Intravenous lidocaine in spine surgery: A meta-analysis of randomized controlled trials von Haratian, Aryan, Musa, Arif, Field, Ryan, Farhan, Saif, Bennett, Collin, Cooke, Christopher, Patel, Rakesh D., Aleem, Ilyas S., Eichler, Martin C., Rajalingam, Karan, Lee, Carlin, Bederman, Samuel

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Sagittal Spinal and Pelvic Parameters in Patients With Scheuermann's Disease: A Preliminary Study von Bederman, S Samuel, Farhan, Saif, Hu, Xiaobang, Lieberman, Isador H, Belanger, Theodore A, Musa, Arif, Eichler, Martin C

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Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders von O'Roak, Brian J., Vives, Laura, Fu, Wenqing, Egertson, Jarrett D., Stanaway, Ian B., Phelps, Ian G., Carvill, Gemma, Kumar, Akash, Lee, Choli, Ankenman, Katy, Munson, Jeff, Hiatt, Joseph B., Turner, Emily H., Levy, Roie, O'Day, Diana R., Krumm, Niklas, Coe, Bradley P., Martin, Beth K., Borenstein, Elhanan, Nickerson, Deborah A., Mefford, Heather C., Doherty, Dan, Akey, Joshua M., Bernier, Raphael, Eichler, Evan E., Shendure, Jay

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The Nuclear Reaction Network WinNet von Reichert, M., Winteler, C., Korobkin, O., Arcones, A., Bliss, J., Eichler, M., Frischknecht, U., Fröhlich, C., Hirschi, R., Jacobi, M., Kuske, J., Martínez-Pinedo, G., Martin, D., Mocelj, D., Rauscher, T., Thielemann, F.-K.

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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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Energy-dependent path of dissipation in nanomechanical resonators von Güttinger, Johannes, Noury, Adrien, Weber, Peter, Eriksson, Axel Martin, Lagoin, Camille, Moser, Joel, Eichler, Christopher, Wallraff, Andreas, Isacsson, Andreas, Bachtold, Adrian

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Recurrent de novo mutations implicate novel genes underlying simplex autism risk von O'Roak, B. J., Stessman, H. A., Boyle, E. A., Witherspoon, K. T., Martin, B., Lee, C., Vives, L., Baker, C., Hiatt, J. B., Nickerson, D. A., Bernier, R., Shendure, J., Eichler, E. E.

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Real World Data in Adaptive Biomedical Innovation: A Framework for Generating Evidence Fit for Decision-Making von Schneeweiss, S, Eichler, H-G, Garcia-Altes, A, Chinn, C, Eggimann, A-V, Garner, S, Goettsch, W, Lim, R, Löbker, W, Martin, D, Müller, T, Park, BJ, Platt, R, Priddy, S, Ruhl, M, Spooner, A, Vannieuwenhuyse, B, Willke, RJ

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Direct pesticide exposure of insects in nature conservation areas in Germany von Brühl, Carsten A., Bakanov, Nikita, Köthe, Sebastian, Eichler, Lisa, Sorg, Martin, Hörren, Thomas, Mühlethaler, Roland, Meinel, Gotthard, Lehmann, Gerlind U. C.

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The complete genome sequence of a Neanderthal from the Altai Mountains von Prüfer, Kay, Racimo, Fernando, Patterson, Nick, Jay, Flora, Sankararaman, Sriram, Sawyer, Susanna, Heinze, Anja, Renaud, Gabriel, Sudmant, Peter H., de Filippo, Cesare, Li, Heng, Mallick, Swapan, Dannemann, Michael, Fu, Qiaomei, Kircher, Martin, Kuhlwilm, Martin, Lachmann, Michael, Meyer, Matthias, Ongyerth, Matthias, Siebauer, Michael, Theunert, Christoph, Tandon, Arti, Moorjani, Priya, Pickrell, Joseph, Mullikin, James C., Vohr, Samuel H., Green, Richard E., Hellmann, Ines, Johnson, Philip L. F., Blanche, Hélène, Cann, Howard, Kitzman, Jacob O., Shendure, Jay, Eichler, Evan E., Lein, Ed S., Bakken, Trygve E., Golovanova, Liubov V., Doronichev, Vladimir B., Shunkov, Michael V., Derevianko, Anatoli P., Viola, Bence, Slatkin, Montgomery, Reich, David, Kelso, Janet, Pääbo, Svante

