A Jeremy Willsey

Author PubWeight™ 31.59^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	De novo mutations revealed by whole-exome sequencing are strongly associated with autism.	Nature	2012	13.61
2	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.	Nat Genet	2013	8.02
3	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	2014	5.30
4	Common genetic variants, acting additively, are a major source of risk for autism.	Mol Autism	2012	2.67
5	Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation.	Am J Hum Genet	2013	1.29
6	Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.	Biol Psychiatry	2013	1.11
7	The developmental transcriptome of the human brain: implications for neurodevelopmental disorders.	Curr Opin Neurol	2014	1.04
8	Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.	Autism Res	2014	0.90