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Connection

Julie Schneider to Mutation

This is a "connection" page, showing publications Julie Schneider has written about Mutation.
Connection Strength

0.566
  1. A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration. Neuropathology. 2020 Dec; 40(6):620-626.
    View in: PubMed
    Score: 0.158
  2. CD33 modulates TREM2: convergence of Alzheimer loci. Nat Neurosci. 2015 Nov; 18(11):1556-8.
    View in: PubMed
    Score: 0.113
  3. A novel GRN mutation (GRN c.708+6_+9delTGAG) in frontotemporal lobar degeneration with TDP-43-positive inclusions: clinicopathologic report of 6 cases. J Neuropathol Exp Neurol. 2014 May; 73(5):467-73.
    View in: PubMed
    Score: 0.102
  4. GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. Neurology. 2012 Nov 06; 79(19):1944-50.
    View in: PubMed
    Score: 0.092
  5. Progranulin mutations in clinical and neuropathological Alzheimer's disease. Alzheimers Dement. 2022 12; 18(12):2458-2467.
    View in: PubMed
    Score: 0.044
  6. Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathol. 2018 12; 136(6):857-872.
    View in: PubMed
    Score: 0.034
  7. The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-e4 carriers. PLoS Genet. 2013; 9(8):e1003685.
    View in: PubMed
    Score: 0.024
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.