PubRank

David W Craig

Author PubWeight™ 156.85‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays. PLoS Genet 2008 20.38
2 A survey of genetic human cortical gene expression. Nat Genet 2007 12.04
3 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
4 Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. Proc Natl Acad Sci U S A 2004 7.70
5 A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. J Clin Psychiatry 2007 7.23
6 GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Neuron 2007 6.88
7 Germline mutations in HOXB13 and prostate-cancer risk. N Engl J Med 2012 5.49
8 Genetic control of individual differences in gene-specific methylation in human brain. Am J Hum Genet 2010 3.91
9 Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet 2008 3.79
10 Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. Am J Hum Genet 2006 3.67
11 Genetic control of human brain transcript expression in Alzheimer disease. Am J Hum Genet 2009 3.35
12 Whole-genome analysis of sporadic amyotrophic lateral sclerosis. N Engl J Med 2007 3.33
13 Common Kibra alleles are associated with human memory performance. Science 2006 3.30
14 Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Neuroimage 2010 3.27
15 Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides. Blood 2012 2.98
16 Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans. Alzheimers Dement 2010 2.79
17 Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. Nat Genet 2009 2.73
18 Voxelwise genome-wide association study (vGWAS). Neuroimage 2010 2.69
19 Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Hum Mol Genet 2010 2.51
20 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. J Neural Transm (Vienna) 2008 2.43
21 Copy number and targeted mutational analysis reveals novel somatic events in metastatic prostate tumors. Genome Res 2010 2.41
22 A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly. Proc Natl Acad Sci U S A 2010 2.12
23 Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage 2010 1.94
24 SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays. Bioinformatics 2006 1.88
25 Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms. PLoS One 2008 1.72
26 Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study. Diabetes 2007 1.58
27 GRM7 variants confer susceptibility to age-related hearing impairment. Hum Mol Genet 2008 1.49
28 A successful social norms campaign to reduce alcohol misuse among college student-athletes. J Stud Alcohol 2006 1.44
29 The Autism Genome Project: goals and strategies. Am J Pharmacogenomics 2005 1.37
30 Sorl1 as an Alzheimer's disease predisposition gene? Neurodegener Dis 2007 1.31
31 Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. Am J Hum Genet 2007 1.24
32 Evidence for an association between KIBRA and late-onset Alzheimer's disease. Neurobiol Aging 2008 1.24
33 Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. PLoS Genet 2011 1.23
34 Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5. Brain 2007 1.23
35 Genome-wide characterization of pancreatic adenocarcinoma patients using next generation sequencing. PLoS One 2012 1.21
36 SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data. BMC Genomics 2005 1.19
37 Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis. Arch Neurol 2009 1.16
38 Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairs. BMC Genomics 2013 1.13
39 A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. Am J Hum Genet 2009 1.11
40 Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. Int J Alzheimers Dis 2011 1.05
41 Autism and increased paternal age related changes in global levels of gene expression regulation. PLoS One 2011 1.03
42 Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Brain Imaging Behav 2012 1.03
43 A pilot study using next-generation sequencing in advanced cancers: feasibility and challenges. PLoS One 2013 0.98
44 Paired tumor and normal whole genome sequencing of metastatic olfactory neuroblastoma. PLoS One 2012 0.95
45 Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease. Br J Haematol 2013 0.95
46 Misperceptions of peer norms as a risk factor for sugar-sweetened beverage consumption among secondary school students. J Am Diet Assoc 2010 0.94
47 SNP-based chromosomal copy number ascertainment following multiple displacement whole-genome amplification. Biotechniques 2007 0.93
48 Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Hum Mol Genet 2007 0.93
49 Induction of pluripotent stem cells from autopsy donor-derived somatic cells. Neurosci Lett 2011 0.91
50 Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite population. Am J Med Genet A 2005 0.89
51 Cerebellar telomere length and psychiatric disorders. Behav Genet 2010 0.88
52 Long insert whole genome sequencing for copy number variant and translocation detection. Nucleic Acids Res 2013 0.86
53 An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicine. Pac Symp Biocomput 2015 0.83
54 Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. Am J Med Genet B Neuropsychiatr Genet 2012 0.83
55 In vitro-differentiated neural cell cultures progress towards donor-identical brain tissue. Hum Mol Genet 2013 0.82
56 Understanding the links between privacy and public data sharing. Nat Methods 2016 0.81
57 Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis. Int J Mol Epidemiol Genet 2009 0.81
58 Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. J Neuroinflammation 2013 0.80
59 Decreased serum arylesterase activity in autism spectrum disorders. Psychiatry Res 2010 0.79
60 Microarray-based genome-wide association studies using pooled DNA. Methods Mol Biol 2011 0.78
61 Open-access synthetic spike-in mRNA-seq data for cancer gene fusions. BMC Genomics 2014 0.78
62 High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35. Birth Defects Res A Clin Mol Teratol 2006 0.78
63 Chromosomal abnormality at 6p25.1-25.3 identifies a susceptibility locus for hypothalamic hamartoma associated with epilepsy. Epilepsy Res 2007 0.78
64 No safe haven: locations of harassment and bullying victimization in middle schools. J Sch Health 2014 0.77
65 Misperception of peer weight norms and its association with overweight and underweight status among adolescents. Prev Sci 2015 0.77
66 Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome Analyzer. Methods Mol Biol 2011 0.75
67 Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer. BMC Med Genomics 2014 0.75
68 Simultaneous characterization of somatic events and HPV-18 integration in a metastatic cervical carcinoma patient using DNA and RNA sequencing. Int J Gynecol Cancer 2014 0.75
69 Statistical comparison framework and visualization scheme for ranking-based algorithms in high-throughput genome-wide studies. J Comput Biol 2009 0.75
70 The nuts and bolts of gene array technology and its application to drug abuse research. Drug Alcohol Depend 2007 0.75