A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort

Overview of attention for article published in BMC Neurology, January 2014

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So far, Dimensions has found 90 publications that cite this research output.

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The most recent citing publications are shown below. View all 90 publications that cite this research output on Dimensions.

Unveiling the interplay of AMPK/SIRT1/PGC-1α axis in brain health: Promising targets against aging and NDDs

Article in Ageing Research Reviews (March 2024)

Peroxisome proliferator-activated receptor gamma coactivator-1 (PGC-1) family in physiological and pathophysiological process and diseases

Article in Signal Transduction and Targeted Therapy (March 2024)

Modification of Huntington’s disease by short tandem repeats

Article in Brain Communications (January 2024)

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