Base-Resolution Analyses of Sequence and Parent-of-Origin Dependent DNA Methylation in the Mouse Genome von Xie, Wei, Barr, Cathy L., Kim, Audrey, Yue, Feng, Lee, Ah Young, Eubanks, James, Dempster, Emma L., Ren, Bing

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A Compendium of Chromatin Contact Maps Reveals Spatially Active Regions in the Human Genome von Schmitt, Anthony D., Hu, Ming, Jung, Inkyung, Xu, Zheng, Qiu, Yunjiang, Tan, Catherine L., Li, Yun, Lin, Shin, Lin, Yiing, Barr, Cathy L., Ren, Bing

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A compendium of promoter-centered long-range chromatin interactions in the human genome von Jung, Inkyung, Schmitt, Anthony, Diao, Yarui, Lee, Andrew J., Liu, Tristin, Yang, Dongchan, Tan, Catherine, Eom, Junghyun, Chan, Marilynn, Chee, Sora, Chiang, Zachary, Kim, Changyoun, Masliah, Eliezer, Barr, Cathy L., Li, Bin, Kuan, Samantha, Kim, Dongsup, Ren, Bing

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EGFR Mutation Promotes Glioblastoma through Epigenome and Transcription Factor Network Remodeling von Liu, Feng, Hon, Gary C., Villa, Genaro R., Turner, Kristen M., Ikegami, Shiro, Yang, Huijun, Ye, Zhen, Li, Bin, Kuan, Samantha, Lee, Ah Young, Zanca, Ciro, Wei, Bowen, Lucey, Greg, Jenkins, David, Zhang, Wei, Barr, Cathy L., Furnari, Frank B., Cloughesy, Timothy F., Yong, William H., Gahman, Timothy C., Shiau, Andrew K., Cavenee, Webster K., Ren, Bing, Mischel, Paul S.

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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies von Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S, Huang, Alden Y, Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M, Hirschtritt, Matthew E, Greenberg, Erica, Muller-Vahl, Kirsten R, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, Hinney, Anke, King, Robert A, Fernandez, Thomas V, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L, Rizzo, Renata, Lyon, Gholson J, McMahon, William M, Batterson, James R, Cath, Danielle C, Malaty, Irene A, Okun, Michael S, Berlin, Cheston, Woods, Douglas W, Lee, Paul C, Jankovic, Joseph, Robertson, Mary M, Gilbert, Donald L, Brown, Lawrence W, Coffey, Barbara J, Dietrich, Andrea, Hoekstra, Pieter J, Kuperman, Samuel, Zinner, Samuel H, Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N, Pato, Michele T, Knowles, James A, Roffman, Joshua L, Smoller, Jordan W, Buckner, Randy L, Willsey, A. Jeremy, Tischfield, Jay A, Heiman, Gary A, Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J, Pauls, David L, Freimer, Nelson B, Neale, Benjamin M, Davis, Lea K, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M

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DNA Variant in the RPGRIP1L Gene Influences Alternative Splicing von Reble, Emma, Feng, Yu, Wigg, Karen G., Barr, Cathy L.

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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome von Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M., Coppola, Giovanni, Bruun, Ruth D., Chouinard, Sylvain, Darrow, Sabrina, Greenberg, Erica, Hirschtritt, Matthew E., Kurlan, Roger, Leckman, James F., Robertson, Mary M., Smit, Jan

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Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology von Alexander, John, Potamianou, Hera, Xing, Jinchuan, Deng, Li, Karagiannidis, Iordanis, Tsetsos, Fotis, Drineas, Petros, Tarnok, Zsanett, Rizzo, Renata, Wolanczyk, Tomasz, Farkas, Luca, Nagy, Peter, Szymanska, Urszula, Androutsos, Christos, Tsironi, Vaia, Koumoula, Anastasia, Barta, Csaba, Sandor, Paul, Barr, Cathy L, Tischfield, Jay, Paschou, Peristera, Heiman, Gary A, Georgitsi, Marianthi

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Association of SLITRK1 to Gilles de la Tourette Syndrome von Miranda, Debora M., Wigg, Karen, Kabia, E. Mameisia, Feng, Yu, Sandor, Paul, Barr, Cathy L.

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The Dyslexia-associated gene KIAA0319L is involved in neuronal migration in the developing chick visual system von Charish, Jason, Harada, Hidekiyo, Chen, Xiaoyan, Wälchli, Thomas, Barr, Cathy L, Monnier, Philippe P

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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture von Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Neale, Benjamin M, Yang, Jian, Lee, S Hong, Evans, Patrick, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Blom, Rianne M, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C, Cath, Danielle C, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Gallagher, Patience J, Garrido, Helena, Geller, Daniel, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian M J, Hounie, Ana G, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Mesa Restrepo, Sandra C, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Romero, Roxana, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H

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Genome‐wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders von Price, Kaitlyn M., Wigg, Karen G., Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, He, Gengming, Kerr, Elizabeth N., Carter, Tasha‐Cate, Guger, Sharon L., Lovett, Maureen W., Strug, Lisa J., Barr, Cathy L.

