PubRank

Stephan J Sanders

Author PubWeight™ 45.96‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
2 Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 2014 5.30
3 De novo mutations in histone-modifying genes in congenital heart disease. Nature 2013 5.15
4 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell 2013 2.94
5 Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013 2.74
6 Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet 2010 2.70
7 Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 2012 2.67
8 Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron 2013 2.45
9 Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol Psychiatry 2011 2.28
10 A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proc Natl Acad Sci U S A 2012 1.85
11 Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. Science 2012 1.65
12 Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. Am J Hum Genet 2012 1.52
13 Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. PLoS Genet 2013 1.48
14 Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Hum Mol Genet 2011 1.22
15 DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Mol Autism 2014 1.20
16 Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biol Psychiatry 2013 1.11
17 Intellectual disability is associated with increased runs of homozygosity in simplex autism. Am J Hum Genet 2013 0.96
18 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
19 Physiological and psychological illness symptoms at high altitude and their relationship with acute mountain sickness: a prospective cohort study. J Travel Med 2012 0.88
20 Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism. Brain Dev 2011 0.82
21 A balanced t(10;15) translocation in a male patient with developmental language disorder. Eur J Med Genet 2011 0.80
22 De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder. Am J Hum Genet 2017 0.75