(Q24610176)

1

0 references

Vassiliki Gkantouna

4

object named as

Vassiliki Gkantouna

0 references

George P Patrinos

9

object named as

George P Patrinos

0 references

author name string

Emmanouil Viennas

2

0 references

Dimitris I Antoniou

3

0 references

Sjozef van Baal

5

0 references

Emanuel F Petricoin

6

0 references

Konstantinos Poulas

Creative Commons Attribution-NonCommercial 2.5 Generic

7

0 references

language of work or name

English

0 references

publication date

January 2011

0 references

published in

Nucleic Acids Research

0 references

volume

39

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page(s)

D926-32

0 references

issue

Database issue

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copyright license

start time

14 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

A new scientific journal linked to a genetic database: towards a novel publication modality

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Realities and expectations of pharmacogenomics and personalized medicine: impact of translating genetic knowledge into clinical practice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Locus-specific database domain and data content analysis: evolution and content maturation toward clinical use.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

ETHNOS : A versatile electronic tool for the development and curation of national genetic databases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Genetic databases and their potential in pharmacogenomics

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

DNA, diseases and databases: disastrously deficient

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

PAHdb: a locus-specific knowledgebase.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Planning the human variome project: the Spain report.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

National and ethnic mutation databases: recording populations' genography

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

Human Gene Mutation Database (HGMD): 2003 update.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013745

A brief survey of software architecture concepts and service oriented architecture

28 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKQ1236

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1093/NAR/GKQ1236

0 references

DBLP publication ID

journals/nar/GeorgitsiVAGBPPTP11

1 reference