1.
Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth
by FROMER, Menachem
American journal of human genetics, 2012, Vol.91 (4), p.597-607
2.
Identification of Small Exonic CNV from Whole-Exome Sequence Data and Application to Autism Spectrum Disorder
by Poultney, Christopher S
American journal of human genetics, 2013, Vol.93 (4), p.607-619
3.
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases
by Chen, Rong
Nature biotechnology, 2016, Vol.34 (5), p.531-538
4.
Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders
by Lim, Elaine T
Neuron (Cambridge, Mass.), 2013, Vol.77 (2), p.235-242
5.
Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression
by Hauberg, Mads Engel
American journal of human genetics, 2017, Vol.100 (6), p.885-894
6.
Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS
by Dobbyn, Amanda
American journal of human genetics, 2018, Vol.102 (6), p.1169-1184
7.
The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders
by Buxbaum, Joseph D
Neuron (Cambridge, Mass.), 2012, Vol.76 (6), p.1052-1056
8.
Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression
by Hauberg, Mads Engel
American journal of human genetics, 2017, Vol.101 (1), p.157-157
