(Q30486431)

21 August 2017

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations (English)

1 reference

21 August 2017

0 references

1 reference

Joseph Borg

2

0 references

Giannis Tzimas

object named as

Giannis Tzimas

10

0 references

Ross Hardison

object named as

Ross C Hardison

12

0 references

Webb Miller

9

object named as

Webb Miller

1 reference

21 August 2017

13

George P Patrinos

1 reference

21 August 2017

1

Belinda Giardine

1 reference

21 August 2017

8

Cathy Riemer

1 reference

21 August 2017

5

Kamran Moradkhani

1 reference

21 August 2017

11

Henri Wajcman

1 reference

21 August 2017

Emmanouil Viennas

3

1 reference

21 August 2017

Cristiana Pavlidis

4

1 reference

21 August 2017

Philippe Joly

6

1 reference

21 August 2017

Marina Bartsakoulia

7

1 reference

21 August 2017

language of work or name

English

0 references

publication date

16 October 2013

1 reference

21 August 2017

Nucleic Acids Research

1 reference

21 August 2017

42

1 reference

21 August 2017

Database issue

1 reference

21 August 2017

D1063-9

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

21 August 2017

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

ENCODE data in the UCSC Genome Browser: year 5 update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

The UCSC Genome Browser database: extensions and updates 2013.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

LOVD v.2.0: the next generation in gene variant databases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

FINDbase: a worldwide database for genetic variation allele frequencies updated

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

PhenCode: connecting ENCODE data with mutations and phenotype

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

CTGA: the database for genetic disorders in Arab populations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

DNA, diseases and databases: disastrously deficient

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3964999

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKT911

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24137000

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobin

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24137000

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKT911

1 reference

journals/nar/GiardineBVPMJBRMTWHP14

21 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

21 August 2017

1 reference