BOSTON, July 29, 2025 /PRNewswire/ -- Athena Diagnostics, the specialty neurology business of Quest Diagnostics (NYSE: DGX), a leading provider of diagnostic information services, today announced a ...

Despite modern high-throughput sequencing, the genetic cause of most rare movement disorders remains unclear. A research team in Bochum and Tübingen has now solved one piece of the puzzle: The ...

An immune-related gene has now been tied to a rare inherited neurological disorder, revealing an overlooked pathway in the ...

The Nature Index 2025 Research Leaders — previously known as Annual Tables — reveal the leading institutions and countries/territories in the natural and health sciences, according to their output in ...

Retrotransposon activity could be one cause of the movement disorder ataxia, a study published on September 6 in Neuron suggests. These so-called jumping genes have the ability to create copies of ...

Spinal cerebellar ataxia 6 (SCA6) is an inherited neurological condition which has a debilitating impact on motor coordination. Affecting around 1 in 100,000 people, the rarity of SCA6 has seen it ...

Genetic analysis of the large patient cohort was conducted in Tübingen under the supervision of Dr. Tobias Haack. Functional characterization of the newly identified disease gene was led by Dr. Jonasz ...