Dale J Hedges

Author PubWeight™ 46.47‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Age at onset in two common neurodegenerative diseases is genetically controlled. Am J Hum Genet 2002 2.90
2 Mammalian non-LTR retrotransposons: for better or worse, in sickness and in health. Genome Res 2008 2.83
3 SVA elements: a hominid-specific retroposon family. J Mol Biol 2005 2.39
4 A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Ann Hum Genet 2009 2.15
5 Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat Rev Cardiol 2013 2.09
6 LINE-1 RNA splicing and influences on mammalian gene expression. Nucleic Acids Res 2006 1.94
7 Estimating the retrotransposition rate of human Alu elements. Gene 2006 1.85
8 Alu elements and hominid phylogenetics. Proc Natl Acad Sci U S A 2003 1.81
9 Active Alu element "A-tails": size does matter. Genome Res 2002 1.79
10 Retrotransposition of Alu elements: how many sources? Trends Genet 2004 1.73
11 Reconstructing the population genetic history of the Caribbean. PLoS Genet 2013 1.68
12 Alu insertion loci and platyrrhine primate phylogeny. Mol Phylogenet Evol 2005 1.49
13 Alu element mutation spectra: molecular clocks and the effect of DNA methylation. J Mol Biol 2004 1.41
14 Genome-wide analysis of the human Alu Yb-lineage. Hum Genomics 2004 1.33
15 Under the genomic radar: the stealth model of Alu amplification. Genome Res 2005 1.31
16 Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet 2013 1.30
17 Diverse cis factors controlling Alu retrotransposition: what causes Alu elements to die? Genome Res 2009 1.26
18 Different evolutionary fates of recently integrated human and chimpanzee LINE-1 retrotransposons. Gene 2006 1.26
19 Multiplex polymerase chain reaction for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA: application in human identification. Anal Biochem 2005 1.17
20 Analysis of the human Alu Ya-lineage. J Mol Biol 2004 1.12
21 Alu repeats increase local recombination rates. BMC Genomics 2009 1.11
22 Identification of repeat structure in large genomes using repeat probability clouds. Anal Biochem 2008 1.07
23 Comprehensive analysis of two Alu Yd subfamilies. J Mol Evol 2003 1.06
24 Analysis of the human Alu Ye lineage. BMC Evol Biol 2005 1.03
25 Characterization of pre-insertion loci of de novo L1 insertions. Gene 2006 1.01
26 Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily. Hum Mutat 2009 0.98
27 Quantitative PCR for DNA identification based on genome-specific interspersed repetitive elements. Genomics 2004 0.97
28 Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays. Anal Biochem 2008 0.96
29 Comprehensive analysis of Alu-associated diversity on the human sex chromosomes. Gene 2003 0.95
30 An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males. Mol Autism 2011 0.92
31 Rescuing Alu: recovery of new inserts shows LINE-1 preserves Alu activity through A-tail expansion. PLoS Genet 2012 0.88
32 Chompy: an infestation of MITE-like repetitive elements in the crocodilian genome. Gene 2005 0.83
33 Evaluating mitochondrial DNA variation in autism spectrum disorders. Ann Hum Genet 2012 0.79
34 Resolution of mixed human DNA samples using mitochondrial DNA sequence variants. Anal Biochem 2004 0.78