Snow cover extent during spring snowmelt in the south-central interior of British Columbia von Smith, Russell S., Scherer, Rob A., Dobson, Don A.

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A food systems approach and qualitative system dynamics model to reveal policy issues within the commercial broiler chicken system in South Africa von Queenan, Kevin, Cuevas, Soledad, Mabhaudhi, Tafadzwanashe, Chimonyo, Michael, Shankar, Bhavani, Slotow, Rob, Häsler, Barbara

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A food systems approach and qualitative system dynamics model to reveal policy issues within the commercial broiler chicken system in South Africa von Queenan, Kevin, Cuevas, Soledad, Mabhaudhi, Tafadzwanashe, Chimonyo, Michael, Shankar, Bhavani, Slotow, Rob, Häsler, Barbara

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Trial registration numbers are underreported in biomedical publications von van de Wetering, Fleur T, Scholten, Rob J P M, Haring, Tamara, Clarke, Michael, Hooft, Lotty

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Extensive glycosylation of ACPA-IgG variable domains modulates binding to citrullinated antigens in rheumatoid arthritis von Rombouts, Yoann, Willemze, Annemiek, van Beers, Joyce J B C, Shi, Jing, Kerkman, Priscilla F, van Toorn, Linda, Janssen, George M C, Zaldumbide, Arnaud, Hoeben, Rob C, Pruijn, Ger J M, Deelder, André M, Wolbink, Gertjan, Rispens, Theo, van Veelen, Peter A, Huizinga, Tom W J, Wuhrer, Manfred, Trouw, Leendert A, Scherer, Hans U, Toes, René E M

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Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND Network von Baribeau, Danielle A., Dupuis, Annie, Paton, Tara A., Hammill, Christopher, Scherer, Stephen W., Schachar, Russell J., Arnold, Paul D., Szatmari, Peter, Nicolson, Rob, Georgiades, Stelios, Crosbie, Jennifer, Brian, Jessica, Iaboni, Alana, Kushki, Azadeh, Lerch, Jason P., Anagnostou, Evdokia

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Identification and characterisation of citrullinated antigen-specific B cells in peripheral blood of patients with rheumatoid arthritis von Kerkman, Priscilla F, Fabre, Emeline, van der Voort, Ellen I H, Zaldumbide, Arnaud, Rombouts, Yoann, Rispens, Theo, Wolbink, Gertjan, Hoeben, Rob C, Spits, Hergen, Baeten, Dominique L P, Huizinga, Tom W J, Toes, René E M, Scherer, Hans U

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Identification of additional trials in prospective trial registers for Cochrane systematic reviews von van Enst, Wynanda A, Scholten, Rob J P M, Hooft, Lotty

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ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal network... von Teunissen, Maria W A, Lewerissa, Elly, van Hugte, Eline J H, Wang, Shan, Ockeloen, Charlotte W, Koolen, David A, Pfundt, Rolph, Marcelis, Carlo L M, Brilstra, Eva, Howe, Jennifer L, Scherer, Stephen W, Le Guillou, Xavier, Bilan, Frédéric, Primiano, Michelle, Roohi, Jasmin, Piton, Amelie, de Saint Martin, Anne, Baer, Sarah, Seiffert, Simone, Platzer, Konrad, Jamra, Rami Abou, Syrbe, Steffen, Doering, Jan H, Lakhani, Shenela, Nangia, Srishti, Gilissen, Christian, Vermeulen, R Jeroen, Rouhl, Rob P W, Brunner, Han G, Willemsen, Marjolein H, Nadif Kasri, Nael

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DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders von Siu, Michelle T., Goodman, Sarah J., Yellan, Isaac, Butcher, Darci T., Jangjoo, Maryam, Grafodatskaya, Daria, Rajendram, Rageen, Lou, Youliang, Zhang, Rujun, Zhao, Chunhua, Nicolson, Rob, Georgiades, Stelios, Szatmari, Peter, Scherer, Stephen W., Roberts, Wendy, Anagnostou, Evdokia, Weksberg, Rosanna

