Inhibitory Plasticity Balances Excitation and Inhibition in Sensory Pathways and Memory Networks von Vogels, T. P., Sprekeler, H., Zenke, F., Clopath, C., Gerstner, W.

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Unmasking Latent Inhibitory Connections in Human Cortex to Reveal Dormant Cortical Memories von Barron, H.C., Vogels, T.P., Emir, U.E., Makin, T.R., O’Shea, J., Clare, S., Jbabdi, S., Dolan, R.J., Behrens, T.E.J.

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Inhibitory synaptic plasticity: spike timing-dependence and putative network function von Vogels, T P, Froemke, R C, Doyon, N, Gilson, M, Haas, J S, Liu, R, Maffei, A, Miller, P, Wierenga, C J, Woodin, M A, Zenke, F, Sprekeler, H

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Neural network dynamics von VOGELS, Tim P, RAJAN, Kanaka, ABBOTT, L. F

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Gating Deficits in Model Networks: A Path to Schizophrenia? von Vogels, T. P., Abbott, L. F.

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Signal Propagation and Logic Gating in Networks of Integrate-and-Fire Neurons von Vogels, Tim P, Abbott, L. F

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Towards democratizing and automating online conferences: lessons from the neuromatch conferences von Achakulvisut, T, Ruangrong, T, Mineault, P, Vogels, TP, Peters, MAK, Poirazi, P, Rozell, C, Wyble, B, Goodman, DFM, Kording, KP

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Think: Theory for Africa von Currin, CB, Khoza, PN, Antrobus, AD, Latham, PE, Vogels, TP, Raimondo, JV

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Search for Majorana neutrinos with the first two years of EXO-200 data von Albert, J B, Auty, D J, Barbeau, P S, Beauchamp, E, Beck, D, Belov, V, Benitez-Medina, C, Bonatt, J, Breidenbach, M, Brunner, T, Burenkov, A, Cao, G F, Chambers, C, Chaves, J, Cleveland, B, Coon, M, Craycraft, A, Daniels, T, Danilov, M, Daugherty, S J, Davis, C G, Davis, J, DeVoe, R, Delaquis, S, Didberidze, T, Dolgolenko, A, Dolinski, M J, Dunford, M, Fairbank, W, Farine, J, Feldmeier, W, Fierlinger, P, Fudenberg, D, Giroux, G, Gornea, R, Graham, K, Gratta, G, Hall, C, Herrin, S, Hughes, M, Jewell, M J, Jiang, X S, Johnson, A, Johnson, T N, Johnston, S, Karelin, A, Kaufman, L J, Killick, R, Koffas, T, Kravitz, S, Kuchenkov, A, Kumar, K S, Leonard, D S, Leonard, F, Licciardi, C, Lin, Y H, MacLellan, R, Marino, M G, Mong, B, Moore, D, Nelson, R, Odian, A, Ostrovskiy, I, Ouellet, C, Piepke, A, Pocar, A, Prescott, C Y, Rivas, A, Rowson, P C, Rozo, M P, Russell, J J, Schubert, A, Sinclair, D, Slutsky, S, Smith, E, Stekhanov, V, Tarka, M, Tolba, T, Tosi, D, Twelker, K, Vogel, P, Vuilleumier, J-L, Waite, A, Walton, J, Walton, T, Weber, M, Wen, L J, Wichoski, U, Wright, J D, Yang, L, Yen, Y-R, Zeldovich, O Ya, Zhao, Y B

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Inhibitory plasticity balances excitation and inhibition in sensory pathways and memory networks von Vogels, TP, Sprekeler, H, Zenke, F, Clopath, C, Gerstner, W

