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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Journal of clinical oncology, 2010-06, Vol.28 (16), p.2682-2689

2010

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Ataxia-telangiectasia mutated (ATM) silencing promotes neuroblastoma progression through a MYCN independent mechanism

Oncotarget, 2015-07, Vol.6 (21), p.18558-18576

2015

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MRD ‐risk stratification mitigates TLX3 prognostic impact in paediatric T‐cell acute lymphoblastic leukaemia: A national cohort analysis

British journal of haematology, 2024-08, Vol.205 (2), p.729-732

2024

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Adapted risk stratification and intensive chemotherapy abrogate the poor prognosis of pediatric B acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 (iAMP21): a National cohort analysis

Leukemia & lymphoma, 2024-02, Vol.65 (2), p.279-282

2024

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Nicolaides–Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion

Cardiology in the young, 2022-05, Vol.32 (5), p.821-823

2022

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NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

European journal of medical genetics, 2019-03, Vol.62 (3), p.204-209

2019

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Similar but different: identical pathology with differing outcome in ‘Not‐so‐identical’ twins

British journal of haematology, 2017-07, Vol.178 (1), p.152-153

2017

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Guidelines for cytogenetic investigations in tumours

European journal of human genetics : EJHG, 2016-01, Vol.24 (1), p.6-13

2016

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De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

American journal of medical genetics. Part A, 2015-05, Vol.167A (5), p.1134-1141

2015

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A retrospective study of myeloid leukaemia in children with Down syndrome in Ireland

Irish journal of medical science, 2020-08, Vol.189 (3), p.979-984

2020

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Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome

Hormone research in paediatrics, 2017-01, Vol.87 (2), p.130-135

2017

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Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

The New England journal of medicine, 1999-06, Vol.340 (25), p.1954-1961

1999

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A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder

BMC medical genetics, 2015-06, Vol.16 (1), p.45-45, Article 45

2015

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Cover Image, Volume 173A, Number 1, January 2017

American journal of medical genetics. Part A, 2017-01, Vol.173 (1), p.i-i

2017

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Bicoronal and metopic craniosynostosis in association with a de novo unbalanced t(2;7) chromosomal translocation

American journal of medical genetics. Part A, 2017-01, Vol.173 (1), p.274-279

2017

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CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16)

Blood, 2005-08, Vol.106 (4), p.1369-1375

2005

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A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9

American journal of medical genetics. Part A, 2005-07, Vol.136A (1), p.31-37

2005

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Cytogenetic characterization of childhood acute lymphoblastic leukemia in Nicaragua

Pediatric blood & cancer, 2009-12, Vol.53 (7), p.1238-1241

2009

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Prediction of chromosomal aneuploidy from gene expression data

Genes chromosomes & cancer, 2007-01, Vol.46 (1), p.75-86

2007

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High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma

Diagnostic molecular pathology, 2013-06, Vol.22 (2), p.76-84

2013

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The PAX5 oncogene is expressed in N-type neuroblastoma cells and increases tumorigenicity of a S-type cell line

Carcinogenesis (New York), 2004-10, Vol.25 (10), p.1839-1846

2004

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The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG)

European journal of haematology, 2007-06, Vol.78 (6), p.468-476

2007

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Vocal cord paralysis in association with 9q34 duplication

Clinical dysmorphology, 2014-07, Vol.23 (3), p.105

2014

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SKY analysis of childhood neural tumors and cell lines demonstrates a susceptibility of aberrant chromosomes to further rearrangements

Cancer letters, 2007-05, Vol.250 (1), p.47-52

2007

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Congenital sacrococcygeal PNET and chemotherapy

Indian journal of medical and paediatric oncology, 2012-07, Vol.33 (3), p.182-184

2012

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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Ataxia-telangiectasia mutated (ATM) silencing promotes neuroblastoma progression through a MYCN independent mechanism

MRD ‐risk stratification mitigates TLX3 prognostic impact in paediatric T‐cell acute lymphoblastic leukaemia: A national cohort analysis

Adapted risk stratification and intensive chemotherapy abrogate the poor prognosis of pediatric B acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 (iAMP21): a National cohort analysis

Nicolaides–Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

Similar but different: identical pathology with differing outcome in ‘Not‐so‐identical’ twins

Guidelines for cytogenetic investigations in tumours

De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

A retrospective study of myeloid leukaemia in children with Down syndrome in Ireland

Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome

Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder

Cover Image, Volume 173A, Number 1, January 2017

Bicoronal and metopic craniosynostosis in association with a de novo unbalanced t(2;7) chromosomal translocation

CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16)

A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9

Cytogenetic characterization of childhood acute lymphoblastic leukemia in Nicaragua

Prediction of chromosomal aneuploidy from gene expression data

High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma

The PAX5 oncogene is expressed in N-type neuroblastoma cells and increases tumorigenicity of a S-type cell line

The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG)

Vocal cord paralysis in association with 9q34 duplication

SKY analysis of childhood neural tumors and cell lines demonstrates a susceptibility of aberrant chromosomes to further rearrangements

Congenital sacrococcygeal PNET and chemotherapy

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