{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,10]],"date-time":"2026-10-10T13:23:32Z","timestamp":1791638612731,"version":"4.3.4"},"reference-count":146,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2013,7,1]],"date-time":"2013-07-01T00:00:00Z","timestamp":1372636800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2013,7,16]],"date-time":"2013-07-16T00:00:00Z","timestamp":1373932800000},"content-version":"vor","delay-in-days":15,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Molecular Aspects of Medicine"],"published-print":{"date-parts":[[2013,7]]},"DOI":"10.1016\/j.mam.2012.06.009","type":"journal-article","created":{"date-parts":[[2012,7,5]],"date-time":"2012-07-05T16:56:42Z","timestamp":1341507402000},"page":"826-840","source":"Crossref","is-referenced-by-count":169,"title":["The role of imprinted genes in humans"],"prefix":"10.1016","volume":"34","author":[{"given":"Miho","family":"Ishida","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gudrun E.","family":"Moore","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.mam.2012.06.009_b0005","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1136\/jmg.2007.053017","article-title":"The genetic aetiology of Silver\u2013Russell syndrome","volume":"45","author":"Abu-Amero","year":"2008","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0010","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1136\/jmg.2009.071316","article-title":"Epigenetic signatures of Silver\u2013Russell syndrome","volume":"47","author":"Abu-Amero","year":"2010","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0015","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1002\/(SICI)1098-2795(199803)49:3<229::AID-MRD2>3.0.CO;2-Q","article-title":"Expression of the insulin-like growth factors and their receptors in term placentas: a comparison between normal and IUGR births","volume":"49","author":"Abu-Amero","year":"1998","journal-title":"Mol. Reprod. Dev."},{"key":"10.1016\/j.mam.2012.06.009_b0020","first-page":"429","article-title":"Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes","volume":"68","author":"Adkins","year":"2010","journal-title":"Pediatr. Res."},{"key":"10.1016\/j.mam.2012.06.009_b0025","doi-asserted-by":"crossref","first-page":"2826","DOI":"10.1093\/humrep\/den310","article-title":"A review of known imprinting syndromes and their association with assisted reproduction technologies","volume":"23","author":"Amor","year":"2008","journal-title":"Hum. Reprod."},{"key":"10.1016\/j.mam.2012.06.009_b0030","doi-asserted-by":"crossref","first-page":"1908","DOI":"10.1007\/s00125-010-1790-0","article-title":"Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight","volume":"53","author":"Andersson","year":"2010","journal-title":"Diabetologia"},{"key":"10.1016\/j.mam.2012.06.009_b0035","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1007\/s00109-006-0131-8","article-title":"Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight","volume":"85","author":"Apostolidou","year":"2007","journal-title":"J. Mol. Med. (Berlin)"},{"key":"10.1016\/j.mam.2012.06.009_b0040","doi-asserted-by":"crossref","first-page":"4724","DOI":"10.1093\/hmg\/ddp435","article-title":"Multilocus methylation analysis in a large cohort of 11p15-related fetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci","volume":"18","author":"Azzi","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0045","doi-asserted-by":"crossref","first-page":"1735","DOI":"10.1016\/j.cub.2008.09.044","article-title":"Global survey of genomic imprinting by transcriptome sequencing","volume":"18","author":"Babak","year":"2008","journal-title":"Curr. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0050","doi-asserted-by":"crossref","first-page":"1610","DOI":"10.1126\/science.270.5242.1610","article-title":"Gametic imprinting in mammals","volume":"270","author":"Barlow","year":"1995","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0055","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1038\/349084a0","article-title":"The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus","volume":"349","author":"Barlow","year":"1991","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0060","doi-asserted-by":"crossref","first-page":"1255","DOI":"10.1172\/JCI19159","article-title":"Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS","volume":"112","author":"Bastepe","year":"2003","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.mam.2012.06.009_b0065","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1038\/ng1487","article-title":"Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib","volume":"37","author":"Bastepe","year":"2005","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0070","doi-asserted-by":"crossref","first-page":"1283","DOI":"10.1086\/320117","article-title":"Paternal uniparental isodisomy of chromosome 20q\u2013and the resulting changes in GNAS1 methylation\u2013as a plausible cause of pseudohypoparathyroidism","volume":"68","author":"Bastepe","year":"2001","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0075","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1111\/j.1399-0004.2010.01514.x","article-title":"Silver\u2013Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues","volume":"80","author":"Begemann","year":"2011","journal-title":"Clin. