Large Autosomal Copy-Number Differences within Unselected Monozygotic Twin Pairs are Rare (Q48380129)

11 February 2018

title

Large Autosomal Copy-Number Differences within Unselected Monozygotic Twin Pairs are Rare (English)

1 reference

11 February 2018

1 reference

11 February 2018

Nick Martin

series ordinal

1 reference

11 February 2018

Grant W Montgomery

0 references

Allan F McRae

1 reference

11 February 2018

language of work or name

English

0 references

publication date

12 January 2015

1 reference

11 February 2018

Twin Research and Human Genetics

published in

1 reference

11 February 2018

volume

1 reference

11 February 2018

issue

1 reference

11 February 2018

page(s)

13-18

1 reference

11 February 2018

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

cites work

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Detectable clonal mosaicism and its relationship to aging and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Human copy number variation and complex genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

A twin approach to unraveling epigenetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

The continuing value of twin studies in the omics era.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Timing of de novo mutagenesis--a twin study of sodium-channel mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Failure to Confirm CNVs as of Aetiological Significance in Twin Pairs Discordant for Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Common variants in the trichohyalin gene are associated with straight hair in Europeans

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Detectable clonal mosaicism from birth to old age and its relationship to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Copy number variation in human health, disease, and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.85

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1017/THG.2014.85

1 reference

11 February 2018

1 reference

11 February 2018