Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q57264082)
Watch
English
Common deletions and SNPs are in linkage disequilibrium in the human genome
scientific article published on 04 December 2005
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
title
Common deletions and SNPs are in linkage disequilibrium in the human genome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
main subject
disequilibrium
1 reference
based on heuristic
inferred from title
linkage disequilibrium
1 reference
based on heuristic
inferred from title
author
David A Hinds
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Kelly A. Frazer
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
author name string
Andrew P Kloek
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Michael Jen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Xiyin Chen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
language of work or name
English
0 references
publication date
4 December 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
page(s)
82-85
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/ng1695
0 references
cites work
Frequency and predictive value of 22q11 deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
21 January 2018
Fine-scale structural variation of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Segmental duplications and copy-number variation in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common inversion under selection in Europeans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
alpha-Synuclein locus triplication causes Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large-scale copy number polymorphism in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of large-scale variation in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of single-nucleotide polymorphisms in coding regions of human genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A population study of chromosome 22q11 deletions in infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of 22q11 microdeletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel α-globin gene arrangement in man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular mechanisms for genomic disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A high-resolution survey of deletion polymorphism in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common deletion polymorphisms in the human genome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recent segmental duplications in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Whole-genome patterns of common DNA variation in three human populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1695
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
PubMed ID
16327809
1 reference
stated in
Europe PubMed Central
PubMed ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
