Systematic Localization of Common Disease-Associated Variation in Regulatory DNA von Maurano, Matthew T., Humbert, Richard, Rynes, Eric, Thurman, Robert E., Haugen, Eric, Wang, Hao, Reynolds, Alex P., Sandstrom, Richard, Qu, Hongzhu, Brody, Jennifer, Shafer, Anthony, Neri, Fidencio, Lee, Kristen, Kutyavin, Tanya, Stehling-Sun, Sandra, Johnson, Audra K., Canfield, Theresa K., Giste, Erika, Diegel, Morgan, Bates, Daniel, Hansen, R. Scott, Neph, Shane, Sabo, Peter J., Heimfeld, Shelly, Raubitschek, Antony, Ziegler, Steven, Cotsapas, Chris, Sotoodehnia, Nona, Glass, Ian, Sunyaev, Shamil R., Kaul, Rajinder, Stamatoyannopoulos, John A.

Volltext

Topologically associating domains are stable units of replication-timing regulation von Pope, Benjamin D., Ryba, Tyrone, Dileep, Vishnu, Yue, Feng, Wu, Weisheng, Denas, Olgert, Vera, Daniel L., Wang, Yanli, Hansen, R. Scott, Canfield, Theresa K., Thurman, Robert E., Cheng, Yong, Gülsoy, Günhan, Dennis, Jonathan H., Snyder, Michael P., Stamatoyannopoulos, John A., Taylor, James, Hardison, Ross C., Kahveci, Tamer, Ren, Bing, Gilbert, David M.

Volltext

An expansive human regulatory lexicon encoded in transcription factor footprints von Neph, Shane, Vierstra, Jeff, Stergachis, Andrew B., Reynolds, Alex P., Haugen, Eric, Vernot, Benjamin, Thurman, Robert E., John, Sam, Sandstrom, Richard, Johnson, Audra K., Maurano, Matthew T., Humbert, Richard, Rynes, Eric, Wang, Hao, Vong, Shinny, Lee, Kristen, Bates, Daniel, Diegel, Morgan, Roach, Vaughn, Dunn, Douglas, Neri, Jun, Schafer, Anthony, Hansen, R. Scott, Kutyavin, Tanya, Giste, Erika, Weaver, Molly, Canfield, Theresa, Sabo, Peter, Zhang, Miaohua, Balasundaram, Gayathri, Byron, Rachel, MacCoss, Michael J., Akey, Joshua M., Bender, M. A., Groudine, Mark, Kaul, Rajinder, Stamatoyannopoulos, John A.

Volltext

Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site von Letessier, Anne, Millot, Gaël A., Koundrioukoff, Stéphane, Lachagès, Anne-Marie, Vogt, Nicolas, Hansen, R. Scott, Malfoy, Bernard, Brison, Olivier, Debatisse, Michelle

Volltext

Sequencing newly replicated DNA reveals widespread plasticity in human replication timing von Hansen, R. Scott, Thomas, Sean, Sandstrom, Richard, Canfield, Theresa K, Thurman, Robert E, Weaver, Molly, Dorschner, Michael O, Gartler, Stanley M, Stamatoyannopoulos, John A

Volltext

Mouse regulatory DNA landscapes reveal global principles of cis-regulatory evolution von Vierstra, Jeff, Rynes, Eric, Sandstrom, Richard, Zhang, Miaohua, Canfield, Theresa, Hansen, R. Scott, Stehling-Sun, Sandra, Sabo, Peter J., Byron, Rachel, Humbert, Richard, Thurman, Robert E., Johnson, Audra K., Vong, Shinny, Lee, Kristen, Bates, Daniel, Neri, Fidencio, Diegel, Morgan, Giste, Erika, Haugen, Eric, Dunn, Douglas, Wilken, Matthew S., Josefowicz, Steven, Samstein, Robert, Chang, Kai-Hsin, Eichler, Evan E., De Bruijn, Marella, Reh, Thomas A., Skoultchi, Arthur, Rudensky, Alexander, Orkin, Stuart H., Papayannopoulou, Thalia, Treuting, Piper M., Selleri, Licia, Kaul, Rajinder, Groudine, Mark, Bender, M. A., Stamatoyannopoulos, John A.

Volltext

Conservation of trans-acting circuitry during mammalian regulatory evolution von Stergachis, Andrew B., Neph, Shane, Sandstrom, Richard, Haugen, Eric, Reynolds, Alex P., Zhang, Miaohua, Byron, Rachel, Canfield, Theresa, Stelhing-Sun, Sandra, Lee, Kristen, Thurman, Robert E., Vong, Shinny, Bates, Daniel, Neri, Fidencio, Diegel, Morgan, Giste, Erika, Dunn, Douglas, Vierstra, Jeff, Hansen, R. Scott, Johnson, Audra K., Sabo, Peter J., Wilken, Matthew S., Reh, Thomas A., Treuting, Piper M., Kaul, Rajinder, Groudine, Mark, Bender, M. A., Borenstein, Elhanan, Stamatoyannopoulos, John A.

Volltext

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals von Ladd, Paula D., Smith, Leslie E., Rabaia, Natalia A., Moore, James M., Georges, Sara A., Hansen, R. Scott, Hagerman, Randi J., Tassone, Flora, Tapscott, Stephen J., Filippova, Galina N.

