Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Papers
(The H4-Index of Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is 17. 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 2022-08-01 to 2026-08-01.)
ArticleCitations
Incorporating patient preferences and burden-of-disease in evaluating ALS drug candidate AMX0035: a Bayesian decision analysis perspective42
Correction34
Clinical and demographical characteristics in a cohort of MND patients treated with riluzole. Differences between tablets and oral suspension32
Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: a ten year follow up study30
The correlation between social support, coping style, advance care planning readiness, and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study27
A novel heterozygous GRN deletion (c.302_315del) associated with behavioral variant frontotemporal dementia27
Development, reliability, validity, and acceptability of the remote administration of the Edinburgh Cognitive and Behavioural ALS Screen (ECAS)27
Single task-level, 2SD-based cutoffs for the Italian version of the Edinburgh Cognitive and Behavioral ALS screen (ECAS)25
The amyotrophic lateral sclerosis-health index (ALS-HI): development and evaluation of a novel outcome measure25
Validity and reliability measures of the Swedish Karolinska version of the Edinburgh Cognitive and Behavioral ALS Screen (SK-ECAS)24
Rapid classification of a novel ALS-causing I149S variant in superoxide dismutase-121
Theme 5 Human Cell Biology and Pathology21
Emerging strategies for interpreting variants of uncertain significance (VUS) in amyotrophic lateral sclerosis20
Challenges in medical care for amyotrophic lateral sclerosis: a survey of physicians from Republic of Bashkortostan (Russia), Belarus, and Kazakhstan20
Theme 7 Pre-Clinical Therapeutic Strategies19
Genetic ancestry and risk allele C9orf72 rs3849942 T for amyotrophic lateral sclerosis in Latin American populations18
Peripheral immunity relate to disease progression and prognosis in amyotrophic lateral sclerosis18
Residential exposure associations with ALS risk, survival, and phenotype: a Michigan-based case-control study17
Epidemiology, clinical features, and management of amyotrophic lateral sclerosis in the neurology department of the Bogodogo University Hospital in Ouagadougou, Burkina Faso17
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