(Q37808466)

23 August 2017

title

Ionising radiation and genetic risks. XVI. A genome-based framework for risk estimation in the light of recent advances in genome research (English)

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23 August 2017

author name string

Krishnaswami Sankaranarayanan

series ordinal

1

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23 August 2017

Hooshang Nikjoo

series ordinal

2

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23 August 2017

publication date

10 November 2010

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International Journal of Radiation Biology

23 August 2017

published in

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23 August 2017

volume

87

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23 August 2017

issue

2

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23 August 2017

page(s)

161-178

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Segmental duplications: organization and impact within the current human genome project assembly

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recent segmental duplications in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Evidence for large inversion polymorphisms in the human genome from HapMap data

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Alu repeats and human genomic diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Large, rare chromosomal deletions associated with severe early-onset obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Role of non-homologous end joining (NHEJ) in maintaining genomic integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mutational and selective effects on copy-number variants in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Missing heritability and strategies for finding the underlying causes of complex disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Structural variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Growing dictyate oocytes, but not early preimplantation embryos, of the mouse display high levels of DNA homologous recombination by single-strand annealing and lack DNA nonhomologous end joining.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Human genetic variation and its contribution to complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Processing of bistranded abasic DNA clusters in gamma-irradiated human hematopoietic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mechanisms for human genomic rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Clustered DNA damage induced by gamma radiation in human fibroblasts (HF19), hamster (V79-4) cells and plasmid DNA is revealed as Fpg and Nth sensitive sites

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A microhomology-mediated break-induced replication model for the origin of human copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Finishing the euchromatic sequence of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mechanisms of DNA double strand break repair and chromosome aberration formation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Population analysis of large copy number variants and hotspots of human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Sensing and repairing DNA double-strand breaks

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

LINE drive. retrotransposition and genome instability

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome assembly comparison identifies structural variants in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

DNA double-strand breaks: signaling, repair and the cancer connection

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Characterization of missing human genome sequences and copy-number polymorphic insertions

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mechanism and regulation of human non-homologous DNA end-joining

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide association studies: potential next steps on a genetic journey

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

An initial map of insertion and deletion (INDEL) variation in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

DNA end resection: many nucleases make light work

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A common sequence motif associated with recombination hot spots and genome instability in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Computational approach for determining the spectrum of DNA damage induced by ionizing radiation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Analysis of 22 deletion breakpoints in dystrophin intron 49.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

The role of double-strand break repair — insights from human genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

The fine-scale and complex architecture of human copy-number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Ku DNA end-binding protein modulates homologous repair of double-strand breaks in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A review of dsb induction data for varying quality radiations

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Coupled homologous and nonhomologous repair of a double-strand break preserves genomic integrity in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Segmental duplications mediate novel, clinically relevant chromosome rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Ionizing radiation and genetic risks. III. Nature of spontaneous and radiation-induced mutations in mammalian in vitro systems and mechanisms of induction of mutations by radiation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Ionizing radiation and genetic risks. II. Nature of radiation-induced mutations in experimental mammalian in vivo systems

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Ionizing radiation and genetic risks. X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human ge

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Molecular mechanisms for constitutional chromosomal rearrangements in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Segmental duplications and copy-number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Alternative end-joining is suppressed by the canonical NHEJ component Xrcc4-ligase IV during chromosomal translocation formation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

On the mechanism of gene amplification induced under stress in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Differential usage of non-homologous end-joining and homologous recombination in double strand break repair

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome architecture, rearrangements and genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Clustered DNA damages induced in isolated DNA and in human cells by low doses of ionizing radiation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Fine-scale structural variation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A comprehensive analysis of common copy-number variations in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Repair of radiation induced DNA double strand breaks by backup NHEJ is enhanced in G2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mobile elements create structural variation: analysis of a complete human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Copy number variations in East-Asian population and their evolutionary and functional implications

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Complex human chromosomal and genomic rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Mendelian disorders and multifactorial traits: the big divide or one for all?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Common deletions and SNPs are in linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Homologous DNA Exchanges in Humans Can Be Explained by the Yeast Double-Strand Break Repair Model: A Study of 17p11.2 Rearrangements Associated with CMT1A and HNPP

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

Complex gene conversion events in germline mutation at human minisatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09553002.2010.518214

10.3109/09553002.2010.518214

21 January 2018

Identifiers

DOI

1 reference

23 August 2017

1 reference