An Expanded View of Complex Traits: From Polygenic to Omnigenic (Q30322686)

23 June 2018

review article

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title

An Expanded View of Complex Traits: From Polygenic to Omnigenic (English)

1 reference

23 June 2018

genome-wide association study

main subject

omics

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23 June 2018

Jonathan K. Pritchard

series ordinal

3

object named as

Jonathan K Pritchard

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23 June 2018

Evan A Boyle

series ordinal

1

object named as

Evan A Boyle

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23 June 2018

language of work or name

English

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publication date

1 June 2017

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23 June 2018

published in

Cell

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23 June 2018

volume

169

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23 June 2018

issue

7

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23 June 2018

page(s)

1177-1186

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23 June 2018

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

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4 July 2018

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Defining the role of common variation in the genomic and biological architecture of adult human height

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Common SNPs explain a large proportion of the heritability for human height

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Common genetic variation and human traits

4 July 2018

1 reference

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4 July 2018

1 reference

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4 July 2018

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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

4 July 2018

1 reference

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Exploring complex networks

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5536862

A genomic screen of autism: evidence for a multilocus etiology

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5536862

Collective dynamics of 'small-world' networks

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5536862

Pleiotropic models of quantitative variation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5536862

Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5536862

Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28622505

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Psychiatric Genomics: An Update and an Agenda

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28622505

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CELL.2017.05.038

1 reference

23 June 2018

PMC publication ID

5536862

1 reference

23 June 2018

PubMed publication ID

28622505

1 reference

23 June 2018