High-resolution haplotype structure in the human genome (Q56002085)

5

object named as

Eric S. Lander

0 references

Mark Joseph Daly

1

object named as

Mark J. Daly

0 references

Stephen F Schaffner

3

object named as

Stephen F. Schaffner

0 references

author name string

Thomas J. Hudson

https://scigraph.springernature.com/pub.10.1038/ng1001-229

4

0 references

language of work or name

English

0 references

publication date

October 2001

0 references

published in

Nature Genetics

0 references

volume

29

0 references

issue

2

0 references

page(s)

229-232

0 references

exact match

0 references

cites work

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Recombinational and mutational hotspots within the human lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Linkage disequilibrium and homozygosity of chromosome segments in finite populations

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Initial sequencing and analysis of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Identification of new single-nucleotide polymorphisms in the thrombin receptor gene and their effects on coronary artery diseases in Koreans

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Allele associations reveal four prominent haplotypes at the human interleukin-6 (IL-6) locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

New polymorphisms in the IL-10 promoter region

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-229

7 January 2021