(Q37970653)

26 August 2017

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

26 August 2017

0 references

1 reference

Marka van Blitterswijk

17

Marka van Blitterswijk

0 references

Wouter van Rheenen

18

Wouter van Rheenen

0 references

Max Koppers

Max Koppers

9

0 references

Dagmar Verbaan

Dagmar Verbaan

39

0 references

Rubén Fernández-Santiago

Rubén Fernández-Santiago

33

0 references

Robin Lemmens

Robin Lemmens

30

0 references

Philip Van Damme

Philip Van Damme

29

0 references

Nicola Ticozzi

Nicola Ticozzi

4

0 references

Claudia Schulte

Claudia Schulte

7

0 references

Stefano Goldwurm

Stefano Goldwurm

27

0 references

Hans Scheffer

Hans Scheffer

15

0 references

Vincenzo Silani

Vincenzo Silani

46

0 references

Thomas Gasser

47

Thomas Gasser

1 reference

26 August 2017

14

Bastiaan R Bloem

1 reference

26 August 2017

44

Daniela Berg

2 references

ORCID Public Data File 2021

26 August 2017

Christine Klein

35

Christine Klein

1 reference

26 August 2017

28

Gianni Pezzoli

1 reference

26 August 2017

41

Peter Heutink

1 reference

26 August 2017

Leonard H van den Berg

56

Leonard H van den Berg

1 reference

26 August 2017

48

Albert C Ludolph

1 reference

26 August 2017

49

Wim Robberecht

1 reference

26 August 2017

5

Peter M Andersen

1 reference

26 August 2017

51

Jan H Veldink

1 reference

26 August 2017

54

John E Landers

1 reference

26 August 2017

10

Frank P Diekstra

1 reference

26 August 2017

52

R Jeroen Pasterkamp

1 reference

26 August 2017

53

Paul I W de Bakker

1 reference

26 August 2017

32

Anna Birve

1 reference

26 August 2017

2

Helenius J Schelhaas

1 reference

26 August 2017

8

Hylke M Blauw

1 reference

26 August 2017

38

Marianne de Visser

1 reference

26 August 2017

13

Pamela Keagle

1 reference

26 August 2017

Anneke J van der Kooi

37

Anneke J van der Kooi

1 reference

26 August 2017

3

Paul W J van Vught

1 reference

26 August 2017

6

Ewout J N Groen

1 reference

26 August 2017

50

Roel A Ophoff

1 reference

26 August 2017

31

Caroline Dahlberg

1 reference

26 August 2017

34

Stefan Waibel

1 reference

26 August 2017

11

Katsumi Fumoto

1 reference

26 August 2017

19

Anne-Marie Wills

1 reference

26 August 2017

45

Robert H Brown

1 reference

26 August 2017

25

Rebecca D Folkerth

1 reference

26 August 2017

Michael A van Es

1

1 reference

26 August 2017

Ashley Lyn LeClerc

12

1 reference

26 August 2017

Bart F L van Nuenen

16

1 reference

26 August 2017

Patrick P Lowe

20

1 reference

26 August 2017

Guo-fu Hu

21

1 reference

26 August 2017

Wenhao Yu

22

1 reference

26 August 2017

Hiroko Kishikawa

23

1 reference

26 August 2017

David Wu

24

1 reference

26 August 2017

Claudio Mariani

26

1 reference

26 August 2017

Markus Weber

36

1 reference

26 August 2017

Jacobus J van Hilten

40

1 reference

26 August 2017

Eric A M Hennekam

42

1 reference

26 August 2017

Edwin Cuppen

43

1 reference

26 August 2017

Bart P van de Warrenburg

55

1 reference

26 August 2017

language of work or name

1 reference

1 December 2011

1 reference

26 August 2017

1 reference

26 August 2017

70

1 reference

26 August 2017

6

1 reference

26 August 2017

964-973

1 reference

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia

26 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Ataxin-2 repeat-length variation and neurodegeneration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Exome sequencing reveals VCP mutations as a cause of familial ALS

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

A neuroprotective role for angiogenin in models of Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Statistical analysis strategies for association studies involving rare variants

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

An estimate of amyotrophic lateral sclerosis heritability using twin data.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Paraoxonase gene mutations in amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Pooled association tests for rare variants in exon-resequencing studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Mutations of optineurin in amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Finding the missing heritability of complex diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

SNCA variants are associated with increased risk for multiple system atrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

A groupwise association test for rare mutations using a weighted sum statistic

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Transcriptional dysregulation in a transgenic model of Parkinson disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Genetics of sporadic amyotrophic lateral sclerosis.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

A new role for angiogenin in neurite growth and pathfinding: implications for amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

alpha-Synuclein locus triplication causes Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

SCA2 may present as levodopa-responsive parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Meta-analysis of Observational Studies in Epidemiology: A Proposal for Reporting

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Progress and challenges in genome-wide association studies in humans

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Evidence for a common pathway linking neurodegenerative diseases.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Angiogenin protects motoneurons against hypoxic injury.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Control of motoneuron survival by angiogenin.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

TDP-43 mutation in familial amyotrophic lateral sclerosis

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

A novel candidate region for ALS on chromosome 14q11.2.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5560057

Absence of angiogenic genes modification in Italian ALS patients

1 September 2018

1 reference

12 December 2020

Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility

1 reference

12 December 2020

Coexistence of parkinsonism, dementia and upper motor neuron syndrome in four Czech patients

1 reference

12 December 2020

A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

1 reference

12 December 2020

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis

1 reference

12 December 2020

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations

1 reference

12 December 2020

A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group

1 reference

12 December 2020

Identifiers

DOI

10.1002/ANA.22611

1 reference

26 August 2017

1 reference

26 August 2017

1 reference