Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transp... von Chai, J-H., Locke, D.P., Greally, J.M., Knoll, J.H.M., Ohta, T., Dunai, J., Yavor, A., Eichler, E.E., Nicholls, R.D.

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A pre-neoplastic epigenetic field defect in HCV-infected liver at transcription factor binding sites and polycomb targets von Wijetunga, N A, Pascual, M, Tozour, J, Delahaye, F, Alani, M, Adeyeye, M, Wolkoff, A W, Verma, A, Greally, J M

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Short Interspersed Transposable Elements (SINEs) are Excluded from Imprinted Regions in the Human Genome von Greally, John M.

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Position Effects Are Influenced by the Orientation of a Transgene with Respect to Flanking Chromatin von Feng, Yong-Qing, Lorincz, Matthew C., Fiering, Steve, Greally, John M., Bouhassira, Eric E.

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A stain upon the silence: genes escaping X inactivation von Brown, Carolyn J., Greally, John M.

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β-globin YAC transgenes exhibit uniform expression levels but position effect variegation in mice von ALAMI, R, GREALLY, J. M, TANIMOTO, K, HWANG, S, FENG, Y.-Q, ENGEL, J. D, FIERING, S, BOUHASSIRA, E. E

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The mouse H19 locus mediates a transition between imprinted and non-imprinted DNA replication patterns von GREALLY, J. M, STARR, D. J, HWANG, S, SONG, L, JAAROLA, M, ZEMEL, S

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Mammalian Linker-Histone Subtypes Differentially Affect Gene Expression in vivo von Alami, Raouf, Fan, Yuhong, Pack, Stephanie, Sonbuchner, Timothy M., Besse, Arnaud, Lin, Qingcong, Greally, John M., Skoultchi, Arthur I., Bouhassira, Eric E.

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The potential role of epigenomic dysregulation in complex human disease von Hatchwell, Eli, Greally, John M

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Genetics of Childhood Disorders: VIII. Making Sense Out of Nonsense von GREALLY, JOHN M., LOMBROSO, PAUL J.

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Epigenetic Abnormalities Associated with a Chromosome 18(q21-q22) Inversion and a Gilles de la Tourette Syndrome Phenotype von State, Matthew W., Greally, John M., Cuker, Adam, Bowers, Peter N., Henegariu, Octavian, Morgan, Thomas M., Gunel, Murat, DiLuna, Michael, King, Robert A., Nelson, Carol, Donovan, Abigail, Anderson, George M., Leckman, James F., Hawkins, Trevor, Pauls, David L., Lifton, Richard P., Ward, David C.

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Genetics of Childhood Disorders: XIII. Genomic Imprinting: The Indelible Mark of the Gamete von GREALLY, JOHN M., STATE, MATTHEW W.

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Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome von GREALLY, J. M

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Epigenomics: beyond CpG islands von Fazzari, Melissa J, Greally, John M

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Applying whole-genome studies of epigenetic regulation to study human disease von Lieb, J.D., Beck, S., Bulyk, M.L., Farnham, P., Hattori, N., Henikoff, S., Liu, X.S., Okumura, K., Shiota, K., Ushijima, T., Greally, J.M.

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Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site von Chai, Jing-Hua, Locke, Devin P, Ohta, Tohru, Greally, John M, Nicholls, Robert D

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Homez, a Homeobox Leucine Zipper Gene Specific to the Vertebrate Lineage von Bayarsaihan, Dashzeveg, Enkhmandakh, Badam, Makeyev, Aleksandr, Greally, John M., Leckman, James F., Ruddle, Frank H.

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A molecular anatomical analysis of mosaic trisomy 16 von GREALLY, J. M, NEISWANGER, K, CUMMINS, J. H, BOONE, L. Y, LENKEY, S. G, WENGER, S. L, LEWIS, J. L, FISCHER, D, PAUL, R. A, STEELE, M. W

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MEN1 tumor-suppressor protein localizes to telomeres during meiosis von Suphapeetiporn, Kanya, Greally, John M., Walpita, Deepika, Ashley, Terry, Bale, Allen E.

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Identification of a Candidate Regulatory Region in the Human CD8 Gene Complex by Colocalization of DNase I Hypersensitive Sites and Matrix Attachment Regions Which Bind SATB1 and G... von Kieffer, Lynda J, Greally, John M, Landres, Inna, Nag, Shanta, Nakajima, Yuko, Kohwi-Shigematsu, Terumi, Kavathas, Paula B

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