Résultats de la recherche - Brie Wamsley
- Résultat(s) 1 - 11 résultats de 11
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1
Early Somatostatin Interneuron Connectivity Mediates the Maturation of Deep Layer Cortical Circuits par Sebnem N. Tuncdemir, Brie Wamsley, Floor J. Stam, Fumitaka Osakada, Martyn Goulding, Edward M. Callaway, Bernardo Rudy, Gord Fishell
Publié 2016Artigo -
2
Rbfox1 Mediates Cell-type-Specific Splicing in Cortical Interneurons par Brie Wamsley, Xavier H. Jaglin, Emilia Favuzzi, Giulia Quattrocolo, Maximiliano José Nigro, Nusrath Yusuf, Alireza Khodadadi‐Jamayran, Bernardo Rudy, Gord Fishell
Publié 2018Artigo -
3
Molecular cascades and cell type–specific signatures in ASD revealed by single-cell genomics par Brie Wamsley, Lucy Bicks, Yuyan Cheng, Riki Kawaguchi, Diana Quintero, Michael Margolis, Jennifer Grundman, Jianyin Liu, Shaohua Xiao, Natalie Hawken, Samantha Mazariegos, Daniel H. Geschwind
Publié 2024Artigo -
4
Translational profiling of hypocretin neurons identifies candidate molecules for sleep regulation par Jasbir S. Dalal, Jee Hoon Roh, Susan E. Maloney, Afua A. Akuffo, Samir Shah, Han Yuan, Brie Wamsley, Wendell B. Jones, Cristina de Guzman Strong, Paul A. Gray, David M. Holtzman, Nathaniel Heintz, Joseph D. Dougherty
Publié 2013Artigo -
5
Neuronal Inactivity Co-opts LTP Machinery to Drive Potassium Channel Splicing and Homeostatic Spike Widening par Boxing Li, Benjamin S. Suutari, Simón D. Sun, Zheng-Yi Luo, Chuan‐Chuan Wei, Nicolas Chenouard, Nataniel J. Mandelberg, Guoan Zhang, Brie Wamsley, Guoling Tian, Sandrine Sanchez, Sikun You, Lianyan Huang, Thomas A. Neubert, Gord Fishell, Richard W. Tsien
Publié 2020Artigo -
6
Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics par Chloe X. Yap, Daniel Vo, Matthew G. Heffel, Arjun Bhattacharya, Cindy Wen, Yuanhao Yang, Kathryn E. Kemper, Jian Zeng, Zhili Zheng, Zhihong Zhu, Eilís Hannon, Dorothea Seiler Vellame, Alice Franklin, Christa Caggiano, Brie Wamsley, Daniel H. Geschwind, Noah Zaitlen, Alexander Gusev, Bogdan Paşaniuc, Jonathan Mill, Chongyuan Luo, Michael J. Gandal
Publié 2024Artigo -
7
Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD par Michael J. Gandal, Jillian R. Haney, Brie Wamsley, Chloe X. Yap, Sepideh Parhami, Prashant S. Emani, Nathan Chang, George Chen, Gil D. Hoftman, Diego de Alba, Gokul Ramaswami, Christopher Hartl, Arjun Bhattacharya, Chongyuan Luo, Ting Jin, Daifeng Wang, Riki Kawaguchi, Diana Quintero, Jing Ou, Ye Wu, Neelroop Parikshak, Vivek Swarup, T. Grant Belgard, Mark Gerstein, Bogdan Paşaniuc, Daniel H. Geschwind
Publié 2022Artigo -
8
Single-cell genomics and regulatory networks for 388 human brains par Prashant S. Emani, Jason Liu, Declan Clarke, Matthew Jensen, Jonathan Warrell, Chirag Gupta, Ran Meng, Che-Yu Lee, Siwei Xu, Cagatay Dursun, Shaoke Lou, Yuhang Chen, Zhiyuan Chu, Timur R. Galeev, Ahyeon Hwang, Yunyang Li, Pengyu Ni, Xiao Zhou, Trygve E. Bakken, Jaroslav Bendl, Lucy Bicks, Tanima Chatterjee, Lijun Cheng, Yuyan Cheng, Yi Dai, Ziheng Duan, Mary Flaherty, John F. Fullard, Michael Gancz, Diego Garrido-Martín, Sophia C. Gaynor-Gillett, Jennifer Grundman, Natalie Hawken, Ella Henry, Gabriel E. Hoffman, Ao Huang, Yunzhe Jiang, Ting Jin, Nikolas L. Jorstad, Riki Kawaguchi, Saniya Khullar, Jianyin Liu, Junhao Liu, Shuang Liu, Shaojie Ma, Michael Margolis, Samantha Mazariegos, Jill E. Moore, Jennifer Moran, Éric Nguyen, Nishigandha Phalke, Milos Pjanic, Henry Pratt, Diana Quintero, Ananya S. Rajagopalan, Tiernon R. Riesenmy, Nicole Shedd, Manman Shi, Megan Spector, Rosemarie Terwilliger, Kyle J. Travaglini, Brie Wamsley, Gaoyuan Wang, Yan Xia, Shaohua Xiao, Andrew C. Yang, Suchen Zheng, Michael J. Gandal, Donghoon Lee, Ed S. Lein, Panos Roussos, Nenad Šestan, Zhiping Weng, Kevin P. White, Hyejung Won, Matthew J. Girgenti, Jing Zhang, Daifeng Wang, Daniel H. Geschwind, Mark Gerstein, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, José Juan Almagro Armenteros, Brian J. Beliveau, Sabina Berretta, Rahul Bharadwaj, Arjun Bhattacharya, Kristen Brennand, Davide Capauto, Frances A. Champagne, Chris Chatzinakos, H. Isaac Chen, Lijun Cheng, Andrew Chess, Jo-fan Chien, Ashley Clement, Leonardo Collado‐Torres, Gregory M. Cooper
Publié 2024Artigo -
9
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders par Benxia Hu, Hyejung Won, Won Mah, Royce Park, Bibi Kassim, Keeley Spiess, Alexey Kozlenkov, Cheynna Crowley, Sirisha Pochareddy, Allison E. Ashley‐Koch, Gregory E. Crawford, Melanie E. Garrett, Lingyun Song, Alexias Safi, Graham D. Johnson, Gregory A. Wray, Timothy E. Reddy, Fernando S. Goes, Peter P. Zandi, Julien Bryois, Andrew E. Jaffe, Amanda J. Price, Nikolay A. Ivanov, Leonardo Collado‐Torres, Thomas M. Hyde, Emily E. Burke, Joel E. Kleiman, Ran Tao, Joo Heon Shin, Kiran Girdhar, Yan Jiang, Marija Kundaković, Leanne Brown, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Alexander W. Charney, Vahram Haroutunian, Barbara K. Lipska, David A. Lewis, Chang-Gyu Hahn, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang, Rujia Dai, Yongjun Wang, Yan Xia, Annie W. Shieh, Chunyu Liu, Kay Grennan, Ramu Vadukapuram, Gina Giase, Dominic Fitzgerald, Lijun Cheng, Miguel Brown, Mimi Brown, Tonya M. Brunetti, Thomas Goodman, Majd Alsayed, Kevin P. White, Mohana Ray, Damon Polioudakis, Brie Wamsley, Jiani Yin, Luis de la Torre-Ubieta, Michael J. Gandal, Vivek Swarup, Stephan Sanders, Matthew W. State, Donna M. Werling, Joon‐Yong An, Brooke Sheppard, A. Jeremy Willsey, Amira Kefi, Eugenio Mattei, Michael Purcaro, Zhiping Weng, J. Russell Moore, Henry Pratt, Jack Huey
Publié 2021Artigo -
10
Revealing the brain's molecular architecture par Allison E. Ashley‐Koch, Gregory E. Crawford, Melanie E. Garrett, Lingyun Song, Alexias Safi, Graham D. Johnson, Gregory A. Wray, Timothy E. Reddy, Fernando S. Goes, Peter P. Zandi, Julien Bryois, Andrew E. Jaffe, Amanda J. Price, Nikolay A. Ivanov, Leonardo Collado‐Torres, Thomas M. Hyde, Emily E. Burke, Joel E. Kleiman, Ran Tao, Joo Heon Shin, Schahram Akbarian, Kiran Girdhar, Yan Jiang, Marija Kundaković, Leanne Brown, Bibi Kassim, Royce Park, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Barbara K. Lipska, David A. Lewis, Vahram Haroutunian, Chang-Gyu Hahn, Alexander W. Charney, Stella Dracheva, Alexey Kozlenkov, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang, Rujia Dai, Annie W. Shieh, Chunyu Liu, Kay Grennan, Yan Xia, Ramu Vadukapuram, Yongjun Wang, Dominic Fitzgerald, Lijun Cheng, M. S. Brown, Mimi Brown, Tonya M. Brunetti, Thomas Goodman, Majd Alsayed, Michael J. Gandal, Daniel H. Geschwind, Hyejung Won, Damon Polioudakis, Brie Wamsley, Jiani Yin, Tarik Hadžić, Luis de la Torre-Ubieta, Vivek Swarup, Stephan Sanders, Matthew W. State, Donna M. Werling, Joon‐Yong An, Brooke Sheppard, A. Jeremy Willsey, Kevin P. White, Mohana Ray, Gina Giase, Amira Kefi, Eugenio Mattei, Michael Purcaro, Zhiping Weng, Jill E. Moore, Henry Pratt, Jack Huey, Tyler Borrman
Publié 2018Artigo -
11
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism par Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt
Publié 2022Revisão
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Biology
Neuroscience
Genetics
Gene
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Alternative splicing
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Chromatin
Developmental psychology
Epigenetics
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Gene expression profiling
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Interneuron
Parvalbumin
Phenotype
RNA
RNA splicing
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Transcriptome