A Methodological Approach to Small Area Estimation for the Behavioral Risk Factor Surveillance System von Pierannunzi, Carol, Xu, Fang, Wallace, Robyn C, Garvin, William, Greenlund, Kurt J, Bartoli, William, Ford, Derek, Eke, Paul, Town, G Machell

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Serine and Lipid Metabolism in Macular Disease and Peripheral Neuropathy von Gantner, Marin L, Eade, Kevin, Wallace, Martina, Handzlik, Michal K, Fallon, Regis, Trombley, Jennifer, Bonelli, Roberto, Giles, Sarah, Harkins-Perry, Sarah, Heeren, Tjebo F.C, Sauer, Lydia, Ideguchi, Yoichiro, Baldini, Michelle, Scheppke, Lea, Dorrell, Michael I, Kitano, Maki, Hart, Barbara J, Cai, Carolyn, Nagasaki, Takayuki, Badur, Mehmet G, Okada, Mali, Woods, Sasha M, Egan, Catherine, Gillies, Mark, Guymer, Robyn, Eichler, Florian, Bahlo, Melanie, Fruttiger, Marcus, Allikmets, Rando, Bernstein, Paul S, Metallo, Christian M, Friedlander, Martin

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Allergic Rhinitis and its Impact on Asthma (ARIA) Guidelines – 2016 Revision von Brożek, Jan L., MD, PhD, Bousquet, Jean, MD, PhD, Agache, Ioana, MD, PhD, Agarwal, Arnav, BHSc, Bachert, Claus, MD PhD, Bosnic-Anticevich, Sinthia, BPharm, PhD, Brignardello-Petersen, Romina, DDS, MSc, PhD, Canonica, G. Walter, MD, Casale, Thomas, MD, Chavannes, Niels H., MD, PhD, Correia de Sousa, Jaime, MD, PhD, Cruz, Alvaro A, Cuello-Garcia, Carlos A., MD, Demoly, Pascal, MD, PhD, Dykewicz, Mark, MD, Etxeandia-Ikobaltzeta, Itziar, PhD, Florez, Ivan D., MD, MSc, Fokkens, Wytske, MD, PhD, Fonseca, Joao, MD, PhD, Hellings, Peter W., MD, PhD, Klimek, Ludger, MD, PhD, Kowalski, Sergio, MD, Kuna, Piotr, MD, PhD, Laisaar, Kaja-Triin, MD, MPH, Larenas-Linnemann, Désirée E., MD, Lødrup Carlsen, Karin C., MD, PhD, Manning, Peter J., MD, Meltzer, Eli, MD, Mullol, Joaquim, MD, PhD, Muraro, Antonella, MD, PhD, O’Hehir, Robyn, PhD, Ohta, Ken, MD, PhD, Panzner, Petr, MD, PhD, Papadopoulos, Nikolaos, MD, PhD, Park, Hae-Sim, MD, PhD, Passalacqua, Gianni, MD, Pawankar, Ruby, MD, PhD, Price, David, MD, Riva, John J., MD, Roldán, Yetiani, MD, Ryan, Dermot, MD, Sadeghirad, Behnam, PharmD, MPH, Samolinski, Boleslaw, MD, PhD, Schmid-Grendelmeier, Peter, MD, Sheikh, Aziz, MD, MSc, Togias, Alkis, MD, Valero, Antonio, MD, PhD, Valiulis, Arunas, MD, PhD, Valovirta, Erkka, MD, PhD, Ventresca, Matthew, MSc, Wallace, Dana, MD, Waserman, Susan, MD, MSc, Wickman, Magnus, MD, Wiercioch, Wojtek, MSc, Yepes-Nuñez, Juan José, MD, MSc, Zhang, Luo, MD, Zhang, Yuan, MPH, Zidarn, Mihaela, MD, MSc, Zuberbier, Torsten, MD, Schünemann, Holger J., MD, PhD, MSc

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A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome von Bassuk, Alexander G., Wallace, Robyn H., Buhr, Aimee, Buller, Andrew R., Afawi, Zaid, Shimojo, Masahito, Miyata, Shingo, Chen, Shan, Gonzalez-Alegre, Pedro, Griesbach, Hilary L., Wu, Shu, Nashelsky, Marcus, Vladar, Eszter K., Antic, Dragana, Ferguson, Polly J., Cirak, Sebahattin, Voit, Thomas, Scott, Matthew P., Axelrod, Jeffrey D., Gurnett, Christina, Daoud, Azhar S., Kivity, Sara, Neufeld, Miriam Y., Mazarib, Aziz, Straussberg, Rachel, Walid, Simri, Korczyn, Amos D., Slusarski, Diane C., Berkovic, Samuel F., El-Shanti, Hatem I.

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Family-Focused Practice and Policy Recommendations to Improve the Inpatient Experience for Patients Undergoing a Stem Cell Transplant von Wallace, Lyndsey J., Olex, Maria M., McAndrew, Natalie S.

