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Home › Research › Topics › whole-exome-sequencing

whole-exome-sequencing

2 studies tagged whole-exome-sequencing, dated 2013-04-23 to 2015-08-05. Bibliography: BibTeX (.bib) · RIS (.ris)

Newest in this topic

  1. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons 2015-08-05
  2. Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment 2013-04-23

Studies

2 studies carry this tag.

Date range

2013 to 2015

Top journals

  • European journal of human genetics : EJHG 1
  • Molecular psychiatry 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. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

    ✓ Peer-reviewed alzhub usefulness score 48 out of 100. European journal of human genetics : EJHG 2015-08-05 Genetics

    Causative variants in APP, PSEN1 or PSEN2 account for a majority of cases of autosomal dominant early-onset Alzheimer disease (ADEOAD, onset before 65 years).

  2. Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment

    ✓ Peer-reviewed alzhub usefulness score 76 out of 100. Molecular psychiatry 2013-04-23 Genetics

    Whole-exome sequencing of individuals with mild cognitive impairment, combined with genotype imputation, was used to identify coding variants other than the apolipoprotein E (APOE) ε4 allele associated with rate of hippocampal volume loss using an extreme trait design.

All topic tags with their study counts