verified SJR 0,957 · Q1 • database Scopus / SJR & Web of Science indexed

United Kingdom · Informa Healthcare

workspace_premium Q1 — Medicine (miscellaneous) lock Subscription

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is a journal indexed in SJR in Medicine (miscellaneous) and Neurology (clinical) with an H index of 89. It has an SJR impact factor of 0,957 and it has a best quartile of Q1. It has an SJR impact factor of 0,957.

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration focuses its scope in these topics and keywords: lateral, amyotrophic, sclerosis, systematic, methods, percutaneous, frequent, juvenile, patients, alsscreening, ...

ISSN: 2167-8421

Publisher: Informa Healthcare

Category: Medicine (miscellaneous)

Indexation: verifiedScopus / SJR verifiedWeb of Science

open_in_new Portal NPD menu_book Guidelines NPD

schedule CountryOfPapers database fields

SJR Impact Factor trending_up

0,957 Q1

H-index 89

Acceptance rate pie_chart

26% Selective

Source Acceptance_Rate

Time to publication hourglass_top

NPD

Field NPD

Publication cost (APC) payments

NPD Subscription

Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

SJR Impact

0,957

H-index

Docs (year)

132

Docs 3y

283

Total refs

3877

Cites 3y

760

Citable 3y

275

Cites/Doc 2y

2.77

Ref/Doc

29.37

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

shield Researcher voice

Name good journals. Call out predatory ones.

Share what peer review, fees, and timelines were really like. Praise fair editors. Flag APC traps, fake metrics, or spam solicitations — with facts from your submission.

Fair & fast peer review Clear APC / no surprise fees Suspected predatory Fake impact claims

rate_review Write an honest review

Researcher reviews

sentiment_dissatisfied No reviews yet — be the first to share an honest experience.

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID * * Only to validate authenticity — identity is not shown publicly.

Best articles by citations

Atlanta metropolitan area amyotrophic lateral sclerosis (ALS) surveillance: incidence and prevalence 2009-2011 and survival characteristics through 2015

Young slow-progressing ALS patients are at higher risk of inappropriate and disease-quickening surgeries

Dropped head syndrome in amyotrophic lateral sclerosis

Dropped head presentation in ALS

Detection of a novel frameshift mutation and regions with homozygosis within ARHGEF28 gene in familial amyotrophic lateral sclerosis

CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum

Cortical contributions to the flail leg syndrome: Pathophysiological insights

Coeliac disease mimicking Amyotrophic Lateral Sclerosis

Clinicopathologic report of ocular involvement in ALS patients with C9orf72 mutation

Clinical varieties and epidemiological aspects of amyotrophic lateral sclerosis in the Caribbean island of Guadeloupe: A new focus of ALS associated with Parkinsonism

Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: An update of LIGALS register

Breaking bad news in amyotrophic lateral sclerosis: The need for medical education

SHOW MORE ARTICLES

Behavioral manifestations in a Brazilian non-demented C9orf72-negative ALS population

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort

Analysis of the C9orf72 gene in spinal muscular atrophy patients

An epidemiological profile of dysarthria incidence and assistive technology use in the living population of people with MND in Scotland

Amyotrophic lateral sclerosis mimic syndrome due to neurosyphilis

ALSUntangled No. 52: Glutathione

ALSUntangled No. 26: Lunasin

Adult onset Sandhoff disease: a rare mimicker of amyotrophic lateral sclerosis

A speech measure for early stratification of fast and slow progressors of bulbar amyotrophic lateral sclerosis: lip movement jitter

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS

A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis

FAQs

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration has an SJR of 0,957 (best quartile Q1) in the CountryOfPapers database.

Immediate OA APC is not available (NPD).

The acceptance rate recorded for Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is 26%.

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Metrics

Name good journals. Call out predatory ones.

Researcher reviews

Best articles by citations

FAQs

What is the SJR of Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration?

What is the APC / publication cost?

What is the acceptance rate?