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0080","doi-asserted-by":"crossref","first-page":"2126","DOI":"10.2337\/diabetes.53.8.2126","article-title":"Variation at the insulin gene VNTR (variable number tandem repeat) polymorphism and early growth: studies in a large Finnish birth cohort","volume":"53","author":"Bennett","year":"2004","journal-title":"Diabetes"},{"key":"10.1016\/j.mam.2012.06.009_b0085","doi-asserted-by":"crossref","first-page":"4709","DOI":"10.1210\/jc.2006-1127","article-title":"IGF-II serum levels are normal in children with Silver\u2013Russell syndrome who frequently carry epimutations at the IGF2 locus","volume":"91","author":"Binder","year":"2006","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0090","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1038\/ejhg.2008.233","article-title":"Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith\u2013Wiedemann syndrome","volume":"17","author":"Bliek","year":"2009","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0095","doi-asserted-by":"crossref","first-page":"934","DOI":"10.1126\/science.1220671","article-title":"Quantitative sequencing of 5-methylcytosine and 5-hydroxymethylcytosine at single-base resolution","volume":"336","author":"Booth","year":"2012","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0100","doi-asserted-by":"crossref","first-page":"96","DOI":"10.1038\/nature02886","article-title":"Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L","volume":"431","author":"Bourc\u2019his","year":"2004","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0105","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1038\/nrg3080","article-title":"Uncovering the role of 5-hydroxymethylcytosine in the epigenome","volume":"13","author":"Branco","year":"2012","journal-title":"Nat. Rev. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0110","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1177\/0885066604269663","article-title":"Current concepts in intrauterine growth restriction","volume":"19","author":"Brodsky","year":"2004","journal-title":"J. Intensive Care Med."},{"key":"10.1016\/j.mam.2012.06.009_b0115","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1002\/ajmg.c.30273","article-title":"Prader\u2013Willi syndrome and Angelman syndrome","volume":"154C","author":"Buiting","year":"2010","journal-title":"Am. J. Med. Genet. C Semin. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0120","doi-asserted-by":"crossref","first-page":"893","DOI":"10.1093\/hmg\/3.6.893","article-title":"Detection of aberrant DNA methylation in unique Prader\u2013Willi syndrome patients and its diagnostic implications","volume":"3","author":"Buiting","year":"1994","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0125","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1038\/ejhg.2008.165","article-title":"Prader\u2013Willi syndrome","volume":"17","author":"Cassidy","year":"2009","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0130","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1136\/jmg.34.5.353","article-title":"Epigenetic modification and uniparental inheritance of H19 in Beckwith\u2013Wiedemann syndrome","volume":"34","author":"Catchpoole","year":"1997","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0135","doi-asserted-by":"crossref","first-page":"496","DOI":"10.1038\/315496a0","article-title":"Differential activity of maternally and paternally derived chromosome regions in mice","volume":"315","author":"Cattanach","year":"1985","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0140","doi-asserted-by":"crossref","first-page":"8292","DOI":"10.1073\/pnas.1532175100","article-title":"Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism","volume":"100","author":"Charalambous","year":"2003","journal-title":"Proc. Nat. Acad. Sci. U.S.A."},{"key":"10.1016\/j.mam.2012.06.009_b0145","doi-asserted-by":"crossref","first-page":"3993","DOI":"10.1210\/jc.2009-2205","article-title":"Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis","volume":"95","author":"Chillambhi","year":"2010","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0150","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1101\/gad.495809","article-title":"Transcription is required for establishment of germline methylation marks at imprinted genes","volume":"23","author":"Chotalia","year":"2009","journal-title":"Gene Dev."},{"key":"10.1016\/j.mam.2012.06.009_b0155","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1002\/ajmg.c.30267","article-title":"Beckwith\u2013Wiedemann syndrome","volume":"154C","author":"Choufani","year":"2010","journal-title":"Am. J. Med. Genet. C Semin. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0160","doi-asserted-by":"crossref","first-page":"3257","DOI":"10.1093\/hmg\/ddp263","article-title":"A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism","volume":"18","author":"de Smith","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0165","doi-asserted-by":"crossref","first-page":"R527","DOI":"10.1016\/S0960-9822(01)00311-6","article-title":"Genomic imprinting: mother maintains methylation marks","volume":"11","author":"Dean","year":"2001","journal-title":"Curr. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0170","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1016\/S1084-9521(02)00141-6","article-title":"Epigenetic reprogramming in early mammalian development and following somatic nuclear transfer","volume":"14","author":"Dean","year":"2003","journal-title":"Semin. Cell Dev. