PubRank

Sampath Arepalli

Author PubWeight™ 70.88‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009 10.34
2 Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. PLoS Genet 2010 8.74
3 Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010 7.87
4 Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol 2012 5.18
5 A genome-wide association study identifies protein quantitative trait loci (pQTLs). PLoS Genet 2008 4.75
6 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol 2007 3.93
7 SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol 2009 3.55
8 Distinct DNA methylation changes highly correlated with chronological age in the human brain. Hum Mol Genet 2011 2.62
9 Genome-wide association study confirms extant PD risk loci among the Dutch. Eur J Hum Genet 2011 2.12
10 A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum Mol Genet 2009 1.93
11 Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). PLoS Genet 2011 1.75
12 Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011 1.65
13 MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies. Hum Mol Genet 2012 1.58
14 Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. Brain 2012 1.50
15 Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene. Arch Neurol 2011 1.48
16 Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. Neurobiol Dis 2012 1.35
17 NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiol Aging 2014 1.32
18 Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies. Nucleic Acids Res 2013 1.25
19 Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients. Proc Natl Acad Sci U S A 2010 1.13
20 SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia. Arch Neurol 2011 0.97
21 Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study. J Neurol Sci 2005 0.93
22 Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry 2014 0.90
23 IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations. Stroke 2007 0.90
24 Assessment of Parkinson's disease risk loci in Greece. Neurobiol Aging 2013 0.84
25 APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis. J Alzheimers Dis 2011 0.82
26 Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease. Neurobiol Aging 2005 0.80
27 ABCA1 polymorphisms and Alzheimer's disease. Neurosci Lett 2007 0.79
28 Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs. BMC Med Genet 2009 0.79
29 Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? Am J Med Genet B Neuropsychiatr Genet 2008 0.77
30 A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome. Mov Disord 2014 0.75