Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variants among patients with motor neuron disease in Lithuania - a retrospective single-center study.

Neurogenetics - 31 Jul 2026

Naktinytė Eva, Vilimienė Ramunė, Valančius Domantas, Baronas Karolis, Zagorskienė Irena, Utkus Algirdas, Klimašauskienė Aušra, Burnytė Birutė

Abstract excerpt

Motor neuron disease (MND) comprises several clinical phenotypes, with amyotrophic lateral sclerosis (ALS) being the most common. Despite the identification of over 40 ALS-associated genes, the pathogenesis remains complex and polygenic. This study evaluated the clinical phenotypes and prevalence of genetic causes in MND patients in Lithuania. We conducted a retrospective single-center study at a tertiary care...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Amyotrophic Lateral Sclerosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to C9orf72 Protein

Share to DNA Repeat Expansion

Share to Genetic Variation

Share to Lithuania

Share to Motor Neuron Disease

Share to Phenotype

Source

Identifiers

PMID: 42536230
DOI: 10.1007/s10048-026-00926-y

Genes

FUS
SOD1
NEK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variants among patients with motor neuron disease in Lithuania - a retrospective single-center study.PMID 42536230Read ↗

Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis CohortSemantic proximity Read ↗

Unraveling the genetic landscape of ALS in Greece: identification of known and novel causative variants in a 353-patient cohort.Semantic proximity Read ↗

Genetic epidemiology of amyotrophic lateral sclerosis in Cyprus: a population-based study.Semantic proximity Read ↗

Genetic variability in sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population.Semantic proximity Read ↗

Genetic Basis of Motor Neuron Diseases: Insights, Clinical Management, and Future DirectionsSemantic proximity Read ↗

Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population.Semantic proximity Read ↗

Genetic Epidemiology of Amyotrophic Lateral Sclerosis in Norway: A 2-Year Population-Based StudySemantic proximity Read ↗

Genotypes and phenotypes of motor neuron disease: an update of the genetic landscape in Scotland.Semantic proximity Read ↗

Genetic Landscape of Amyotrophic Lateral Sclerosis in Czech Patients.Semantic proximity Read ↗

A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK.Semantic proximity Read ↗

Genetics of Motor Neuron Disease in New ZealandSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.