Published in PLoS One on December 12, 2007
Genome-wide DNA methylation profiling reveals novel epigenetically regulated genes and non-coding RNAs in human testicular cancer. Br J Cancer (2010) 1.86
Endonuclease-sensitive regions of human spermatozoal chromatin are highly enriched in promoter and CTCF binding sequences. Genome Res (2009) 1.79
DNA methylation profiles of ovarian epithelial carcinoma tumors and cell lines. PLoS One (2010) 1.65
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders. PLoS One (2012) 1.64
Array-based DNA methylation profiling in follicular lymphoma. Leukemia (2009) 1.63
Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men. Eur J Hum Genet (2010) 1.48
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Epigenetics meets endocrinology. J Mol Endocrinol (2011) 1.30
Oxidative DNA damage impairs global sperm DNA methylation in infertile men. J Assist Reprod Genet (2009) 1.25
Novel insights into DNA methylation features in spermatozoa: stability and peculiarities. PLoS One (2012) 1.16
Integrative DNA methylation and gene expression analyses identify DNA packaging and epigenetic regulatory genes associated with low motility sperm. PLoS One (2011) 1.13
Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm. Hum Reprod (2010) 1.12
Assisted reproduction treatment and epigenetic inheritance. Hum Reprod Update (2012) 1.11
Identification of preferential target sites for human DNA methyltransferases. Nucleic Acids Res (2010) 1.06
Idiopathic male infertility is strongly associated with aberrant promoter methylation of methylenetetrahydrofolate reductase (MTHFR). PLoS One (2010) 1.04
Analysing the sperm epigenome: roles in early embryogenesis and assisted reproduction. Nat Rev Urol (2012) 0.97
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Environmentally induced epigenetic transgenerational inheritance of male infertility. Curr Opin Genet Dev (2014) 0.95
Human endometrial DNA methylome is cycle-dependent and is associated with gene expression regulation. Mol Endocrinol (2014) 0.92
Integrating the multiple dimensions of genomic and epigenomic landscapes of cancer. Cancer Metastasis Rev (2010) 0.90
Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives. Asian J Androl (2014) 0.88
Epigenetic regulation of the RHOX homeobox gene cluster and its association with human male infertility. Hum Mol Genet (2013) 0.87
Elevated levels of DNA methylation at the OPRM1 promoter in blood and sperm from male opioid addicts. J Opioid Manag (2011) 0.87
Imprinting methylation errors in ART. Reprod Med Biol (2014) 0.84
Epigenetic regulatory mechanisms associated with infertility. Obstet Gynecol Int (2010) 0.83
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health. Clin Epigenetics (2015) 0.83
Variable imprinting of the MEST gene in human preimplantation embryos. Eur J Hum Genet (2012) 0.82
Male-mediated developmental toxicity. Asian J Androl (2013) 0.81
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Male reprotoxicity and endocrine disruption. EXS (2012) 0.80
Biomarkers of chemotherapy-induced testicular damage. Fertil Steril (2013) 0.80
Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring. Reprod Biol Endocrinol (2015) 0.80
Toxoplasma gondii decreases the reproductive fitness in mice. PLoS One (2014) 0.80
Genome-wide promoter methylation profile of human testis and epididymis: identified from cell-free seminal DNA. BMC Genomics (2013) 0.79
Male reproductive cancers and infertility: a mutual relationship. Int J Mol Sci (2015) 0.79
Broad DNA methylation changes of spermatogenesis, inflammation and immune response-related genes in a subgroup of sperm samples for assisted reproduction. Andrology (2013) 0.79
DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcription. PLoS One (2011) 0.78
A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART). J Assist Reprod Genet (2014) 0.76
Repeated assessment by high-throughput assay demonstrates that sperm DNA methylation levels are highly reproducible. Fertil Steril (2011) 0.76
Integrative DNA methylation and gene expression analysis identifies discoidin domain receptor 1 association with idiopathic nonobstructive azoospermia. Fertil Steril (2014) 0.76
Stability of the human sperm DNA methylome to folic acid fortification and short-term supplementation. Hum Reprod (2016) 0.75
DNA methylation in spermatogenesis and male infertility. Exp Ther Med (2016) 0.75