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy von Lower, Karen M, Lütcherath, Viggo, Gécz, Jozef, Frints, Suzanna G.M, Partington, Michael, Strømme, Petter, Scheffer, Ingrid E, Gedeon, Ági K, Lewis, Suzanne M.E, Turner, Gillian, Fryns, Jean-Pierre, Sutherland, Grant R, Wallace, Robyn H, Mangelsdorf, Marie E, Shaw, Marie A, Mulley, John C, Bruyere, Helene

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Myeloablative Autologous Stem-Cell Transplantation for Severe Scleroderma von Sullivan, Keith M, Goldmuntz, Ellen A, Keyes-Elstein, Lynette, McSweeney, Peter A, Pinckney, Ashley, Welch, Beverly, Mayes, Maureen D, Nash, Richard A, Crofford, Leslie J, Eggleston, Barry, Castina, Sharon, Griffith, Linda M, Goldstein, Julia S, Wallace, Dennis, Craciunescu, Oana, Khanna, Dinesh, Folz, Rodney J, Goldin, Jonathan, St. Clair, E. William, Seibold, James R, Phillips, Kristine, Mineishi, Shin, Simms, Robert W, Ballen, Karen, Wener, Mark H, Georges, George E, Heimfeld, Shelly, Hosing, Chitra, Forman, Stephen, Kafaja, Suzanne, Silver, Richard M, Griffing, Leroy, Storek, Jan, LeClercq, Sharon, Brasington, Richard, Csuka, Mary E, Bredeson, Christopher, Keever-Taylor, Carolyn, Domsic, Robyn T, Kahaleh, M. Bashar, Medsger, Thomas, Furst, Daniel E

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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations von Scheffer, Ingrid E., Harkin, Louise A., Grinton, Bronwyn E., Dibbens, Leanne M., Turner, Samantha J., Zielinski, Marta A., Xu, Ruwei, Jackson, Graeme, Adams, Judith, Connellan, Mary, Petrou, Steven, Wellard, R. Mark, Briellmann, Regula S., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

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Management of anaphylaxis due to COVID‐19 vaccines in the elderly von Bousquet, Jean, Agache, Ioana, Blain, Hubert, Jutel, Marek, Del Giacco, Stefano, Czarlewski, Wienczyslawa, Abdul Latiff, Amir Hamzah, Annesi‐Maesano, Isabella, Atanaskovic‐Markovic, Marina, Bachert, Claus, Barbaud, Annick, Bedbrook, Anna, Bennoor, Kazi S., Berghea, Elena Camelia, Bindslev‐Jensen, Carsten, Bonini, Sergio, Bosnic‐Anticevich, Sinthia, Brockow, Knut, Camargos, Paulo, Canonica, G. Walter, Carriazo, Ana, Casale, Thomas, Caubet, Jean‐Christoph, Cherubini, Antonio, Christoff, George, Chu, Derek K., Cruz, Alvaro A., El‐Gamal†, Yehia, Ebisawa, Motohiro, Eberlein, Bernadette, Farrell, John, Fonseca, Joao A., Gavazzi, Gaëtan, Gawlik, Radoslaw, Gelincik, Asli, Gemicioğlu, Bilun, Gotua, Maia, Guérin, Olivier, Haahtela, Tari, Hoffmann‐Sommergruber, Karin, Hoffmann, Hans Jürgen, Hofmann, Maja, Hrubisko, Martin, Ispayeva, Zhanat, Ivancevich, Juan Carlos, Knol, Edward, Kuna, Piotr, Kvedariene, Violeta, Le Moing, Vincent, Louis, Renaud, Lourenco, Olga, Mahler, Vera, Matucci, Andrea, Milenkovic, Branislava, Mortz, Charlotte G., Neffen, Hugo, O’Hehir, Robyn E., Okamoto, Yoshitaka, Ollert, Markus, Palomares, Oscar, Papadopoulos, Nikolaos G., Panzner, Petr, Petrovic, Mirko, Pfaar, Oliver, Reynes, Jacques, Roller‐Winsberger, Regina E., Rolland, Yves, Rottem, Menachem, Salles, Nathalie, Santos, Alexandra F., Sarquis, Faradiba, Sastre, Joaquin, M. G. A. Schols, Jos, Scichilone, Nicola, Sediva, Anna, Shamji, Mohamed H., Skypala, Isabel, Smolinska, Sylwia, Sokolowska, Milena, Sousa‐Pinto, Bernardo, Sova, Milan, Stelmach, Rafael, Suppli Ulrik, Charlotte, Todo‐Bom, Ana Maria, Toppila‐Salmi, Sanna, Tsiligianni, Ioanna, Torres, Maria, Untersmayr, Eva, Urrutia Pereira, Marilyn, Valiulis, Arunas, Vitte, Joana, Vultaggio, Alessandra, Walusiak‐Skorupa, Jolanta, Wang, De‐Yun, Waserman, Susan, Yorgancioglu, Arzu, Yusuf, Osman M., Zernotti, Mario, Chivato, Tomas, Zuberbier, Torsten