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The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals von Giannuzzi, Giuliana, Schmidt, Paul J., Porcu, Eleonora, Willemin, Gilles, Munson, Katherine M., Nuttle, Xander, Earl, Rachel, Chrast, Jacqueline, Hoekzema, Kendra, Risso, Davide, Männik, Katrin, De Nittis, Pasquelena, Baratz, Ethan D., Herault, Yann, Gao, Xiang, Philpott, Caroline C., Bernier, Raphael A., Kutalik, Zoltan, Fleming, Mark D., Eichler, Evan E., Reymond, Alexandre

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Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies von Miller, David T., Adam, Margaret P., Aradhya, Swaroop, Biesecker, Leslie G., Brothman, Arthur R., Carter, Nigel P., Church, Deanna M., Crolla, John A., Eichler, Evan E., Epstein, Charles J., Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M., Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B., Kok, Klaas, Krantz, Ian D., Kuhn, Robert M., Lee, Charles, Ostell, James M., Rosenberg, Carla, Scherer, Stephen W., Spinner, Nancy B., Stavropoulos, Dimitri J., Tepperberg, James H., Thorland, Erik C., Vermeesch, Joris R., Waggoner, Darrel J., Watson, Michael S., Martin, Christa Lese, Ledbetter, David H.

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Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants von Girirajan, Santhosh, Rosenfeld, Jill A, Coe, Bradley P, Parikh, Sumit, Friedman, Neil, Goldstein, Amy, Filipink, Robyn A, McConnell, Juliann S, Angle, Brad, Meschino, Wendy S, Nezarati, Marjan M, Asamoah, Alexander, Jackson, Kelly E, Gowans, Gordon C, Martin, Judith A, Carmany, Erin P, Stockton, David W, Schnur, Rhonda E, Penney, Lynette S, Martin, Donna M, Raskin, Salmo, Leppig, Kathleen, Thiese, Heidi, Smith, Rosemarie, Aberg, Erika, Niyazov, Dmitriy M, Escobar, Luis F, El-Khechen, Dima, Johnson, Kisha D, Lebel, Robert R, Siefkas, Kiana, Ball, Susie, Shur, Natasha, McGuire, Marianne, Brasington, Campbell K, Spence, J. Edward, Martin, Laura S, Clericuzio, Carol, Ballif, Blake C, Shaffer, Lisa G, Eichler, Evan E

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Haplotype-resolved diverse human genomes and integrated analysis of structural variation von Ebert, Peter, Audano, Peter A, Zhu, Qihui, Rodriguez-Martin, Bernardo, Porubsky, David, Bonder, Marc Jan, Sulovari, Arvis, Ebler, Jana, Zhou, Weichen, Serra Mari, Rebecca, Yilmaz, Feyza, Zhao, Xuefang, Hsieh, PingHsun, Lee, Joyce, Kumar, Sushant, Lin, Jiadong, Rausch, Tobias, Chen, Yu, Ren, Jingwen, Santamarina, Martin, Höps, Wolfram, Ashraf, Hufsah, Chuang, Nelson T, Yang, Xiaofei, Munson, Katherine M, Lewis, Alexandra P, Fairley, Susan, Tallon, Luke J, Clarke, Wayne E, Basile, Anna O, Byrska-Bishop, Marta, Corvelo, André, Evani, Uday S, Lu, Tsung-Yu, Chaisson, Mark J P, Chen, Junjie, Li, Chong, Brand, Harrison, Wenger, Aaron M, Ghareghani, Maryam, Harvey, William T, Raeder, Benjamin, Hasenfeld, Patrick, Regier, Allison A, Abel, Haley J, Hall, Ira M, Flicek, Paul, Stegle, Oliver, Gerstein, Mark B, Tubio, Jose M C, Mu, Zepeng, Li, Yang I, Shi, Xinghua, Hastie, Alex R, Ye, Kai, Chong, Zechen, Sanders, Ashley D, Zody, Michael C, Talkowski, Michael E, Mills, Ryan E, Devine, Scott E, Lee, Charles, Korbel, Jan O, Marschall, Tobias, Eichler, Evan E

