Tongue base suspension in children with cerebral palsy and obstructive sleep apnea von Hartzell, Larry David, Guillory, Ryan M, Munson, Patrick David, Dunham, Andrew K, Bower, Charles Michael, Richter, Gresham Thomas

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Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly von Aneichyk, Tatsiana, Hendriks, William T., Yadav, Rachita, Shin, David, Gao, Dadi, Vaine, Christine A., Collins, Ryan L., Domingo, Aloysius, Currall, Benjamin, Stortchevoi, Alexei, Multhaupt-Buell, Trisha, Penney, Ellen B., Cruz, Lilian, Dhakal, Jyotsna, Brand, Harrison, Hanscom, Carrie, Antolik, Caroline, Dy, Marisela, Ragavendran, Ashok, Underwood, Jason, Cantsilieris, Stuart, Munson, Katherine M., Eichler, Evan E., Acuña, Patrick, Go, Criscely, Jamora, R. Dominic G., Rosales, Raymond L., Church, Deanna M., Williams, Stephen R., Garcia, Sarah, Klein, Christine, Müller, Ulrich, Wilhelmsen, Kirk C., Timmers, H. T. Marc, Sapir, Yechiam, Wainger, Brian J., Henderson, Daniel, Ito, Naoto, Weisenfeld, Neil, Jaffe, David, Sharma, Nutan, Breakefield, Xandra O., Ozelius, Laurie J., Bragg, D. Cristopher, Talkowski, Michael E.

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Whole blood gene expression and atrial fibrillation: the Framingham Heart Study von Lin, Honghuang, Yin, Xiaoyan, Lunetta, Kathryn L, Dupuis, Josée, McManus, David D, Lubitz, Steven A, Magnani, Jared W, Joehanes, Roby, Munson, Peter J, Larson, Martin G, Levy, Daniel, Ellinor, Patrick T, Benjamin, Emelia J

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Assembly of 43 human Y chromosomes reveals extensive complexity and variation von Hallast, Pille, Ebert, Peter, Loftus, Mark, Yilmaz, Feyza, Audano, Peter A., Logsdon, Glennis A., Bonder, Marc Jan, Zhou, Weichen, Höps, Wolfram, Kim, Kwondo, Li, Chong, Hoyt, Savannah J., Dishuck, Philip C., Porubsky, David, Tsetsos, Fotios, Kwon, Jee Young, Zhu, Qihui, Munson, Katherine M., Hasenfeld, Patrick, Harvey, William T., Lewis, Alexandra P., Kordosky, Jennifer, Hoekzema, Kendra, O’Neill, Rachel J., Korbel, Jan O., Tyler-Smith, Chris, Eichler, Evan E., Shi, Xinghua, Beck, Christine R., Marschall, Tobias, Konkel, Miriam K., Lee, Charles

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes von Glessner, Joseph T., Wang, Kai, Cai, Guiqing, Korvatska, Olena, Kim, Cecilia E., Wood, Shawn, Zhang, Haitao, Estes, Annette, Brune, Camille W., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Reichert, Jennifer, Crawford, Emily L., Munson, Jeffrey, Sleiman, Patrick M. A., Chiavacci, Rosetta, Annaiah, Kiran, Thomas, Kelly, Hou, Cuiping, Glaberson, Wendy, Flory, James, Otieno, Frederick, Garris, Maria, Soorya, Latha, Klei, Lambertus, Piven, Joseph, Meyer, Kacie J., Anagnostou, Evdokia, Sakurai, Takeshi, Game, Rachel M., Rudd, Danielle S., Zurawiecki, Danielle, McDougle, Christopher J., Davis, Lea K., Miller, Judith, Posey, David J., Michaels, Shana, Kolevzon, Alexander, Silverman, Jeremy M., Bernier, Raphael, Levy, Susan E., Schultz, Robert T., Dawson, Geraldine, Owley, Thomas, McMahon, William M., Wassink, Thomas H., Sweeney, John A., Nurnberger, John I., Coon, Hilary, Sutcliffe, James S., Minshew, Nancy J., Grant, Struan F. A., Bucan, Maja, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Schellenberg, Gerard D., Hakonarson, Hakon

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Human-specific tandem repeat expansion and differential gene expression during primate evolution von Sulovari, Arvis, Li, Ruiyang, Audano, Peter A., Porubsky, David, Vollger, Mitchell R., Logsdon, Glennis A., Warren, Wesley C., Pollen, Alex A., Chaisson, Mark J. P., Eichler, Evan E.

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Gaps and complex structurally variant loci in phased genome assemblies von Porubsky, David, Vollger, Mitchell R, Harvey, William T, Rozanski, Allison N, Ebert, Peter, Hickey, Glenn, Hasenfeld, Patrick, Sanders, Ashley D, Stober, Catherine, Korbel, Jan O, Paten, Benedict, Marschall, Tobias, Eichler, Evan E

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Impact and characterization of serial structural variations across humans and great apes von Höps, Wolfram, Rausch, Tobias, Jendrusch, Michael, Korbel, Jan O., Sedlazeck, Fritz J.

