(Q57249752)

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Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

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Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases (English)

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Philippe Froguel

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Philippe Froguel

12

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author name string

Adam J. de Smith

1

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Anya Tsalenko

2

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Nick Sampas

3

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Alicia Scheffer

4

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N. Alice Yamada

5

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Peter Tsang

6

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Amir Ben-Dor

7

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Zohar Yakhini

8

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Richard J. Ellis

9

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Laurakay Bruhn

10

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Stephen Laderman

11

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Alexandra I.F. Blakemore

13

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publication date

31 July 2007

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Human Molecular Genetics

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16

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2783-2794

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23

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Whole-genome patterns of common DNA variation in three human populations

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Detection of large-scale variation in the human genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

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

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Common deletion polymorphisms in the human genome.

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Global variation in copy number in the human genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Large-scale copy number polymorphism in the human genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Segmental duplications and copy-number variation in the human genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Fine-scale structural variation of the human genome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

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

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Trisomy 12 in Epstein-Barr virus-transformed lymphoblastoid cell lines of normal individuals and patients with nonhematologic malignancies

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Efficient calculation of interval scores for DNA copy number data analysis

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Lipoprotein lipase-mediated uptake and degradation of low density lipoproteins by fibroblasts and macrophages

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Mapping of a novel human carbonyl reductase, CBR3, and ribosomal pseudogenes to human chromosome 21q22.2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

A novel nk-2-related transcription factor associated with human fetal liver and hepatocellular carcinoma

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Evolutionary expansion and divergence in the ZNF91 subfamily of primate-specific zinc finger genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Mitochondrial genome variation and the origin of modern humans

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Bias of selection on human copy-number variants

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

A common inversion under selection in Europeans

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Pharmacogenomics and individualized drug therapy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Challenges and standards in integrating surveys of structural variation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

The UCSC Genome Browser Database

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

GOstat: find statistically overrepresented Gene Ontologies within a group of genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Human genomics: In search of normality

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM208

21 January 2018

Identifiers

10.1093/HMG/DDM208

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