Age-dependent microRNA control of synaptic plasticity in 22q11 deletion syndrome and schizophrenia by Earls, Laurie R, Fricke, R Gaines, Yu, Jing, Berry, Raymond B, Baldwin, Lisa T, Zakharenko, Stanislav S

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Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome by Earls, Laurie R, Bayazitov, Ildar T, Fricke, Robert G, Berry, Raymond B, Illingworth, Elizabeth, Mittleman, Guy, Zakharenko, Stanislav S

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Coenzyme Q protects Caenorhabditis elegans GABA neurons from calcium-dependent degeneration by Earls, Laurie R., Hacker, Mallory L., Watson, Joseph D., Miller, David M., Bargmann, Cornelia

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Non-coding RNA regulation of synaptic plasticity and memory: Implications for aging by Earls, Laurie R, Westmoreland, Joby J, Zakharenko, Stanislav S

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A Synaptic Function Approach to Investigating Complex Psychiatric Diseases by Earls, Laurie R., Zakharenko, Stanislav S.

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SCYL2 Protects CA3 Pyramidal Neurons from Excitotoxicity during Functional Maturation of the Mouse Hippocampus by Gingras, Sebastien, Earls, Laurie R, Howell, Sherie, Smeyne, Richard J, Zakharenko, Stanislav S, Pelletier, Stephane

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INSIGHTS INTO SCHIZOPHRENIA FROM 22Q11DS MOUSE MODELS by Earls, Laurie R, Zakharenko, Stanislav

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Age-dependent expression pattern in the mammalian brain of a novel, small peptide encoded in the 22q11.2 deletion syndrome region by Kragness, Sabrina, Harrison, Mark A.A., Westmoreland, Joby J., Burstain, Adam, Earls, Laurie R.

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Homologs of genes expressed in Caenorhabditis elegans GABAergic neurons are also found in the developing mouse forebrain by Hammock, Elizabeth A D, Eagleson, Kathie L, Barlow, Susan, Earls, Laurie R, Miller, 3rd, David M, Levitt, Pat

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RGS9-2 Modulates D2 Dopamine Receptor-Mediated Ca2+ Channel Inhibition in Rat Striatal Cholinergic Interneurons by Cabrera-Vera, Theresa M., Hernandez, Salvador, Earls, Laurie R., Medkova, Martina, Sundgren-Andersson, Anna K., Surmeier, D. James, Hamm, Heidi E., Exton, John H.

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Non-coding RNA regulation of synaptic plasticity and memory: Implications for aging: Non-coding RNA in Aging by EARLS, Laurie R, WESTMORELAND, Joby J, ZAKHARENKO, Stanislav S

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RGS9-2 modulates D sub(2) dopamine receptor-mediated Ca super(2+) channel inhibition in rat striatal cholinergic interneurons by Cabrera-Vera, Theresa M, Hernandez, Salvador, Earls, Laurie R, Medkova, Martina, Sundgren-Andersson, Anna K, Surmeier, DJames, Hamm, Heidi E

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RGS9-2 modulates D 2 dopamine receptor-mediated Ca 2+ channel inhibition in rat striatal cholinergic interneurons by Cabrera-Vera, Theresa M., Hernandez, Salvador, Earls, Laurie R., Medkova, Martina, Sundgren-Andersson, Anna K., Surmeier, D. James, Hamm, Heidi E.

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Mapping child growth failure across low- and middle-income countries by Kinyoki, Damaris K, Osgood-Zimmerman, Aaron E, Pickering, Brandon V, Schaeffer, Lauren E, Marczak, Laurie B, Lazzar-Atwood, Alice, Collison, Michael L

