{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T01:23:38Z","timestamp":1790472218377,"version":"4.1.0"},"reference-count":144,"publisher":"The Company of Biologists","license":[{"start":{"date-parts":[[2021,5,18]],"date-time":"2021-05-18T00:00:00Z","timestamp":1621296000000},"content-version":"am","delay-in-days":503,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["GM051279"],"award-info":[{"award-number":["GM051279"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>Genomic imprinting, a phenomenon where the two parental alleles are regulated differently, is observed in mammals, marsupials and a few other species, including seed-bearing plants. Dysregulation of genomic imprinting can cause developmental disorders such as Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syndrome (SRS). In this review, we discuss 1) how various (epi)genetic lesions lead to the dysregulation of clinically relevant imprinted loci and 2) how such perturbations may contribute to the developmental defects in BWS and SRS. Given that the regulatory mechanisms of most imprinted clusters are well conserved between mice and humans, numerous mouse models of BWS and SRS have been generated. These mouse models are key to understanding how mutations at imprinted loci result in pathological phenotypes in humans, although there are some limitations. This review focuses on how the biological findings obtained from innovative mouse models explain clinical features of BWS and SRS.<\/jats:p>","DOI":"10.1242\/dmm.044123","type":"journal-article","created":{"date-parts":[[2020,5,18]],"date-time":"2020-05-18T12:15:10Z","timestamp":1589804110000},"source":"Crossref","is-referenced-by-count":44,"title":["Modeling human epigenetic disorders in mice: Beckwith-Wiedemann Syndrome and Silver-Russell Syndrome"],"prefix":"10.1242","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0514-3516","authenticated-orcid":false,"given":"Suhee","family":"Chang","sequence":"first","affiliation":[{"name":"Epigenetics Institute, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9410-5222","authenticated-orcid":false,"given":"Marisa S.","family":"Bartolomei","sequence":"additional","affiliation":[{"name":"Epigenetics Institute, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2020,1,1]]},"reference":[{"key":"2021042700254877400_DMM044123C1","doi-asserted-by":"publisher","first-page":"105","DOI":"10.1002\/humu.23131","article-title":"11p15 ICR1 Partial Deletions Associated with IGF2\/H19 DMR Hypomethylation and Silver\u2013Russell Syndrome","volume":"38","author":"Abi Habib","year":"2017","journal-title":"Hum. 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