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0175","doi-asserted-by":"crossref","first-page":"13734","DOI":"10.1073\/pnas.241522698","article-title":"Conservation of methylation reprogramming in mammalian development: aberrant reprogramming in cloned embryos","volume":"98","author":"Dean","year":"2001","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1016\/j.mam.2012.06.009_b0180","doi-asserted-by":"crossref","first-page":"e1002600","DOI":"10.1371\/journal.pgen.1002600","article-title":"Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective","volume":"8","author":"Deveale","year":"2012","journal-title":"PLoS Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0185","doi-asserted-by":"crossref","first-page":"e1709","DOI":"10.1371\/journal.pone.0001709","article-title":"SnoRNA Snord116 (Pwcr1\/MBII-85) deletion causes growth deficiency and hyperphagia in mice","volume":"3","author":"Ding","year":"2008","journal-title":"PLoS One"},{"key":"10.1016\/j.mam.2012.06.009_b0190","doi-asserted-by":"crossref","first-page":"235","DOI":"10.4161\/epi.9019","article-title":"Differential expression of imprinted genes in normal and IUGR human placentas","volume":"4","author":"Diplas","year":"2009","journal-title":"Epigenetics"},{"key":"10.1016\/j.mam.2012.06.009_b0195","doi-asserted-by":"crossref","first-page":"1526","DOI":"10.1095\/biolreprod62.6.1526","article-title":"Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo","volume":"62","author":"Doherty","year":"2000","journal-title":"Biol. Reprod."},{"key":"10.1016\/j.mam.2012.06.009_b0200","doi-asserted-by":"crossref","first-page":"2476","DOI":"10.1093\/humrep\/dem172","article-title":"Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study","volume":"22","author":"Doornbos","year":"2007","journal-title":"Hum. Reprod."},{"key":"10.1016\/j.mam.2012.06.009_b0205","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1038\/ng0598-98","article-title":"Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon longitudinal study of pregnancy and childhood","volume":"19","author":"Dunger","year":"1998","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0210","doi-asserted-by":"crossref","first-page":"450","DOI":"10.1007\/BF00441965","article-title":"Wiedemann\u2013Beckwith syndrome","volume":"147","author":"Engstrom","year":"1988","journal-title":"Eur. J. Pediatr."},{"key":"10.1016\/j.mam.2012.06.009_b0215","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1055\/s-0032-1307417","article-title":"Role of ART in imprinting disorders","volume":"30","author":"Eroglu","year":"2012","journal-title":"Semin. Reprod. Med."},{"key":"10.1016\/j.mam.2012.06.009_b0220","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1186\/1471-213X-7-116","article-title":"Assisted reproductive technology affects developmental kinetics, H19 imprinting control region methylation and H19 gene expression in individual mouse embryos","volume":"7","author":"Fauque","year":"2007","journal-title":"BMC Dev. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0225","doi-asserted-by":"crossref","first-page":"426","DOI":"10.1038\/ng988","article-title":"Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1","volume":"32","author":"Fitzpatrick","year":"2002","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0230","doi-asserted-by":"crossref","first-page":"2313","DOI":"10.2337\/diabetes.51.7.2313","article-title":"A putative functional polymorphism in the IGF-I gene: association studies with type 2 diabetes, adult height, glucose tolerance, and fetal growth in UK populations","volume":"51","author":"Frayling","year":"2002","journal-title":"Diabetes"},{"key":"10.1016\/j.mam.2012.06.009_b0235","doi-asserted-by":"crossref","first-page":"430","DOI":"10.1038\/ng.567","article-title":"Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight","volume":"42","author":"Freathy","year":"2010","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0240","doi-asserted-by":"crossref","first-page":"e1001015","DOI":"10.1371\/journal.pgen.1001015","article-title":"The importance of imprinting in the human placenta","volume":"6","author":"Frost","year":"2010","journal-title":"PLoS Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0245","doi-asserted-by":"crossref","first-page":"1003","DOI":"10.1038\/ng1629","article-title":"Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver\u2013Russell syndrome","volume":"37","author":"Gicquel","year":"2005","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0250","doi-asserted-by":"crossref","first-page":"1377","DOI":"10.1093\/hmg\/2.9.1377","article-title":"Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader\u2013Willi patients","volume":"2","author":"Glenn","year":"1993","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0255","doi-asserted-by":"crossref","first-page":"360","DOI":"10.1016\/j.ghir.2005.06.016","article-title":"Association between birth weight, body mass index and IGF2\/ApaI polymorphism","volume":"15","author":"Gomes","year":"2005","journal-title":"Growth Horm. IGF Res."