(Q34344661)

1 August 2017

title

Genotator: a disease-agnostic tool for genetic annotation of disease (English)

1 reference

1 August 2017

7

Peter J Tonellato

1 reference

1 August 2017

Dennis P Wall

1

1 reference

1 August 2017

Rimma Pivovarov

2

1 reference

1 August 2017

Mark Tong

3

1 reference

1 August 2017

Jae-Yoon Jung

4

1 reference

1 August 2017

Vincent A Fusaro

5

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1 August 2017

Todd F DeLuca

6

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1 August 2017

publication date

29 October 2010

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1 August 2017

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1 August 2017

volume

3

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1 August 2017

page(s)

50

1 reference

https://scigraph.springernature.com/pub.10.1186/1755-8794-3-50

1 August 2017

exact match

0 references

cites work

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Case-control study of the parkin gene in early-onset Parkinson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Phenotypic associations of tau and ApoE in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Association of DRD3 and GRIN2B with impulse control and related behaviors in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Effect of APOE genotype on amyloid plaque load and gray matter volume in Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Earlier onset of Alzheimer's disease: risk polymorphisms within PRNP, PRND, CYP46, and APOE genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

APOE and APOC1 promoter polymorphisms and the risk of Alzheimer disease in African American and Caribbean Hispanic individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Association of MTHFR gene polymorphism C677T with susceptibility to late-onset Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

Association between BDNF Val66Met polymorphism and Alzheimer disease, dementia with Lewy bodies, and Pick disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-3-50

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990725

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990725

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990725

Point mutation analysis of the FMR-1 gene in autism

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2990725

Pharmacogenomics in Alzheimer's disease

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21034472

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21034472

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8794-3-50

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference