PubRank

Michael E Zwick

Author PubWeight™ 50.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Microarray-based genomic selection for high-throughput resequencing. Nat Methods 2007 9.62
2 Haplotype inference in random population samples. Am J Hum Genet 2002 8.07
3 Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 2014 5.30
4 Structure and complexity of a bacterial transcriptome. J Bacteriol 2009 3.55
5 Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics 2004 1.72
6 Genomic characterization of the Yersinia genus. Genome Biol 2010 1.63
7 Microarray-based mutation detection in the dystrophin gene. Hum Mutat 2008 1.39
8 SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics 2010 1.36
9 Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions. Ann Hum Genet 2009 1.32
10 Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay. J Clin Invest 2011 1.19
11 Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. Am J Med Genet A 2010 1.16
12 Targeted sequencing of the human X chromosome exome. Genomics 2011 1.06
13 A genome sequencing center in every lab. Eur J Hum Genet 2005 1.05
14 Rapid identification of genetic modifications in Bacillus anthracis using whole genome draft sequences generated by 454 pyrosequencing. PLoS One 2010 0.99
15 Copy number abnormalities in sporadic canine colorectal cancers. Genome Res 2010 0.95
16 Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLoS One 2010 0.93
17 Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci. Arthritis Rheum 2013 0.93
18 Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease. J Pediatr Gastroenterol Nutr 2014 0.92
19 Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. J Med Genet 2012 0.90
20 Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse. G3 (Bethesda) 2012 0.88
21 Empirical evaluation of oligonucleotide probe selection for DNA microarrays. PLoS One 2010 0.84
22 Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder. Hum Mol Genet 2012 0.83
23 Microarray oligonucleotide probe designer (MOPeD): A web service. Open Access Bioinformatics 2010 0.81
24 Evaluating rare variants in complex disorders using next-generation sequencing. Curr Psychiatry Rep 2013 0.80
25 Applying rapid genome sequencing technologies to characterize pathogen genomes. Anal Chem 2008 0.80
26 Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture. Inflamm Bowel Dis 2012 0.79
27 Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes. Hum Mutat 2014 0.75
28 A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic Galactosemia. JIMD Rep 2015 0.75