(Q35207544)

7 August 2017

1 reference

title

Haplotypes and the systematic analysis of genetic variation in genes and genomes (English)

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7 August 2017

1 reference

Margret R Hoehe

1

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7 August 2017

1 September 2003

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7 August 2017

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7 August 2017

4

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7 August 2017

5

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7 August 2017

547-570

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A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

7 August 2017

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Phenylketonuria. Population genetics of a disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Global patterns of linkage disequilibrium at the CD4 locus and modern human origins

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

X chromosome evidence for ancient human histories

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Sequence variation in the human angiotensin converting enzyme.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Sequence variability and candidate gene analysis in complex disease: association of mu opioid receptor gene variation with substance dependence

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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/10.2217%2F14622416.4.5.547

Haplotype variation and linkage disequilibrium in 313 human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Recombinational and mutational hotspots within the human lipoprotein lipase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Research suggests importance of haplotypes over SNPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The Sequence of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Extent and distribution of linkage disequilibrium in three genomic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Linkage disequilibrium: what history has to tell us.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Is there a paradigm shift in genetics? Lessons from the study of human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Human genome sequence variation and the influence of gene history, mutation and recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Haplotype blocks and linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Variation in recombination rate across the genome: evidence and implications

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Unraveling heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Detecting recent positive selection in the human genome from haplotype structure

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Linkage disequilibrium in humans: models and data

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Haplotype analysis in population genetics and association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Robustness of inference of haplotype block structure.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

A dynamic programming algorithm for haplotype block partitioning

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

How many diseases does it take to map a gene with SNPs?

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The predictive power of haplotypes in clinical response

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Binge eating as a major phenotype of melanocortin 4 receptor gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The extent of linkage disequilibrium in four populations with distinct demographic histories

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Linkage disequilibrium and the mapping of complex human traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

An SNP map of human chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

DNA sequence variation in a non-coding region of low recombination on the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Is selection responsible for the low level of variation in the last intron of the ZFY locus?

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Adjusting the focus on human variation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Evidence for positive selection and population structure at the human MAO-A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Human populations show reduced DNA sequence variation at the factor IX locus

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

On the allelic spectrum of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

The allelic architecture of human disease genes: common disease-common variant... or not?

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Population genetic structure of variable drug response

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Phenogenetic drift and the evolution of genotype-phenotype relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

SNP frequencies in human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

Notes from the SNP vs. haplotype front

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.4.5.547

21 January 2018

Identifiers

DOI

10.2217/14622416.4.5.547

1 reference

release_apruf5cjdrhm5okvjmd36kftqm

7 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/apruf5cjdrhm5okvjmd36kftqm

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

12943464

1 reference

PubMed ID

12943464