Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies (Q24567762)

11

0 references

George P Patrinos

12

object named as

George P Patrinos

0 references

Vassiliki Gkantouna

3

object named as

Vassiliki Gkantouna

0 references

author name string

Emmanouil Viennas

2

0 references

Cristiana Pavlidis

4

0 references

Marina Bartsakoulia

5

0 references

Zafeiria-Marina Ioannou

6

0 references

Ilham Ratbi

7

0 references

Abdelaziz Sefiani

8

0 references

John Tsaknakis

9

0 references

Konstantinos Poulas

Creative Commons Attribution-NonCommercial 3.0 Unported

10

0 references

language of work or name

English

0 references

publication date

January 2014

0 references

published in

Nucleic Acids Research

0 references

volume

42

0 references

issue

Database issue

0 references

page(s)

D1020-6

0 references

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

1 reference

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FINDbase: a worldwide database for genetic variation allele frequencies updated

24 March 2017

1 reference

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Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain

24 March 2017

1 reference

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

24 March 2017

1 reference

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Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey

24 March 2017

1 reference

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

27 September 2017

1 reference

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

27 September 2017

1 reference

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

27 September 2017

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Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database

27 September 2017

1 reference

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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=3964978

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

27 September 2017

1 reference

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Pharmacogenetics: a practical role in predicting antiretroviral drug toxicity?

27 September 2017

1 reference

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The Human Gene Mutation Database: 2008 update

27 September 2017

1 reference

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PAHdb: a locus-specific knowledgebase.

30 May 2018

1 reference

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National and ethnic mutation databases: recording populations' genography

30 May 2018

1 reference

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

28 November 2018

1 reference

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A brief survey of software architecture concepts and service oriented architecture

28 November 2018

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Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKT1125

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1093/NAR/GKT1125

1 reference

journals/nar/PapadopoulosVGPBIRSTPTP14

3493532

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

3493532

1 reference

1 reference

1 reference