{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T16:32:09Z","timestamp":1791045129935,"version":"4.1.0"},"reference-count":42,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2009,6]]},"DOI":"10.1097\/gco.0b013e32832d7b95","type":"journal-article","created":{"date-parts":[[2009,5,21]],"date-time":"2009-05-21T07:34:40Z","timestamp":1242891280000},"page":"201-206","source":"Crossref","is-referenced-by-count":36,"title":["Epigenetics and assisted reproduction"],"prefix":"10.1097","volume":"21","author":[{"given":"Louise","family":"Wilkins-Haug","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-3-20210129","doi-asserted-by":"crossref","first-page":"1723","DOI":"10.1101\/gr.6584707","article-title":"Computational and experimental identification of novel human imprinted genes","volume":"17","author":"Luedi","year":"2007","journal-title":"Genome Res"},{"key":"R2-3-20210129","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1159\/000056752","article-title":"The role of imprinted genes in fetal growth","volume":"81","author":"Miozzo","year":"2002","journal-title":"Biol Neonate"},{"key":"R3-3-20210129","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1002\/bdrc.20039","article-title":"Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction","volume":"75","author":"Arnaud","year":"2005","journal-title":"Birth Defects Res C Embryo Today"},{"key":"R4-3-20210129","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1113\/jphysiol.2002.033274","article-title":"Regulation of supply and demand for maternal nutrients in mammals by imprinted genes","volume":"547","author":"Reik","year":"2003","journal-title":"J Physiol"},{"key":"R5-3-20210129","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1113\/jphysiol.2006.104968","article-title":"Placental adaptive responses and fetal programming","volume":"572","author":"Myatt","year":"2006","journal-title":"J Physiol"},{"issue":"Suppl 3","key":"R6-3-20210129","first-page":"50","article-title":"Imprinted genes, placental development and fetal growth","volume":"65","author":"Fowden","year":"2006","journal-title":"Horm Res"},{"key":"R7-3-20210129","doi-asserted-by":"crossref","first-page":"172","DOI":"10.1006\/dbio.2001.0501","article-title":"Dynamic reprogramming of DNA methylation in the early mouse embryo","volume":"241","author":"Santos","year":"2002","journal-title":"Dev Biol"},{"key":"R8-3-20210129","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1086\/341096","article-title":"Intracytoplasmic sperm injection may increase the risk of imprinting defects","volume":"71","author":"Cox","year":"2002","journal-title":"Am J Hum Genet"},{"key":"R9-3-20210129","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1086\/346030","article-title":"Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection","volume":"72","author":"Orstavik","year":"2003","journal-title":"Am J Hum Genet"},{"key":"R10-3-20210129","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1136\/jmg.2004.026930","article-title":"Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples","volume":"42","author":"Ludwig","year":"2005","journal-title":"J Med Genet"},{"key":"R11-3-20210129","doi-asserted-by":"crossref","first-page":"3237","DOI":"10.1093\/humrep\/dem268","article-title":"A survey of assisted reproductive technology births and imprinting disorders","volume":"22","author":"Bowdin","year":"2007","journal-title":"Hum Reprod"},{"key":"R12-3-20210129","doi-asserted-by":"crossref","first-page":"1662","DOI":"10.1016\/j.fertnstert.2007.09.005","article-title":"Growth and development of children born after in vitro fertilization","volume":"90","author":"Ceelen","year":"2008","journal-title":"Fertil Steril"},{"key":"R13-3-20210129","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1111\/j.1399-0004.1994.tb04219.x","article-title":"Clinical features and natural history of Beckwith\u2013Wiedemann syndrome: presentation of 74 new cases","volume":"46","author":"Elliott","year":"1994","journal-title":"Clin Genet"},{"key":"R14-3-20210129","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1002\/ajmg.c.30058","article-title":"Beckwith\u2013Wiedemann syndrome","volume":"137","author":"Weksberg","year":"2005","journal-title":"Am J Med Genet C Semin Med Genet"},{"key":"R15-3-20210129","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1086\/346031","article-title":"Association of in vitro fertilization with Beckwith\u2013Wiedemann syndrome and epigenetic alterations of LIT1 and H19","volume":"72","author":"DeBaun","year":"2003","journal-title":"Am J Hum Genet"},{"key":"R16-3-20210129","doi-asserted-by":"crossref","first-page":"1338","DOI":"10.1086\/374824","article-title":"In vitro fertilization may increase the risk of Beckwith\u2013Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene","volume":"72","author":"Gicquel","year":"2003","journal-title":"Am J Hum Genet"},{"key":"R17-3-20210129","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1136\/jmg.40.1.62","article-title":"Beckwith\u2013Wiedemann syndrome and assisted reproduction technology (ART)","volume":"40","author":"Maher","year":"2003","journal-title":"J Med Genet"},{"key":"R18-3-20210129","doi-asserted-by":"crossref","first-page":"1009","DOI":"10.1093\/humrep\/dei405","article-title":"Assisted reproductive therapies and imprinting disorders: a preliminary