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Global mortality of snakebite envenoming between 1990 and 2019 by Roberts, Nicholas L. S., Johnson, Emily K., Zeng, Scott M., Hamilton, Erin B., Abdoli, Amir, Alahdab, Fares, Alipour, Vahid, Ancuceanu, Robert, Andrei, Catalina Liliana, Anvari, Davood, Arabloo, Jalal, Ausloos, Marcel, Awedew, Atalel Fentahun, Badiye, Ashish D., Bakkannavar, Shankar M., Bhalla, Ashish, Bhardwaj, Nikha, Bhardwaj, Pankaj, Bhaumik, Soumyadeep, Bijani, Ali, Boloor, Archith, Cai, Tianji, Carvalho, Felix, Chu, Dinh-Toi, Couto, Rosa A. S., Dai, Xiaochen, Desta, Abebaw Alemayehu, Do, Hoa Thi, Earl, Lucas, Eftekhari, Aziz, Esmaeilzadeh, Firooz, Farzadfar, Farshad, Fernandes, Eduarda, Filip, Irina, Foroutan, Masoud, Franklin, Richard Charles, Gaidhane, Abhay Motiramji, Gebregiorgis, Birhan Gebresillassie, Gebremichael, Berhe, Ghashghaee, Ahmad, Golechha, Mahaveer, Hamidi, Samer, Haque, Syed Emdadul, Hayat, Khezar, Herteliu, Claudiu, Ilesanmi, Olayinka Stephen, Islam, M. Mofizul, Jagnoor, Jagnoor, Kanchan, Tanuj, Kapoor, Neeti, Khan, Ejaz Ahmad, Khatib, Mahalaqua Nazli, Khundkar, Roba, Krishan, Kewal, Kumar, G. Anil, Kumar, Nithin, Landires, Iván, Lim, Stephen S., Madadin, Mohammed, Maled, Venkatesh, Manafi, Navid, Marczak, Laurie B., Menezes, Ritesh G., Meretoja, Tuomo J., Miller, Ted R., Mohammadian-Hafshejani, Abdollah, Mokdad, Ali H., Monteiro, Francis N. P., Moradi, Maryam, Nayak, Vinod C., Nguyen, Cuong Tat, Nguyen, Huong Lan Thi, Nuñez-Samudio, Virginia, Ostroff, Samuel M., Padubidri, Jagadish Rao, Pham, Hai Quang, Pinheiro, Marina, Pirestani, Majid, Quazi Syed, Zahiruddin, Rabiee, Navid, Radfar, Amir, Rahimi-Movaghar, Vafa, Rao, Sowmya J., Rastogi, Prateek, Rawaf, David Laith, Rawaf, Salman, Reiner, Robert C., Sahebkar, Amirhossein, Samy, Abdallah M., Sawhney, Monika, Schwebel, David C., Senthilkumaran, Subramanian, Shaikh, Masood Ali, Skryabin, Valentin Yurievich, Skryabina, Anna Aleksandrovna, Soheili, Amin, Stokes, Mark A., Thapar, Rekha, Tovani-Palone, Marcos Roberto, Tran, Bach Xuan

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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision by Baldridge, Dustin, Wangler, Michael F, Bowman, Angela N, Yamamoto, Shinya, Schedl, Tim, Pak, Stephen C, Postlethwait, John H, Shin, Jimann, Solnica-Krezel, Lilianna, Bellen, Hugo J, Westerfield, Monte

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Macrocephaly and developmental delay caused by missense variants in RAB5C by Koop, Klaas, Yuan, Weimin, Tessadori, Federico, Rodriguez-Polanco, Wilmer R, Grubbs, Jeremy, Zhang, Bo, Osmond, Matt, Graham, Gail, Sawyer, Sarah, Conboy, Erin, Vetrini, Francesco, Treat, Kayla, Płoski, Rafal, Pienkowski, Victor Murcia, Kłosowska, Anna, Fieg, Elizabeth, Krier, Joel, Mallebranche, Coralie, Alban, Ziegler, Aldinger, Kimberly A, Ritter, Deborah, Macnamara, Ellen, Sullivan, Bonnie, Herriges, John, Alaimo, Joseph T, Helbig, Catherine, Ellis, Colin A, van Eyk, Clare, Gecz, Jozef, Farrugia, Daniel, Osei-Owusu, Ikeoluwa, Adès, Lesley, van den Boogaard, Marie-Jose, Fuchs, Sabine, Bakker, Jeroen, Duran, Karen, Dawson, Zachary D, Lindsey, Anika, Huang, Huiyan, Baldridge, Dustin, Silverman, Gary A, Grant, Barth D, Raizen, David, van Haaften, Gijs, Pak, Stephen C, Rehmann, Holger, Schedl, Tim, van Hasselt, Peter

