(Q51562888)

7 April 2018

title

Call for participation in the neurogenetics consortium within the Human Variome Project. (English)

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9

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Sherifa A Hamed

11

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Francesc Palau

15

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Peter Robinson

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Antonio Salas

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Jorge Amigo

22

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Mary G. Sweeney

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object named as

Mary G Sweeney

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author name string

Andrea Haworth

1

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Lars Bertram

2

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Paola Carrera

3

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Joanna L Elson

4

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Corey D Braastad

5

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Diane W Cox

6

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Marc Cruts

7

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Johann T den Dunnen

8

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John K Fink

10

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Henry Houlden

12

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Dennis R Johnson

13

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Karen Nuytemans

14

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Dipa L Raja Rayan

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Birgitt Schüle

19

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Michael O Woods

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Richard G H Cotton

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Maria-Jesus Sobrido

24

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publication date

1 June 2011

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7 April 2018

published in

Neurogenetics

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volume

12

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issue

3

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7 April 2018

page(s)

169-173

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7 April 2018

https://scigraph.springernature.com/pub.10.1007/s10048-011-0287-4

exact match

0 references

cites work

Recommendations of the 2006 Human Variome Project meeting

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

Planning the human variome project: the Spain report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

GENETICS. The Human Variome Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0287-4

10.1007/S10048-011-0287-4

21 January 2018

Identifiers

DOI

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7 April 2018

release_vo4yleyjgvffpgn75if345pnuu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vo4yleyjgvffpgn75if345pnuu

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

21630033

1 reference

7 April 2018