British survey","volume":"21","author":"Sutcliffe","year":"2006","journal-title":"Hum Reprod"},{"key":"R19-3-20210129","doi-asserted-by":"crossref","first-page":"526","DOI":"10.1086\/423902","article-title":"Beckwith\u2013Wiedemann syndrome and IVF: a case\u2013control study","volume":"75","author":"Halliday","year":"2004","journal-title":"Am J Hum Genet"},{"key":"R20-3-20210129","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1002\/bdra.20547","article-title":"Isolated fetal omphalocele, Beckwith\u2013Wiedemann syndrome, and assisted reproductive technologies","volume":"85","author":"Wilkins-Haug","year":"2009","journal-title":"Birth Defects Res A Clin Mol Teratol"},{"key":"R21-3-20210129","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1016\/j.fertnstert.2004.07.964","article-title":"Association between Beckwith\u2013Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients","volume":"83","author":"Chang","year":"2005","journal-title":"Fertil Steril"},{"key":"R22-3-20210129","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":"R23-3-20210129","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":"R24-3-20210129","doi-asserted-by":"crossref","first-page":"262","DOI":"10.1007\/s00439-006-0205-2","article-title":"A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus","volume":"120","author":"Mackay","year":"2006","journal-title":"Hum Genet"},{"key":"R25-3-20210129","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1097\/01.AOG.0000114989.84822.51","article-title":"Perinatal outcomes in singletons following in vitro fertilization: a meta-analysis","volume":"103","author":"Jackson","year":"2004","journal-title":"Obstet Gynecol"},{"key":"R26-3-20210129","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 U S A"},{"key":"R27-3-20210129","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"},{"issue":"6\u20137","key":"R28-3-20210129","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":"R29-3-20210129","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":"R30-3-20210129","doi-asserted-by":"crossref","first-page":"5275","DOI":"10.1210\/en.2006-0288","article-title":"Epigenetic regulation of human trophoblastic cell migration and invasion","volume":"147","author":"Rahnama","year":"2006","journal-title":"Endocrinology"},{"key":"R31-3-20210129","doi-asserted-by":"crossref","first-page":"549","DOI":"10.1091\/mbc.e05-08-0818","article-title":"Unique suppression of prostaglandin H synthase-2 expression by inhibition of histone deacetylation, specifically in human amnion but not adjacent choriodecidua","volume":"17","author":"Mitchell","year":"2006","journal-title":"Mol Biol Cell"},{"issue":"5","key":"R32-3-20210129","doi-asserted-by":"crossref","first-page":"68R","DOI":"10.1203\/pdr.0b013e318045764c","article-title":"Could epigenetics play a role in the developmental origins of health and disease?","volume":"61","author":"Cutfield","year":"2007","journal-title":"Pediatr Res"},{"key":"R33-3-20210129","doi-asserted-by":"crossref","first-page":"627","DOI":"10.1016\/S0093-691X(99)00263-0","article-title":"Improving the safety of embryo technologies: possible role of genomic imprinting","volume":"53","author":"Young","year":"2000","journal-title":"Theriogenology"},{"key":"R34-3-20210129","first-page":"240","article-title":"Ubiquitin and ubiquitin\u2013protein conjugates are present in human cytotrophoblast throughout gestation","volume":"4","author":"Bebington","year":"2000","journal-title":"Early Pregnancy"},{"key":"R35-3-20210129","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1093\/hmg\/ddm280","article-title":"Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development","volume":"17","author":"Rivera","year":"2008","journal-title":"Hum Mol Genet"},{"key":"R36-3-20210129","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":"R37-3-20210129","doi-asserted-by":"crossref","first-page":"1653","DOI":"10.1093\/hmg\/ddn055","article-title":"Superovulation alters the expression of imprinted genes in the midgestation mouse placenta","volume":"17","author":"Fortier","year":"2008","journal-title":"Hum Mol Genet"},{"key":"R38-3-20210129","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":"R39-3-20210129","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1093\/molehr\/gal040","article-title":"Genetic imprinting during impaired spermatogenesis","volume":"12","author":"Hartmann","year":"2006","journal-title":"Mol Hum Reprod"},{"key":"R40-3-20210129","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":"R41-3-20210129","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":"R42-3-20210129","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"}],"container-title":["Current Opinion in Obstetrics &amp; Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.1097\/GCO.0b013e32832d7b95","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,6]],"date-time":"2026-08-06T17:53:36Z","timestamp":1786038816000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00001703-200906000-00003"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,6]]},"references-count":42,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2009]]}},"URL":"https:\/\/doi.org\/10.1097\/gco.0b013e32832d7b95","relation":{},"ISSN":["1040-872X"],"issn-type":[{"value":"1040-872X","type":"print"}],"subject":[],"published":{"date-parts":[[2009,6]]}}}