Volltext

X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis von HANSEN, R. Scott

Volltext

The DNMT3B DNA Methyltransferase Gene Is Mutated in the ICF Immunodeficiency Syndrome von Hansen, R. Scott, Wijmenga, Cisca, Luo, Ping, Stanek, Ann M., Canfield, Theresa K., Corry M. R. Weemaes, Gartler, Stanley M.

Volltext

The accessible chromatin landscape of the human genome von Thurman, Robert E., Rynes, Eric, Humbert, Richard, Vierstra, Jeff, Maurano, Matthew T., Haugen, Eric, Sheffield, Nathan C., Stergachis, Andrew B., Wang, Hao, Vernot, Benjamin, Garg, Kavita, John, Sam, Sandstrom, Richard, Bates, Daniel, Boatman, Lisa, Canfield, Theresa K., Diegel, Morgan, Dunn, Douglas, Ebersol, Abigail K., Frum, Tristan, Giste, Erika, Johnson, Audra K., Johnson, Ericka M., Kutyavin, Tanya, Lajoie, Bryan, Lee, Bum-Kyu, Lee, Kristen, London, Darin, Lotakis, Dimitra, Neph, Shane, Neri, Fidencio, Nguyen, Eric D., Qu, Hongzhu, Reynolds, Alex P., Roach, Vaughn, Safi, Alexias, Sanchez, Minerva E., Sanyal, Amartya, Shafer, Anthony, Simon, Jeremy M., Song, Lingyun, Vong, Shinny, Weaver, Molly, Yan, Yongqi, Zhang, Zhancheng, Zhang, Zhuzhu, Lenhard, Boris, Tewari, Muneesh, Dorschner, Michael O., Hansen, R. Scott, Navas, Patrick A., Stamatoyannopoulos, George, Iyer, Vishwanath R., Lieb, Jason D., Sunyaev, Shamil R., Akey, Joshua M., Sabo, Peter J., Kaul, Rajinder, Furey, Terrence S., Dekker, Job, Crawford, Gregory E., Stamatoyannopoulos, John A.

Volltext

Hairpin-Bisulfite PCR: Assessing Epigenetic Methylation Patterns on Complementary Strands of Individual DNA Molecules von Laird, Charles D., Pleasant, Nicole D., Clark, Aaron D., Sneeden, Jessica L., K. M. Anwarul Hassan, Manley, Nathan C., Vary, Jay C., Morgan, Todd, Hansen, R. Scott, Stöger, Reinhard

Volltext

Late-replicating heterochromatin is characterized by decreased cytosine methylation in the human genome von Suzuki, Masako, Oda, Mayumi, Ramos, María-Paz, Pascual, Marién, Lau, Kevin, Stasiek, Edyta, Agyiri, Frederick, Thompson, Reid F, Glass, Jacob L, Jing, Qiang, Sandstrom, Richard, Fazzari, Melissa J, Hansen, R Scott, Stamatoyannopoulos, John A, McLellan, Andrew S, Greally, John M

Volltext

Dosage regulation of the active X chromosome in human triploid cells von Deng, Xinxian, Nguyen, Di Kim, Hansen, R Scott, Van Dyke, Daniel L, Gartler, Stanley M, Disteche, Christine M

Volltext

Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR von Miner, Brooks E., Stöger, Reinhard J., Burden, Alice F., Laird, Charles D., Hansen, R. Scott

Volltext

Analysis of Human Syndromes with Disordered Chromatin Reveals the Impact of Heterochromatin on the Efficacy of ATM-Dependent G2/M Checkpoint Arrest von Brunton, Holly, Goodarzi, Aaron A., Noon, Angela T., Shrikhande, Amruta, Hansen, R. Scott, Jeggo, Penny A., Shibata, Atsushi

Volltext

Hemimethylation and Non-CpG Methylation Levels in a Promoter Region of Human LINE-1 (L1) Repeated Elements von Burden, Alice F., Manley, Nathan C., Clark, Aaron D., Gartler, Stanley M., Laird, Charles D., Hansen, R. Scott

Volltext

DNase I hypersensitivity analysis of the mouse brain and retina identifies region-specific regulatory elements von Wilken, Matthew S, Brzezinski, Joseph A, La Torre, Anna, Siebenthall, Kyle, Thurman, Robert, Sabo, Peter, Sandstrom, Richard S, Vierstra, Jeff, Canfield, Theresa K, Hansen, R Scott, Bender, Michael A, Stamatoyannopoulos, John, Reh, Thomas A

Volltext

A genome-wide map of adeno-associated virus–mediated human gene targeting von Deyle, David R, Hansen, R Scott, Cornea, Anda M, Li, Li B, Burt, Amber A, Alexander, Ian E, Sandstrom, Richard S, Stamatoyannopoulos, John A, Wei, Chia-Lin, Russell, David W

Volltext

Genetic variation in ICF syndrome: Evidence for genetic heterogeneity von Wijmenga, Cisca, Hansen, R. Scott, Gimelli, Giorgio, Björck, Erik J., Davies, E. Graham, Valentine, David, Belohradsky, Bernd H., van Dongen, Jacques J., Smeets, Dominique F.C.M., van den Heuvel, Lambert P.W.J., Luyten, Jan A.F.M., Strengman, Eric, Weemaes, Corry, Pearson, Peter L.

Volltext