| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
|
Nat Genet
|
2007
|
12.62
|
|
2
|
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
|
Nature
|
2010
|
12.27
|
|
3
|
Bayesian refinement of association signals for 14 loci in 3 common diseases.
|
Nat Genet
|
2012
|
3.31
|
|
4
|
Associations with early-life socio-economic position in adult DNA methylation.
|
Int J Epidemiol
|
2011
|
2.67
|
|
5
|
The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study.
|
J Allergy Clin Immunol
|
2008
|
2.53
|
|
6
|
Transgenerational response to nutrition, early life circumstances and longevity.
|
Eur J Hum Genet
|
2007
|
2.27
|
|
7
|
Genetic information and testing in insurance and employment: technical, social and ethical issues.
|
Eur J Hum Genet
|
2003
|
1.45
|
|
8
|
The search for genenotype/phenotype associations and the phenome scan.
|
Paediatr Perinat Epidemiol
|
2005
|
1.38
|
|
9
|
Transgenerational epigenetic inheritance: how important is it?
|
Nat Rev Genet
|
2013
|
1.32
|
|
10
|
Prevalence of mitochondrial 1555A-->G mutation in European children.
|
N Engl J Med
|
2009
|
1.32
|
|
11
|
Parental and grandparental ages in the autistic spectrum disorders: a birth cohort study.
|
PLoS One
|
2010
|
1.23
|
|
12
|
Contribution of variants in the small heterodimer partner gene to birthweight, adiposity, and insulin levels: mutational analysis and association studies in multiple populations.
|
Diabetes
|
2003
|
1.01
|
|
13
|
Childhood abuse is associated with methylation of multiple loci in adult DNA.
|
BMC Med Genomics
|
2014
|
0.95
|
|
14
|
Differences between blood donors and a population sample: implications for case-control studies.
|
Int J Epidemiol
|
2013
|
0.87
|
|
15
|
Prevalence and audiological features in carriers of GJB2 mutations, c.35delG and c.101T>C (p.M34T), in a UK population study.
|
BMJ Open
|
2012
|
0.86
|
|
16
|
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3].
|
Am J Med Genet
|
2002
|
0.82
|
|
17
|
Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome.
|
Eur J Hum Genet
|
2003
|
0.80
|
|
18
|
The anthropometry of children and adolescents may be influenced by the prenatal smoking habits of their grandmothers: a longitudinal cohort study.
|
Am J Hum Biol
|
2014
|
0.79
|
|
19
|
The insulin gene variable number of tandem repeat: associations and interactions with childhood body fat mass and insulin secretion in normal children.
|
J Clin Endocrinol Metab
|
2006
|
0.79
|
|
20
|
Jean Golding and Paediatric and Perinatal Epidemiology: practising what she preaches.
|
Paediatr Perinat Epidemiol
|
2012
|
0.75
|