Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children

[1]  M. Maghnie,et al.  Diagnosis and management of Silver–Russell syndrome: first international consensus statement , 2017, Nature Reviews Endocrinology.

[2]  D. Postma,et al.  Epigenome-Wide Meta-Analysis of Methylation in Children Related to Prenatal NO2 Air Pollution Exposure , 2016, Environmental health perspectives.

[3]  R. Weksberg,et al.  EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome , 2016, European Journal of Human Genetics.

[4]  G. Castellani,et al.  Erratum: A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data , 2016, Aging.

[5]  Tom R. Gaunt,et al.  Longitudinal analysis of DNA methylation associated with birth weight and gestational age , 2015, Human molecular genetics.

[6]  J. Ilonen,et al.  Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes , 2015, Clinical Epigenetics.

[7]  Enrico Giampieri,et al.  A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data , 2015, Aging.

[8]  P. Stanier,et al.  Genome-wide methylation analysis in Silver–Russell syndrome patients , 2015, Human Genetics.

[9]  T. Lind,et al.  Maternal body mass index in early pregnancy and offspring asthma, rhinitis and eczema up to 16 years of age , 2014, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[10]  Rafael A. Irizarry,et al.  Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays , 2014, Bioinform..

[11]  J. Kere,et al.  Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7 , 2013, Epigenetics.

[12]  A. Stevens,et al.  3-M syndrome: a growth disorder associated with IGF2 silencing , 2013, Endocrine connections.

[13]  T. Ideker,et al.  Genome-wide methylation profiles reveal quantitative views of human aging rates. , 2013, Molecular cell.

[14]  Eurie L. Hong,et al.  Annotation of functional variation in personal genomes using RegulomeDB , 2012, Genome research.

[15]  J. Kere,et al.  Differential DNA Methylation in Purified Human Blood Cells: Implications for Cell Lineage and Studies on Disease Susceptibility , 2012, PloS one.

[16]  A. Oshlack,et al.  SWAN: Subset-quantile Within Array Normalization for Illumina Infinium HumanMethylation450 BeadChips , 2012, Genome Biology.

[17]  Peter A. Jones Functions of DNA methylation: islands, start sites, gene bodies and beyond , 2012, Nature Reviews Genetics.

[18]  Steven J. M. Jones,et al.  Mutations in EZH2 cause Weaver syndrome. , 2012, American journal of human genetics.

[19]  L. Dunkel,et al.  New Finnish growth references for children and adolescents aged 0 to 20 years: Length/height-for-age, weight-for-length/height, and body mass index-for-age , 2011, Annals of medicine.

[20]  R. Oakey,et al.  The role of imprinted genes in humans , 2011, Genome Biology.

[21]  E. Kjeldsen,et al.  The combined expression of HOXA4 and MEIS1 is an independent prognostic factor in patients with AML , 2009, European journal of haematology.

[22]  T. Eggermann Silver-Russell and Beckwith-Wiedemann Syndromes: Opposite (Epi)Mutations in 11p15 Result in Opposite Clinical Pictures , 2009, Hormone Research in Paediatrics.

[23]  C. Gieger,et al.  Identification of ten loci associated with height highlights new biological pathways in human growth , 2008, Nature Genetics.

[24]  C. Lindgren,et al.  Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR. , 2008, Clinical chemistry.

[25]  Jim Stalker,et al.  A Novel CpG Island Set Identifies Tissue-Specific Methylation at Developmental Gene Loci , 2008, PLoS biology.

[26]  A. Hartemink,et al.  Computational and experimental identification of novel human imprinted genes. , 2007, Genome research.

[27]  C. Férec,et al.  Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: A new patient presenting with normal growth , 2007, American journal of medical genetics. Part A.

[28]  T. Eggermann,et al.  (Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation? , 2006, European journal of medical genetics.

[29]  D. Oscier,et al.  Promoter hypermethylation silences expression of the HoxA4 gene and correlates with IgVh mutational status in CLL , 2006, Leukemia.

[30]  B. Hamel,et al.  Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. , 2006, American journal of human genetics.

[31]  T. Eggermann,et al.  Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain , 2005, Journal of Medical Genetics.

[32]  C. Gicquel,et al.  Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome , 2005, Nature Genetics.

[33]  W. Lam,et al.  Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells , 2005, Nature Genetics.

[34]  L. Shaffer,et al.  Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia. , 1998, American journal of human genetics.

[35]  T. Eggermann,et al.  Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy , 1997, Human Genetics.

[36]  R. Trembath,et al.  Maternal uniparental disomy 7 in Silver-Russell syndrome. , 1997, Journal of medical genetics.

[37]  K. Méhes,et al.  Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. , 1995, Human molecular genetics.

[38]  R. Behringer,et al.  Homeotic transformation of cervical vertebrae in Hoxa-4 mutant mice. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[39]  J. Kere,et al.  Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. , 1994, American journal of human genetics.

[40]  M. Capecchi,et al.  Targeted disruptions of the murine Hoxa-4 and Hoxa-6 genes result in homeotic transformations of components of the vertebral column , 1994, Mechanisms of Development.

[41]  E. Lewis,et al.  The 1991 Albert Lasker Medical Awards. Clusters of master control genes regulate the development of higher organisms. , 1992, JAMA.

[42]  J. Innis,et al.  Human HOX gene disorders. , 2014, Molecular genetics and metabolism.

[43]  Cheng Li,et al.  Adjusting batch effects in microarray expression data using empirical Bayes methods. , 2007, Biostatistics.

[44]  Gordon K. Smyth,et al.  limma: Linear Models for Microarray Data , 2005 .

[45]  Alex E. Lash,et al.  Gene Expression Omnibus: NCBI gene expression and hybridization array data repository , 2002, Nucleic Acids Res..

[46]  David M. Evans,et al.  Genome-wide association analysis identifies 20 loci that influence adult height , 2008, Nature Genetics.