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Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese von Gratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J, Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K, Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J, Ran, Shu, Reutens, David C, Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H, Wheeler, Lawrie, Wu, Jinyu, Yang, Jian, Xu, Huji, Visscher, Peter M, Bartlett, Perry F, Brown, Matthew A, Wray, Naomi R, Fan, Dongsheng

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The role of affective commitment and political skill in the work interfering with family (WIF) conflict – voluntary turnover relationship von Yang, Jun, Bently, Jeffery R., Treadway, Darren C., Brouer, Robyn L., Wallace, Angela

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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy von Müller, Ulrich, Schellenberg, Gerard D, Höglinger, Günter U, Melhem, Nadine M, Dickson, Dennis W, Sleiman, Patrick M A, Wang, Li-San, Klei, Lambertus, Rademakers, Rosa, de Silva, Rohan, Litvan, Irene, Riley, David E, van Swieten, John C, Heutink, Peter, Wszolek, Zbigniew K, Uitti, Ryan J, Vandrovcova, Jana, Hurtig, Howard I, Gross, Rachel G, Maetzler, Walter, Goldwurm, Stefano, Tolosa, Eduardo, Borroni, Barbara, Pastor, Pau, Cantwell, Laura B, Han, Mi Ryung, Dillman, Allissa, van der Brug, Marcel P, Gibbs, J Raphael, Cookson, Mark R, Hernandez, Dena G, Singleton, Andrew B, Farrer, Matthew J, Yu, Chang-En, Golbe, Lawrence I, Revesz, Tamas, Hardy, John, Lees, Andrew J, Devlin, Bernie, Hakonarson, Hakon

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Truncation of the GABAA-Receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus von HARKIN, Louise A, BOWSER, David N, SCHEFFER, Ingrid E, PETROU, Steven, DIBBENS, Leanne M, SINGH, Rita, PHILLIPS, Fiona, WALLACE, Robyn H, RICHARDS, Michaella C, WILLIAMS, David A, MULLEY, John C, BERKOVIC, Samuel F

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An Immune-Inflammation Gene Expression Signature in Prostate Tumors of Smokers von Prueitt, Robyn L, Wallace, Tiffany A, Glynn, Sharon A, Yi, Ming, Tang, Wei, Luo, Jun, Dorsey, Tiffany H, Stagliano, Katherine E, Gillespie, John W, Hudson, Robert S, Terunuma, Atsushi, Shoe, Jennifer L, Haines, Diana C, Yfantis, Harris G, Han, Misop, Martin, Damali N, Jordan, Symone V, Borin, James F, Naslund, Michael J, Alexander, Richard B, Stephens, Robert M, Loffredo, Christopher A, Lee, Dong H, Putluri, Nagireddy, Sreekumar, Arun, Hurwitz, Arthur A, Ambs, Stefan

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PGRMC1 effects on metabolism, genomic mutation and CpG methylation imply crucial roles in animal biology and disease von Thejer, Bashar M, Adhikary, Partho P, Teakel, Sarah L, Fang, Johnny, Weston, Paul A, Gurusinghe, Saliya, Anwer, Ayad G, Gosnell, Martin, Jazayeri, Jalal A, Ludescher, Marina, Gray, Lesley-Ann, Pawlak, Michael, Wallace, Robyn H, Pant, Sameer D, Wong, Marie, Fischer, Tamas, New, Elizabeth J, Fehm, Tanja N, Neubauer, Hans, Goldys, Ewa M, Quinn, Jane C, Weston, Leslie A, Cahill, Michael A

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Multiplex families with epilepsy: Success of clinical and molecular genetic characterization von Afawi, Zaid, Oliver, Karen L, Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y, Helbig, Katherine L, Goldberg-Stern, Hadassa, Misk, Adel J, Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H, Mangelsdorf, Marie, MacPherson, James N, Carvill, Gemma L, Mefford, Heather C, Jackson, Graeme D, Scheffer, Ingrid E, Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E, Corbett, Mark, Mulley, John C, Dibbens, Leanne M, Korczyn, Amos D, Berkovic, Samuel F

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Evidence for global teleconnections in a late Pleistocene speleothem record of water balance and vegetation change at Sudwala Cave, South Africa von Green, Helen, Pickering, Robyn, Drysdale, Russell, Johnson, Brett C., Hellstrom, John, Wallace, Malcolm

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Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families von Marini, Carla, Scheffer, Ingrid E., Crossland, Kathryn M., Grinton, Bronwyn E., Phillips, Fiona L., McMahon, Jacinta M., Turner, Samantha J., Dean, Joanne T., Kivity, Sara, Mazarib, Aziz, Neufeld, Miriam Y., Korczyn, Amos D., Harkin, Louise A., Dibbens, Leanne M., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B von WALLACE, R. H, SCHEFFER, I. E, PARASIVAM, G, BARNETT, S, WALLACE, G. B, SUTHERLAND, G. R, BERKOVIC, S. F, MULLEY, J. C

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