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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder von C Yuen, Ryan K, Merico, Daniele, Bookman, Matt, L Howe, Jennifer, Thiruvahindrapuram, Bhooma, Patel, Rohan V, Whitney, Joe, Deflaux, Nicole, Bingham, Jonathan, Wang, Zhuozhi, Pellecchia, Giovanna, Buchanan, Janet A, Walker, Susan, Marshall, Christian R, Uddin, Mohammed, Zarrei, Mehdi, Deneault, Eric, D'Abate, Lia, Chan, Ada J S, Koyanagi, Stephanie, Paton, Tara, Pereira, Sergio L, Hoang, Ny, Engchuan, Worrawat, Higginbotham, Edward J, Ho, Karen, Lamoureux, Sylvia, Li, Weili, MacDonald, Jeffrey R, Nalpathamkalam, Thomas, Sung, Wilson W L, Tsoi, Fiona J, Wei, John, Xu, Lizhen, Tasse, Anne-Marie, Kirby, Emily, Van Etten, William, Twigger, Simon, Roberts, Wendy, Drmic, Irene, Jilderda, Sanne, Modi, Bonnie MacKinnon, Kellam, Barbara, Szego, Michael, Cytrynbaum, Cheryl, Weksberg, Rosanna, Zwaigenbaum, Lonnie, Woodbury-Smith, Marc, Brian, Jessica, Senman, Lili, Iaboni, Alana, Doyle-Thomas, Krissy, Thompson, Ann, Chrysler, Christina, Leef, Jonathan, Savion-Lemieux, Tal, Smith, Isabel M, Liu, Xudong, Nicolson, Rob, Seifer, Vicki, Fedele, Angie, Cook, Edwin H, Dager, Stephen, Estes, Annette, Gallagher, Louise, Malow, Beth A, Parr, Jeremy R, Spence, Sarah J, Vorstman, Jacob, Frey, Brendan J, Robinson, James T, Strug, Lisa J, Fernandez, Bridget A, Elsabbagh, Mayada, Carter, Melissa T, Hallmayer, Joachim, Knoppers, Bartha M, Anagnostou, Evdokia, Szatmari, Peter, Ring, Robert H, Glazer, David, Pletcher, Mathew T, Scherer, Stephen W

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Structural Variation of Chromosomes in Autism Spectrum Disorder von Marshall, Christian R., Noor, Abdul, Vincent, John B., Lionel, Anath C., Feuk, Lars, Skaug, Jennifer, Shago, Mary, Moessner, Rainald, Pinto, Dalila, Ren, Yan, Thiruvahindrapduram, Bhooma, Fiebig, Andreas, Schreiber, Stefan, Friedman, Jan, Ketelaars, Cees E.J., Vos, Yvonne J., Ficicioglu, Can, Kirkpatrick, Susan, Nicolson, Rob, Sloman, Leon, Summers, Anne, Gibbons, Clare A., Teebi, Ahmad, Chitayat, David, Weksberg, Rosanna, Thompson, Ann, Vardy, Cathy, Crosbie, Vicki, Luscombe, Sandra, Baatjes, Rebecca, Zwaigenbaum, Lonnie, Roberts, Wendy, Fernandez, Bridget, Szatmari, Peter, Scherer, Stephen W.

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Ion Neutral Mass Spectrometer Results from the First Flyby of Titan von Waite, J. Hunter, Niemann, Hasso, Yelle, Roger V, Kasprzak, Wayne T, Cravens, Thomas E, Luhmann, Janet G, McNutt, Ralph L, Ip, Wing-Huen, Gell, David, De La Haye, Virginie, Můller-Wordag, Ingo, Magee, Brian, Borggren, Nathan, Ledvina, Steve, Fletcher, Greg, Walter, Erin, Miller, Ryan, Scherer, Stefan, Thorpe, Rob, Xu, Jing, Block, Bruce, Arnett, Ken

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An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell Composition von Jangjoo, Maryam, Goodman, Sarah J, Choufani, Sanaa, Trost, Brett, Scherer, Stephen W, Kelley, Elizabeth, Ayub, Muhammad, Nicolson, Rob, Georgiades, Stelios, Crosbie, Jennifer, Schachar, Russell, Anagnostou, Evdokia, Grunebaum, Eyal, Weksberg, Rosanna

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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression von Lowther, Chelsea, Speevak, Marsha, Armour, Christine M., Goh, Elaine S., Graham, Gail E., Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata J.M., Schultz, Lee-Anne, Morra, Antonella, Nicolson, Rob, Bikangaga, Peter, Samdup, Dawa, Zaazou, Mostafa, Boyd, Kerry, Jung, Jack H., Siu, Victoria, Rajguru, Manjulata, Goobie, Sharan, Tarnopolsky, Mark A., Prasad, Chitra, Dick, Paul T., Hussain, Asmaa S., Walinga, Margreet, Reijenga, Renske G., Gazzellone, Matthew, Lionel, Anath C., Marshall, Christian R., Scherer, Stephen W., Stavropoulos, Dimitri J., McCready, Elizabeth, Bassett, Anne S.

