(Q22337172)

4 July 2017

title

Are rare variants responsible for susceptibility to complex diseases? (English)

1 reference

4 July 2017

Pritchard JK

1

J K

Pritchard

1 reference

4 July 2017

language of work or name

English

0 references

publication date

12 June 2001

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

69

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4 July 2017

issue

1

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4 July 2017

page(s)

124-137

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Estimate of the mutation rate per nucleotide in humans

4 July 2017

cites work

1 reference

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A genomic screen of autism: evidence for a multilocus etiology

19 March 2017

1 reference

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Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

19 March 2017

1 reference

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Searching for genetic determinants in the new millennium

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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When did the human population size start increasing?

19 March 2017

1 reference

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Compensatory mutations, antibiotic resistance and the population genetics of adaptive evolution in bacteria

19 March 2017

1 reference

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The future of genetic studies of complex human diseases

19 March 2017

1 reference

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Patterns of genetic variation in Mendelian and complex traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Adjusting the focus on human variation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

A coalescent approach to study linkage disequilibrium between single-nucleotide polymorphisms

27 September 2017

1 reference

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Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B.

27 September 2017

1 reference

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Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia B.

27 September 2017

1 reference

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Epidemiology of neurofibromatosis type 1.

27 September 2017

1 reference

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The power of association studies to detect the contribution of candidate genetic loci to variation in complex traits

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

High genomic deleterious mutation rates in hominids

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

The sampling distribution of disease-associated alleles.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

The genealogy of samples in models with selection

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Linkage strategies for genetically complex traits. II. The power of affected relative pairs

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Linkage strategies for genetically complex traits. I. Multilocus models

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Fitness of RNA virus decreased by Muller's ratchet

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

A test for epistasis among induced mutations in Caenorhabditis elegans

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Frequency in relatives for an all‐or‐none trait

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Low nucleotide diversity in man

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Perfect simulation from population genetic models with selection

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Genealogies and weak purifying selection.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226027

Population genetics--making sense out of sequence

29 November 2018

1 reference

12 December 2020

Effect of allelic heterogeneity on the power of the transmission disequilibrium test

1 reference

12 December 2020

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

1 reference

12 December 2020

The new genomics: global views of biology

1 reference

12 December 2020

Linkage disequilibrium mapping of complex disease: fantasy or reality?

1 reference

12 December 2020

Identifiers

DOI

10.1086/321272

1 reference

OpenCitations bibliographic resource ID

4 July 2017

412025

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference