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Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome

Angela Sparago, Flavia Cerrato, Maria Vernucci, Giovanni Battista Ferrero, Margherita Silengo, Andrea Riccio

Nature Genetics · 2004 · 366 citations · 12 references

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12

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

Adam C. Bell, Gary Felsenfeld · Nature · 2000 · 1.7K citations

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CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

Amy T. Hark, Christopher J. Schoenherr, David J. Katz et al. · Nature · 2000 · 1.5K citations

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Deletion of the <i>H19</i> differentially methylated domain results in loss of imprinted expression of <i>H19</i> and <i>Igf2</i>

Joanne L. Thorvaldsen, Kristen L. Duran, Marisa S. Bartolomei · Genes & Development · 1998 · 646 citations · Full text

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Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Karin Buiting, Shinji Saitoh, Bärbel Dittrich et al. · Nature Genetics · 1995 · 598 citations

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Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

Chandrasekhar Kanduri, Vinod Pant, Dmitri Loukinov et al. · Current Biology · 2000 · 446 citations · Full text

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