},{"key":"10.1016\/j.mam.2012.06.009_b0260","doi-asserted-by":"crossref","first-page":"682","DOI":"10.1126\/science.1190831","article-title":"Sex-specific parent-of-origin allelic expression in the mouse brain","volume":"329","author":"Gregg","year":"2010","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0265","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1126\/science.1190830","article-title":"High-resolution analysis of parent-of-origin allelic expression in the mouse brain","volume":"329","author":"Gregg","year":"2010","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0270","doi-asserted-by":"crossref","first-page":"6079","DOI":"10.1073\/pnas.97.11.6079","article-title":"Oral administration of a corticotropin-releasing hormone receptor antagonist significantly attenuates behavioral, neuroendocrine, and autonomic responses to stress in primates","volume":"97","author":"Habib","year":"2000","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1016\/j.mam.2012.06.009_b0275","doi-asserted-by":"crossref","first-page":"877","DOI":"10.1038\/nature06714","article-title":"Chromatin dynamics during epigenetic reprogramming in the mouse germ line","volume":"452","author":"Hajkova","year":"2008","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0280","doi-asserted-by":"crossref","first-page":"1983","DOI":"10.1242\/dev.129.8.1983","article-title":"Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice","volume":"129","author":"Hata","year":"2002","journal-title":"Development"},{"key":"10.1016\/j.mam.2012.06.009_b0285","doi-asserted-by":"crossref","first-page":"2734","DOI":"10.1210\/jc.2006-1948","article-title":"Study of association between common variation in the insulin-like growth factor 2 gene and indices of obesity and body size in middle-aged men and women","volume":"92","author":"Heude","year":"2007","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0290","doi-asserted-by":"crossref","first-page":"1607","DOI":"10.1101\/gad.1667008","article-title":"Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development","volume":"22","author":"Hirasawa","year":"2008","journal-title":"Gene Dev."},{"key":"10.1016\/j.mam.2012.06.009_b0295","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1111\/j.1365-2443.2006.00943.x","article-title":"Oocyte growth-dependent progression of maternal imprinting in mice","volume":"11","author":"Hiura","year":"2006","journal-title":"Genes Cells"},{"key":"10.1016\/j.mam.2012.06.009_b0300","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1016\/j.tig.2007.07.003","article-title":"Construction and evolution of imprinted loci in mammals","volume":"23","author":"Hore","year":"2007","journal-title":"Trends Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0305","doi-asserted-by":"crossref","first-page":"2041","DOI":"10.1002\/ajmg.a.32364","article-title":"Mechanisms of imprinting of the Prader\u2013Willi\/Angelman region","volume":"146A","author":"Horsthemke","year":"2008","journal-title":"Am. J. Med. Genet. A"},{"key":"10.1016\/j.mam.2012.06.009_b0310","doi-asserted-by":"crossref","first-page":"829","DOI":"10.1016\/S0092-8674(01)00280-X","article-title":"Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene","volume":"104","author":"Howell","year":"2001","journal-title":"Cell"},{"key":"10.1016\/j.mam.2012.06.009_b0315","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1016\/j.ajhg.2012.02.021","article-title":"Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight","volume":"90","author":"Ishida","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0320","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1038\/nature06146","article-title":"Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation","volume":"449","author":"Jia","year":"2007","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0325","doi-asserted-by":"crossref","first-page":"e1000992","DOI":"10.1371\/journal.pgen.1000992","article-title":"The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers","volume":"6","author":"Kagami","year":"2010","journal-title":"PLoS Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0330","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1038\/ng.2007.56","article-title":"Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes","volume":"40","author":"Kagami","year":"2008","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0335","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1111\/j.1651-2227.2006.00120.x","article-title":"Insulin-like growth factor 2 (IGF2) and IGF2 receptor gene variants are associated with fetal growth","volume":"96","author":"Kaku","year":"2007","journal-title":"Acta Paediatr."},{"key":"10.1016\/j.mam.2012.06.009_b0340","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1093\/hmg\/9.3.453","article-title":"The cell cycle control gene ZAC\/PLAGL1 is imprinted \u2013 a strong candidate gene for transient neonatal diabetes","volume":"9","author":"Kamiya","year":"2000","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0345","doi-asserted-by":"crossref","first-page":"900","DOI":"10.1038\/nature02633","article-title":"Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting","volume":"429","author":"Kaneda","year":"2004","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0350","doi-asserted-by":"crossref","first-page":"366","DOI":"10.1111\/j.1399-0004.2012.01844.x","article-title":"Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2\/H19 in Silver\u2013Russell syndrome","volume":"81","author":"Kannenberg","year":"2012","journal-title":"Clin. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0355","doi-asserted-by":"crossref","first-page":"5656","DOI":"10.1093\/nar\/gkp613","article-title":"YY1\u2019s role in DNA methylation of Peg3 and Xist","volume":"37","author":"Kim","year":"2009","journal-title":"Nucleic Acids Res."