PubRank

Ronald J Trent

Author PubWeight™ 25.95‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Melanesian and Asian origins of Polynesians: mtDNA and Y chromosome gradients across the Pacific. Mol Biol Evol 2006 2.98
2 Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians. Am J Hum Genet 2008 2.02
3 Demographic history of Oceania inferred from genome-wide data. Curr Biol 2010 1.93
4 The impact of the Austronesian expansion: evidence from mtDNA and Y chromosome diversity in the Admiralty Islands of Melanesia. Mol Biol Evol 2008 1.41
5 The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes. Hum Genet 2005 1.29
6 A gene-environment study of the paraoxonase 1 gene and pesticides in amyotrophic lateral sclerosis. Neurotoxicology 2006 1.25
7 Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. Am J Hum Genet 2012 1.05
8 Genetic susceptibility to environmental toxicants in ALS. Am J Med Genet B Neuropsychiatr Genet 2007 1.05
9 A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2009 0.95
10 Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study. Neuroreport 2012 0.95
11 Patterns of DNA mutations and ALK rearrangement in resected node negative lung adenocarcinoma. J Thorac Oncol 2013 0.93
12 Identification of a candidate genetic variant for the high prevalence of type II diabetes in Polynesians. Eur J Hum Genet 2007 0.92
13 A polymorphism in the poliovirus receptor gene differs in motor neuron disease. Neuroreport 2004 0.87
14 Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis. Neuromuscul Disord 2009 0.86
15 Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset. Hum Genet 2012 0.83
16 Diagnostic validation of a familial hypercholesterolaemia cohort provides a model for using targeted next generation DNA sequencing in the clinical setting. Pathology 2014 0.81
17 Are metallothionein genes silenced in ALS? Toxicol Lett 2006 0.81
18 An analysis of the entire SOD1 gene in sporadic ALS. Neuromuscul Disord 2008 0.81
19 TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochem Biophys Res Commun 2012 0.81
20 Altered immunoglobulin expression and functional silencing of self-reactive B lymphocytes in transgenic mice. J Immunol 2009 0.80
21 Molecular characterisation of neonatal cardiac hypertrophy and its regression. Cardiol Young 2004 0.78
22 Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics 2013 0.77
23 DHPLC can be used to detect low-level mutations in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2010 0.77
24 Can ALS-associated C9orf72 repeat expansions be diagnosed on a blood DNA test alone? PLoS One 2013 0.75
25 Screening the metallothionein III gene in sporadic amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2005 0.75