(Q53842374)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

title

Exome sequencing uncovers hidden pathways in familial and sporadic ALS (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

6 March 2020

main subject

1 reference

based on heuristic

inferred from title

author

Conceicao Bettencourt

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

author name string

Henry Houlden

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

language of work or name

English

0 references

publication date

1 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

page(s)

611-613

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

Advances in treating amyotrophic lateral sclerosis: insights from pathophysiological studies

6 March 2020

cites work

1 reference

Dissection of genetic factors associated with amyotrophic lateral sclerosis

21 January 2018

1 reference

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

21 January 2018

1 reference

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

21 January 2018

1 reference

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

21 January 2018

1 reference

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.

21 January 2018

1 reference

Amyotrophic lateral sclerosis: an update on recent genetic insights

21 January 2018

1 reference

Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2.

21 January 2018

1 reference

Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis.

21 January 2018

1 reference

Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia

21 January 2018

1 reference

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders

21 January 2018

1 reference

Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NN.4012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25919956%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference