Published in Behav Genet on January 10, 2006
Age-related decline in brain resources modulates genetic effects on cognitive functioning. Front Neurosci (2008) 1.33
A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. Mol Psychiatry (2012) 1.22
The effects of cholesterol on learning and memory. Neurosci Biobehav Rev (2010) 1.05
Endophenotypes in normal brain morphology and Alzheimer's disease: a review. Neuroscience (2009) 1.02
Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia. J Alzheimers Dis (2010) 0.93
Apolipoprotein E epsilon4 influences on episodic recall and brain structures in aging pilots. Neurobiol Aging (2008) 0.89
Age-related and depot-specific changes in white adipose tissue of growth hormone receptor-null mice. J Gerontol A Biol Sci Med Sci (2013) 0.84
Both odor identification and ApoE-ε4 contribute to normative cognitive aging. Psychol Aging (2011) 0.82
Influences of APOE ε4 and expertise on performance of older pilots. Psychol Aging (2011) 0.81
Use of genetic variation as biomarkers for Alzheimer's disease. Ann N Y Acad Sci (2009) 0.79
Effects of epsilon4 on object recognition in the non-demented elderly. Curr Aging Sci (2010) 0.77
A meta-analysis of heritability of cognitive aging: minding the "missing heritability" gap. Neuropsychol Rev (2015) 0.76
Gene-Environment Interplay in Physical, Psychological, and Cognitive Domains in Mid to Late Adulthood: Is APOE a Variability Gene? Behav Genet (2015) 0.75
Global variation in copy number in the human genome. Nature (2006) 57.50
Detection of large-scale variation in the human genome. Nat Genet (2004) 49.18
The diploid genome sequence of an individual human. PLoS Biol (2007) 44.80
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Origins and functional impact of copy number variation in the human genome. Nature (2009) 23.63
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet (2008) 15.51
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet (2010) 13.70
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27
Prepublication data sharing. Nature (2009) 12.24
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Copy number variation: new insights in genome diversity. Genome Res (2006) 8.66
Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet (2012) 7.59
Integrative annotation of 21,037 human genes validated by full-length cDNA clones. PLoS Biol (2004) 7.17
Genome assembly comparison identifies structural variants in the human genome. Nat Genet (2006) 6.93
Role of genes and environments for explaining Alzheimer disease. Arch Gen Psychiatry (2006) 6.68
Heritability of adult body height: a comparative study of twin cohorts in eight countries. Twin Res (2003) 6.43
Air pollution and lung cancer incidence in 17 European cohorts: prospective analyses from the European Study of Cohorts for Air Pollution Effects (ESCAPE). Lancet Oncol (2013) 6.12
Challenges and standards in integrating surveys of structural variation. Nat Genet (2007) 6.05
Complex SNP-related sequence variation in segmental genome duplications. Nat Genet (2004) 5.90
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. Am J Hum Genet (2008) 5.53
Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res (2006) 5.50
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet (2012) 4.73
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma. Nat Genet (2009) 4.52
The Database of Genomic Variants: a curated collection of structural variation in the human genome. Nucleic Acids Res (2013) 4.42
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat Genet (2012) 4.37
Locus Reference Genomic sequences: an improved basis for describing human DNA variants. Genome Med (2010) 4.19
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet (2014) 4.13
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes (2010) 4.07
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet (2002) 4.03
Personality and major depression: a Swedish longitudinal, population-based twin study. Arch Gen Psychiatry (2006) 3.94
Public data archives for genomic structural variation. Nat Genet (2010) 3.92
Copy-number variation in control population cohorts. Hum Mol Genet (2007) 3.88
Identification of seven loci affecting mean telomere length and their association with disease. Nat Genet (2013) 3.87
New models for large prospective studies: is there a better way? Am J Epidemiol (2012) 3.85
Effect of low doses of ionising radiation in infancy on cognitive function in adulthood: Swedish population based cohort study. BMJ (2004) 3.67
The Swedish Twin Registry in the third millennium: an update. Twin Res Hum Genet (2006) 3.58
Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci. PLoS Genet (2007) 3.47
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet (2010) 3.37
