(Q33350714)

26 July 2017

title

The human genome puzzle - the role of copy number variation in somatic mosaicism (English)

1 reference

26 July 2017

Hasmik Mkrtchyan

1

1 reference

26 July 2017

Madeleine Gross

2

1 reference

26 July 2017

Sophie Hinreiner

3

1 reference

26 July 2017

Anna Polytiko

4

1 reference

26 July 2017

Marina Manvelyan

5

1 reference

26 July 2017

Kristin Mrasek

6

1 reference

26 July 2017

Nadezda Kosyakova

7

1 reference

26 July 2017

Elisabeth Ewers

8

1 reference

26 July 2017

Heike Nelle

9

1 reference

26 July 2017

Thomas Liehr

10

1 reference

26 July 2017

Samarth Bhatt

11

1 reference

26 July 2017

Karen Thoma

12

1 reference

26 July 2017

Erich Gebhart

13

1 reference

26 July 2017

Sylvia Wilhelm

14

1 reference

26 July 2017

Raimund Fahsold

15

1 reference

26 July 2017

Marianne Volleth

16

1 reference

26 July 2017

Anja Weise

17

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26 July 2017

publication date

1 September 2010

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26 July 2017

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26 July 2017

volume

11

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26 July 2017

issue

6

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26 July 2017

page(s)

426-431

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Early embryonic chromosome instability results in stable mosaic pattern in human tissues

26 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

In situ genetic analysis of cellular chimerism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Chromosomal mosaicism goes global

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Extensive genomic copy number variation in embryonic stem cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Copy number variation and evolution in humans and chimpanzees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Paired-end mapping reveals extensive structural variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Aneuploidy and confined chromosomal mosaicism in the developing human brain.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Global variation in copy number in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Copy number variation: new insights in genome diversity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Chromosomal variation in mammalian neuronal cells: known facts and attractive hypotheses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Bias of selection on human copy-number variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Structural variation in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Fine-scale structural variation of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Large-scale copy number polymorphism in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Steps involved in immortalization and tumorigenesis in human B-lymphoblastoid cell lines transformed by Epstein-Barr virus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Allelic exclusion in B and T lymphopoiesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Chromosome instability is common in human cleavage-stage embryos.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3018723

Somatic mosaicism for copy number variation in differentiated human tissues

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21358987

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

What a difference copy number variation makes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21358987

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2174/138920210793176047

1 reference

26 July 2017

1 reference

26 July 2017

1 reference