PubRank

David J Cutler

Author PubWeight™ 209.83‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 85.39
2 A note on exact tests of Hardy-Weinberg equilibrium. Am J Hum Genet 2005 18.98
3 Genome-wide detection and characterization of positive selection in human populations. Nature 2007 17.27
4 Microarray-based genomic selection for high-throughput resequencing. Nat Methods 2007 9.62
5 Haplotype inference in random population samples. Am J Hum Genet 2002 8.07
6 Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies. Nat Genet 2004 5.78
7 Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 2014 5.30
8 A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet 2008 5.28
9 A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature 2005 4.92
10 Genomic alterations in cultured human embryonic stem cells. Nat Genet 2005 3.89
11 Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. Am J Hum Genet 2003 2.51
12 Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arrays. Genome Res 2004 2.47
13 Microdeletions of 3q29 confer high risk for schizophrenia. Am J Hum Genet 2010 2.38
14 Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus. Hum Mol Genet 2003 1.87
15 Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics 2004 1.72
16 Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology 2006 1.71
17 Haplotype and missing data inference in nuclear families. Genome Res 2004 1.69
18 Microarray-based resequencing of multiple Bacillus anthracis isolates. Genome Biol 2004 1.61
19 Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. Genome Biol 2008 1.61
20 Population bottlenecks as a potential major shaping force of human genome architecture. PLoS Genet 2007 1.47
21 An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome. J Mol Diagn 2006 1.40
22 SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics 2010 1.36
23 Aberrant gating of photic input to the suprachiasmatic circadian pacemaker of mice lacking the VPAC2 receptor. J Neurosci 2004 1.30
24 Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies. Am J Hum Genet 2007 1.23
25 Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. Am J Med Genet A 2010 1.16
26 Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis. Hum Mol Genet 2008 1.12
27 Autosomal recessive causes likely in early-onset Alzheimer disease. Arch Neurol 2011 1.08
28 Targeted sequencing of the human X chromosome exome. Genomics 2011 1.06
29 On the probability that a novel variant is a disease-causing mutation. Genome Res 2005 1.02
30 What is a suitable dissolution method for drug nanoparticles? Pharm Res 2008 1.01
31 Pharmacokinetic parameter prediction from drug structure using artificial neural networks. Int J Pharm 2004 0.95
32 Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLoS One 2010 0.93
33 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
34 Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease. J Pediatr Gastroenterol Nutr 2014 0.92
35 Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase. Hum Mol Genet 2009 0.92
36 The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry. PLoS One 2011 0.91
37 Mometasone furoate degradation and metabolism in human biological fluids and tissues. Biopharm Drug Dispos 2003 0.90
38 Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse. G3 (Bethesda) 2012 0.88
39 Population demographic history can cause the appearance of recombination hotspots. Am J Hum Genet 2012 0.87
40 Population genetics identifies challenges in analyzing rare variants. Genet Epidemiol 2015 0.87
41 Empirical evaluation of oligonucleotide probe selection for DNA microarrays. PLoS One 2010 0.84
42 Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder. Hum Mol Genet 2012 0.83
43 Genistein cooperates with the histone deacetylase inhibitor vorinostat to induce cell death in prostate cancer cells. BMC Cancer 2012 0.82
44 Microarray oligonucleotide probe designer (MOPeD): A web service. Open Access Bioinformatics 2010 0.81
45 Simultaneous neutron scattering and Raman scattering. Appl Spectrosc 2009 0.80
46 Variation in the lymphotoxin-alpha/tumor necrosis factor locus modifies risk of erythema nodosum in sarcoidosis. J Invest Dermatol 2009 0.80
47 A model of binding on DNA microarrays: understanding the combined effect of probe synthesis failure, cross-hybridization, DNA fragmentation and other experimental details of affymetrix arrays. BMC Genomics 2012 0.79
48 Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture. Inflamm Bowel Dis 2012 0.79
49 Association study of serotonin pathway genes in attempted suicide. Am J Med Genet B Neuropsychiatr Genet 2011 0.79
50 Paraoxonase-1 polymorphisms in Alzheimer's disease, Parkinson's disease, and AD-PD spectrum diseases. Neurobiol Aging 2010 0.79
51 Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression. Am J Med Genet B Neuropsychiatr Genet 2007 0.76
52 Multiple pharmacokinetic parameter prediction for a series of cephalosporins. J Pharm Sci 2003 0.76
53 A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic Galactosemia. JIMD Rep 2015 0.75
54 A comprehensive search for recombinogenic motifs in the human genome. PLoS One 2013 0.75
55 Integrating Next-Generation Genomic Sequencing and Mass Spectrometry to Estimate Allele-Specific Protein Abundance in Human Brain. J Proteome Res 2017 0.75
56 Selective descriptor pruning for QSAR/QSPR studies using artificial neural networks. J Comput Chem 2003 0.75
57 Focused-ion-beam milling: a novel approach to probing the interior of particles used for inhalation aerosols. Pharm Res 2007 0.75
58 Dissolution kinetic behavior of drug nanoparticles and their conformity to the diffusion model. Langmuir 2008 0.75