Genetic influence on human lifespan and longevity. Hum Genet (2006) 3.27
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat Biotechnol (2011) 3.25
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Depression in older adults. Annu Rev Clin Psychol (2009) 3.07
A Swedish national twin study of lifetime major depression. Am J Psychiatry (2006) 3.06
Geographical structure and differential natural selection among North European populations. Genome Res (2009) 3.03
Prevalence, heritability, and prospective risk factors for anorexia nervosa. Arch Gen Psychiatry (2006) 3.02
Cancer as a risk factor for long-term cognitive deficits and dementia. J Natl Cancer Inst (2005) 3.02
Telomere length predicts survival independent of genetic influences. Aging Cell (2007) 3.01
Genetic variation in the vasopressin receptor 1a gene (AVPR1A) associates with pair-bonding behavior in humans. Proc Natl Acad Sci U S A (2008) 2.97
Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet (2013) 2.92
Cardiovascular fitness in males at age 18 and risk of serious depression in adulthood: Swedish prospective population-based study. Br J Psychiatry (2012) 2.86
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet (2013) 2.83
The genome-wide patterns of variation expose significant substructure in a founder population. Am J Hum Genet (2008) 2.79
Towards a comprehensive structural variation map of an individual human genome. Genome Biol (2010) 2.79
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain. Nat Struct Mol Biol (2011) 2.73
Cardiovascular diseases and risk of hip fracture. JAMA (2009) 2.69
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies. Int J Epidemiol (2010) 2.44
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction. Nat Genet (2005) 2.32
Global and unbiased detection of splice junctions from RNA-seq data. Genome Biol (2010) 2.32
Strategies and issues in the detection of pathway enrichment in genome-wide association studies. Hum Genet (2009) 2.31
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome. Proc Natl Acad Sci U S A (2008) 2.22
Age-related somatic structural changes in the nuclear genome of human blood cells. Am J Hum Genet (2012) 2.15
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet (2012) 2.12
Polymorphisms associated with asthma are inversely related to glioblastoma multiforme. Cancer Res (2005) 2.11
No evidence for heritability of Parkinson disease in Swedish twins. Neurology (2004) 2.10
Genetic and environmental influences on mothering of adolescents: a comparison of two samples. Dev Psychol (2004) 1.99
The sources of co-morbidity between major depression and generalized anxiety disorder in a Swedish national twin sample. Psychol Med (2006) 1.93
HGVbaseG2P: a central genetic association database. Nucleic Acids Res (2008) 1.90
Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. Biol Psychiatry (2011) 1.89
Genetic liability to fractures in the elderly. Arch Intern Med (2005) 1.88
Genome-wide association study of smoking initiation and current smoking. Am J Hum Genet (2009) 1.87
Complete ascertainment of dementia in the Swedish Twin Registry: the HARMONY study. Neurobiol Aging (2005) 1.85
Likelihood ratio tests in behavioral genetics: problems and solutions. Behav Genet (2006) 1.80
Quantitative genetic analysis of latent growth curve models of cognitive abilities in adulthood. Dev Psychol (2005) 1.79
Systems medicine and integrated care to combat chronic noncommunicable diseases. Genome Med (2011) 1.78
How heritable is Alzheimer's disease late in life? Findings from Swedish twins. Ann Neurol (2004) 1.77
Gastroesophageal reflux disease in monozygotic and dizygotic twins. Gastroenterology (2002) 1.76
Linkage disequilibrium patterns vary substantially among populations. Eur J Hum Genet (2005) 1.73
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet (2013) 1.72
A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One (2012) 1.72
Treatment of generalized anxiety disorder in older adults. J Consult Clin Psychol (2003) 1.71
Comorbid type 2 diabetes mellitus and hypertension exacerbates cognitive decline: evidence from a longitudinal study. Age Ageing (2004) 1.71
Genetic influences on exercise participation in 37,051 twin pairs from seven countries. PLoS One (2006) 1.71
Obesity and hormone-dependent tumors: cohort and co-twin control studies based on the Swedish Twin Registry. Int J Cancer (2003) 1.71
Depression as a risk factor or prodromal feature for dementia? Findings in a population-based sample of Swedish twins. Psychol Aging (2009) 1.70
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A (2006) 1.70
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Med (2013) 1.70