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Computational pan-genomics: status, promises and challenges von Marschall, Tobias, Marz, Manja, Abeel, Thomas, Dijkstra, Louis, Dutilh, Bas E, Ghaffaari, Ali, Kersey, Paul, Kloosterman, Wigard P, Mäkinen, Veli, Novak, Adam M, Paten, Benedict, Porubsky, David, Rivals, Eric, Alkan, Can, Baaijens, Jasmijn A, Paul I W De Bakker, Boeva, Valentina, Bonnal, Raoul J P, Chiaromonte, Francesca, Chikhi, Rayan, Ciccarelli, Francesca D, Cijvat, Robin, Datema, Erwin, Van Duijn, Cornelia M, Eichler, Evan E, Ernst, Corinna, Eskin, Eleazar, Garrison, Erik, El-Kebir, Mohammed, Klau, Gunnar W, Korbel, Jan O, Eric-Wubbo Lameijer, Langmead, Benjamin, Martin, Marcel, Medvedev, Paul, Mu, John C, Neerincx, Pieter, Ouwens, Klaasjan, Peterlongo, Pierre, Pisanti, Nadia, Rahmann, Sven, Raphael, Ben, Reinert, Knut, de Ridder, Dick, de Ridder, Jeroen, Schlesner, Matthias, Schulz-Trieglaff, Ole, Sanders, Ashley D, Sheikhizadeh, Siavash, Shneider, Carl, Smit, Sandra, Valenzuela, Daniel, Wang, Jiayin, Wessels, Lodewyk, Zhang, Ying, Guryev, Victor, Vandin, Fabio, Ye, Kai, Schönhuth, Alexander

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Treatment of lung infection in patients with cystic fibrosis: Current and future strategies von Döring, Gerd, Flume, Patrick, Heijerman, Harry, Elborn, J. Stuart

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Snow heterogeneous reactivity of bromide with ozone lost during snow metamorphism von Edebeli, Jacinta, Trachsel, Jürg C, Avak, Sven E, Ammann, Markus, Schneebeli, Martin, Eichler, Anja, Bartels-Rausch, Thorsten

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Paroxetine decreases platelet serotonin storage and platelet function in human beings von Hergovich, Nicole, Aigner, Martin, Eichler, Hans‐Georg, Entlicher, Jesusa, Drucker, Christa, Jilma, Bernd

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No recovery in the biomass of flying insects over the last decade in German nature protected areas von Mühlethaler, Roland, Köthe, Sebastian, Hörren, Thomas, Sorg, Martin, Eichler, Lisa, Lehmann, Gerlind U. C.

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A family study implicates GBE1 in the etiology of autism spectrum disorder von Fanjul‐Fernández, Miriam, Brown, Natasha J., Hickey, Peter, Diakumis, Peter, Rafehi, Haloom, Bozaoglu, Kiymet, Green, Cherie C., Rattray, Audrey, Young, Savannah, Alhuzaimi, Dana, Mountford, Hayley S., Gillies, Greta, Lukic, Vesna, Vick, Tanya, Finlay, Keri, Coe, Bradley P., Eichler, Evan E., Delatycki, Martin B., Wilson, Sarah J., Bahlo, Melanie, Scheffer, Ingrid E., Lockhart, Paul J.

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