NF1 microdeletion breakpoints are clustered at flanking repetitive sequences von DORSCHNER, M. O, SYBERT, V. P, WEAVER, M, PLETCHER, B. A, STEPHENS, K

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Genomic profiling of anaplastic meningioma identifies recurrent genetic alterations with relevance to lower‐grade meningioma von Cimino, P. J., Yoda, R. A., Wirsching, H.‐G., Warrick, J. I., Dorschner, M. O., Ferreira, M.

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Comparative analysis of two Nramp loci from rainbow trout von Dorschner, M O, Phillips, R B

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High levels of MHC class II allelic diversity in lake trout from Lake Superior von Dorschner, MO, Duris, T, Bronte, CR, Burnham Curtis, MK, Phillips, RB

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Lack of effect of beta-naphthoflavone on induction of Nramp genes in adult rainbow trout Oncorhynchus mykiss von Dasmahapatra, A.K, Wimpee, B.A.B, Budsberg, K.J, Dorschner, M.O, Phillips, R.B, Hutz, R.J

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Discovery of Functional Noncoding Elements by Digital Analysis of Chromatin Structure von Sabo, Peter J., Hawrylycz, Michael, Wallace, James C., Humbert, Richard, Yu, Man, Shafer, Anthony, Kawamoto, Janelle, Hall, Robert, Mack, Joshua, Dorschner, Michael O., McArthur, Michael, Stamatoyannopoulos, John A., Gartler, Stanley M.

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Sequence analysis of the mitochondrial DNA control region of ciscoes (genus Coregonus): taxonomic implications for the Great Lakes species flock von REED, KENT M., DORSCHNER, MICHAEL O., TODD, THOMAS N., PHILLIPS, RUTH B.

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Genome-Wide Identification of DNasel Hypersensitive Sites Using Active Chromatin Sequence Libraries von Sabo, Peter J., Humbert, Richard, Hawrylycz, Michael, Wallace, James C., Dorschner, Michael O., McArthur, Michael, Stamatoyannopoulos, John A., Davie, Earl W.

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The zebrafish mutant gene chardonnay (cdy) encodes divalent metal transporter 1 (DMT1) von Donovan, Adriana, Brownlie, Alison, Dorschner, Michael O., Zhou, Yi, Pratt, Stephen J., Paw, Barry H., Phillips, Ruth B., Thisse, Christine, Thisse, Bernard, Zon, Leonard I.

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Gammaretroviral Vector Integration Occurs Overwhelmingly Within and Near DNase Hypersensitive Sites von MINGDONG LIU, CHANG LONG LI, STAMATOYANNOPOULOS, George, DORSCHNER, Michael O, HUMBERT, Richard, STAMATOYANNOPOULOS, John A, EMERY, David W

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Genomic context of paralogous recombination hotspots mediating recurrent NF1 region microdeletion von Forbes, Stephen H., Dorschner, Michael O., Le, Rosalynda, Stephens, Karen

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Diagnosis of Five Spinocerebellar Ataxia Disorders by Multiplex Amplification and Capillary Electrophoresis von Dorschner, Michael O., Barden, Deborah, Stephens, Karen

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Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries von Sabo, Peter J, Humbert, Richard, Hawrylycz, Michael, Wallace, James C, Dorschner, Michael O, McArthur, Michael, Stamatoyannopoulos, John A

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Rare loss of function variants in candidate genes and risk of colorectal cancer von Rosenthal, EA, Shirts, BH, Amendola, LM, Horike-Pyne, M, Robertson, PD, Hisama, FM, Bennett, RL, Dorschner, MO, Nickerson, DA, Stanaway, IB, Nassir, R, Vickers, KT, Li, C, Grady, WM, Peters, U, Jarvik, GP, NHLBI GO Exome Sequencing Project

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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

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Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome von Lieberman-Aiden, Erez, van Berkum, Nynke L, Williams, Louise, Imakaev, Maxim, Ragoczy, Tobias, Telling, Agnes, Amit, Ido, Lajoie, Bryan R, Sabo, Peter J, Dorschner, Michael O, Sandstrom, Richard, Bernstein, Bradley, Bender, M.A, Groudine, Mark, Gnirke, Andreas, Stamatoyannopoulos, John, Mirny, Leonid A, Lander, Eric S, Dekker, Job

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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 von Carvill, Gemma L, Heavin, Sinéad B, Yendle, Simone C, McMahon, Jacinta M, O'Roak, Brian J, Cook, Joseph, Khan, Adiba, Dorschner, Michael O, Weaver, Molly, Calvert, Sophie, Malone, Stephen, Wallace, Geoffrey, Stanley, Thorsten, Bye, Ann M E, Bleasel, Andrew, Howell, Katherine B, Kivity, Sara, Mackay, Mark T, Rodriguez-Casero, Victoria, Webster, Richard, Korczyn, Amos, Afawi, Zaid, Zelnick, Nathanel, Lerman-Sagie, Tally, Lev, Dorit, Møller, Rikke S, Gill, Deepak, Andrade, Danielle M, Freeman, Jeremy L, Sadleir, Lynette G, Shendure, Jay, Berkovic, Samuel F, Scheffer, Ingrid E, Mefford, Heather C

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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.

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Genome-scale mapping of DNase I sensitivity in vivo using tiling DNA microarrays von Stamatoyannopoulos, John A, Sabo, Peter J, Kuehn, Michael S, Thurman, Robert, Johnson, Brett E, Johnson, Ericka M, Cao, Hua, Yu, Man, Rosenzweig, Elizabeth, Goldy, Jeff, Haydock, Andrew, Weaver, Molly, Shafer, Anthony, Lee, Kristin, Neri, Fidencio, Humbert, Richard, Singer, Michael A, Richmond, Todd A, Dorschner, Michael O, McArthur, Michael, Hawrylycz, Michael, Green, Roland D, Navas, Patrick A, Noble, William S

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Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies von Amendola, Laura M., Muenzen, Kathleen, Biesecker, Leslie G., Bowling, Kevin M., Cooper, Greg M., Dorschner, Michael O., Driscoll, Catherine, Foreman, Ann Katherine M., Golden-Grant, Katie, Greally, John M., Hindorff, Lucia, Kanavy, Dona, Jobanputra, Vaidehi, Johnston, Jennifer J., Kenny, Eimear E., McNulty, Shannon, Murali, Priyanka, Ou, Jeffrey, Powell, Bradford C., Rehm, Heidi L., Rolf, Bradley, Roman, Tamara S., Van Ziffle, Jessica, Guha, Saurav, Abhyankar, Avinash, Crosslin, David, Venner, Eric, Yuan, Bo, Zouk, Hana, Jarvik, Gail P.

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