GWASdb: a database for human genetic variants identified by genome-wide association studies (Q35630781)

9 August 2017

GWASdb: a database for human genetic variants identified by genome-wide association studies (English)

1 reference

genome-wide association study

9 August 2017

0 references

0 references

6

Meredith Yeager

0 references

Ee Lyn Lim

object named as

Ee Lyn Lim

4

0 references

Junwen Wang

object named as

Junwen Wang

10

0 references

Stephen Chanock

9

object named as

Stephen J Chanock

1 reference

9 August 2017

1

Mulin Jun Li

1 reference

9 August 2017

2

Panwen Wang

1 reference

9 August 2017

8

Pak Chung Sham

1 reference

9 August 2017

Xiaorong Liu

3

1 reference

9 August 2017

Zhangyong Wang

5

1 reference

9 August 2017

Maria P Wong

7

1 reference

9 August 2017

language of work or name

English

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publication date

1 December 2011

1 reference

9 August 2017

Nucleic Acids Research

1 reference

9 August 2017

40

1 reference

9 August 2017

D1047-54

1 reference

9 August 2017

Database issue

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

9 August 2017

start time

12 May 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factor

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

A knowledge-based weighting framework to boost the power of genome-wide association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

New tools and methods for direct programmatic access to the dbSNP relational database

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

A map of human genome variation from population-scale sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

FastPval: a fast and memory efficient program to calculate very low P-values from empirical distribution.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Integrating common and rare genetic variation in diverse human populations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Varietas: a functional variation database portal

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Cytoscape Web: an interactive web-based network browser

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

GWAS analyzer: integrating genotype, phenotype and public annotation data for genome-wide association study analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SCAN: SNP and copy number annotation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNP@Evolution: a hierarchical database of positive selection on the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

A genome-wide association study of hypertension and blood pressure in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

From disease ontology to disease-ontology lite: statistical methods to adapt a general-purpose ontology for the test of gene-ontology associations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNPit: a federated data integration system for the purpose of functional SNP annotation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

HGVbaseG2P: a central genetic association database

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

UniPROBE: an online database of protein binding microarray data on protein-DNA interactions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

F-SNP: computationally predicted functional SNPs for disease association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

CTCFBSDB: a CTCF-binding site database for characterization of vertebrate genomic insulators

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

The NCBI dbGaP database of genotypes and phenotypes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

The role of site accessibility in microRNA target recognition

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

PharmGKB: a logical home for knowledge relating genotype to drug response phenotype

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

VISTA Enhancer Browser--a database of tissue-specific human enhancers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

Search for basonuclin target genes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNPselector: a web tool for selecting SNPs for genetic association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

The genetic association database

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

JASPAR: an open-access database for eukaryotic transcription factor binding profiles

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

TRANSFAC: transcriptional regulation, from patterns to profiles

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

pfSNP: An integrated potentially functional SNP resource that facilitates hypotheses generation through knowledge syntheses.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

A navigator for human genome epidemiology.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245026

SNP Function Portal: a web database for exploring the function implication of SNP alleles

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKR1182

SNPxGE2: a database for human 3-way SNP-expression associations

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKR1182

A mammalian promoter model links cis elements to genetic networks

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22139925

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An open access database of genome-wide association results

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22139925

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

ssSNPTarget: genome-wide splice-site Single Nucleotide Polymorphism database

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22139925

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKR1182

1 reference

journals/nar/LiWLLWYWSCW12

9 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

9 August 2017

1 reference