Different Levels of DNA Methylation Detected in Human Sperms after Morphological Selection Using High Magnification Microscopy. Biomed Res Int (2016) 0.75
Potential Role of Methylation Marker in Glioma Supporting Clinical Decisions. Int J Mol Sci (2016) 0.75
From the Cover: Sperm Molecular Biomarkers Are Sensitive Indicators of Testicular Injury following Subchronic Model Toxicant Exposure. Toxicol Sci (2016) 0.75
Factors associated with aberrant imprint methylation and oligozoospermia. Sci Rep (2017) 0.75
Comparison of in vitro fertilization outcomes in ICSI cycles after human sperm preparation by density gradient centrifugation and direct micro swim-up without centrifugation. JBRA Assist Reprod (2017) 0.75
Rapid method for the isolation of mammalian sperm DNA. Biotechniques (2015) 0.75
Global methylation status of sperm DNA in carriers of chromosome structural aberrations. Asian J Androl (2016) 0.75
The role of epigenetics in idiopathic male infertility. J Assist Reprod Genet (2016) 0.75
Non-Invasive Approaches to Epigenetic-Based Sperm Selection. Med Sci Monit (2017) 0.75
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Genetic and epigenetic regulators of pluripotency. Cell (2007) 7.47
Epigenetic reprogramming in mouse primordial germ cells. Mech Dev (2002) 6.67
A molecular programme for the specification of germ cell fate in mice. Nature (2002) 5.67
Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops. Nat Genet (2004) 5.47
Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse. Genesis (2003) 5.19
Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission. Proc Natl Acad Sci U S A (2003) 4.70
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet (2003) 4.25
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat Genet (1994) 4.04
Sperm morphology, motility, and concentration in fertile and infertile men. N Engl J Med (2001) 3.97
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Allele-specific expression of imprinted genes in mouse migratory primordial germ cells. Mech Dev (2002) 3.30
Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2. Cancer Res (2002) 3.21
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Hum Mol Genet (2001) 3.07
Incidence and main causes of infertility in a resident population (1,850,000) of three French regions (1988-1989). Hum Reprod (1991) 2.98
Retracted Transgenerational epigenetic imprinting of the male germline by endocrine disruptor exposure during gonadal sex determination. Endocrinology (2006) 2.93
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Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells. Development (2002) 2.55
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Epigenetic decisions in mammalian germ cells. Science (2007) 1.88
Timing of establishment of paternal methylation imprints in the mouse. Genomics (2004) 1.84
Gene expression dynamics during germline specification in mice identified by quantitative single-cell gene expression profiling. Biol Reprod (2006) 1.78
Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS. J Clin Invest (2003) 1.77
Reprogramming of primordial germ cells begins before migration into the genital ridge, making these cells inadequate donors for reproductive cloning. Proc Natl Acad Sci U S A (2003) 1.73
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Retrotransposon silencing by DNA methylation can drive mammalian genomic imprinting. PLoS Genet (2007) 1.70
Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib. Nat Genet (2004) 1.68
A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. Genomics (2001) 1.64
Genomic imprinting in disruptive spermatogenesis. Lancet (2004) 1.62
Methylation dynamics of repetitive DNA elements in the mouse germ cell lineage. Genomics (2003) 1.58
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region. Genomics (2000) 1.51
A unique configuration of genome-wide DNA methylation patterns in the testis. Proc Natl Acad Sci U S A (2006) 1.46
Establishment of male-specific epigenetic information. Gene (2005) 1.42
Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis. Hum Mol Genet (2000) 1.40
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour. Br J Cancer (2005) 1.39
Gamete imprinting: setting epigenetic patterns for the next generation. Reprod Fertil Dev (2006) 1.36
Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB. Hum Mol Genet (2004) 1.26
Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome. Eur J Hum Genet (2001) 1.25