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Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneity von Raviram, Ramya, Raman, Anugraha, Preissl, Sebastian, Ning, Jiangfang, Wu, Shaoping, Koga, Tomoyuki, Zhang, Kai, Brennan, Cameron W, Zhu, Chenxu, Luebeck, Jens, Van Deynze, Kinsey, Han, Jee Yun, Hou, Xiaomeng, Ye, Zhen, Mischel, Anna K, Li, Yang Eric, Fang, Rongxin, Baback, Tomas, Mugford, Joshua, Han, Claudia Z, Glass, Christopher K, Barr, Cathy L, Mischel, Paul S, Bafna, Vineet, Escoubet, Laure, Ren, Bing, Chen, Clark C

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Language Difficulties in School-Age Children With Developmental Dyslexia von Price, Kaitlyn M., Wigg, Karen G., Misener, Virginia L., Clarke, Antoine, Yeung, Natalie, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Lovett, Maureen W., Barr, Cathy L.

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Identification of brain cell types underlying genetic association with word reading and correlated traits von Price, Kaitlyn M., Wigg, Karen G., Nigam, Anukrati, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Lovett, Maureen W., Strug, Lisa J., Tripathy, Shreejoy J., Barr, Cathy L.

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Language and reading impairments are associated with increased prevalence of non‐right‐handedness von Abbondanza, Filippo, Dale, Philip S., Wang, Carol A., Hayiou‐Thomas, Marianna E., Toseeb, Umar, Koomar, Tanner S., Wigg, Karen G., Feng, Yu, Price, Kaitlyn M., Kerr, Elizabeth N., Guger, Sharon L., Lovett, Maureen W., Strug, Lisa J., Bergen, Elsje, Dolan, Conor V., Tomblin, J. Bruce, Moll, Kristina, Schulte‐Körne, Gerd, Neuhoff, Nina, Warnke, Andreas, Fisher, Simon E., Barr, Cathy L., Michaelson, Jacob J., Boomsma, Dorret I., Snowling, Margaret J., Hulme, Charles, Whitehouse, Andrew J. O., Pennell, Craig E., Newbury, Dianne F., Stein, John, Talcott, Joel B., Bishop, Dorothy V. M., Paracchini, Silvia

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Validating psychiatric endophenotypes: Inhibitory control and attention deficit hyperactivity disorder von Crosbie, Jennifer, Pérusse, Daniel, Barr, Cathy L., Schachar, Russell J.

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Synaptic processes and immune-related pathways implicated in Tourette syndrome von Yu, Dongmei, Sul, Jae Hoon, Huang, Alden Y., Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy A., Aschauer, Harald, Barr, Cathy L., Grados, Marco A., Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Rizzo, Renata, McMahon, William M., Batterson, James R., Cath, Danielle C., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Lee, Paul C., Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Dietrich, Andrea, Hoekstra, Pieter J., Kuperman, Samuel, Wagner, Michael, Knowles, James A., Jeremy Willsey, A., Tischfield, Jay A., Heiman, Gary A., Cox, Nancy J., Freimer, Nelson B., Davis, Lea K., Mathews, Carol A., Scharf, Jeremiah M., Paschou, Peristera, Coppola, Giovanni, Darrow, Sabrina, Davis, Lea K., Dion, Yves, Freimer, Nelson B., Greenberg, Erica, Kurlan, Roger, Leckman, James F., Malaty, Irene A., Neale, Benjamin M., Okun, Michael S., Rouleau, Guy A., Smit, Jan H., Aschauer, Harald Aschauer Harald, Barta, Csaba, Depienne, Christel, Konstantinidis, Anastasios, Müller-Vahl, Kirsten, Paschou, Peristera, Wolanczyk, Tomasz, Brown, Lawrence, Fernandez, Thomas V., Garcia-Delgar, Blanca, Gilbert, Donald, Grice, Dorothy E., Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Leventhal, Bennett L., Madruga-Garrido, Marcos, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Willsey, A. Jeremy, Zinner, Samuel, Aschauer, Harald, Fernandez, Thomas, Heiman, Gary, Hoekstra, Pieter, Tischfield, Jay

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Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder von Barr, Cathy L, Xu, Chun, Kroft, Jamie, Feng, Yu, Wigg, Karen, Zai, Gwyneth, Tannock, Rosemary, Schachar, Russell, Malone, Molly, Roberts, Wendy, Nöthen, Markus M, Grünhage, Frank, Vandenbergh, David J, Uhl, George, Sunohara, Glen, King, Nicole, Kennedy, James L

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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities von Price, Kaitlyn M., Wigg, Karen G., Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Fisher, Simon E., Lovett, Maureen W., Strug, Lisa J., Barr, Cathy L.

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