(Q34673398)

3 August 2017

1 reference

title

How many SNPs does a genome-wide haplotype map require? (English)

1 reference

3 August 2017

Benjamin A. Salisbury

object named as

Benjamin Salisbury

2

0 references

Richard S. Judson

object named as

Richard Judson

1

0 references

author name string

Julie Schneider

3

1 reference

PubMed ID

12052145

3 August 2017

Andreas Windemuth

4

1 reference

PubMed ID

12052145

3 August 2017

J Claiborne Stephens

5

1 reference

3 August 2017

1 May 2002

1 reference

3 August 2017

1 reference

3 August 2017

3

1 reference

3 August 2017

379-391

1 reference

3 August 2017

3

1 reference

Haplotype variation and linkage disequilibrium in 313 human genes

3 August 2017

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

The Sequence of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

New goals for the U.S. Human Genome Project: 1998-2003.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Single nucleotide polymorphism libraries: why and how are we building them?

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Genetic epidemiology of single-nucleotide polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Irresistible force meets immovable object: SNP mapping of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

The predictive power of haplotypes in clinical response

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Sequence variation in the human angiotensin converting enzyme.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Estimation of myriad haplotype frequencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

A New Statistical Method for Haplotype Reconstruction from Population Data

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Linguistics. From the mouths (and hands) of babes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

A Mathematical Theory of Communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Gene index analysis of the human genome estimates approximately 120,000 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Assessment of the total number of human transcription units.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

HGBASE: a database of SNPs and other variations in and around human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Accessing genetic variation: genotyping single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Searching for genetic determinants in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Linkage disequilibrium and the mapping of complex human traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

GENOMICS: Genetic Association by Whole-Genome Analysis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14622416.3.3.379

21 January 2018

Identifiers

DOI

10.1517/14622416.3.3.379

1 reference

3 August 2017

1 reference

PubMed ID

12052145