Relaxation of IGF2 imprinting in Wilms tumours associated with specific changes in IGF2 methylation. Oncogene (1999) 1.25
YY1 as a controlling factor for the Peg3 and Gnas imprinted domains. Genomics (2006) 1.23
Transposon silencing and imprint establishment in mammalian germ cells. Cold Spring Harb Symp Quant Biol (2004) 1.17
Retracted Androgen activates PEG10 to promote carcinogenesis in hepatic cancer cells. Oncogene (2007) 1.08
Influence of global sperm DNA methylation on IVF results. Hum Reprod (2005) 1.08
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Structural characterization of Rasgrf1 and a novel linked imprinted locus. Gene (2002) 1.07
Complex patterns of inheritance of an imprinted murine transgene suggest incomplete germline erasure. Nucleic Acids Res (2000) 1.07
Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus. J Biol Chem (2001) 1.05
Developmental changes in methylation of spermatogenesis-specific genes include reprogramming in the epididymis. Nat Genet (1994) 1.03
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. Hum Genet (2004) 1.00
Effect of transient embryonic in vivo exposure to the endocrine disruptor methoxychlor on embryonic and postnatal testis development. J Androl (2003) 0.99
A CTCF-binding silencer regulates the imprinted genes AWT1 and WT1-AS and exhibits sequential epigenetic defects during Wilms' tumourigenesis. Hum Mol Genet (2007) 0.97
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Evaluation of a large cohort of men presenting for a screening semen analysis. Fertil Steril (2000) 0.92
Genetic imprinting during impaired spermatogenesis. Mol Hum Reprod (2006) 0.91
Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior. Genomics (2001) 0.90
The human Y chromosome and male infertility. Results Probl Cell Differ (2000) 0.88
The effect of epigenetic sperm abnormalities on early embryogenesis. Asian J Androl (2006) 0.88
Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer. Cytogenet Genome Res (2006) 0.84
Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI). Int J Androl (2001) 0.81
Allele-specific methylation at the promoter-associated CpG island of mouse Copg2. Mamm Genome (2003) 0.79
Genes and male infertility: what can go wrong? J Androl (2003) 0.77
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med (2013) 19.87
Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. Cancer Cell (2010) 16.12
Integrated genomic characterization of endometrial carcinoma. Nature (2013) 14.29
CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet (2006) 13.63
The somatic genomic landscape of glioblastoma. Cell (2013) 11.73
Absolute quantification of somatic DNA alterations in human cancer. Nat Biotechnol (2012) 10.87
Epigenetic stem cell signature in cancer. Nat Genet (2006) 9.62
Pan-cancer patterns of somatic copy number alteration. Nat Genet (2013) 7.73
Analysis of repetitive element DNA methylation by MethyLight. Nucleic Acids Res (2005) 6.49
Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer. Genome Res (2010) 6.03
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas. N Engl J Med (2015) 5.71
Regions of focal DNA hypermethylation and long-range hypomethylation in colorectal cancer coincide with nuclear lamina-associated domains. Nat Genet (2011) 5.70
Genome-scale analysis of aberrant DNA methylation in colorectal cancer. Genome Res (2011) 4.84
Precision and performance characteristics of bisulfite conversion and real-time PCR (MethyLight) for quantitative DNA methylation analysis. J Mol Diagn (2006) 4.68
Prenatal tobacco smoke exposure affects global and gene-specific DNA methylation. Am J Respir Crit Care Med (2009) 4.44
Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage. Nat Biotechnol (2011) 3.97
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet (2010) 3.93
Survival and development of neonatal rat cardiomyocytes transplanted into adult myocardium. J Mol Cell Cardiol (2002) 3.79
Cooperativity between DNA methyltransferases in the maintenance methylation of repetitive elements. Mol Cell Biol (2002) 3.61
DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons. PLoS One (2007) 3.30
Association of breast cancer DNA methylation profiles with hormone receptor status and response to tamoxifen. Cancer Res (2004) 3.23
Interplay between the cancer genome and epigenome. Cell (2013) 3.05
Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma. N Engl J Med (2015) 3.00
Inferring tumour purity and stromal and immune cell admixture from expression data. Nat Commun (2013) 2.94
Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns. Hum Mol Genet (2009) 2.85
Cigarette smoking and colorectal cancer risk by molecularly defined subtypes. J Natl Cancer Inst (2010) 2.38
Population-based case-control study of recreational drug use and testis cancer risk confirms an association between marijuana use and nonseminoma risk. Cancer (2012) 2.33
Low-level processing of Illumina Infinium DNA Methylation BeadArrays. Nucleic Acids Res (2013) 2.19
Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening. Cancer Epidemiol Biomarkers Prev (2008) 2.12
Long-term epigenetic therapy with oral zebularine has minimal side effects and prevents intestinal tumors in mice. Cancer Prev Res (Phila) (2008) 2.04
DNA methylation as a biomarker for cardiovascular disease risk. PLoS One (2010) 2.04
Bis-SNP: combined DNA methylation and SNP calling for Bisulfite-seq data. Genome Biol (2012) 2.02
Null association between histology of first and second primary malignancies in men with bilateral testicular germ cell tumors. Am J Epidemiol (2013) 2.00
Breast cancer DNA methylation profiles in cancer cells and tumor stroma: association with HER-2/neu status in primary breast cancer. Cancer Res (2006) 1.99
Epigenetic analysis of KSHV latent and lytic genomes. PLoS Pathog (2010) 1.94
A comparison of cluster analysis methods using DNA methylation data. Bioinformatics (2004) 1.94
Analysis of the association between CIMP and BRAF in colorectal cancer by DNA methylation profiling. PLoS One (2009) 1.90
DNA hypomethylation and ovarian cancer biology. Cancer Res (2004) 1.75
Meta-analysis identifies four new loci associated with testicular germ cell tumor. Nat Genet (2013) 1.74
Complete genetic suppression of polyp formation and reduction of CpG-island hypermethylation in Apc(Min/+) Dnmt1-hypomorphic Mice. Cancer Res (2002) 1.73
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer. Nat Commun (2013) 1.73
The landscape of microsatellite instability in colorectal and endometrial cancer genomes. Cell (2013) 1.68
DNA methylation profiles of ovarian epithelial carcinoma tumors and cell lines. PLoS One (2010) 1.65
Sensitive detection of DNA methylation. Ann N Y Acad Sci (2003) 1.65
Hypomethylation and hypermethylation of DNA in Wilms tumors. Oncogene (2002) 1.59
Role of methionine adenosyltransferase 2A and S-adenosylmethionine in mitogen-induced growth of human colon cancer cells. Gastroenterology (2007) 1.56
Smad3 deficiency promotes tumorigenesis in the distal colon of ApcMin/+ mice. Cancer Res (2006) 1.52
Combination of molecular alterations and smoking intensity predicts bladder cancer outcome: a report from the Los Angeles Cancer Surveillance Program. Cancer (2013) 1.51
Vitamin C promotes widespread yet specific DNA demethylation of the epigenome in human embryonic stem cells. Stem Cells (2010) 1.50
Shorter androgen receptor CAG repeat lengths associated with cryptorchidism risk among Hispanic white boys. J Clin Endocrinol Metab (2011) 1.50
Unique DNA methylation patterns distinguish noninvasive and invasive urothelial cancers and establish an epigenetic field defect in premalignant tissue. Cancer Res (2010) 1.47
Environmental epigenetics: prospects for studying epigenetic mediation of exposure-response relationships. Hum Genet (2012) 1.47
Discovery of multi-dimensional modules by integrative analysis of cancer genomic data. Nucleic Acids Res (2012) 1.46
MethyLight. Methods Mol Biol (2009) 1.45
Dietary sources of N-nitroso compounds and bladder cancer risk: findings from the Los Angeles bladder cancer study. Int J Cancer (2013) 1.45
Alterations of immune response of Non-Small Cell Lung Cancer with Azacytidine. Oncotarget (2013) 1.44
Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer. Cancer Res (2009) 1.43
The Influence of Screening for Precancerous Lesions on Family-Based Genetic Association Tests: An Example of Colorectal Polyps and Cancer. Am J Epidemiol (2015) 1.42
DNA methylation analysis by digital bisulfite genomic sequencing and digital MethyLight. Nucleic Acids Res (2008) 1.42
An epidemiologic and genomic investigation into the obesity paradox in renal cell carcinoma. J Natl Cancer Inst (2013) 1.42
Hierarchical clustering of lung cancer cell lines using DNA methylation markers. Cancer Epidemiol Biomarkers Prev (2002) 1.38
Distinct methylation profiles of glioma subtypes. Int J Cancer (2003) 1.38
Kaiso contributes to DNA methylation-dependent silencing of tumor suppressor genes in colon cancer cell lines. Cancer Res (2008) 1.36
