(Q35748382)

10 August 2017

title

Age-related somatic structural changes in the nuclear genome of human blood cells (English)

1 reference

10 August 2017

21

1 reference

10 August 2017

22

Vilmantas Giedraitis

0 references

Jennifer R Harris

12

object named as

Jennifer R Harris

1 reference

10 August 2017

28

Jan P Dumanski

1 reference

10 August 2017

1

Lars A Forsberg

1 reference

10 August 2017

27

Devin Absher

1 reference

10 August 2017

10

Dorret Boomsma

1 reference

10 August 2017

24

Martin Ingelsson

1 reference

10 August 2017

26

Nancy L Pedersen

1 reference

10 August 2017

23

Lars Lannfelt

1 reference

10 August 2017

Themistocles L Assimes

16

object named as

Themistocles L Assimes

1 reference

10 August 2017

Chiara Rasi

2

1 reference

10 August 2017

Hamid R Razzaghian

3

1 reference

10 August 2017

Geeta Pakalapati

4

1 reference

10 August 2017

Lindsay Waite

5

1 reference

10 August 2017

Krista Stanton Thilbeault

6

1 reference

10 August 2017

Anna Ronowicz

7

1 reference

10 August 2017

Nathan E Wineinger

8

1 reference

10 August 2017

Hemant K Tiwari

9

1 reference

10 August 2017

Maxwell P Westerman

11

1 reference

10 August 2017

Robert Lyle

13

1 reference

10 August 2017

Magnus Essand

14

1 reference

10 August 2017

Fredrik Eriksson

15

1 reference

10 August 2017

Carlos Iribarren

17

1 reference

10 August 2017

Eric Strachan

18

1 reference

10 August 2017

Terrance P O'Hanlon

19

1 reference

10 August 2017

Lisa G Rider

20

1 reference

10 August 2017

Arkadiusz Piotrowski

25

1 reference

10 August 2017

language of work or name

English

0 references

publication date

2 February 2012

1 reference

American Journal of Human Genetics

10 August 2017

published in

1 reference

10 August 2017

volume

90

1 reference

10 August 2017

issue

2

1 reference

10 August 2017

page(s)

217-228

1 reference

Structural genetic variation in the context of somatic mosaicism

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Somatic mosaicism in healthy human tissues

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: a report on 62 cases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Unraveling the molecular pathophysiology of myelodysplastic syndromes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

De novo rates and selection of large copy number variation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Evolution of the mutation rate

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Somatic gene mutation and human disease other than cancer: an update

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Evolution in health and medicine Sackler colloquium: Somatic evolutionary genomics: mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

B-cell diversity decreases in old age and is correlated with poor health status

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Cytogenetic features in myelodysplastic syndromes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Genomic rearrangements and sporadic disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Recurrent DNA inversion rearrangements in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Clinical relevance of cytogenetics in myelodysplastic syndromes.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Epigenetic differences arise during the lifetime of monozygotic twins

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

The influence of age on T cell generation and TCR diversity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Circular binary segmentation for the analysis of array-based DNA copy number data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Mechanisms and consequences of somatic mosaicism in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

A new non-linear normalization method for reducing variability in DNA microarray experiments

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Chromosome translocations and covert leukemic clones are generated during normal fetal development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Loss of telomeric DNA during aging of normal and trisomy 21 human lymphocytes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Telomeres shorten during ageing of human fibroblasts

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Frequency of human sperm carrying structural aberrations of chromosome 1 increases with advancing age.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Mitochondrial DNA deletions and the aging heart.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Whole-genome genotyping with the single-base extension assay

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276669

Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients

25 September 2018

1 reference

12 December 2020

Frequency of new copy number variation in humans

1 reference

12 December 2020

Somatic mosaicism for copy number variation in differentiated human tissues

1 reference

12 December 2020

Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms

1 reference

12 December 2020

10.1016/J.AJHG.2011.12.009

Identifiers

DOI

1 reference

release_eoze6r7wxre2tovhgkypwbiz4q

10 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/eoze6r7wxre2tovhgkypwbiz4q

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3276669

1 reference

10 August 2017

1 reference