(Q42611572)

English

The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.

scientific article published on 13 September 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

3 November 2017

The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era. (English)

1 reference

Europe PubMed Central

3 November 2017

0 references

0 references

object named as

Myles Byrne

5

0 references

object named as

Juha Muilu

12

0 references

object named as

Teppo Varilo

3

0 references

author name string

Anne Polvi

1

1 reference

Europe PubMed Central

3 November 2017

Henna Linturi

2

1 reference

Europe PubMed Central

3 November 2017

Anna-Kaisa Anttonen

4

1 reference

Europe PubMed Central

3 November 2017

Ivo F A C Fokkema

6

1 reference

Europe PubMed Central

3 November 2017

Henrikki Almusa

7

1 reference

Europe PubMed Central

3 November 2017

Anthony Metzidis

8

1 reference

Europe PubMed Central

3 November 2017

Kristiina Avela

9

1 reference

Europe PubMed Central

3 November 2017

Pertti Aula

10

1 reference

Europe PubMed Central

3 November 2017

Marjo Kestilä

11

1 reference

Europe PubMed Central

3 November 2017

publication date

13 September 2013

1 reference

Europe PubMed Central

3 November 2017

1 reference

Europe PubMed Central

3 November 2017

34

1 reference

Europe PubMed Central

3 November 2017

11

1 reference

Europe PubMed Central

3 November 2017

1458-1466

1 reference

Europe PubMed Central

3 November 2017

Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

VarioML framework for comprehensive variation data representation and exchange

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Locus Reference Genomic sequences: an improved basis for describing human DNA variants.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Mutation nomenclature

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Quantifying the use of bioresources for promoting their sharing in scientific research

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Genetic markers and population history: Finland revisited

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Human Variome Project country nodes: documenting genetic information within a country

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Molecular genetics of the Finnish disease heritage.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Comparison of solution-based exome capture methods for next generation sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Guidelines for establishing locus specific databases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

21 January 2018

Finnish Disease Heritage I: characteristics, causes, background

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

7 January 2021

based on heuristic

inferred from DOI database lookup

Finnish Disease Heritage II: population prehistory and genetic roots of Finns

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

7 January 2021

based on heuristic

inferred from DOI database lookup

The Finnish Disease Heritage III: the individual diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22389

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.22389

1 reference

Europe PubMed Central

3 November 2017

1 reference

Europe PubMed Central

3 November 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42611572&oldid=1575610464"