De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder by Dong, Shan, Walker, Michael F, Carriero, Nicholas J, DiCola, Michael, Willsey, A Jeremy, Ye, Adam Y, Waqar, Zainulabedin, Gonzalez, Luis E, Overton, John D, Frahm, Stephanie, Keaney, 3rd, John F, Teran, Nicole A, Dea, Jeanselle, Mandell, Jeffrey D, Hus Bal, Vanessa, Sullivan, Catherine A, DiLullo, Nicholas M, Khalil, Rehab O, Gockley, Jake, Yuksel, Zafer, Sertel, Sinem M, Ercan-Sencicek, A Gulhan, Gupta, Abha R, Mane, Shrikant M, Sheldon, Michael, Brooks, Andrew I, Roeder, Kathryn, Devlin, Bernie, State, Matthew W, Wei, Liping, Sanders, Stephan J

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No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti... by Murdoch, John D, Gupta, Abha R, Sanders, Stephan J, Walker, Michael F, Keaney, John, Fernandez, Thomas V, Murtha, Michael T, Anyanwu, Samuel, Ober, Gordon T, Raubeson, Melanie J, DiLullo, Nicholas M, Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A Jeremy, Choe, So-Yeon, Neale, Benjamin M, Daly, Mark J, State, Matthew W

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism by Sanders, Stephan J., Murtha, Michael T., Gupta, Abha R., Murdoch, John D., Raubeson, Melanie J., Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, DiLullo, Nicholas M., Parikshak, Neelroop N., Stein, Jason L., Walker, Michael F., Ober, Gordon T., Teran, Nicole A., Song, Youeun, El-Fishawy, Paul, Murtha, Ryan C., Choi, Murim, Overton, John D., Bjornson, Robert D., Carriero, Nicholas J., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.

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Neurogenetic analysis of childhood disintegrative disorder by Gupta, Abha R, Westphal, Alexander, Yang, Daniel Y J, Sullivan, Catherine A W, Eilbott, Jeffrey, Zaidi, Samir, Voos, Avery, Vander Wyk, Brent C, Ventola, Pam, Waqar, Zainulabedin, Fernandez, Thomas V, Ercan-Sencicek, A Gulhan, Walker, Michael F, Choi, Murim, Schneider, Allison, Hedderly, Tammy, Baird, Gillian, Friedman, Hannah, Cordeaux, Cara, Ristow, Alexandra, Shic, Frederick, Volkmar, Fred R, Pelphrey, Kevin A

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The contribution of de novo coding mutations to autism spectrum disorder by Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali T., Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jeffrey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael

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Facing Current Conditions: Employing Voting Rights Act Preclearance to Protect Reproductive Rights by Walker, Michael F

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci by Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.

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Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons by Griesi-Oliveira, K, Acab, A, Gupta, A R, Sunaga, D Y, Chailangkarn, T, Nicol, X, Nunez, Y, Walker, M F, Murdoch, J D, Sanders, S J, Fernandez, T V, Ji, W, Lifton, R P, Vadasz, E, Dietrich, A, Pradhan, D, Song, H, Ming, G-l, Gu, X, Haddad, G, Marchetto, M C N, Spitzer, N, Passos-Bueno, M R, State, M W, Muotri, A R

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In Vitro Cultivation of Microphallus turgidus (Trematoda: Microphallidae) from Metacercaria to Ovigerous Adult with Continuation of the Life Cycle in the Laboratory by Pung, Oscar J, Burger, Ashley R, Walker, Michael F, Barfield, Whitney L, Lancaster, Micah H, Jarrous, Christina E

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De Novo Coding Variants Are Strongly Associated with Tourette Disorder by Willsey, A. Jeremy, Yu, Dongmei, King, Robert A., Dietrich, Andrea, Xing, Jinchuan, Richer, Petra, Smith, Louw, Dong, Shan, Samocha, Kaitlin E., Bohnenpoll, Julia, Bromberg, Yana, Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Deng, Li, Dong, Shan, Elzerman, Lonneke, Fernandez, Thomas V., Fründt, Odette, Garcia-Delgar, Blanca, Gedvilaite, Erika, Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hoekstra, Pieter J., Hong, Hyun Ju, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lamerz, Andreas, Ludolph, Andrea G., Lühr da Silva, Claudia, Madruga-Garrido, Marcos, Mir, Pablo, Münchau, Alexander, Murphy, Tara L., Nasello, Cara, Openneer, Thaïra J.C., Plessen, Kerstin J., Richer, Petra, Roessner, Veit, Sanders, Stephan, Smith, Louw, Song, Dong-Ho, State, Matthew W., Stolte, Anne Marie, Sun, Nawei, Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Walker, Michael F., Wanderer, Sina, Wang, Shuoguo, Willsey, A. Jeremy, Woods, Martin, Xing, Jinchuan, Zhang, Yeting, Zhou, Anbo, Zinner, Samuel H., Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Cath, Danielle C., Chouinard, Sylvain, Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Illmann, Cornelia, Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Posthuma, Danielle, Ramensky, Vasily, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Singer, Harvey S., Yu, Dongmei, Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Tischfield, Jay A., Scharf, Jeremiah M., State, Matthew W., Heiman, Gary A.

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No evidence for association of Autism with rare heterozygous point mutations in contactin-associated protein-like 2 by Murdoch, John D, Gupta, Abha R, Sanders, Stephan J, Walker, Michael F, Keaney, John, Fernandez, Thomas V, Murtha, Michael T, Anyanwu, Samuel, Ober, Gordon T, Raubeson, Melanie J, DiLullo, Nicholas M, Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A. Jeremy, Choe, So-Yeon, Neale, Benjamin M, Daly, Mark J, State, Matthew W

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No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 ( CNTNAP2 ), or in Other Contactin-Associated Proteins or Contac... by Murdoch, John D, Gupta, Abha R, Sanders, Stephan J, Walker, Michael F, Keaney, John, Fernandez, Thomas V, Murtha, Michael T, Anyanwu, Samuel, Ober, Gordon T, Raubeson, Melanie J, DiLullo, Nicholas M, Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A Jeremy, Choe, So-Yeon, Neale, Benjamin M, Daly, Mark J, State, Matthew W

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Why should neuroscientists worry about iron? The emerging role of ferroptosis in the pathophysiology of neuroprogressive diseases by Morris, Gerwyn, Berk, Michael, Carvalho, André F., Maes, Michael, Walker, Adam J., Puri, Basant K.

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Bacterial microbiota of the upper respiratory tract and childhood asthma by Depner, Martin, PhD, Ege, Markus J., MD, Cox, Michael J., PhD, Dwyer, Sarah, PhD, Walker, Alan W., PhD, Birzele, Lena T, Genuneit, Jon, MD, Horak, Elisabeth, MD, Braun-Fahrländer, Charlotte, MD, Danielewicz, Hanna, MD, PhD, Maier, Raina M., PhD, Moffatt, Miriam F., PhD, Cookson, William O., MD, Heederik, Dick, PhD, von Mutius, Erika, MD, Legatzki, Antje, PhD

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Investigation and amelioration of long-term instrumental drifts in water vapor and nitrous oxide measurements from the Aura Microwave Limb Sounder (MLS) and their implications for... by Livesey, Nathaniel J, Read, William G, Froidevaux, Lucien, Lambert, Alyn, Santee, Michelle L, Schwartz, Michael J, Millán, Luis F, Jarnot, Robert F, Wagner, Paul A, Hurst, Dale F, Walker, Kaley A, Sheese, Patrick E, Nedoluha, Gerald E

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An endocannabinoid mechanism for stress-induced analgesia by Piomelli, Daniele, Tarzia, Giorgio, Hohmann, Andrea G, Mangieri, Regina, Duranti, Andrea, Tontini, Andrea, Krey, Jocelyn F, Neely, Mark H, Crystal, Jonathon D, Suplita, Richard L, Mor, Marco, Bolton, Nathan M, Fegley, Darren, Holmes, Philip V, Michael Walker, J

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Syntrophus conductive pili demonstrate that common hydrogen-donating syntrophs can have a direct electron transfer option by Walker, David J. F., Nevin, Kelly P., Holmes, Dawn E., Rotaru, Amelia-Elena, Ward, Joy E., Woodard, Trevor L., Zhu, Jiaxin, Ueki, Toshiyuki, Nonnenmann, Stephen S., McInerney, Michael J., Lovley, Derek R.

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Whole genome deep sequencing of HIV-1 reveals the impact of early minor variants upon immune recognition during acute infection by Henn, Matthew R, Boutwell, Christian L, Charlebois, Patrick, Lennon, Niall J, Power, Karen A, Macalalad, Alexander R, Berlin, Aaron M, Malboeuf, Christine M, Ryan, Elizabeth M, Gnerre, Sante, Zody, Michael C, Erlich, Rachel L, Green, Lisa M, Berical, Andrew, Wang, Yaoyu, Casali, Monica, Streeck, Hendrik, Bloom, Allyson K, Dudek, Tim, Tully, Damien, Newman, Ruchi, Axten, Karen L, Gladden, Adrianne D, Battis, Laura, Kemper, Michael, Zeng, Qiandong, Shea, Terrance P, Gujja, Sharvari, Zedlack, Carmen, Gasser, Olivier, Brander, Christian, Hess, Christoph, Günthard, Huldrych F, Brumme, Zabrina L, Brumme, Chanson J, Bazner, Suzane, Rychert, Jenna, Tinsley, Jake P, Mayer, Ken H, Rosenberg, Eric, Pereyra, Florencia, Levin, Joshua Z, Young, Sarah K, Jessen, Heiko, Altfeld, Marcus, Birren, Bruce W, Walker, Bruce D, Allen, Todd M

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Improved transcriptome sampling pinpoints 26 ancient and more recent polyploidy events in Caryophyllales, including two allopolyploidy events by Yang, Ya, Moore, Michael J., Brockington, Samuel F., Mikenas, Jessica, Olivieri, Julia, Walker, Joseph F., Smith, Stephen A.

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The kynurenine pathway in major depressive disorder, bipolar disorder, and schizophrenia: a meta-analysis of 101 studies by Marx, Wolfgang, McGuinness, Amelia J., Rocks, Tetyana, Ruusunen, Anu, Cleminson, Jasmine, Walker, Adam J., Gomes-da-Costa, Susana, Lane, Melissa, Sanches, Marsal, Diaz, Alexandre P., Tseng, Ping-Tao, Lin, Pao-Yen, Berk, Michael, Clarke, Gerard, O’Neil, Adrienne, Jacka, Felice, Stubbs, Brendon, Carvalho, André F., Quevedo, João, Soares, Jair C., Fernandes, Brisa S.

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