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Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons
Schafer, Simon T., Paquola, Apua C. M., Stern, Shani, Gosselin, David, Ku, Manching, Pena, Monique, Kuret, Thomas J. M., Liyanage, Marvin, Mansour, Abed AlFatah, Jaeger, Baptiste N., Marchetto, Maria C., Glass, Christopher K., Mertens, Jerome, Gage, Fred H.
Published in Nature neuroscience (01.02.2019)
Published in Nature neuroscience (01.02.2019)
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Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Gandal, Michael J., Zhang, Pan, Hadjimichael, Evi, Walker, Rebecca L., Chen, Chao, Liu, Shuang, Won, Hyejung, van Bakel, Harm, Varghese, Merina, Wang, Yongjun, Shieh, Annie W., Haney, Jillian, Parhami, Sepideh, Belmont, Judson, Kim, Minsoo, Moran Losada, Patricia, Khan, Zenab, Mleczko, Justyna, Xia, Yan, Dai, Rujia, Wang, Daifeng, Yang, Yucheng T., Xu, Min, Fish, Kenneth, Hof, Patrick R., Warrell, Jonathan, Fitzgerald, Dominic, White, Kevin, Jaffe, Andrew E., Peters, Mette A., Gerstein, Mark, Liu, Chunyu, Iakoucheva, Lilia M., Pinto, Dalila, Geschwind, Daniel H., Ashley-Koch, Allison E., Crawford, Gregory E., Garrett, Melanie E., Song, Lingyun, Safi, Alexias, Johnson, Graham D., Wray, Gregory A., Reddy, Timothy E, Goes, Fernando S., Zandi, Peter, Bryois, Julien, Jaffe, Andrew E., Price, Amanda J., Ivanov, Nikolay A., Collado-Torres, Leonardo, Hyde, Thomas M., Burke, Emily E., Kleiman, Joel E., Tao, Ran, Shin, Joo Heon, Akbarian, Schahram, Girdhar, Kiran, Jiang, Yan, Kundakovic, Marija, Brown, Leanne, Kassim, Bibi S., Park, Royce B., Wiseman, Jennifer R, Zharovsky, Elizabeth, Jacobov, Rivka, Devillers, Olivia, Flatow, Elie, Hoffman, Gabriel E., Lipska, Barbara K., Lewis, David A., Haroutunian, Vahram, Hahn, Chang-Gyu, Charney, Alexander W., Dracheva, Stella, Kozlenkov, Alexey, Belmont, Judson, DelValle, Diane, Francoeur, Nancy, Hadjimichael, Evi, Pinto, Dalila, van Bakel, Harm, Roussos, Panos, Fullard, John F., Bendl, Jaroslav, Hauberg, Mads E., Mangravite, Lara M, Peters, Mette A., Chae, Yooree, Peng, Junmin, Niu, Mingming, Wang, Xusheng, Webster, Maree J., Beach, Thomas G., Chen, Chao, Jiang, Yi, Dai, Rujia, Shieh, Annie W., Liu, Chunyu, Grennan, Kay S., Xia, Yan
Published in Science (American Association for the Advancement of Science) (14.12.2018)
Published in Science (American Association for the Advancement of Science) (14.12.2018)
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
C Yuen, Ryan K, Merico, Daniele, Bookman, Matt, L Howe, Jennifer, Thiruvahindrapuram, Bhooma, Patel, Rohan V, Whitney, Joe, Deflaux, Nicole, Bingham, Jonathan, Wang, Zhuozhi, Pellecchia, Giovanna, Buchanan, Janet A, Walker, Susan, Marshall, Christian R, Uddin, Mohammed, Zarrei, Mehdi, Deneault, Eric, D'Abate, Lia, Chan, Ada J S, Koyanagi, Stephanie, Paton, Tara, Pereira, Sergio L, Hoang, Ny, Engchuan, Worrawat, Higginbotham, Edward J, Ho, Karen, Lamoureux, Sylvia, Li, Weili, MacDonald, Jeffrey R, Nalpathamkalam, Thomas, Sung, Wilson W L, Tsoi, Fiona J, Wei, John, Xu, Lizhen, Tasse, Anne-Marie, Kirby, Emily, Van Etten, William, Twigger, Simon, Roberts, Wendy, Drmic, Irene, Jilderda, Sanne, Modi, Bonnie MacKinnon, Kellam, Barbara, Szego, Michael, Cytrynbaum, Cheryl, Weksberg, Rosanna, Zwaigenbaum, Lonnie, Woodbury-Smith, Marc, Brian, Jessica, Senman, Lili, Iaboni, Alana, Doyle-Thomas, Krissy, Thompson, Ann, Chrysler, Christina, Leef, Jonathan, Savion-Lemieux, Tal, Smith, Isabel M, Liu, Xudong, Nicolson, Rob, Seifer, Vicki, Fedele, Angie, Cook, Edwin H, Dager, Stephen, Estes, Annette, Gallagher, Louise, Malow, Beth A, Parr, Jeremy R, Spence, Sarah J, Vorstman, Jacob, Frey, Brendan J, Robinson, James T, Strug, Lisa J, Fernandez, Bridget A, Elsabbagh, Mayada, Carter, Melissa T, Hallmayer, Joachim, Knoppers, Bartha M, Anagnostou, Evdokia, Szatmari, Peter, Ring, Robert H, Glazer, David, Pletcher, Mathew T, Scherer, Stephen W
Published in Nature neuroscience (01.04.2017)
Published in Nature neuroscience (01.04.2017)
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Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Krupp, Deidre R., Barnard, Rebecca A., Duffourd, Yannis, Evans, Sara A., Mulqueen, Ryan M., Bernier, Raphael, Rivière, Jean-Baptiste, Fombonne, Eric, O’Roak, Brian J.
Published in American journal of human genetics (07.09.2017)
Published in American journal of human genetics (07.09.2017)
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Paternally inherited cis-regulatory structural variants are associated with autism
Brandler, William M., Antaki, Danny, Gujral, Madhusudan, Kleiber, Morgan L., Whitney, Joe, Maile, Michelle S., Hong, Oanh, Chapman, Timothy R., Tan, Shirley, Tandon, Prateek, Pang, Timothy, Tang, Shih C., Vaux, Keith K., Yang, Yan, Harrington, Eoghan, Juul, Sissel, Turner, Daniel J., Thiruvahindrapuram, Bhooma, Kaur, Gaganjot, Wang, Zhuozhi, Kingsmore, Stephen F., Gleeson, Joseph G., Bisson, Denis, Kakaradov, Boyko, Telenti, Amalio, Venter, J. Craig, Corominas, Roser, Toma, Claudio, Cormand, Bru, Rueda, Isabel, Guijarro, Silvina, Messer, Karen S., Nievergelt, Caroline M., Arranz, Maria J., Courchesne, Eric, Pierce, Karen, Muotri, Alysson R., Iakoucheva, Lilia M., Hervas, Amaia, Scherer, Stephen W., Corsello, Christina, Sebat, Jonathan
Published in Science (American Association for the Advancement of Science) (20.04.2018)
Published in Science (American Association for the Advancement of Science) (20.04.2018)
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Maternal Gestational Diabetes Mellitus and Newborn DNA Methylation: Findings From the Pregnancy and Childhood Epigenetics Consortium
Howe, Caitlin G., Cox, Bianca, