(Q42352511)

27 October 2017

GWAS: heritability missing in action? (English)

1 reference

genome-wide association study

27 October 2017

0 references

1 reference

2

1 reference

27 October 2017

Angus J Clarke

1

1 reference

27 October 2017

17 March 2010

1 reference

European Journal of Human Genetics

27 October 2017

1 reference

27 October 2017

18

1 reference

27 October 2017

8

1 reference

27 October 2017

859-861

1 reference

Finding the missing heritability of complex diseases

27 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Origins and functional impact of copy number variation in the human genome

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Epistasis and its implications for personal genetics.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

From genotypes to genometypes: putting the genome back in genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Using biological networks to search for interacting loci in genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Personal genomes: The case of the missing heritability

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Extending genome-wide association studies to copy-number variation

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Large recurrent microdeletions associated with schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Rare chromosomal deletions and duplications increase risk of schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Strong association of de novo copy number mutations with sporadic schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Common and rare variants in multifactorial susceptibility to common diseases

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Positive selection in the human genome: from genome scans to biological significance

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

The success of the genome-wide association approach: a brief story of a long struggle

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Association between microdeletion and microduplication at 16p11.2 and autism

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Scan of human genome reveals no new Loci under ancient balancing selection

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

The genetic architecture of quantitative traits: lessons from Drosophila

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Popper revisited: GWAS here, last year.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987389

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

17 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.35

A limited role for balancing selection

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20234388

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hypotheses in genome-wide association scans

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20234388

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2010.35

1 reference

PMC publication ID

2987389

Dimensions Publication ID

27 October 2017

0 references

1 reference

PMC publication ID

2987389

27 October 2017

PubMed publication ID

20234388

1 reference

PMC publication ID

2987389