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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder by Barish, Scott, Senturk, Mumine, Schoch, Kelly, Minogue, Amanda L, Lopergolo, Diego, Fallerini, Chiara, Harland, Jake, Seemann, Jacob H, Stong, Nicholas, Kranz, Peter G, Kansagra, Sujay, Mikati, Mohamad A, Jasien, Joan, El-Dairi, Mays, Galluzzi, Paolo, Ariani, Francesca, Renieri, Alessandra, Mari, Francesca, Wangler, Michael F, Arur, Swathi, Jiang, Yong-Hui, Yamamoto, Shinya, Shashi, Vandana, Bellen, Hugo J

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Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder by Mignot, Cyril, Littlejohn, Rebecca O., Bademci, Guney, Balasubramanyam, Ashok, Beck, Anita, Berg-Rood, Beverly, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Butte, Manish J., Peter Chang, Ta Chen, D'Souza, Precilla, Dasari, Surendra, Dayal, Jyoti G., Dell'Angelica, Esteban C., Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Earl, Dawn, Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Goddard, Page C., Golden-Grant, Katie, Grajewski, Alana, Hadley, Don, Hahn, Sihoun, Halley, Meghan C., High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Hutchison, Sarah, Izumi, Kosuke, Jarvik, Gail P., Jayadev, Suman, Jean-Marie, Orpa, Kennedy, Jennifer, Ketkar, Shamika, Kohane, Isaac S., Kohler, Jennefer N., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Levitt, Roy, Liu, Pengfei, Longo, Nicola, Loscalzo, Joseph, Macnamara, Ellen F., Maduro, Valerie V., Manolio, Teri A., Marth, Gabor, Martin, Beth A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Morava, Eva, Nakano-Okuno, Mariko, Newman, John H., Nickerson, Deborah, Oglesbee, Devin, Pallais, J. Carl, Phillips, John A., Rosenwasser, Natalie, Schedl, Timothy, Shashi, Vandana, Sisco, Kathy, Solem, Emily, Solnica-Krezel, Lilianna, Solomon, Ben, Sullivan, Jennifer A., Sweetser, David A., Sybert, Virginia, Tekin, Mustafa, Telischi, Fred, Tran, Alyssa A., Ungar, Rachel A., Vanderver, Adeline, Velinder, Matt, Viskochil, Dave, Wallace, Stephanie, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Ward, Patricia A., Hubshman, Monika Weisz, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Sarret, Catherine, Platzer, Konrad, Fischer, Susann, Granadillo, Jorge L., Schreiner, Elisabeth

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EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder by Forghani, Irman, Adam, Margaret, Azamian, Mahshid S., Baker, Eva, Baldridge, Dustin, Bale, Jim, Beck, Anita, Berg‐Rood, Beverly, Berry, Gerard T., Bican, Anna, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Chang, Ta Chen Peter, Cogan, Joy D., Colley, Heather A., D'Souza, Precilla, Dasari, Surendra, Dell'Angelica, Esteban C., Duncan, Laura, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Fernandez, Liliana, Fieg, Elizabeth L., Forghani, Irman, Gochuico, Bernadette, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Kohler, Jennefer N., Krakow, Deborah, Kravets, Elijah, Koziura, Mary, Lam, Byron, Lam, Christina, Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Lee, Hane, Levitt, Roy, Liu, Pengfei, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Majcherska, Marta M., Manolio, Teri A., Marth, Gabor, Martínez‐Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McConkie‐Rosell, Allyn, McGee, Elisabeth, Might, Matthew, Mirzaa, Ghayda, Moretti, Paolo M., Mosbrook‐Davis, Deborah, Murdock, David R., Nieves‐Rodriguez, Shirley, Parker, Neil H., Phillips, John A., Power, Bradley, Pusey, Barbara N., Quinlan, Aaron, Raskind, Wendy, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Solem, Emily, Stoler, Joan M., Sun, Angela, Tabor, Holly K., Tan, Amelia L. M., Telischi, Fred, Tifft, Cynthia J., Toro, Camilo, Tucker, Brianna M., Vogel, Tiphanie P., Wambach, Jennifer, Wang, Lee‐kai, Wegner, Daniel, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Zein, Wadih, Zuchner, Stephan

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