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Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders von Baribeau, Danielle A., Dupuis, Annie, Paton, Tara A., Scherer, Stephen W., Schachar, Russell J., Arnold, Paul D., Szatmari, Peter, Nicolson, Rob, Georgiades, Stelios, Crosbie, Jennifer, Brian, Jessica, Iaboni, Alana, Lerch, Jason, Anagnostou, Evdokia

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A large data resource of genomic copy number variation across neurodevelopmental disorders von Zarrei, Mehdi, Burton, Christie L., Engchuan, Worrawat, Young, Edwin J., Higginbotham, Edward J., MacDonald, Jeffrey R., Trost, Brett, Chan, Ada J. S., Walker, Susan, Lamoureux, Sylvia, Heung, Tracy, Mojarad, Bahareh A., Kellam, Barbara, Paton, Tara, Faheem, Muhammad, Miron, Karin, Lu, Chao, Wang, Ting, Samler, Kozue, Wang, Xiaolin, Costain, Gregory, Hoang, Ny, Pellecchia, Giovanna, Wei, John, Patel, Rohan V., Thiruvahindrapuram, Bhooma, Roifman, Maian, Merico, Daniele, Goodale, Tara, Drmic, Irene, Speevak, Marsha, Howe, Jennifer L., Yuen, Ryan K. C., Buchanan, Janet A., Vorstman, Jacob A. S., Marshall, Christian R., Wintle, Richard F., Rosenberg, David R., Hanna, Gregory L., Woodbury-Smith, Marc, Cytrynbaum, Cheryl, Zwaigenbaum, Lonnie, Elsabbagh, Mayada, Flanagan, Janine, Fernandez, Bridget A., Carter, Melissa T., Szatmari, Peter, Roberts, Wendy, Lerch, Jason, Liu, Xudong, Nicolson, Rob, Georgiades, Stelios, Weksberg, Rosanna, Arnold, Paul D., Bassett, Anne S., Crosbie, Jennifer, Schachar, Russell, Stavropoulos, Dimitri J., Anagnostou, Evdokia, Scherer, Stephen W.

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Comprehensive genomic characterization defines human glioblastoma genes and core pathways von McLendon, Roger, Friedman, Allan, Bigner, Darrell, Brat, Daniel J, M Mastrogianakis, Gena, Lehman, Norman, Aldape, Ken, Bogler, Oliver, Nazareth, Lynn, Hall, Otis, Zhu, Yiming, Jhangiani, Shalini, San Lucas, Anthony, Kovar, Christie, Dinh, Huyen, Santibanez, Jireh, Joshi, Vandita, Wilkinson, Jane, Onofrio, Robert, Ardlie, Kristin, Gabriel, Stacey, Ding, Li, McLellan, Michael D, Shi, Xiaoqi, Abbott, Rachel, Fulton, Lucinda, Meyer, Rick, Osborne, John R, Dunford-Shore, Brian H, Delehaunty, Kim, Swift, Gary, Pohl, Craig, Leong, Shin, Haipek, Carrie, Schmidt, Heather, Vickery, Tammi, Chinwalla, Asif, Weinstock, George M, Mardis, Elaine R, Verhaak, Roel GW, O'Kelly, Michael, Beroukhim, Rameen, Carter, Scott, Chiang, Derek, Gould, Josh, Korn, Josh, Mermel, Craig, Monti, Stefano, Nguyen, Huy, Parkin, Melissa, Stransky, Nicolas, Meyerson, Matthew, Protopopov, Alexei, Zhang, Jianhua, Perna, Ilana, Yao, Jun, Kim, Hyunsoo, Kohane, Isaac S, Seidman, Jon, Kucherlapati, Raju, Laird, Peter W, Cope, Leslie, Herman, James G, Weisenberger, Daniel J, Mi Yi, Joo, Southwick, Audrey, Aggarwal, Amita, Brooks, James D, Spellman, Paul T, Marr, Henry, Gi Choi, Yoon, Wang, Victoria, Robinson, Mark, Peng, Vivian, Fontenay, Gerald V, Parvin, Bahram, Speed, Terence P, Gray, Joe W, Brennan, Cameron, Olshen, Adam, Schultz, Nikolaus, Stukalov, Alexey, Cerami, Ethan, Qin, Li-Xuan, Ladanyi, Marc, Neil Hayes, D, Topal, Michael D, Shi, Yan, Penny, Robert, Lenkiewicz, Elizabeth, Morris, Scott, Kahn, Ari, Chen, Jessica, Nassau, David, Hickey, Erin, Vockley, Joseph, Vaught, Jim, Madhavan, Subhashree, Guyer, Mark, Thomson, Elizabeth

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Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes von Woodbury-Smith, Marc, Nicolson, Rob, Zarrei, Mehdi, Yuen, Ryan K. C., Walker, Susan, Howe, Jennifer, Uddin, Mohammed, Hoang, Ny, Buchanan, Janet A., Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W.

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The southwestern surgical congress multi-center trial on suspected common duct stones von Frazee, Richard, Regner, Justin, Truitt, Michael S., Agrawal, Vaidehi, Swope, Megan, Burlew, Clay Cothren, Dissanaike, Sharmila, Vangipurum, Divya, Bruns, Brandon, O'Meara, Lindsay, Stivers, John, Kwok, Amy, Grover, Brandon T., Kothari, Shanu N., Cibari, Chris, Dunn, Julie, McIntyre, Robert C., Wright, Frank, Scherer, Elizabeth P., Crane, Christopher, Schroeppel, Thomas J., Callaghan, Emma, Gordy, Stephanie, Todd, Rob

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