Sex differential in methylation patterns of selected genes in Singapore Chinese. Hum Genet (2005) 1.35
DNA methylation profiles of gastric carcinoma characterized by quantitative DNA methylation analysis. Lab Invest (2007) 1.34
Genome-wide association study identifies multiple loci associated with bladder cancer risk. Hum Mol Genet (2013) 1.34
Rebuilding a damaged heart: long-term survival of transplanted neonatal rat cardiomyocytes after myocardial infarction and effect on cardiac function. Circulation (2002) 1.32
Correlation of pathologic features with CpG island methylator phenotype (CIMP) by quantitative DNA methylation analysis in colorectal carcinoma. Am J Surg Pathol (2006) 1.29
Identification of a panel of sensitive and specific DNA methylation markers for squamous cell lung cancer. Mol Cancer (2008) 1.24
Combined bisulfite restriction analysis (COBRA). Methods Mol Biol (2002) 1.20
Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23. Hum Mol Genet (2013) 1.19
Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels. Hum Genet (2002) 1.19
DNA methyltransferase deficiency modifies cancer susceptibility in mice lacking DNA mismatch repair. Mol Cell Biol (2002) 1.18
Dnmt1 deficiency leads to enhanced microsatellite instability in mouse embryonic stem cells. Nucleic Acids Res (2004) 1.17
LINE-1 methylation in plasma DNA as a biomarker of activity of DNA methylation inhibitors in patients with solid tumors. Epigenetics (2009) 1.17
Meat intake, cooking-related mutagens and risk of colorectal adenoma in a sigmoidoscopy-based case-control study. Carcinogenesis (2004) 1.16
Genome-scale discovery of DNA-methylation biomarkers for blood-based detection of colorectal cancer. PLoS One (2012) 1.14
The methylenetetrahydrofolate reductase C677T mutation induces cell-specific changes in genomic DNA methylation and uracil misincorporation: a possible molecular basis for the site-specific cancer risk modification. Int J Cancer (2009) 1.14
Identification of a panel of sensitive and specific DNA methylation markers for lung adenocarcinoma. Mol Cancer (2007) 1.14
Genetic variations on chromosomes 5p15 and 15q25 and bladder cancer risk: findings from the Los Angeles-Shanghai bladder case-control study. Carcinogenesis (2010) 1.12
A review of cancer in U.S. Hispanic populations. Cancer Prev Res (Phila) (2012) 1.11
DNA methylation profile of 28 potential marker loci in malignant mesothelioma. Lung Cancer (2007) 1.11
Ovarian cancer early detection claims are biased. Clin Cancer Res (2008) 1.10
The role of DNA methylation in the development and progression of lung adenocarcinoma. Dis Markers (2007) 1.09
The mutagenic potential of duodenoesophageal reflux. Ann Surg (2005) 1.08
Rapid and quantitative method of allele-specific DNA methylation analysis. Biotechniques (2006) 1.08
A phase 1 clinical trial of vorinostat in combination with decitabine in patients with acute myeloid leukaemia or myelodysplastic syndrome. Br J Haematol (2014) 1.08
Distinct DNA methylation profiles in malignant mesothelioma, lung adenocarcinoma, and non-tumor lung. Lung Cancer (2005) 1.06
Water intake and bladder cancer risk in Los Angeles County. Int J Cancer (2008) 1.05
RUNX3 methylation reveals that bladder tumors are older in patients with a history of smoking. Cancer Res (2008) 1.05
Mild depletion of dietary folate combined with other B vitamins alters multiple components of the Wnt pathway in mouse colon. J Nutr (2007) 1.04
Lower risk in parous women suggests that hormonal factors are important in bladder cancer etiology. Cancer Epidemiol Biomarkers Prev (2011) 1.04
DNA hypermethylation of ESR1 and PGR in breast cancer: pathologic and epidemiologic associations. Cancer Epidemiol Biomarkers Prev (2009) 1.04
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases. J Mol Diagn (2010) 1.04
Associations between intake of folate and related micronutrients with molecularly defined colorectal cancer risks in the Iowa Women's Health Study. Nutr Cancer (2012) 1.03
Gene-specific methylation and subsequent risk of colorectal adenomas among participants of the polyp prevention trial. Cancer Epidemiol Biomarkers Prev (2005) 1.01
Analysis of complex methylation data. Methods (2002) 1.00
Shape selectivity in the assembly of lithographically designed colloidal particles. J Am Chem Soc (2007) 1.00
A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32. Blood (2011) 0.99