(Q29614584)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

30 April 2017

0 references

24

Daly MJ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

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26

Altshuler D

1 reference

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25

Gabriel SB

1 reference

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11

Elliott AL

1 reference

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9

Maller JB

1 reference

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10

Kirby A

1 reference

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17

Collins PJ

1 reference

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author name string

McCarroll SA

1

1 reference

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Kuruvilla FG

2

1 reference

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Korn JM

3

1 reference

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Cawley S

4

1 reference

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Nemesh J

5

1 reference

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Wysoker A

6

1 reference

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Shapero MH

7

1 reference

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de Bakker PI

8

1 reference

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Parkin M

12

1 reference

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Hubbell E

13

1 reference

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Webster T

14

1 reference

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Mei R

15

1 reference

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Veitch J

16

1 reference

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Handsaker R

18

1 reference

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Lincoln S

19

1 reference

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Nizzari M

20

1 reference

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Blume J

21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

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Jones KW

22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

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Rava R

23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

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language of work or name

1 reference

30 April 2017

publication date

October 2008

1 reference

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30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

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volume

40

1 reference

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page(s)

1166-74

1 reference

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issue

10

1 reference

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Large-scale copy number polymorphism in the human genome

30 April 2017

cites work

1 reference

Detection of large-scale variation in the human genome

1 May 2017

1 reference

Fine-scale structural variation of the human genome

1 May 2017

1 reference

Segmental duplications and copy-number variation in the human genome

1 May 2017

1 reference

Global variation in copy number in the human genome

1 May 2017

1 reference

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

1 May 2017

1 reference

Mapping and sequencing of structural variation from eight human genomes

1 May 2017

1 reference

Copy-number variation and association studies of human disease

1 May 2017

1 reference

A haplotype map of the human genome

1 May 2017

1 reference

A second generation human haplotype map of over 3.1 million SNPs

1 May 2017

1 reference

A strategy for oligonucleotide microarray probe reduction

1 May 2017

1 reference

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 May 2017

1 reference

Population stratification of a common APOBEC gene deletion polymorphism

1 May 2017

1 reference

Diet and the evolution of human amylase gene copy number variation

1 May 2017

1 reference

Genotype, haplotype and copy-number variation in worldwide human populations

1 May 2017

1 reference

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 May 2017

1 reference

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 May 2017

1 reference

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 May 2017

1 reference

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

1 reference

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

7 January 2021

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

7 January 2021

Redundancy in genotyping arrays

1 reference

7 January 2021

Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes

1 reference

7 January 2021

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

1 reference

7 January 2021

Mutational and selective effects on copy-number variants in the human genome

1 reference

7 January 2021

Copy-number analysis goes more than skin deep

1 reference

7 January 2021

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

1 reference

7 January 2021

Challenges and standards in integrating surveys of structural variation

1 reference

7 January 2021

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

1 reference

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

Identifiers

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

228863

1047420273

0 references

228863

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18776908

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017