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Lapatinib versus trastuzumab in combination with neoadjuvant anthracycline-taxane-based chemotherapy (GeparQuinto, GBG 44): a randomised phase 3 trial von Untch, Michael, Prof, Loibl, Sibylle, MD, Bischoff, Joachim, MD, Eidtmann, Holger, MD, Kaufmann, Manfred, Prof, Blohmer, Jens-Uwe, Prof, Hilfrich, Jörn, Prof, Strumberg, Dirk, Prof, Fasching, Peter A, Prof, Kreienberg, Rolf, Prof, Tesch, Hans, Prof, Hanusch, Claus, MD, Gerber, Bernd, Prof, Rezai, Mahdi, MD, Jackisch, Christian, Prof, Huober, Jens, Prof, Kühn, Thorsten, Prof, Nekljudova, Valentina, PhD, von Minckwitz, Gunter, Prof

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NXY-059 for Acute Ischemic Stroke von Lees, Kennedy R, Zivin, Justin A, Ashwood, Tim, Davalos, Antonio, Davis, Stephen M, Diener, Hans-Christoph, Grotta, James, Lyden, Patrick, Shuaib, Ashfaq, Hårdemark, Hans-Göran, Wasiewski, Warren W

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Inhibitory synaptic plasticity: spike timing-dependence and putative network function von Vogels, T. P, Froemke, R. C, Doyon, N, Gilson, M, Haas, J. S, Liu, R, Maffei, A, Miller, P, Wierenga, C. J, Woodin, M. A, Zenke, F, Sprekeler, H

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Genome sequencing and analysis of the model grass Brachypodium distachyon von Salse, Jerome J., Murat, Florent, Abrouk, Michaël M., Chapman, Elisabeth E.J., Sibout, Richard, Hematy, Kian K., Mouille, Gregory G., Höfte, Herman, Belcram, Harry H., Charles, Mathieu, Chalhoub, Boulos B.

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Antenatal Dexamethasone for Early Preterm Birth in Low-Resource Countries von Oladapo, Olufemi T, Vogel, Joshua P, Piaggio, Gilda, Nguyen, My-Huong, Althabe, Fernando, Gülmezoglu, A Metin, Bahl, Rajiv, Rao, Suman P N, De Costa, Ayesha, Gupta, Shuchita, Baqui, Abdullah H, Khanam, Rasheda, Shahidullah, Mohammod, Chowdhury, Saleha B, Ahmed, Salahuddin, Begum, Nazma, D Roy, Arunangshu, Shahed, M A, Jaben, Iffat A, Yasmin, Farida, Rahman, M Mozibur, Ara, Anjuman, Khatoon, Soofia, Ara, Gulshan, Akter, Shaheen, Akhter, Nasreen, Dey, Probhat R, Sabur, M Abdus, Azad, Mohammad T, Choudhury, Shahana F, Matin, M A, Goudar, Shivaprasad S, Dhaded, Sangappa M, Metgud, Mrityunjay C, Pujar, Yeshita V, Somannavar, Manjunath S, Vernekar, Sunil S, Herekar, Veena R, Bidri, Shailaja R, Mathapati, Sangamesh S, Patil, Preeti G, Patil, Mallanagouda M, Gudadinni, Muttappa R, Bijapure, Hidaytullah R, Mallapur, Ashalata A, Katageri, Geetanjali M, Chikkamath, Sumangala B, Yelamali, Bhuvaneshwari C, Pol, Ramesh R, Misra, Sujata S, Das, Leena, Nanda, Saumya, Nayak, Rashmita B, Singh, Bipsa, Qureshi, Zahida, Were, Fredrick, Osoti, Alfred, Gwako, George, Laving, Ahmed, Kinuthia, John, Mohamed, Hafsa, Aliyan, Nawal, Barassa, Adelaide, Kibaru, Elizabeth, Mbuga, Margaret, Thuranira, Lydia, Githua, Njoroge J, Lusweti, Bernadine, Ayede, Adejumoke I, Falade, Adegoke G, Adesina, Olubukola A, Agunloye, Atinuke M, Iyiola, Oluwatosin O, Sanni, Wilfred, Ejinkeonye, Ifeyinwa K, Idris, Hadiza A, Okoli, Chinyere V, Irinyenikan, Theresa A, Olubosede, Omolayo A, Bello, Olaseinde, Omololu, Olufemi M, Olutekunbi, Olanike A, Akintan, Adesina L, Owa, Olorunfemi O, Oluwafemi, Rosena O, Eniowo, Ireti P, Fabamwo, Adetokunbo O, Disu, Elizabeth A, Agbara, Joy O, Adejuyigbe, Ebunoluwa A, Kuti, Oluwafemi, Anyabolu, Henry C, Awowole, Ibraheem O, Fehintola, Akintunde O, Kuti, Bankole P, Isah, Anthony D, Olateju, Eyinade K, Abiodun, Olusanya, Dedeke, Olabisi F, Akinkunmi, Francis B