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Rare A2ML1 variants confer susceptibility to otitis media von Santos-Cortez, Regie Lyn P, Chiong, Charlotte M, Reyes-Quintos, Ma Rina T, Tantoco, Ma Leah C, Wang, Xin, Acharya, Anushree, Abbe, Izoduwa, Giese, Arnaud P, Smith, Joshua D, Allen, E Kaitlynn, Li, Biao, Cutiongco-de la Paz, Eva Maria, Garcia, Marieflor Cristy, Llanes, Erasmo Gonzalo D V, Labra, Patrick John, Gloria-Cruz, Teresa Luisa I, Chan, Abner L, Wang, Gao T, Daly, Kathleen A, Shendure, Jay, Bamshad, Michael J, Nickerson, Deborah A, Patel, Janak A, Riazuddin, Saima, Sale, Michele M, Chonmaitree, Tasnee, Ahmed, Zubair M, Abes, Generoso T, Leal, Suzanne M

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Mako: A Graph-based Pattern Growth Approach to Detect Complex Structural Variants von Lin, Jiadong, Yang, Xiaofei, Kosters, Walter, Xu, Tun, Jia, Yanyan, Wang, Songbo, Zhu, Qihui, Ryan, Mallory, Guo, Li, Zhang, Chengsheng, Gerstein, Mark B., Sanders, Ashley D., Zody, Micheal C., Talkowski, Michael E., Mills, Ryan E., Korbel, Jan O., Marschall, Tobias, Ebert, Peter, Audano, Peter A., Rodriguez-Martin, Bernardo, Porubsky, David, Jan Bonder, Marc, Sulovari, Arvis, Ebler, Jana, Zhou, Weichen, Serra Mari, Rebecca, Yilmaz, Feyza, Zhao, Xuefang, Hsieh, PingHsun, Lee, Joyce, Kumar, Sushant, Rausch, Tobias, Chen, Yu, Chong, Zechen, Munson, Katherine M., Chaisson, Mark J.P., Chen, Junjie, Shi, Xinghua, Wenger, Aaron M., Harvey, William T., Hansenfeld, Patrick, Regier, Allison, Hall, Ira M., Flicek, Paul, Hastie, Alex R., Fairely, Susan, Lee, Charles, Devine, Scott E., Eichler, Evan E., Ye, Kai

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Congenital nasal pyriform aperture stenosis and ocular albinism co-occurring in a sibship with a maternally-inherited 97 kb Xp22.2 microdeletion von Somsen, David, Davis-Keppen, Laura, Crotwell, Patricia, Flanagan, Jason, Munson, Patrick, Stein, Quinn

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Congenital nasal pyriform aperture stenosis and ocular albinism co-occurring in a sibship with a maternally-inherited 97kb Xp22.2 microdeletion von Somsen, David, Davis-Keppen, Laura, Crotwell, Patricia, Flanagan, Jason, Munson, Patrick, Stein, Quinn

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements von Szatmari, Peter, Paterson, Andrew D, Zwaigenbaum, Lonnie, Roberts, Wendy, Brian, Jessica, Liu, Xiao-Qing, Vincent, John B, Skaug, Jennifer L, Thompson, Ann P, Senman, Lili, Feuk, Lars, Qian, Cheng, Bryson, Susan E, Jones, Marshall B, Marshall, Christian R, Scherer, Stephen W, Vieland, Veronica J, Bartlett, Christopher, Mangin, La Vonne, Goedken, Rhinda, Segre, Alberto, Pericak-Vance, Margaret A, Cuccaro, Michael L, Gilbert, John R, Wright, Harry H, Abramson, Ruth K, Betancur, Catalina, Bourgeron, Thomas, Gillberg, Christopher, Leboyer, Marion, Buxbaum, Joseph D, Davis, Kenneth L, Hollander, Eric, Silverman, Jeremy M, Hallmayer, Joachim, Lotspeich, Linda, Sutcliffe, James S, Haines, Jonathan L, Folstein, Susan E, Piven, Joseph, Wassink, Thomas H, Sheffield, Val, Geschwind, Daniel H, Bucan, Maja, Brown, W Ted, Cantor, Rita M, Constantino, John N, Gilliam, T Conrad, Herbert, Martha, Lajonchere, Clara, Ledbetter, David H, Lese-Martin, Christa, Miller, Janet, Nelson, Stan, Samango-Sprouse, Carol A, Spence, Sarah, State, Matthew, Tanzi, Rudolph E, Coon, Hilary, Dawson, Geraldine, Devlin, Bernie, Estes, Annette, Flodman, Pamela, Klei, Lambertus, McMahon, William M, Minshew, Nancy, Munson, Jeff, Korvatska, Elena, Rodier, Patricia M, Schellenberg, Gerard D, Smith, Moyra, Spence, M Anne, Stodgell, Chris, Tepper, Ping Guo, Wijsman, Ellen M, Yu, Chang-En, Rogé, Bernadette, Mantoulan, Carine, Wittemeyer, Kerstin, Poustka, Annemarie, Felder, Bärbel, Klauck, Sabine M, Schuster, Claudia, Poustka, Fritz, Bölte, Sven, Feineis-Matthews, Sabine, Herbrecht, Evelyn, Schmötzer, Gabi, Tsiantis, John, Papanikolaou, Katerina, Maestrini, Elena, Bacchelli, Elena, Blasi, Francesca, Carone, Simona, Toma, Claudio, Van Engeland, Herman, de Jonge, Maretha, Kemner, Chantal, Koop, Frederieke, Koop, Frederike