},{"key":"10.1016\/j.mam.2012.06.009_b0360","doi-asserted-by":"crossref","first-page":"2542","DOI":"10.1093\/hmg\/ddm187","article-title":"Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients","volume":"16","author":"Kobayashi","year":"2007","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0365","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1038\/nature08625","article-title":"Parental origin of sequence variants associated with complex diseases","volume":"462","author":"Kong","year":"2009","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0370","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1016\/j.anngen.2004.03.006","article-title":"Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting","volume":"47","author":"Kotzot","year":"2004","journal-title":"Ann. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0375","doi-asserted-by":"crossref","first-page":"1215","DOI":"10.1515\/JPEM.2004.17.9.1215","article-title":"Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10","volume":"17","author":"Kukuvitis","year":"2004","journal-title":"J. Pediatr. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0380","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1016\/j.placenta.2011.11.018","article-title":"Ontogeny of growth-regulating genes in the placenta","volume":"33","author":"Kumar","year":"2012","journal-title":"Placenta"},{"key":"10.1016\/j.mam.2012.06.009_b0385","doi-asserted-by":"crossref","first-page":"2953","DOI":"10.1101\/gad.8.24.2953","article-title":"Loss of the imprinted IGF2\/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality","volume":"8","author":"Lau","year":"1994","journal-title":"Gene Dev."},{"key":"10.1016\/j.mam.2012.06.009_b0390","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1038\/2464","article-title":"Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest","volume":"20","author":"Lefebvre","year":"1998","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0395","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1038\/375034a0","article-title":"Disruption of imprinting caused by deletion of the H19 gene region in mice","volume":"375","author":"Leighton","year":"1995","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0400","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1159\/000090818","article-title":"How imprinting centres work","volume":"113","author":"Lewis","year":"2006","journal-title":"Cytogenet. Genome Res."},{"key":"10.1016\/j.mam.2012.06.009_b0405","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1126\/science.284.5412.330","article-title":"Regulation of maternal behavior and offspring growth by paternally expressed Peg3","volume":"284","author":"Li","year":"1999","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0410","doi-asserted-by":"crossref","first-page":"547","DOI":"10.1016\/j.devcel.2008.08.014","article-title":"A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints","volume":"15","author":"Li","year":"2008","journal-title":"Dev. Cell"},{"key":"10.1016\/j.mam.2012.06.009_b0415","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1038\/ng1233","article-title":"Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12","volume":"35","author":"Lin","year":"2003","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0420","doi-asserted-by":"crossref","first-page":"503","DOI":"10.1007\/s00439-002-0718-2","article-title":"Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of birth weight","volume":"110","author":"Lindsay","year":"2002","journal-title":"Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0425","doi-asserted-by":"crossref","first-page":"804","DOI":"10.1086\/429932","article-title":"A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS","volume":"76","author":"Linglart","year":"2005","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0430","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1093\/hmg\/ddi009","article-title":"Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB","volume":"14","author":"Liu","year":"2005","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0435","doi-asserted-by":"crossref","first-page":"839","DOI":"10.1093\/hmg\/ddh104","article-title":"Gene-specific timing and epigenetic memory in oocyte imprinting","volume":"13","author":"Lucifero","year":"2004","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0440","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1038\/ng.187","article-title":"Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57","volume":"40","author":"Mackay","year":"2008","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0445","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1007\/s00439-001-0671-5","article-title":"Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus","volume":"110","author":"Mackay","year":"2002","journal-title":"Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0450","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1002\/ajmg.c.30272","article-title":"Transient neonatal diabetes mellitus type 1","volume":"154C","author":"Mackay","year":"2010","journal-title":"Am. J. Med. Genet. C Semin. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0455","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1038\/13767","article-title":"Absence of genome-wide changes in DNA methylation during development of the zebrafish","volume":"23","author":"Macleod","year":"1999","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0460","doi-asserted-by":"crossref","first-page":"3020","DOI":"10.1210\/jc.2011-1048","article-title":"Clinical review: pseudohypoparathyroidism: diagnosis and treatment","volume":"96","author":"Mantovani","year":"2011","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0465","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1093\/hmg\/ddp465","article-title":"Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner","volume":"19","author":"Market-Velker","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0470","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1093\/molehr\/gam093","article-title":"Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia","volume":"14","author":"Marques","year":"2008","journal-title":"Mol. Hum. Reprod."},{"key":"10.1016\/j.mam.2012.06.009_b0475","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1016\/j.ajog.2006.08.027","article-title":"Altered gene expression patterns in intrauterine growth restriction: potential role of hypoxia","volume":"196","author":"McCarthy","year":"2007","journal-title":"Am. J. Obstet. Gynecol."},{"key":"10.1016\/j.mam.2012.06.009_b0480","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1186\/1756-8935-3-2","article-title":"Distinguishing epigenetic marks of developmental and imprinting regulation","volume":"3","author":"McEwen","year":"2010","journal-title":"Epigenetics Chromatin"},{"key":"10.1016\/j.mam.2012.06.009_b0485","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/0092-8674(84)90313-1","article-title":"Completion of mouse embryogenesis requires both the maternal and paternal genomes","volume":"37","author":"McGrath","year":"1984","journal-title":"Cell"},{"key":"10.1016\/j.mam.2012.06.009_b0490","doi-asserted-by":"crossref","first-page":"540","DOI":"10.1016\/j.placenta.2005.07.004","article-title":"Unbalanced placental expression of imprinted genes in human intrauterine growth restriction","volume":"27","author":"McMinn","year":"2006","journal-title":"Placenta"},{"key":"10.1016\/j.mam.2012.06.009_b0495","doi-asserted-by":"crossref","first-page":"543","DOI":"10.1086\/318192","article-title":"Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?","volume":"68","author":"Mergenthaler","year":"2001","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0500","doi-asserted-by":"crossref","first-page":"e1000423","DOI":"10.1371\/journal.pgen.1000423","article-title":"Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith\u2013Wiedemann Syndrome)","volume":"5","author":"Meyer","year":"2009","journal-title":"PLoS Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0505","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1210\/jc.2003-030605","article-title":"Lack of support for a role of the insulin gene variable number of tandem repeats minisatellite (INS-VNTR) locus in fetal growth or type 2 diabetes-related intermediate traits in United Kingdom populations","volume":"89","author":"Mitchell","year":"2004","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0510","doi-asserted-by":"crossref","first-page":"6623","DOI":"10.1073\/pnas.0511031103","article-title":"Limited evolutionary conservation of imprinting in the human placenta","volume":"103","author":"Monk","year":"2006","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1016\/j.mam.2012.06.009_b0515","doi-asserted-by":"crossref","first-page":"E810","DOI":"10.1210\/jc.2010-2316","article-title":"Variants near CCNL1\/LEKR1 and in ADCY5 and fetal growth characteristics in different trimesters","volume":"96","author":"Mook-Kanamori","year":"2011","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0520","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/0168-9525(91)90040-W","article-title":"Genomic imprinting in mammalian development: a parental tug-of-war","volume":"7","author":"Moore","year":"1991","journal-title":"Trends Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0525","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1002\/humu.10237","article-title":"Epigenetic detection of human chromosome 14 uniparental disomy","volume":"22","author":"Murphy","year":"2003","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.mam.2012.06.009_b0530","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1038\/ncb1519","article-title":"PGC7\/Stella protects against DNA demethylation in early embryogenesis","volume":"9","author":"Nakamura","year":"2007","journal-title":"Nat. Cell Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0535","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1038\/ng0195-12","article-title":"Characteristics of imprinted genes","volume":"9","author":"Neumann","year":"1995","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0540","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/S0092-8674(00)81656-6","article-title":"DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development","volume":"99","author":"Okano","year":"1999","journal-title":"Cell"},{"key":"10.1016\/j.mam.2012.06.009_b0545","doi-asserted-by":"crossref","first-page":"714","DOI":"10.1038\/nature05987","article-title":"DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA","volume":"448","author":"Ooi","year":"2007","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0550","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1007\/s00335-008-9139-4","article-title":"Imprinted noncoding RNAs","volume":"19","author":"Peters","year":"2008","journal-title":"Mamm. Genome"},{"key":"10.1016\/j.mam.2012.06.009_b0555","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1186\/1471-2156-6-22","article-title":"Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans","volume":"6","author":"Petry","year":"2005","journal-title":"BMC Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0560","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1007\/s00439-011-1005-x","article-title":"Maternally transmitted fetal H19 variants and associations with birth weight","volume":"130","author":"Petry","year":"2011","journal-title":"Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0565","doi-asserted-by":"crossref","first-page":"682","DOI":"10.1002\/bdra.20795","article-title":"The role of imprinted genes in fetal growth abnormalities","volume":"91","author":"Piedrahita","year":"2011","journal-title":"Birth Defects Res. A Clin. Mol. Teratol."