Published in Epigenetics on November 18, 2013
Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23. Am J Hum Genet (2015) 0.84
Genome-wide methylation analysis in Silver-Russell syndrome patients. Hum Genet (2015) 0.83
Epigenetics of Aging and Alzheimer's Disease: Implications for Pharmacogenomics and Drug Response. Int J Mol Sci (2015) 0.79
New developments in Silver-Russell syndrome and implications for clinical practice. Epigenomics (2016) 0.79
FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset. Orphanet J Rare Dis (2016) 0.75
Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment. Epigenetics (2016) 0.75
PEG10 overexpression induced by E2F-1 promotes cell proliferation, migration, and invasion in pancreatic cancer. J Exp Clin Cancer Res (2017) 0.75
lumi: a pipeline for processing Illumina microarray. Bioinformatics (2008) 17.19
Functions of DNA methylation: islands, start sites, gene bodies and beyond. Nat Rev Genet (2012) 15.21
Role for DNA methylation in genomic imprinting. Nature (1993) 12.65
A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression. Nature (2011) 11.59
Genomic imprinting: parental influence on the genome. Nat Rev Genet (2001) 11.50
The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets. Bioinformatics (2009) 10.30
Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis. BMC Bioinformatics (2010) 7.78
Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome. Epigenetics (2011) 7.38
Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility. PLoS One (2012) 5.03
A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am J Med Genet (1980) 4.22
Computational and experimental identification of novel human imprinted genes. Genome Res (2007) 3.50
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat Genet (2005) 2.64
The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet (1999) 2.63
Mammalian genomic imprinting. Cold Spring Harb Perspect Biol (2011) 2.59
Age-associated DNA methylation in pediatric populations. Genome Res (2012) 2.53
The sonic hedgehog-patched-gli pathway in human development and disease. Am J Hum Genet (2000) 2.42
Silencing by imprinted noncoding RNAs: is transcription the answer? Trends Genet (2007) 2.29
The function of non-coding RNAs in genomic imprinting. Development (2009) 2.21
A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster. Blood (2009) 2.18
Beckwith-Wiedemann syndrome. Am J Med Genet C Semin Med Genet (2010) 2.15
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet (2001) 2.06
Genomic imprinting in mammals: emerging themes and established theories. PLoS Genet (2006) 1.99
Prader-Willi syndrome and Angelman syndrome. Am J Med Genet C Semin Med Genet (2010) 1.95
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet (2009) 1.86
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark. Hum Mol Genet (2003) 1.80
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution. PLoS Genet (2007) 1.79
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet (2000) 1.78
A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. Genomics (2001) 1.64
Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. Genome Res (2003) 1.61
Homeobox genes in normal and malignant cells. J Cell Physiol (2001) 1.54
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. Eur J Hum Genet (2010) 1.37
Human PEG1/MEST, an imprinted gene on chromosome 7. Hum Mol Genet (1997) 1.36
Genomic landscape of human allele-specific DNA methylation. Proc Natl Acad Sci U S A (2012) 1.34
A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids. Genomics (2003) 1.29
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing. Genome Res (2008) 1.28
6q24 transient neonatal diabetes. Rev Endocr Metab Disord (2010) 1.27
Studying the epigenome using next generation sequencing. J Med Genet (2011) 1.25
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome. Am J Hum Genet (2000) 1.25
A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region. Am J Hum Genet (2000) 1.20
The role of imprinted genes in humans. Mol Aspects Med (2012) 1.19
Global analysis of uniparental disomy using high density genotyping arrays. J Med Genet (2005) 1.18
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Hum Genet (1999) 1.16
Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype? J Med Genet (2001) 1.14
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency. Am J Hum Genet (2007) 1.13
Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome. Am J Hum Genet (2000) 1.12
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics (1997) 1.10
Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes. Hum Mol Genet (2011) 1.09
Identification of six putative human transporters with structural similarity to the drug transporter SLC22 family. Genomics (2007) 1.09
Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. Am J Hum Genet (1994) 1.07
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia. Am J Hum Genet (1998) 1.04
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. Eur J Hum Genet (2001) 1.04
Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14. Epigenetics (2008) 1.03
Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation. Hum Mol Genet (2009) 1.02
Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies. J Clin Endocrinol Metab (2008) 1.01
Silver-Russell syndrome. Arch Dis Child (2011) 0.99
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome. J Med Genet (2003) 0.98
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15. Genome Res (2010) 0.97
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues. J Med Genet (2004) 0.95
Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause. Pediatrics (2002) 0.95
Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growth. Am J Med Genet A (2007) 0.89
Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation. Am J Med Genet A (2012) 0.89
Segmental maternal UPD(7q) in Silver-Russell syndrome. Clin Genet (2008) 0.86
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed. Mamm Genome (2002) 0.85
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues. Hum Mol Genet (2008) 0.85
Methylation profiling in individuals with Russell-Silver syndrome. Am J Med Genet A (2010) 0.85
The adaptor protein SH2B3 (Lnk) negatively regulates neurite outgrowth of PC12 cells and cortical neurons. PLoS One (2011) 0.84
Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome. Clin Genet (2012) 0.83
Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases. Epigenetics (2010) 0.82
Mosaic maternal uniparental isodisomy for chromosome 7q21-qter. Clin Genet (2006) 0.80
No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation. J Pediatr Endocrinol Metab (2007) 0.79
Expression analysis of proline rich 15 (Prr15) in mouse and human gastrointestinal tumors. Mol Carcinog (2011) 0.77