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Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes von Liu, Xiao-Qing, Paterson, Andrew D, Szatmari, Peter

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Whole Blood Gene Expression and Atrial Fibrillation: The Framingham Heart Study von Lin, Honghuang, Yin, Xiaoyan, Lunetta, Kathryn L, Dupuis, Josée, McManus, David D, Lubitz, Steven A, Magnani, Jared W, Joehanes, Roby, Munson, Peter J, Larson, Martin G, Levy, Daniel, Ellinor, Patrick T, Benjamin, Emelia J

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Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders von Anney, Richard J L, Kenny, Elaine M, O'Dushlaine, Colm, Yaspan, Brian L, Parkhomenka, Elena, Buxbaum, Joseph D, Sutcliffe, James, Gill, Michael, Gallagher, Louise

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MACROCYCLIC COMPOUNDS, COMPOSITIONS, AND METHODS OF USING THEREOF von BORCHERDING, David, GUESSREGEN, Stefan, GAO, Zhongli, CAUSSANEL, Franck, GOOD, Andrew, DEVILLERS, Ingrid, SCHWINK, Lothar, RACKELMANN, Nils, THURAIRATNAM, Sukanthini, HIRTH, Brad, LIU, Jinyu, HURLBUT, Greg, GENEVOIS-BORELLA, Arielle, TOPALOV, George, THOMPSON, Fabienne, RUF, Sven, MACOR, John, VAZ, Roy, LI, Yi, BERNARDELLI, Patrick, LIAO, Junkai, GLOMBIK, Heiner, NICOLAI, Eric, RUVINSKY, Anatoly, MUNSON, Mark, KOTHE, Michael, PODESCHWA, Michael, SLOWINSKI, Franck

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MACROCYCLIC COMPOUNDS, COMPOSITIONS AND METHODS OF USING THEREOF von BORCHERDING, David, GUESSREGEN, Stefan, GAO, Zhongli, CAUSSANEL, Franck, GOOD, Andrew, BERNADELLI, Patrick, DEVILLERS, Ingrid, SCHWINK, Lothar, RACKELMANN, Nils, THURAIRATNAM, Sukanthini, HIRTH, Brad, LIU, Jinyu, HURLBUT, Greg, GENEVOIS-BORELLA, Arielle, TOPALOV, George, THOMPSON, Fabienne, RUF, Sven, MACOR, John, VAZ, Roy, LI, Yi, LIAO, Junkai, GLOMBIK, Heiner, NICOLAI, Eric, RUVINSKY, Anatoly, MUNSON, Mark, KOTHE, Michael, PODESCHWA, Michael, SLOWINSKI, Franck

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Assembly of 43 human Y chromosomes reveals extensive complexity and variation von Hallast, Pille, Ebert, Peter, Loftus, Mark, Yilmaz, Feyza, Audano, Peter A., Logsdon, Glennis A., Bonder, Marc Jan, Zhou, Weichen, Höps, Wolfram, Kim, Kwondo, Li, Chong, Dishuck, Philip, Porubsky, David, Tsetsos, Fotios, Kwon, Jee Young, Zhu, Qihui, Munson, Katherine M., Hasenfeld, Patrick, Harvey, William T., Lewis, Alexandra P., Kordosky, Jennifer, Hoekzema, Kendra, (HGSVC), Human Genome Structural Variation Consortium, Korbel, Jan O., Tyler-Smith, Chris, Eichler, Evan E., Shi, Xinghua, Beck, Christine R., Marschall, Tobias, Konkel, Miriam K., Lee, Charles, Hoyt, Savannah J., O’Neill, Rachel J.

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COMPUESTOS, COMPOSICIONES Y MÉTODOS DE USO DE LOS MISMOS von HIRTH, BRAD, KOTHE, MICHAEL, LIU, JINYU, RACKELMANN, NILS, GENEVOIS-BORELLA, ARIELLE, GLOMBIK, HEINER, BERNARDELLI, PATRICK, RUVINSKY, ANATOLY, PODESCHWA, MICHAEL, THURAIRATNAM, SUKANTHINI, RUF, SVEN, BORCHERDING, DAVID, DEVILLERS, INGRID, GUESSREGEN, STEFAN, MACOR, JOHN, GOOD, ANDREW, LI, YI, GAO, ZHONGLI, NICOLAI, ERIC, SLOWINSKI, FRANCK, THOMPSON, FABIENNE, TOPALOV, GEORGE, SCHWINK, LOTHAR, MUNSON, MARK, CAUSSANEL, FRANCK, LIAO, JUNKAI, VAZ, ROY, HURLBUT, GREG

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