},{"key":"10.1016\/j.mam.2012.06.009_b0570","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1097\/00003081-199203000-00015","article-title":"Intrauterine growth retardation: definition, classification, and etiology","volume":"35","author":"Pollack","year":"1992","journal-title":"Clin. Obstet. Gynecol."},{"key":"10.1016\/j.mam.2012.06.009_b0575","doi-asserted-by":"crossref","first-page":"33002","DOI":"10.1074\/jbc.274.46.33002","article-title":"Recombinant human DNA (cytosine-5) methyltransferase. I. Expression, purification, and comparison of de novo and maintenance methylation","volume":"274","author":"Pradhan","year":"1999","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.mam.2012.06.009_b0580","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1126\/science.1063443","article-title":"Epigenetic reprogramming in mammalian development","volume":"293","author":"Reik","year":"2001","journal-title":"Science"},{"key":"10.1016\/j.mam.2012.06.009_b0585","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1038\/35047554","article-title":"Genomic imprinting: parental influence on the genome","volume":"2","author":"Reik","year":"2001","journal-title":"Nat. Rev. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0590","first-page":"741","article-title":"Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader\u2013Willi syndromes","volume":"54","author":"Reis","year":"1994","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0595","doi-asserted-by":"crossref","first-page":"E863","DOI":"10.1210\/jc.2011-2804","article-title":"A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A\/B GNAS and Autosomal Dominant Pseudohypoparathyroidism Type Ib","volume":"97","author":"Richard","year":"2012","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.mam.2012.06.009_b0600","doi-asserted-by":"crossref","first-page":"809","DOI":"10.1007\/s10577-005-1015-4","article-title":"Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32","volume":"13","author":"Rosa","year":"2005","journal-title":"Chromosome Res."},{"key":"10.1016\/j.mam.2012.06.009_b0605","doi-asserted-by":"crossref","first-page":"902","DOI":"10.1136\/jmg.2006.042135","article-title":"The epigenetic imprinting defect of patients with Beckwith\u2013Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region","volume":"43","author":"Rossignol","year":"2006","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0610","doi-asserted-by":"crossref","first-page":"719","DOI":"10.1038\/ng.158","article-title":"Prader\u2013Willi phenotype caused by paternal deficiency for the HBII-85 C\/D box small nucleolar RNA cluster","volume":"40","author":"Sahoo","year":"2008","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0615","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1093\/humrep\/del316","article-title":"Aberrant DNA methylation of imprinted loci in superovulated oocytes","volume":"22","author":"Sato","year":"2007","journal-title":"Hum. Reprod."},{"key":"10.1016\/j.mam.2012.06.009_b0620","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1002\/(SICI)1097-4652(200001)182:1<62::AID-JCP7>3.0.CO;2-X","article-title":"Soluble insulin-like growth factor II\/mannose 6-phosphate receptor inhibits DNA synthesis in insulin-like growth factor II sensitive cells","volume":"182","author":"Scott","year":"2000","journal-title":"J. Cell. Physiol."},{"key":"10.1016\/j.mam.2012.06.009_b0625","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1159\/000090815","article-title":"Genomic imprinting in plants and mammals: how life history constrains convergence","volume":"113","author":"Scott","year":"2006","journal-title":"Cytogenet. Genome Res."},{"key":"10.1016\/j.mam.2012.06.009_b0630","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1017\/S0016672300035333","article-title":"Genome imprinting phenomena on mouse chromosome 7","volume":"56","author":"Searle","year":"1990","journal-title":"Genet. Res."},{"key":"10.1016\/j.mam.2012.06.009_b0635","doi-asserted-by":"crossref","first-page":"1424","DOI":"10.1093\/hmg\/ddp049","article-title":"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","volume":"18","author":"Shiura","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0640","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1016\/j.pcl.2009.03.004","article-title":"Developmental origins of adult disease","volume":"56","author":"Simmons","year":"2009","journal-title":"Pediatr. Clin. North Am."