Asymptomatic Renal Cell Carcinoma as a Finding of Bardet Biedl Syndrome von Zaldivar, Renzo A., Neale, Matthew D., Evans, William E., Pulido, Jose S.

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A Hierarchical Combination of Factors Shapes the Genome-wide Topography of Yeast Meiotic Recombination Initiation von Pan, Jing, Sasaki, Mariko, Kniewel, Ryan, Murakami, Hajime, Blitzblau, Hannah G., Tischfield, Sam E., Zhu, Xuan, Neale, Matthew J., Jasin, Maria, Socci, Nicholas D., Hochwagen, Andreas, Keeney, Scott

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An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder von Werling, Donna M., Brand, Harrison, An, Joon-Yong, Stone, Matthew R., Zhu, Lingxue, Glessner, Joseph T., Collins, Ryan L., Dong, Shan, Layer, Ryan M., Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace B., Wang, Harold Z., Currall, Benjamin B., Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn A., Gilson, Michael C., Yadav, Rachita, Handsaker, Robert E., Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D., Nowakowski, Tomasz J., Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F., Waterman, Matthew J., He, Xin, Kriegstein, Arnold R., Rubenstein, John L., Sestan, Nenad, McCarroll, Steven A., Neale, Benjamin M., Coon, Hilary, Willsey, A. Jeremy, Buxbaum, Joseph D., Daly, Mark J., State, Matthew W., Quinlan, Aaron R., Marth, Gabor T., Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E., Sanders, Stephan J.

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Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

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An inventory of atomic species in the atmosphere of WASP-121b using UVES high-resolution spectroscopy von Merritt, Stephanie R, Gibson, Neale P, Nugroho, Stevanus K, de Mooij, Ernst J W, Hooton, Matthew J, Lothringer, Joshua D, Matthews, Shannon M, Mikal-Evans, Thomas, Nikolov, Nikolay, Sing, David K, Watson, Chris A

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A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

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Dihydrogen Activation by Lithium‐ and Sodium‐Aluminyls von Evans, Matthew J., Anker, Mathew D., McMullin, Claire L., Neale, Sam E., Coles, Martyn P.

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Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder von An, Joon-Yong, Lin, Kevin, Zhu, Lingxue, Werling, Donna M, Dong, Shan, Brand, Harrison, Wang, Harold Z, Zhao, Xuefang, Schwartz, Grace B, Collins, Ryan L, Currall, Benjamin B, Dastmalchi, Claudia, Dea, Jeanselle, Duhn, Clif, Gilson, Michael C, Klei, Lambertus, Liang, Lindsay, Markenscoff-Papadimitriou, Eirene, Pochareddy, Sirisha, Ahituv, Nadav, Buxbaum, Joseph D, Coon, Hilary, Daly, Mark J, Kim, Young Shin, Marth, Gabor T, Neale, Benjamin M, Quinlan, Aaron R, Rubenstein, John L, Sestan, Nenad, State, Matthew W, Willsey, A Jeremy, Talkowski, Michael E, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J

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AAV-expressed eCD4-Ig provides durable protection from multiple SHIV challenges von Gardner, Matthew R., Kattenhorn, Lisa M., Kondur, Hema R., von Schaewen, Markus, Dorfman, Tatyana, Chiang, Jessica J., Haworth, Kevin G., Decker, Julie M., Alpert, Michael D., Bailey, Charles C., Neale, Ernest S., Fellinger, Christoph H., Joshi, Vinita R., Fuchs, Sebastian P., Martinez-Navio, Jose M., Quinlan, Brian D., Yao, Annie Y., Mouquet, Hugo, Gorman, Jason, Zhang, Baoshan, Poignard, Pascal, Nussenzweig, Michel C., Burton, Dennis R., Kwong, Peter D., Piatak, Michael, Lifson, Jeffrey D., Gao, Guangping, Desrosiers, Ronald C., Evans, David T., Hahn, Beatrice H., Ploss, Alexander, Cannon, Paula M., Seaman, Michael S., Farzan, Michael

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Hierarchical Genetic Organization of Human Cortical Surface Area von Chen, Chi-Hua, Gutierrez, E. D., Thompson, Wes, Panizzon, Matthew S., Jernigan, Terry L., Eyler, Lisa T., Fennema-Notestine, Christine, Jak, Amy J., Neale, Michael C., Franz, Carol E., Lyons, Michael J., Grant, Michael D., Fischi, Bruce, Seidman, Larry J., Tsuang, Ming T., Kremen, William S., Dale, Anders M.

