Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosity. (Q53094146)

11 May 2018

title

Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosity. (English)

1 reference

11 May 2018

1 reference

14

1 reference

11 May 2018

Brian F Meyer

22

1 reference

11 May 2018

Fowzan S Alkuraya

24

object named as

Fowzan S Alkuraya

1 reference

11 May 2018

18

Ranad Shaheen

1 reference

11 May 2018

Dorota Monies

13

object named as

Dorota Monies

1 reference

11 May 2018

author name string

Hanif G Khalak

1

1 reference

11 May 2018

Salma M Wakil

2

1 reference

11 May 2018

Faiqa Imtiaz

3

1 reference

11 May 2018

Khushnooda Ramzan

4

1 reference

11 May 2018

Batoul Baz

5

1 reference

11 May 2018

Abeer Almostafa

6

1 reference

11 May 2018

Samya Hagos

7

1 reference

11 May 2018

Fatema Alzahrani

8

1 reference

11 May 2018

Nada Abu-Dhaim

9

1 reference

11 May 2018

Leen Abu Safieh

10

1 reference

11 May 2018

Latifa Al-Jbali

11

1 reference

11 May 2018

Mohammed S Al-Hamed

12

1 reference

11 May 2018

Mohammed S Al-Dosari

15

1 reference

11 May 2018

Namik Kaya

16

1 reference

11 May 2018

Hanan Shamseldin

17

1 reference

11 May 2018

May Al-Rashed

19

1 reference

11 May 2018

Mais Hashem

20

1 reference

11 May 2018

Nada Al-Tassan

21

1 reference

11 May 2018

Anas M Alazami

23

1 reference

11 May 2018

language of work or name

English

0 references

publication date

5 January 2012

1 reference

11 May 2018

published in

Genetics in Medicine

1 reference

11 May 2018

volume

14

1 reference

11 May 2018

issue

5

1 reference

11 May 2018

page(s)

515-519

1 reference

11 May 2018

https://scigraph.springernature.com/pub.10.1038/gim.2011.28

exact match

0 references

cites work

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Personalized copy number and segmental duplication maps using next-generation sequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

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/10.1038%2FGIM.2011.28

Diversity of human copy number variation and multicopy genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

The clinical context of copy number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Copy number variation at 1q21.1 associated with neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

A double hit implicates DIAPH3 as an autism risk gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

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/10.1038%2FGIM.2011.28

Genetic analysis of human embryos by metaphase comparative genomic hybridization (mCGH) improves efficiency of IVF by increasing embryo implantation rate and reducing multiple pregnancies and spontaneous miscarriages

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.28

21 January 2018

Identifiers

DOI

10.1038/GIM.2011.28

1 reference

11 May 2018

release_s7lvcswb2rfv7dut2arjoqt6oq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/s7lvcswb2rfv7dut2arjoqt6oq

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

22241088

1 reference

11 May 2018