2014
MOLECULAR CHARACTERIZATION OF 14 COMPLEX KARYOTYPES IN A COHORT OF 115 PEDIATRIC PATIENTS WITH ACUTE MYELOID LEUKEMIA 2014
ESTUDO CITOGENÉTICO E EPIDEMIOLÓGICO DE 30 PACIENTES PEDIÁTRICOS COM LEUCEMIA PROMIELÓCITICA AGUDA NO BRASIL 2014
NOVEL VARIANT THREE-WAY T(8;13;21)(Q22;Q33;Q22) REVEALED IN A CHILD WITH ACUTE MYELOID LEUKEMIA FAB AML-M2: A CONTRIBUTION BY MOLECULAR APPROACHES 2014
Expression Profiling of Selected Polycomb Complex Genes in Childhood Acute Myeloid Leukemia Revealed an Overexpression of EZH2 in Acute Promyelocytic Leukemia 2013
Cytogenetic and molecular studies of childhood acute myeloid leukemia to identify diagnostic and prognostic biomarkers 2013
Rare, complex and cryptical chrmosomal rearrangements involving the MLL gene: Cytogenetic and molecular studies in 12 Brazilian children with acute leukemia 2013
Different MLL rearrangements at diagnosis of AML-M5 and relapse detected in a child: ins(11;1)(q23;q21q31) and t(11;19)(q23;p13) 2012
A rare t(8;17)(q21;q12) with the loss of p53 gene in a child with myeloid sarcoma that present involvement of bone marrow. 2012
Cytogenetic and molecular studies in karyotypes presenting cryptical abnormalities in childhood acute myeloid leukemia. 2012
A T-ALL childhood case with a complex t(9;9) and homozygous deletion of CDKN2A gene associated to a philadelphia-positive minor subclone. 2012
. Estudo citogenético e molecular revelou anormalidades cromossômicas crípticas e heterogeneidade. 2012
Cytogenetic and multicolor FISH studies revealed an cryptic rearrangment of the chromosome 6 in addition to a t(15;17)(q22;q21) in a child with acute promyelocytic leukemia. 2012
Caracterização citogenética molecular de rearranjos complexos ou raros do gene MLL em leucemias agudas da infância. 2012
Improved childhood Acute Myeloid Leukemia chromosomic profile with the application of Multicolor Banding Chromosome 2012
Análise citogenética de casos de leucemia promielocítica aguda da infância no Brasil através do emprego da técnica de multicolor FISH. 2012
Secondary chromosomic abnormalities to t(8;14)(q24;q32) study by multicolor banding FISH in an early relapsed childhood Burkitt lymphoma/leukemia case. 2011
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis 2010
A new complex karyotype 45,X,-Y,t(8;22;21)(q21.3;q13.3;q22.12),der(22)t(1;22)(q23;q13.3): a new cryptic variant t(8;21) associated with secondary abnormality in a child with acute myeloid leukemia (AML M2) 2010
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 2010
Rearrangement Between the Immunoglobulin Heavy Gene and Chromosome 6p21 Region in a Child with Progenitor B Acute Lymphoblastic Leukemia (PBC-ALL) and a Complex Karyotype 2010
Chromosomic profile study of Brazilian Childhood Acute Myeloid Leukemia 2010
CYTOGENETIC PROFILE OF CHILDHOOD ACUTE MYELOID LEUKEMIA IN BRAZIL 2009
MOLECULAR CYTOGENETIC STUDIES DETECTED COMPLEX NEAR-TRIPLOID KARYOTYPE IN A CHILD WITH ACUTE 2009
BANDING AND MOLECULAR CYTOGENETICS STUDIES IN INFANTS WITH DOWN SYNDROME SUFFERING ACUTE MEGAKARYOCITIC LEUKEMIA 2009
ASSOCIATION BETWEEN CONVENCIONAL AND MOLECULAR CYTOGENETICS IN THE STUDY OF 4 CASES OF CHILDHOOD AML 2009
COMPLEX KARYOTYPE IN AN INFANT WITH ACUTE MEGAKARYOBLASTIC LEUKEMIA AND NEUROFIBROMATOSIS TYPE 1 2009
Consecutive cytogenetic analyzes of 39 cases of childhood Acute Lymphoblastic Leukemia in Rio de Janeiro 2009
Banding and Molecular cytogenetic (MCB and FISH) studies in a baby with acute lymphoblastic leukemia presenting a complex karyotype including t(11;19)(q23;p13) 2008
MCB identifies inv(16) associated with dic(22) chromosome ina child with acute myeloid leukemia FAB M4-Eo 2008
Detecção de um caso de uma LMA De lactente com t(11;19)(q23;p23) "masked", utilizando multicolor FISH (MCB) 2007
. Estudo cromossômico consecutivo multicêntrico da Leucemia Mielóide aguda da Infância: Resultados preliminares 2007
Estudo cromossômico multicêntrico da leucemia mielóide aguda da infância. Relato de 22 casos. 2006
Conventional cytogenetic and molecular studies (FISH and multicolor banding) detected a rearrangement of CBFB-MYH11 fusion in an original cryptical chromosomal abnormality involved chromosome 1 and 16 in one infant with acute myeloid leukemia 2006
Estudo cromossômico de um lactente com Síndrome de Down, envolvendo a região (q21) do cromossomo 1 em um caso de Leucemia Megacarioblástica Aguda 2005
A Hipodiploidia na Leucemia Linfoblástica Aguda na infância. Apresentação de oito casos 2005
Variabilidade Genética da Leucemia Linfoblástica Aguda do tipo L3 na Infância 2004
Estudo cromossômico e imunofenotípico da Leucemia Linfoblástica Aguda do tipo T na infância: relato de 13 casos 2004
Comparação das características clínicas, laboratoriais, imunofenotípicas e citogenéticas de 50 casos de LLA de origem B com hiperdiploidia tipo I e II 2004
Anátomo-patologia de ovário de um caprino mocho pseudo-hermafrodita 60,XX 2002
Anátomo-patologia de testículos de cabras mochas pseudo-hermafroditas 60, XX 2002
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