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Home › Research › Topics › c9orf72

c9orf72

2 studies tagged c9orf72, dated 2014-06-27 to 2019-02-01. Bibliography: BibTeX (.bib) · RIS (.ris)

Newest in this topic

  1. Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity 2019-02-01
  2. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis 2014-06-27

Studies

2 studies carry this tag.

Date range

2014 to 2019

Top journals

  • Annals of neurology 1
  • Science (New York, N.Y.) 1

Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.

  1. Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity

    ✓ Peer-reviewed alzhub usefulness score 43 out of 100. Science (New York, N.Y.) 2019-02-01 Brain scans and imaging

    How hexanucleotide GGGGCC (G 4 C 2 ) repeat expansions in C9orf72 cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) is not understood.

  2. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis

    ✓ Peer-reviewed alzhub usefulness score 67 out of 100. Annals of neurology 2014-06-27 Genetics

    We identified common genetic variants in C9orf72, but in addition in UNC13A that are shared between ALS and FTD.

All topic tags with their study counts