Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence (Q24796448)

2

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Stephen W. Scherer

7

object named as

Stephen W Scherer

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Jeffrey R MacDonald

object named as

Jeffrey R MacDonald

4

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author name string

Joseph Cheung

1

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Razi Khaja

3

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Ken Lau

5

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Lap-Chee Tsui

https://scigraph.springernature.com/pub.10.1186/gb-2003-4-4-r25

6

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language of work or name

English

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publication date

2003

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published in

Genome Biology

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volume

4

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issue

4

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page(s)

R25

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exact match

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cites work

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Initial sequencing and analysis of the human genome

7 April 2017

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The evolutionary fate and consequences of duplicate genes

7 April 2017

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

7 April 2017

1 reference

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Recent segmental duplications in the human genome

7 April 2017

1 reference

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Genome architecture, rearrangements and genomic disorders

7 April 2017

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The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

7 April 2017

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A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

28 September 2017

1 reference

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Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation

28 September 2017

1 reference

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Segmental duplications and the evolution of the primate genome

28 September 2017

1 reference

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A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

28 September 2017

1 reference

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Positive selection of a gene family during the emergence of humans and African apes

28 September 2017

1 reference

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Segmental duplications: an 'expanding' role in genomic instability and disease

28 September 2017

1 reference

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Segmental duplications: organization and impact within the current human genome project assembly

28 September 2017

1 reference

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Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

28 September 2017

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Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

28 September 2017

1 reference

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28 September 2017

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The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=154576

Discovery of the human genome sequence in the public and private databases.

28 November 2018

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A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=154576

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12702206

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12702206

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12702206

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2003-4-4-R25

1 reference

Dimensions Publication ID

228839

1025892956

0 references

228839

1 reference

1 reference

1 reference