Rare variants in PLXNA4 and Parkinson's disease (Q37296750)

19 August 2017

Rare variants in PLXNA4 and Parkinson's disease (English)

1 reference

19 August 2017

8

1 reference

19 August 2017

16

1 reference

19 August 2017

3

Darina Czamara

0 references

Claudia Trenkwalder

18

Claudia Trenkwalder

0 references

Bertram Müller-Myhsok

17

Daniel Christian Ellwanger

Bertram Müller-Myhsok

0 references

Daniel C Ellwanger

4

0 references

Eva C. Schulte

Eva C Schulte

1

0 references

Juliane Winkelmann

Juliane Winkelmann

19

0 references

Annette Peters

Annette Peters

15

0 references

Brit Mollenhauer

7

Brit Mollenhauer

1 reference

19 August 2017

9

Peter Lichtner

1 reference

19 August 2017

Immanuel Stahl

2

1 reference

19 August 2017

Sebastian Eck

5

1 reference

19 August 2017

Elisabeth Graf

6

1 reference

19 August 2017

Dietrich Haubenberger

10

1 reference

19 August 2017

Walter Pirker

11

1 reference

19 August 2017

Thomas Brücke

12

1 reference

19 August 2017

Benjamin Bereznai

13

1 reference

19 August 2017

Maria J Molnar

14

1 reference

19 August 2017

language of work or name

English

0 references

publication date

11 November 2013

1 reference

19 August 2017

1 reference

19 August 2017

8

1 reference

19 August 2017

11

1 reference

19 August 2017

e79145

1 reference

Creative Commons Attribution 4.0 International

19 August 2017

start time

11 November 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

VPS35 mutations in Parkinson disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Exome sequencing reveals VCP mutations as a cause of familial ALS

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

MutationTaster evaluates disease-causing potential of sequence alterations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

A method and server for predicting damaging missense mutations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Secreted semaphorins control spine distribution and morphogenesis in the postnatal CNS.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

A cross-study transcriptional analysis of Parkinson's disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Plexin-A3 and plexin-A4 restrict the migration of sympathetic neurons but not their neural crest precursors.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Pathway-based approaches for analysis of genomewide association studies

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

High-resolution whole-genome association study of Parkinson disease.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Plexin-a4 mediates axon-repulsive activities of both secreted and transmembrane semaphorins and plays roles in nerve fiber guidance

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Human non-synonymous SNPs: server and survey

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Analysis of gene expression in Parkinson's disease: possible involvement of neurotrophic support and axon guidance in dopaminergic cell death

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Interactions between plexin-A2, plexin-A4, and semaphorin 6A control lamina-restricted projection of hippocampal mossy fibers

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Aberrant trajectory of ascending dopaminergic pathway in mice lacking Nkx2.1.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823607

Increased risk of Parkinson's disease in parents and siblings of patients

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24244438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial Parkinson's disease: a clinical genetic analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24244438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24244438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0079145

1 reference

19 August 2017

0 references

1 reference

19 August 2017

PubMed publication ID

24244438

1 reference