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High-resolution haplotype structure in the human genome
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scholarly article
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title
High-resolution haplotype structure in the human genome
(English)
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author
John D. Rioux
object named as
John D. Rioux
series ordinal
2
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Eric Lander
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5
object named as
Eric S. Lander
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Mark Joseph Daly
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1
object named as
Mark J. Daly
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Stephen F Schaffner
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3
object named as
Stephen F. Schaffner
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author name string
Thomas J. Hudson
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4
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language of work or name
English
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publication date
October 2001
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published in
Nature Genetics
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volume
29
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page(s)
229-232
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issue
2
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exact match
https://scigraph.springernature.com/pub.10.1038/ng1001-229
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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
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Recombinational and mutational hotspots within the human lipoprotein lipase gene
1 reference
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https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
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https://api.crossref.org/works/10.1038%2FNG1001-229
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7 January 2021
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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
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7 January 2021
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Linkage disequilibrium and homozygosity of chromosome segments in finite populations
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7 January 2021
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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
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reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes
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Crossref
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https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Initial sequencing and analysis of the human genome
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https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness
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reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Identification of new single-nucleotide polymorphisms in the thrombin receptor gene and their effects on coronary artery diseases in Koreans
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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inferred from DOI database lookup
Allele associations reveal four prominent haplotypes at the human interleukin-6 (IL-6) locus
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reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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New polymorphisms in the IL-10 promoter region
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium
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https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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inferred from DOI database lookup
Linkage disequilibrium in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haplotype tagging for the identification of common disease genes
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1001-229
retrieved
7 January 2021
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Identifiers
DOI
10.1038/NG1001-229
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PubMed ID
11586305
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ResearchGate publication ID
11763944
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