(Q52888757)

English

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia.

scientific article published on 16 January 2016

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

5

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

author name string

Kristina B Lundin

1

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Linda Olsson

2

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Setareh Safavi

3

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Andrea Biloglav

4

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Bertil Johansson

6

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

publication date

16 January 2016

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

55

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

5

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

472-479

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

Common fragile sites as targets for chromosome rearrangements

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies

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Mosaicism and uniparental disomy in prenatal diagnosis

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Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

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Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

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High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.

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Human chromosome fragility

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Runs of homozygosity in European populations

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A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia.

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Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

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Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia

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21 January 2018

Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011.

1 reference

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21 January 2018

Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.

1 reference

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21 January 2018

High hyperdiploid childhood acute lymphoblastic leukemia

1 reference

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21 January 2018

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

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The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

1 reference

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High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

1 reference

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21 January 2018

Mitotic recombination in haematological malignancy.

1 reference

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Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

1 reference

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21 January 2018

Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia

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21 January 2018

Acquired uniparental disomy in myeloproliferative neoplasms

1 reference

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21 January 2018

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies

1 reference

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21 January 2018

A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

21 January 2018

Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships

1 reference

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21 January 2018

Uniparental disomy and human disease: an overview.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

21 January 2018

Uniparental isodisomy due to duplication of chromosome 21 occuring in somatic cells monosomic for chromosome 21

1 reference

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21 January 2018

Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia

1 reference

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21 January 2018

Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia

1 reference

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21 January 2018

A new genetic concept: uniparental disomy and its potential effect, isodisomy

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

7 January 2021

based on heuristic

inferred from DOI database lookup

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

7 January 2021

based on heuristic

inferred from DOI database lookup

Integrated analysis of gene copy number, copy neutral LOH, and microRNA profiles in adult acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

7 January 2021

based on heuristic

inferred from DOI database lookup

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22349

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.22349

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 May 2018

http://europepmc.org/abstract/MED/26773847

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