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

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Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations von Kurata, Harley T., Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Bolkier, Yoav, Dickson, Patricia, Donald, Kirsten A., Eliyahu, Aviva, Emrick, Lisa, Odent, Sylvie, Ortiz-Gonzalez, Xilma, Rosenfeld, Jill A., Skraban, Cara, Alejandro, Mercedes E., Azamian, Mahshid S., Chao, Hsiao-Tuan, Dai, Hongzheng, Dhar, Shweta U., Karaviti, Lefkothea, Lee, Brendan H., Rosenfeld, Jill A., Scott, Daryl A., Wangler, Michael F., Eng, Christine M., Sullivan, Kathleen, Goldstein, David B., McConkie-Rosell, Allyn, Schoch, Kelly, Shashi, Vandana, Beggs, Alan H., Cobban, Laurel A., Cooper, Cynthia M., Fieg, Elizabeth L., Korrick, Susan, Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Stoler, Joan M., Nagy, Anna, Dasari, Surendra, Lanpher, Brendan C., Bivona, Stephanie, Isasi, Rosario, Levitt, Roy, Tekin, Mustafa, Thorson, Willa, Eckstein, David J., Mamounas, Laura A., D’Souza, Precilla, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Macnamara, Ellen F., Maduro, Valerie V., Nath, Avi, Baker, Eva, Power, Bradley, Mosbrook-Davis, Deborah, Rossignol, Francis, Yousef, Muhammad, Amendola, Laura, Bamshad, Michael, Beck, Anita, Bennett, Jimmy, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Jarvik, Gail P., Jarvik, Jeffrey, Mefford, Heather, Merritt, J. Lawrence, Raskind, Wendy, Sybert, Virginia, Wener, Mark, Wenger, Tara, Fisher, Paul G., Reuter, Chloe M., Smith, Kevin S., Zastrow, Diane B., Nakano-Okuno, Mariko, Whitlock, Jordan, Butte, Manish J., Fogel, Brent L., Krakow, Deborah, Lee, Hane, Palmer, Christina G.S., Papp, Jeanette C., Woods, Jeremy D., Andrews, Ashley, Pace, Laura, Viskochil, Dave, Bican, Anna, Kennedy, Jennifer, Cogan, Joy D., Cole, F. Sessions, Kiley, Dana, Sisco, Kathy, Schedl, Timothy, Solnica-Krezel, Lilianna, Pitt, Geoffrey S.

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Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science von Schoch, Kelly, Esteves, Cecilia, Bican, Anna, Spillmann, Rebecca, Cope, Heidi, McConkie-Rosell, Allyn, Walley, Nicole, Fernandez, Liliana, Kohler, Jennefer N., Bonner, Devon, Reuter, Chloe, Stong, Nicholas, Mulvihill, John J., Novacic, Donna, Wolfe, Lynne, Abdelbaki, Ayat, Toro, Camilo, Tifft, Cyndi, Malicdan, May, Gahl, William, Liu, Pengfei, Newman, John, Goldstein, David B., Hom, Jason, Sampson, Jacinda, Wheeler, Matthew T., Cogan, Joy, Bernstein, Jonathan A., Adams, David R., McCray, Alexa T., Shashi, Vandana

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Clinical management guidelines for Friedreich ataxia: best practice in rare diseases von Corben, Louise A, Collins, Veronica, Milne, Sarah, Farmer, Jennifer, Musheno, Ann, Lynch, David, Subramony, Sub, Pandolfo, Massimo, Schulz, Jörg B, Lin, Kim, Delatycki, Martin B

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