Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles (Q36718902)

15 August 2017

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

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15 August 2017

15

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15 August 2017

17

Gert-Jan B van Ommen

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Arkadiusz Piotrowski

Arkadiusz Piotrowski

2

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Robin Andersson

Robin Andersson

4

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Jan Dumański

Jan P Dumanski

22

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Dorret Boomsma

18

Dorret I Boomsma

1 reference

15 August 2017

21

Karin Wirdefeldt

1 reference

15 August 2017

19

Nancy L Pedersen

1 reference

15 August 2017

8

Johanna Sandgren

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15 August 2017

16

Jan Komorowski

1 reference

15 August 2017

5

Stephen Erickson

1 reference

15 August 2017

Teresita Díaz de Ståhl

6

Teresita Diaz de Ståhl

1 reference

15 August 2017

9

Desiree von Tell

1 reference

15 August 2017

Carl E G Bruder

1

1 reference

15 August 2017

Antoinet A C J Gijsbers

3

1 reference

15 August 2017

Uwe Menzel

7

1 reference

15 August 2017

Andrzej Poplawski

10

1 reference

15 August 2017

Michael Crowley

11

1 reference

15 August 2017

Chiquito Crasto

12

1 reference

15 August 2017

E Christopher Partridge

13

1 reference

15 August 2017

Hemant Tiwari

14

1 reference

15 August 2017

Johan T den Dunnen

20

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15 August 2017

language of work or name

English

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publication date

14 February 2008

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American Journal of Human Genetics

15 August 2017

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15 August 2017

82

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15 August 2017

3

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15 August 2017

763-771

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

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Major changes in our DNA lead to major changes in our thinking

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Complete ascertainment of Parkinson disease in the Swedish Twin Registry

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Recurrent DNA inversion rearrangements in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Strong association of de novo copy number mutations with autism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Global variation in copy number in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

30 September 2017

The LCB Data Warehouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Epigenetic differences arise during the lifetime of monozygotic twins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Detection of large-scale variation in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Large-scale copy number polymorphism in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Somatic gene mutation and human disease other than cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Mechanisms and consequences of somatic mosaicism in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

The Swedish Twin Registry: a unique resource for clinical, epidemiological and genetic studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Mechanisms for differences in monozygous twins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Some causes of genotypic and phenotypic discordance in monozygotic twin pairs

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Netherlands Twin Register: from twins to twin families.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Genetic abnormalities and clinical outcome in chronic lymphocytic leukemia.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Epigenetics and twins: three variations on the theme.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

Chromosomal imbalances in familial chronic lymphocytic leukaemia: a comparative genomic hybridisation analysis.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427204

A tiling resolution DNA microarray with complete coverage of the human genome

5 September 2018

1 reference

12 December 2020

Frequency of new copy number variation in humans

1 reference

12 December 2020

Twin registries: an ongoing success story

1 reference

12 December 2020

A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders

1 reference

12 December 2020

10.1016/J.AJHG.2007.12.011

Identifiers

DOI

1 reference

15 August 2017

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15 August 2017

1 reference