},{"key":"10.1016\/j.mam.2012.06.009_b0645","doi-asserted-by":"crossref","first-page":"e235","DOI":"10.1371\/journal.pgen.0030235","article-title":"Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation","volume":"3","author":"Skryabin","year":"2007","journal-title":"PLoS Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0650","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1006\/dbio.2001.0560","article-title":"DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos","volume":"243","author":"Stancheva","year":"2002","journal-title":"Dev. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0655","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1111\/j.1365-2265.2009.03659.x","article-title":"Microarray analysis of placental tissue in intrauterine growth restriction","volume":"72","author":"Struwe","year":"2010","journal-title":"Clin. Endocrinol. (Oxf.)"},{"key":"10.1016\/j.mam.2012.06.009_b0660","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1038\/308548a0","article-title":"Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis","volume":"308","author":"Surani","year":"1984","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0665","doi-asserted-by":"crossref","first-page":"1135","DOI":"10.1016\/S0960-9822(00)00704-1","article-title":"Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12","volume":"10","author":"Takada","year":"2000","journal-title":"Curr. Biol."},{"key":"10.1016\/j.mam.2012.06.009_b0670","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1007\/s11154-010-9150-4","article-title":"6q24 transient neonatal diabetes","volume":"11","author":"Temple","year":"2010","journal-title":"Rev Endocr Metab Disord"},{"key":"10.1016\/j.mam.2012.06.009_b0675","first-page":"316","article-title":"Exomphalos-macroglossia-gigantism syndrome in Jamaican infants","volume":"119","author":"Thorburn","year":"1970","journal-title":"Am. J. Dis. Child."},{"key":"10.1016\/j.mam.2012.06.009_b0680","doi-asserted-by":"crossref","first-page":"3693","DOI":"10.1101\/gad.12.23.3693","article-title":"Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2","volume":"12","author":"Thorvaldsen","year":"1998","journal-title":"Gene Dev."},{"key":"10.1016\/j.mam.2012.06.009_b0685","doi-asserted-by":"crossref","first-page":"648","DOI":"10.1038\/ejhg.2009.246","article-title":"Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci","volume":"18","author":"Turner","year":"2010","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0690","doi-asserted-by":"crossref","first-page":"1036","DOI":"10.1016\/S0140-6736(02)08067-4","article-title":"Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight","volume":"359","author":"Vaessen","year":"2002","journal-title":"Lancet"},{"key":"10.1016\/j.mam.2012.06.009_b0695","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1038\/ng.493","article-title":"The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes","volume":"42","author":"Wallace","year":"2010","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0700","doi-asserted-by":"crossref","first-page":"e3839","DOI":"10.1371\/journal.pone.0003839","article-title":"Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain","volume":"3","author":"Wang","year":"2008","journal-title":"PLoS One"},{"key":"10.1016\/j.mam.2012.06.009_b0705","doi-asserted-by":"crossref","first-page":"4068","DOI":"10.1073\/pnas.0500702102","article-title":"Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis","volume":"102","author":"Webster","year":"2005","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1016\/j.mam.2012.06.009_b0710","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1002\/ajmg.c.30058","article-title":"Beckwith\u2013Wiedemann syndrome","volume":"137C","author":"Weksberg","year":"2005","journal-title":"Am. J. Med. Genet. C Semin. Med. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0715","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1038\/ng1731","article-title":"Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster","volume":"38","author":"Williamson","year":"2006","journal-title":"Nat. Genet."},{"key":"10.1016\/j.mam.2012.06.009_b0720","doi-asserted-by":"crossref","first-page":"745","DOI":"10.1038\/39631","article-title":"Imprinted expression of the Igf2r gene depends on an intronic CpG island","volume":"389","author":"Wutz","year":"1997","journal-title":"Nature"},{"key":"10.1016\/j.mam.2012.06.009_b0725","doi-asserted-by":"crossref","first-page":"1711","DOI":"10.1101\/gr.161600","article-title":"Novel imprinted DLK1\/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2\/H19 regulation","volume":"10","author":"Wylie","year":"2000","journal-title":"Genome Res."},{"key":"10.1016\/j.mam.2012.06.009_b0730","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1038\/ng0598-25","article-title":"A mouse model for Prader\u2013Willi syndrome imprinting-centre mutations","volume":"19","author":"Yang","year":"1998","journal-title":"Nat. Genet."}],"container-title":["Molecular Aspects of Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0098299712000817?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0098299712000817?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2022,1,20]],"date-time":"2022-01-20T08:39:38Z","timestamp":1642667978000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0098299712000817"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,7]]},"references-count":146,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2013,7]]}},"alternative-id":["S0098299712000817"],"URL":"https:\/\/doi.org\/10.1016\/j.mam.2012.06.009","relation":{},"ISSN":["0098-2997"],"issn-type":[{"value":"0098-2997","type":"print"}],"subject":[],"published":{"date-parts":[[2013,7]]}}}