PubRank

Jennifer K Lowe

Author PubWeight™ 57.64‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011 10.61
2 Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature 2011 10.16
3 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
4 Whole population, genome-wide mapping of hidden relatedness. Genome Res 2008 4.72
5 Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell 2013 2.87
6 Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 2012 2.67
7 A 1-Mb resolution radiation hybrid map of the canine genome. Proc Natl Acad Sci U S A 2003 2.30
8 Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia. Nat Genet 2006 2.07
9 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. Heart Rhythm 2009 1.91
10 Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. Hum Mol Genet 2002 1.78
11 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arterioscler Thromb Vasc Biol 2008 1.63
12 DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Am J Hum Genet 2011 1.62
13 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
14 Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae. Proc Natl Acad Sci U S A 2009 1.13
15 Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biol Psychiatry 2013 1.11
16 Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum Mol Genet 2010 0.98
17 Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder. Int Rev Neurobiol 2013 0.91
18 Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. Mol Autism 2014 0.91
19 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
20 Linkage mapping of canine rod cone dysplasia type 2 (rcd2) to CFA7, the canine orthologue of human 1q32. Invest Ophthalmol Vis Sci 2006 0.85
21 European admixture on the Micronesian island of Kosrae: lessons from complete genetic information. Eur J Hum Genet 2009 0.83