Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Papers
(The H4-Index of Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is 16. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
Rapid classification of a novel ALS-causing I149S variant in superoxide dismutase-141
Low plasma hyaluronan is associated with faster functional decline in patients with amyotrophic lateral sclerosis31
The amyotrophic lateral sclerosis-health index (ALS-HI): development and evaluation of a novel outcome measure30
Clinical and demographical characteristics in a cohort of MND patients treated with riluzole. Differences between tablets and oral suspension29
Expanding the clinical and genetic spectrum of SQSTM1-related disorders in family with personality disorder and frontotemporal dementia28
Correction22
The correlation between social support, coping style, advance care planning readiness, and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study21
Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: a ten year follow up study19
Validity and reliability measures of the Swedish Karolinska version of the Edinburgh Cognitive and Behavioral ALS Screen (SK-ECAS)19
Incorporating patient preferences and burden-of-disease in evaluating ALS drug candidate AMX0035: a Bayesian decision analysis perspective18
Single task-level, 2SD-based cutoffs for the Italian version of the Edinburgh Cognitive and Behavioral ALS screen (ECAS)17
Amyotrophic lateral sclerosis mortality rates in Latin America and the Caribbean: a meta-analysis17
Development, reliability, validity, and acceptability of the remote administration of the Edinburgh Cognitive and Behavioural ALS Screen (ECAS)17
Genetic ancestry and risk allele C9orf72 rs3849942 T for amyotrophic lateral sclerosis in Latin American populations17
Impact of occupational categories on the incidence of amyotrophic lateral sclerosis in Sardinia Island, Italy17
Residential exposure associations with ALS risk, survival, and phenotype: a Michigan-based case-control study17
Geographical clusters of amyotrophic lateral sclerosis and the Bradford Hill criteria16
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