(Q33390788)

26 July 2017

1 reference

title

Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases (English)

1 reference

26 July 2017

5

Marta Gwinn

1 reference

26 July 2017

4

Muin J Khoury

1 reference

26 July 2017

2

Anja Wulf

1 reference

26 July 2017

Wei Yu

1

1 reference

PubMed ID

19063745

26 July 2017

Tiebin Liu

series ordinal

3

1 reference

26 July 2017

8 December 2008

1 reference

26 July 2017

1 reference

26 July 2017

9

1 reference

26 July 2017

1

1 reference

29 June 2019

page(s)

528

1 reference

Creative Commons Attribution 2.0 Generic

26 July 2017

start time

1 December 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

describes a project that uses

SQL

1 reference

26 June 2022

https://europepmc.org/article/PMC/PMC2613935

based on heuristic

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2105-9-528

0 references

cites work

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

Genetic susceptibility to cancer: the role of polymorphisms in candidate genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

A HapMap harvest of insights into the genetics of common disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

An open source infrastructure for managing knowledge and finding potential collaborators in a domain-specific subset of PubMed, with an example from human genome epidemiology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

SNP genotyping: technologies and biomedical applications

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

SNPs3D: candidate gene and SNP selection for association studies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

Realizing the promise of genomics in biomedical research

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

G2D: a tool for mining genes associated with disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

Assessing the function of genetic variants in candidate gene association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

A navigator for human genome epidemiology.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613935

The continued need to synthesize the results of genetic associations across multiple studies

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19063745

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-9-528

1 reference

26 July 2017

journals/bmcbi/YuWLKG08

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

1046825227

0 references

Fatcat ID

release_6d5p7a26mzd2lc5s5c5eh5xdly

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6d5p7a26mzd2lc5s5c5eh5xdly

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

2613935

1 reference

26 July 2017

1 reference

PubMed ID

19063745