PubRank

Naomi R Wray

Author PubWeight™ 137.23‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009 33.26
2 Heritability in the genomics era--concepts and misconceptions. Nat Rev Genet 2008 13.42
3 Estimating missing heritability for disease from genome-wide association studies. Am J Hum Genet 2011 8.95
4 A versatile gene-based test for genome-wide association studies. Am J Hum Genet 2010 8.44
5 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
6 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 7.44
7 A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 2012 6.34
8 Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet 2012 5.78
9 Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Hum Mol Genet 2009 3.53
10 Comparing apples and oranges: equating the power of case-control and quantitative trait association studies. Genet Epidemiol 2010 2.13
11 Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet 2012 1.96
12 Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet 2013 1.68
13 Estimation of SNP heritability from dense genotype data. Am J Hum Genet 2013 1.64
14 A better coefficient of determination for genetic profile analysis. Genet Epidemiol 2012 1.63
15 Estimation and partition of heritability in human populations using whole-genome analysis methods. Annu Rev Genet 2013 1.41
16 Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder. J Clin Psychiatry 2015 1.40
17 Translation elongation factor eEF1A2 is a potential oncoprotein that is overexpressed in two-thirds of breast tumours. BMC Cancer 2005 1.33
18 A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. Am J Psychiatry 2011 1.32
19 Sporadic cases are the norm for complex disease. Eur J Hum Genet 2009 1.31
20 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. Eur J Hum Genet 2010 1.27
21 Underestimated effect sizes in GWAS: fundamental limitations of single SNP analysis for dichotomous phenotypes. PLoS One 2011 1.19
22 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. Biol Psychol 2010 1.12
23 Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nat Genet 2013 1.10
24 Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. Am J Hum Genet 2013 1.07
25 Genetic and environmental influences on the co-morbidity between depression, panic disorder, agoraphobia, and social phobia: a twin study. Depress Anxiety 2009 1.07
26 Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy. PLoS One 2013 1.02
27 Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia. Schizophr Bull 2013 1.01
28 A genome-wide association study of sleep habits and insomnia. Am J Med Genet B Neuropsychiatr Genet 2013 0.98
29 Genetic differences between five European populations. Hum Hered 2010 0.98
30 Shared temperament risk factors for anorexia nervosa: a twin study. Psychosom Med 2007 0.95
31 Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PLoS One 2012 0.94
32 New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol 2015 0.93
33 Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample. Am J Med Genet B Neuropsychiatr Genet 2010 0.92
34 Sex differences in symptoms of depression in unrelated individuals and opposite-sex twin and sibling pairs. Twin Res Hum Genet 2006 0.91
35 A recessive genetic model and runs of homozygosity in major depressive disorder. Am J Med Genet B Neuropsychiatr Genet 2014 0.91
36 Empirical evaluation of the genetic similarity of samples from twin registries in Australia and the Netherlands using 359 STRP markers. Twin Res Hum Genet 2006 0.89
37 Epigenetic Signatures of Cigarette Smoking. Circ Cardiovasc Genet 2016 0.88
38 Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One 2013 0.88
39 Hypermethylation in the ZBTB20 gene is associated with major depressive disorder. Genome Biol 2014 0.88
40 NFIB-mediated repression of the epigenetic factor Ezh2 regulates cortical development. J Neurosci 2014 0.87
41 Overlap of expression quantitative trait loci (eQTL) in human brain and blood. BMC Med Genomics 2014 0.87
42 Research review: the role of cytokines in depression in adolescents: a systematic review. J Child Psychol Psychiatry 2013 0.87
43 Response to Amar J. Klar: The chromosome 1;11 translocation provides the best evidence supporting genetic etiology for schizophrenia and bipolar affective disorders. Genetics 2003 0.86
44 Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression. Am J Med Genet B Neuropsychiatr Genet 2009 0.86
45 Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorder. Biol Psychiatry 2006 0.85
46 Testing the role of circadian genes in conferring risk for psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet 2014 0.84
47 Applying polygenic risk scores to postpartum depression. Arch Womens Ment Health 2014 0.82
48 Glutamate cysteine ligase (GCL) and self reported depression: an association study from the HUNT. J Affect Disord 2011 0.82
49 A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability. Am J Med Genet B Neuropsychiatr Genet 2013 0.81
50 Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits. PLoS One 2013 0.81
51 Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. Eur J Hum Genet 2012 0.78
52 Conventional multipoint nonparametric linkage analysis is not necessarily inherently biased. Am J Hum Genet 2004 0.77
53 Phenotypic and discordant-monozygotic analyses of stress and perceived social support as antecedents to or sequelae of risk for depression. Twin Res Hum Genet 2009 0.75
54 Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Sci Transl Med 2022 0.75
55 Concepts and Misconceptions about the Polygenic Additive Model Applied to Disease. Hum Hered 2016 0.75
56 The epigenetic clock and telomere length are independently associated with chronological age and mortality. Int J Epidemiol 2017 0.75