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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Genetic topography of brain morphology von Chen, Chi-Hua, Fiecas, Mark, Gutierrez, E. D., Panizzon, Matthew S., Eyler, Lisa T., Vuoksimaa, Eero, Thompson, Wesley K., Fennema-Notestine, Christine, Hagler, Donald J., Jernigan, Terry L., Neale, Michael C., Franz, Carol E., Lyons, Michael J., Fischl, Bruce, Tsuang, Ming T., Dale, Anders M., Kremen, William S.

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Genetic Influences on Cortical Regionalization in the Human Brain von Chen, Chi-Hua, Panizzon, Matthew S., Eyler, Lisa T., Jernigan, Terry L., Thompson, Wes, Fennema-Notestine, Christine, Jak, Amy J., Neale, Michael C., Franz, Carol E., Hamza, Samar, Lyons, Michael J., Grant, Michael D., Fischl, Bruce, Seidman, Larry J., Tsuang, Ming T., Kremen, William S., Dale, Anders M.

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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes von Wang, Qingbo, Pierce-Hoffman, Emma, Cummings, Beryl B., Alföldi, Jessica, Francioli, Laurent C., Gauthier, Laura D., Hill, Andrew J., O’Donnell-Luria, Anne H., Karczewski, Konrad J., MacArthur, Daniel G.

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Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders von Lim, Elaine T., Raychaudhuri, Soumya, Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, MacArthur, Daniel G., Neale, Benjamin M., Kirby, Andrew, Ruderfer, Douglas M., Fromer, Menachem, Lek, Monkol, Liu, Li, Flannick, Jason, Ripke, Stephan, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Hawes, Alicia, Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Dinh, Huyen, Gross, Shannon, Wang, Li-San, Lin, Chiao-Feng, Valladares, Otto, Gabriel, Stacey B., dePristo, Mark, Altshuler, David M., Purcell, Shaun M., State, Matthew W., Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Daly, Mark J.

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Distinct Genetic Influences on Cortical Surface Area and Cortical Thickness von Panizzon, Matthew S., Fennema-Notestine, Christine, Eyler, Lisa T., Jernigan, Terry L., Prom-Wormley, Elizabeth, Neale, Michael, Jacobson, Kristen, Lyons, Michael J., Grant, Michael D., Franz, Carol E., Xian, Hong, Tsuang, Ming, Fischl, Bruce, Seidman, Larry, Dale, Anders, Kremen, William S.

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Quantum Confined Electron–Phonon Interaction in Silicon Nanocrystals von Sagar, D. M, Atkin, Joanna M, Palomaki, Peter K. B, Neale, Nathan R, Blackburn, Jeffrey L, Johnson, Justin C, Nozik, Arthur J, Raschke, Markus B, Beard, Matthew C

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Evaluating drug targets through human loss-of-function genetic variation von Minikel, Eric Vallabh, Karczewski, Konrad J., Martin, Hilary C., Cummings, Beryl B., Whiffin, Nicola, Rhodes, Daniel, Alföldi, Jessica, Trembath, Richard C., van Heel, David A., Daly, Mark J., Schreiber, Stuart L., MacArthur, Daniel G.

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Potassium Aluminyl Promoted Carbonylation of Ethene von Evans, Matthew J., Neale, Samuel E., Anker, Mathew D., McMullin, Claire L., Coles, Martyn P.

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Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heter... von Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Law, Matthew H, Nandakumar, Priyanka, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Olsen, Catherine M, Neale, Rachel E, Fitzgerald, Rebecca, Thrift, Aaron P, Vaughan, Thomas L, Buas, Matthew F, Hinds, David A, Gharahkhani, Puya, Kendall, Bradley J, MacGregor, Stuart, Fitzgerald, Rebecca, Buas, Matt, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Bird, Nigel C, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Whiteman, David C, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Clark, Sarah K, Elson, Sarah L, Fletez-Brant, Kipper, Fontanillas, Pierre, Furlotte, Nicholas A, Gandhi, Pooja M, Heilbron, Karl, Hicks, Barry, Hinds, David A, Huber, Karen E, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, Luff, Marie K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Mozaffari, Sahar V, Nandakumar, Priyanka, Noblin, Elizabeth S, Northover, Carrie AM, O'Connell, Jared, Petrakovitz, Aaron A, Pitts, Steven J, David Poznik, G., Fah Sathirapongsasuti, J, Shastri, Anjali J, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Tunney, Robert J, Vacic, Vladimir, Wang, Xin, Zare, Amir S

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