Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association (Q33735944)

29 July 2017

Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association (English)

1 reference

29 July 2017

Marina Sirota

3

0 references

Atul Butte

series ordinal

4

object named as

Atul J Butte

1 reference

29 July 2017

Rong Chen

1

1 reference

PubMed ID

21042586

29 July 2017

Eugene V Davydov

series ordinal

2

1 reference

PubMed ID

21042586

29 July 2017

language of work or name

English

0 references

publication date

22 October 2010

1 reference

29 July 2017

1 reference

29 July 2017

5

1 reference

29 July 2017

10

1 reference

29 July 2017

e13574

1 reference

Creative Commons Attribution 4.0 International

29 July 2017

start time

22 October 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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Gene expression variability within and between human populations and implications toward disease susceptibility

14 July 2018

1 reference

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Synthetic associations in the context of genome-wide association scan signals

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Clinical assessment incorporating a personal genome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Rare variants create synthetic genome-wide associations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Silent (synonymous) SNPs: should we care about them?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

McKusick's Online Mendelian Inheritance in Man (OMIM)

14 July 2018

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

14 July 2018

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

14 July 2018

1 reference

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Human polymorphism at microRNAs and microRNA target sites

14 July 2018

1 reference

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A "silent" polymorphism in the MDR1 gene changes substrate specificity

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

The MeSH translation maintenance system: structure, interface design, and implementation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

The genetic association database

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

The Unified Medical Language System (UMLS): integrating biomedical terminology

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

The human genome browser at UCSC

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

dbSNP: the NCBI database of genetic variation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Population-specific susceptibility to Crohn's disease and ulcerative colitis; dominant and recessive relative risks in the Japanese population

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

The Human Gene Mutation Database: 2008 update

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

Association of TNFSF15 with Crohn's disease in Koreans

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2962641

An open access database of genome-wide association results

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21042586

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0013574

1 reference

29 July 2017

0 references

1 reference

29 July 2017

1 reference

PubMed ID

21042586