Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

1. 10.

   The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment · 2015

2. 12.

   CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function · 2012

3. 15.

   Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples · 2014

4. 28.

   Qualimap 2: advanced multi-sample quality control for high-throughput sequencing data · 2015

5. 36.

   DELLY: structural variant discovery by integrated paired-end and split-read analysis · 2012

6. 40.

   The Database of Genomic Variants: a curated collection of structural variation in the human genome · 2013

7. 43.

   Analysis of protein-coding genetic variation in 60,706 humans · 2016

8. 44.

   The Ensembl Variant Effect Predictor · 2016

9. 53.

   The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology · 2017

10. 64.

    Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia · 2018

11. 66.

    GENCODE reference annotation for the human and mouse genomes · 2018

12. 69.

    Detection of long repeat expansions from PCR-free whole-genome sequence data · 2017

13. 72.

    Vcfanno: fast, flexible annotation of genetic variants · 2016

14. 78.

    Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program · 2021

67 more references, whose wording the paper’s licence keeps private.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.