Published in Hum Mol Genet on July 01, 2003
Intra-individual change over time in DNA methylation with familial clustering. JAMA (2008) 6.17
DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project. PLoS Biol (2004) 4.96
Epigenetics and assisted reproductive technology: a call for investigation. Am J Hum Genet (2004) 2.41
Allele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genome. PLoS Genet (2007) 1.71
Epigenetic variation during the adult lifespan: cross-sectional and longitudinal data on monozygotic twin pairs. Aging Cell (2012) 1.55
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer. Hum Mol Genet (2008) 1.47
Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology. PLoS Genet (2010) 1.36
C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene. J Infect Dis (2011) 1.21
Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes. PLoS One (2009) 1.14
Human imprinted chromosomal regions are historical hot-spots of recombination. PLoS Genet (2006) 1.12
DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease? BMC Med Genomics (2012) 1.11
Influence of mom and dad: quantitative genetic models for maternal effects and genomic imprinting. Genetics (2006) 1.05
Identification of the human homolog of the imprinted mouse Air non-coding RNA. Genomics (2008) 0.99
The new field of epigenomics: implications for cancer and other common disease research. Cold Spring Harb Symp Quant Biol (2004) 0.98
Effect of insulin-like growth factor gene polymorphisms alone or in interaction with diabetes on the risk of pancreatic cancer. Cancer Epidemiol Biomarkers Prev (2008) 0.97
DNA methylation at differentially methylated regions of imprinted genes is resistant to developmental programming by maternal nutrition. Epigenetics (2012) 0.97
Genetics, individuality, and medicine in the 21st century. Am J Hum Genet (2004) 0.94
The epigenetic lorax: gene-environment interactions in human health. Epigenomics (2012) 0.92
Aberrant promoter hypermethylation of PBRM1, BAP1, SETD2, KDM6A and other chromatin-modifying genes is absent or rare in clear cell RCC. Epigenetics (2013) 0.89
DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults. Clin Epigenetics (2012) 0.87
Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2. BMC Genet (2011) 0.86
DNA methylation as a mechanism of nutritional plasticity: limited support from horned beetles. J Exp Zool B Mol Dev Evol (2012) 0.84
Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors. Mamm Genome (2005) 0.83
Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking. PLoS One (2010) 0.83
Retracted Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region. Nucleic Acids Res (2006) 0.81
Bayesian model selection for characterizing genomic imprinting effects and patterns. Bioinformatics (2009) 0.79
Epithelial cancers in the post-genomic era: should we reconsider our lifestyle? Cancer Metastasis Rev (2013) 0.78
Asymmetric strand segregation: epigenetic costs of genetic fidelity? PLoS Genet (2009) 0.78
Breast cancer risk and imprinting methylation in blood. Clin Epigenetics (2015) 0.77
Quantitative genetics of genomic imprinting: a comparison of simple variance derivations, the effects of inbreeding, and response to selection. G3 (Bethesda) (2011) 0.76
Genome-wide random regression analysis for parent-of-origin effects of body composition allometries in mouse. Sci Rep (2017) 0.75
Intra-individual change over time in DNA methylation with familial clustering. JAMA (2008) 6.17
Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science (2003) 4.48
Future research directions in acute lung injury: summary of a National Heart, Lung, and Blood Institute working group. Am J Respir Crit Care Med (2003) 3.75
Identification of a herpes simplex labialis susceptibility region on human chromosome 21. J Infect Dis (2008) 2.24
DNA methylation and gene expression differences in children conceived in vitro or in vivo. Hum Mol Genet (2009) 1.92
Genetic and haplotype diversity among wild-derived mouse inbred strains. Genome Res (2004) 1.86
Community engagement and informed consent in the International HapMap project. Community Genet (2007) 1.73
Neuropathy target esterase gene mutations cause motor neuron disease. Am J Hum Genet (2008) 1.66
Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements. Hum Mol Genet (2005) 1.65
Conserved DNA methylation in Gadd45a(-/-) mice. Epigenetics (2009) 1.59
Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet (2001) 1.59
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet (2003) 1.50
Ethnicity and human genetic linkage maps. Am J Hum Genet (2004) 1.50
Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology. PLoS Genet (2010) 1.36
A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia. J Clin Invest (2005) 1.33
Fine Mapping and Identification of BMI Loci in African Americans. Am J Hum Genet (2013) 1.27
Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes (2003) 1.24
C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene. J Infect Dis (2011) 1.21
SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex. Immunogenetics (2004) 1.15
Human imprinted chromosomal regions are historical hot-spots of recombination. PLoS Genet (2006) 1.12
DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease? BMC Med Genomics (2012) 1.11
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry (2012) 1.08
Natural selection and the evolution of genome imprinting. Annu Rev Genet (2003) 1.05
A longitudinal study of X-inactivation ratio in human females. Hum Genet (2004) 1.05
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population. PLoS One (2013) 1.03
Predicting wear and blood metal ion levels in metal-on-metal hip resurfacing. J Orthop Res (2013) 1.03
Explaining inter-individual variability in phenotype: is epigenetics up to the challenge? Epigenetics (2010) 1.02
X chromosome effect on maternal recombination and meiotic drive in the mouse. Genetics (2002) 1.00
The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11. Genetics (2005) 0.99
Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation. Arch Ophthalmol (2006) 0.96
Maternal transmission ratio distortion at the mouse Om locus results from meiotic drive at the second meiotic division. Genetics (2005) 0.95
The Arg16Gly polymorphism of the beta2-adrenergic receptor and left ventricular systolic function. Am J Hypertens (2003) 0.94
Epigenetic differences in normal colon mucosa of cancer patients suggest altered dietary metabolic pathways. Cancer Prev Res (Phila) (2012) 0.94
The epigenetic lorax: gene-environment interactions in human health. Epigenomics (2012) 0.92
Hybrid vigor and transgenerational epigenetic effects on early mouse embryo phenotype. Biol Reprod (2008) 0.91
Ooplasmic donation in humans: the potential for epigenic modifications. Hum Reprod (2002) 0.91
From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project. Annu Rev Genomics Hum Genet (2008) 0.90
Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol (2013) 0.87
Genes with aberrant expression in murine preneoplastic intestine show epigenetic and expression changes in normal mucosa of colon cancer patients. Cancer Prev Res (Phila) (2013) 0.86
Setting priorities for genomic research. Science (2004) 0.86
Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth. Biol Reprod (2014) 0.85
The unfolded protein response contributes to preimplantation mouse embryo death in the DDK syndrome. Biol Reprod (2009) 0.83
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings. Invest Ophthalmol Vis Sci (2002) 0.82
PRDM9 sticks its zinc fingers into recombination hotspots and between species. F1000 Biol Rep (2010) 0.82
Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Hum Genet (2004) 0.82
Human X-chromosome inactivation pattern distributions fit a model of genetically influenced choice better than models of completely random choice. Eur J Hum Genet (2013) 0.80
Recapitulation of the ovum mutant (Om) phenotype and loss of Om locus polarity in cloned mouse embryos. Biol Reprod (2004) 0.77
Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations. Acta Diabetol (2009) 0.76
Developmental potential as a criterion for understanding and defining embryos. Conn Law Rev (2004) 0.75