Major changes in our DNA lead to major changes in our thinking (Q36863509)

16 August 2017

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title

Major changes in our DNA lead to major changes in our thinking (English)

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16 August 2017

Jonathan Sebat

1

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language of work or name

English

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publication date

1 July 2007

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16 August 2017

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16 August 2017

volume

39

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16 August 2017

issue

7 Suppl

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16 August 2017

page(s)

S3-5

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Detection of large-scale variation in the human genome

16 August 2017

cites work

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Large-scale copy number polymorphism in the human genome

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Fine-scale structural variation of the human genome

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Common deletion polymorphisms in the human genome.

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

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Chemical characterization of element 112

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Global variation in copy number in the human genome

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7 January 2021

An SNP map of the human genome generated by reduced representation shotgun sequencing

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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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7 January 2021

The origin and behavior of mutable loci in maize

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Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

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7 January 2021

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

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7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

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

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

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7 January 2021

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

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7 January 2021

Strong association of de novo copy number mutations with autism

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

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A genomic screen of autism: evidence for a multilocus etiology

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Reproductive fitness in familial schizophrenia

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Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

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De-novo mutation in hereditary motor and sensory neuropathy type I.

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7 January 2021

Processes of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion.

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7 January 2021

Lack of RH C/E expression in the Rhesus D--phenotype is the result of a gene deletion

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7 January 2021

Tandem array of human visual pigment genes at Xq28

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7 January 2021

Molecular genetics of inherited variation in human color vision

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Genomic rearrangements and sporadic disease

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7 January 2021

Copy-number variation and association studies of human disease

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7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

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https://api.crossref.org/works/10.1038%2FNG2095

7 January 2021

Identifiers

DOI

10.1038/NG2095

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16 August 2017

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