PubRank

Michael A van Es

Author PubWeight™ 33.37‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Lancet Neurol 2010 3.61
2 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. Nat Genet 2010 2.56
3 Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen. Lancet Neurol 2008 2.54
4 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Proc Natl Acad Sci U S A 2009 2.03
5 Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. BMC Genomics 2009 1.72
6 Evidence for an oligogenic basis of amyotrophic lateral sclerosis. Hum Mol Genet 2012 1.62
7 Gene-network analysis identifies susceptibility genes related to glycobiology in autism. PLoS One 2009 1.23
8 Analysis of genome-wide copy number variation in Irish and Dutch ALS populations. Hum Mol Genet 2008 1.12
9 FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. Arch Neurol 2010 1.08
10 A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet 2010 1.06
11 Alzheimer's disease beyond APOE. Nat Genet 2009 1.02
12 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Neurobiol Aging 2012 1.02
13 Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. Hum Reprod 2009 1.01
14 A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Hum Mol Genet 2013 0.98
15 Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. PLoS One 2012 0.95
16 UNC13A is a modifier of survival in amyotrophic lateral sclerosis. Neurobiol Aging 2011 0.95
17 A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Hum Mol Genet 2010 0.92
18 VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient. Neurobiol Aging 2012 0.91
19 Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients. Neurobiol Aging 2011 0.90
20 H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis. Neurobiol Aging 2012 0.87
21 Genetic overlap between apparently sporadic motor neuron diseases. PLoS One 2012 0.84
22 Amyotrophic lateral sclerosis is not linked to multiple sclerosis in a population based study. J Neurol Neurosurg Psychiatry 2013 0.83
23 C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis. Ann Neurol 2014 0.83
24 Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3. Neurobiol Aging 2012 0.82
25 Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle. Amyotroph Lateral Scler Frontotemporal Degener 2013 0.77
26 Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients. Neurobiol Aging 2012 0.76
27 Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis. Neurobiol Aging 2010 0.76
28 Mutational analysis of TARDBP in Parkinson's disease. Neurobiol Aging 2012 0.75