Alison J Coffey

Author PubWeight™ 42.28^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.	Nature	2010	12.27
2	Target-enrichment strategies for next-generation sequencing.	Nat Methods	2010	8.78
3	The DNA sequence of the human X chromosome.	Nature	2005	6.97
4	Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.	Am J Hum Genet	2005	1.78
5	Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study.	Lancet Neurol	2006	1.54
6	Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder.	PLoS One	2011	1.27
7	A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling.	PLoS One	2012	1.16
8	Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.	PLoS Genet	2009	1.16
9	Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.	Blood	2013	1.15
10	Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance.	Pharmacogenet Genomics	2006	0.97
11	An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studies.	PLoS One	2011	0.91
12	Physical and transcript map of the hereditary prostate cancer region at xq27.	Genomics	2002	0.88
13	Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach.	Pharmacogenet Genomics	2007	0.87
14	Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing data.	Hum Genet	2011	0.85
15	DNA rescue by the vectorette method.	Methods Mol Biol	2003	0.83
16	The association between polymorphisms in RLIP76 and drug response in epilepsy.	Pharmacogenomics	2007	0.79
17	Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.	Basic Res Cardiol	2013	0.75
18	Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS).	Epilepsy Res	2011	0.75