Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
Etherton, Mark R, Blaiss, Cory A, Powell, Craig M, Südhof, Thomas C
Published in Proceedings of the National Academy of Sciences - PNAS (20.10.2009)
Published in Proceedings of the National Academy of Sciences - PNAS (20.10.2009)
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Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission
Kouser, Mehreen, Speed, Haley E, Dewey, Colleen M, Reimers, Jeremy M, Widman, Allie J, Gupta, Natasha, Liu, Shunan, Jaramillo, Thomas C, Bangash, Muhammad, Xiao, Bo, Worley, Paul F, Powell, Craig M
Published in The Journal of neuroscience (20.11.2013)
Published in The Journal of neuroscience (20.11.2013)
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Effects of heterozygous deletion of autism-related gene Cullin-3 in mice
Xia, Qiang-Qiang, Walker, Angela K, Song, Chenghui, Wang, Jing, Singh, Anju, Mobley, James A, Xuan, Zhong X, Singer, Jeffrey D, Powell, Craig M
Published in PloS one (10.07.2023)
Published in PloS one (10.07.2023)
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Journal Article
"Déjà vu" in an autism gene mouse model modifies social mores
Xia, Qiang-Qiang, Sekar, Prathibha, Powell, Craig M
Published in Neuron (Cambridge, Mass.) (04.05.2022)
Published in Neuron (Cambridge, Mass.) (04.05.2022)
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Journal Article
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
Blundell, Jacqueline, Blaiss, Cory A, Etherton, Mark R, Espinosa, Felipe, Tabuchi, Katsuhiko, Walz, Christopher, Bolliger, Marc F, Sudhof, Thomas C, Powell, Craig M
Published in The Journal of neuroscience (10.02.2010)
Published in The Journal of neuroscience (10.02.2010)
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Journal Article
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
Tabuchi, Katsuhiko, Blundell, Jacqueline, Etherton, Mark R., Hammer, Robert E., Liu, Xinran, Powell, Craig M., Südhof, Thomas C.
Published in Science (American Association for the Advancement of Science) (05.10.2007)
Published in Science (American Association for the Advancement of Science) (05.10.2007)
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Pharmacological Inhibition of mTORC1 Suppresses Anatomical, Cellular, and Behavioral Abnormalities in Neural-Specific Pten Knock-Out Mice
Zhou, Jing, Blundell, Jacqueline, Ogawa, Shiori, Kwon, Chang-Hyuk, Zhang, Wei, Sinton, Christopher, Powell, Craig M, Parada, Luis F
Published in The Journal of neuroscience (11.02.2009)
Published in The Journal of neuroscience (11.02.2009)
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Phelan-McDermid syndrome: a classification system after 30 years of experience
Phelan, Katy, Boccuto, Luigi, Powell, Craig M, Boeckers, Tobias M, van Ravenswaaij-Arts, Conny, Rogers, R Curtis, Sala, Carlo, Verpelli, Chiara, Thurm, Audrey, Bennett, Jr, William E, Winrow, Christopher J, Garrison, Sheldon R, Toro, Roberto, Bourgeron, Thomas
Published in Orphanet journal of rare diseases (29.01.2022)
Published in Orphanet journal of rare diseases (29.01.2022)
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Kctd13 deletion reduces synaptic transmission via increased RhoA
Escamilla, Christine Ochoa, Filonova, Irina, Walker, Angela K., Xuan, Zhong X., Holehonnur, Roopashri, Espinosa, Felipe, Liu, Shunan, Thyme, Summer B., López-García, Isabel A., Mendoza, Dorian B., Usui, Noriyoshi, Ellegood, Jacob, Eisch, Amelia J., Konopka, Genevieve, Lerch, Jason P., Schier, Alexander F., Speed, Haley E., Powell, Craig M.
Published in Nature (London) (09.11.2017)
Published in Nature (London) (09.11.2017)
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Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Levy, Tess, Foss-Feig, Jennifer H, Betancur, Catalina, Siper, Paige M, Trelles-Thorne, Maria del Pilar, Halpern, Danielle, Frank, Yitzchak, Lozano, Reymundo, Layton, Christina, Britvan, Bari, Bernstein, Jonathan A, Buxbaum, Joseph D, Berry-Kravis, Elizabeth, Powell, Craig M, Srivastava, Siddharth, Sahin, Mustafa, Soorya, Latha, Thurm, Audrey, Kolevzon, Alexander
Published in Human molecular genetics (21.02.2022)
Published in Human molecular genetics (21.02.2022)
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Journal Article
Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits
Speed, Haley E, Kouser, Mehreen, Xuan, Zhong, Reimers, Jeremy M, Ochoa, Christine F, Gupta, Natasha, Liu, Shunan, Powell, Craig M
Published in The Journal of neuroscience (01.07.2015)
Published in The Journal of neuroscience (01.07.2015)
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Journal Article
Aortic Root Dilation and Genotype Associations in Phelan-McDermid Syndrome
Gluckman, Jake, Levy, Tess, Friedman, Kate, Garces, Francesca, Filip-Dhima, Rajna, Quinlan, Aisling, Iannotti, Isabelle, Pekar, Margaret, Hernandez, Alexandra Lopez, Nava, Madison T, Kravets, Elijah, Siegel, Abigail, Bernstein, Jonathan A, Berry-Kravis, Elizabeth, Powell, Craig M, Soorya, Latha Valluripalli, Thurm, Audrey, Srivastava, Siddharth, Buxbaum, Joseph D, Sahin, Mustafa, Kolevzon, Alexander, Gelb, Bruce D
Published in American journal of medical genetics. Part A (11.09.2024)
Published in American journal of medical genetics. Part A (11.09.2024)
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Journal Article
Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity
Araujo, Daniel J, Toriumi, Kazuya, Escamilla, Christine O, Kulkarni, Ashwinikumar, Anderson, Ashley G, Harper, Matthew, Usui, Noriyoshi, Ellegood, Jacob, Lerch, Jason P, Birnbaum, Shari G, Tucker, Haley O, Powell, Craig M, Konopka, Genevieve
Published in The Journal of neuroscience (08.11.2017)
Published in The Journal of neuroscience (08.11.2017)
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