Enzymatic approaches and bisulfite sequencing cannot distinguish between 5-methylcytosine and 5-hydroxymethylcytosine in DNA von Nestor, Colm, Ruzov, Alexey, Meehan, Richard R, Dunican, Donncha S

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Redistribution of H3K27me3 upon DNA hypomethylation results in de-repression of Polycomb target genes von Reddington, James P, Perricone, Sara M, Nestor, Colm E, Reichmann, Judith, Youngson, Neil A, Suzuki, Masako, Reinhardt, Diana, Dunican, Donncha S, Prendergast, James G, Mjoseng, Heidi, Ramsahoye, Bernard H, Whitelaw, Emma, Greally, John M, Adams, Ian R, Bickmore, Wendy A, Meehan, Richard R

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The CXXC-TET bridge - mind the methylation gap von Dunican, Donncha S, Pennings, Sari, Meehan, Richard R

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The interaction of xKaiso with xTcf3: a revised model for integration of epigenetic and Wnt signalling pathways von Ruzov, Alexey, Hackett, Jamie A, Prokhortchouk, Anna, Reddington, James P, Madej, Monika J, Dunican, Donncha S, Prokhortchouk, Egor, Pennings, Sari, Meehan, Richard R

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Senescent cells harbour features of the cancer epigenome von Cruickshanks, Hazel A., McBryan, Tony, Nelson, David M., VanderKraats, Nathan D., Shah, Parisha P., van Tuyn, John, Singh Rai, Taranjit, Brock, Claire, Donahue, Greg, Dunican, Donncha S., Drotar, Mark E., Meehan, Richard R., Edwards, John R., Berger, Shelley L., Adams, Peter D.

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Rapid reprogramming of epigenetic and transcriptional profiles in mammalian culture systems von Nestor, Colm E, Ottaviano, Raffaele, Reinhardt, Diana, Cruickshanks, Hazel A, Mjoseng, Heidi K, McPherson, Rhoanne C, Lentini, Antonio, Thomson, John P, Dunican, Donncha S, Pennings, Sari, Anderton, Stephen M, Benson, Mikael, Meehan, Richard R

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Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybri... von DUNICAN, Donncha S, MCWILLIAM, Peter, TIGHE, Orna, PARLE-MCDERMOTT, Anne, CROKE, David T

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Expression of a large LINE-1-driven antisense RNA is linked to epigenetic silencing of the metastasis suppressor gene TFPI-2 in cancer von Cruickshanks, Hazel A, Vafadar-Isfahani, Natasha, Dunican, Donncha S, Lee, Andy, Sproul, Duncan, Lund, Jonathan N, Meehan, Richard R, Tufarelli, Cristina

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Activation of transcription factor circuity in 2i-induced ground state pluripotency is independent of repressive global epigenetic landscapes von Shukla, Ruchi, Mjoseng, Heidi K, Thomson, John P, Kling, Simon, Sproul, Duncan, Dunican, Donncha S, Ramsahoye, Bernard, Wongtawan, Tuempong, Treindl, Fridolin, Templin, Markus F, Adams, Ian R, Pennings, Sari, Meehan, Richard R

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Lsh regulates LTR retrotransposon repression independently of Dnmt3b function von Dunican, Donncha S, Cruickshanks, Hazel A, Suzuki, Masako, Semple, Colin A, Davey, Tracey, Arceci, Robert J, Greally, John, Adams, Ian R, Meehan, Richard R

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Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques von Thomson, John P, Hunter, Jennifer M, Nestor, Colm E, Dunican, Donncha S, Terranova, Rémi, Moggs, Jonathan G, Meehan, Richard R

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Apoptosis and DNA methylation von Meng, Huan X, Hackett, James A, Nestor, Colm, Dunican, Donncha S, Madej, Monika, Reddington, James P, Pennings, Sari, Harrison, David J, Meehan, Richard R

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Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques von Thomson, J. P., Hunter, J. M., Nestor, C. E., Dunican, D. S., Terranova, R., Moggs, J. G., Meehan, R. R.

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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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Correction: Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA... von Dunican, Donncha S, McWilliam, Peter, Tighe, Orna, Parle-McDermott, Anne, Croke, David T

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Gene expression differences between the microsatellite instability phenotypes in colorectal cancer revealed by high-density cDNA array hybridization von Dunican, Donncha S, McWilliam, Peter, Tighe, Orna, Parle-McDermott, Anne, Croke, David T

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Genetic diversity within the R408W phenylketonuria mutation lineages in Europe von Tighe, Orna, Dunican, Donncha, O'Neill, Charles, Bertorelle, Giorgio, Beattie, Diane, Graham, Colin, Zschocke, Johannes, Cali, Francesco, Romano, Valentino, Hrabincova, Eva, Kozak, Libor, Nechyporenko, Marina, Livshits, Ludmilla, Guldberg, Per, Jurkowska, Monika, Zekanowski, Cezary, Perez, Belen, Desviat, Lourdes Ruiz, Ugarte, Magdalena, Kučinskas, Vaidutis, Knappskog, Per, Treacy, Eileen, Naughten, Eileen, Tyfield, Linda, Byck, Susan, Scriver, Charles R., Mayne, Philip D., Croke, David T.

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