SimHap GUI: an intuitive graphical user interface for genetic association analysis (Q33396011)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

review article

1 reference

title

SimHap GUI: an intuitive graphical user interface for genetic association analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

main subject

graphical user interface

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Kim Carter

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Pamela A McCaskie

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

25 December 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

557

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 2.0 Generic

19 January 2020

copyright license

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

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2105-9-557

0 references

cites work

Polymorphisms of the matrix metalloproteinase 9 gene and abdominal aortic aneurysm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Does high C-reactive protein concentration increase atherosclerosis? The Whitehall II Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Inflammation, insulin resistance, and diabetes--Mendelian randomization using CRP haplotypes points upstream

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Analysis of variants in DNA damage signalling genes in bladder cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Association between cytokine gene polymorphisms and outcomes in renal transplantation: a meta-analysis of individual patient data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

IL18 haplotypes are associated with serum IL-18 concentrations in a population-based study and a cohort of individuals with premature coronary heart 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=2639440

Macrophage migration inhibitory factor in acute lung injury: expression, biomarker, and associations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Computer programs for population genetics data analysis: a survival guide

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Genome-wide association studies for common diseases and complex traits

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Fine genetic mapping using haplotype analysis and the missing data problem

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery 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=2639440

15-Lipoxygenase gene variants are associated with carotid plaque but not carotid intima-media thickness.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Melanocortin 1 receptor (MC1R) genotype influences erythemal sensitivity to psoralen-ultraviolet A photochemotherapy.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Comprehensive analysis of 22 XPC polymorphisms and bladder cancer risk.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Polymorphisms of the Interleukin-6 Gene Promoter and Abdominal Aortic Aneurysm

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Cholesteryl ester transfer protein gene haplotypes, plasma high-density lipoprotein levels and the risk of coronary heart disease

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

Association Between Osteopontin and Human Abdominal Aortic Aneurysm

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

The C-480T hepatic lipase polymorphism is associated with HDL-C but not with risk of coronary heart disease

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2639440

A common interleukin 18 haplotype is associated with higher body mass index in subjects with diabetes and coronary heart disease

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19109877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19109877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19109877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-9-557

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

journals/bmcbi/CarterMP08

19 January 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19109877%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference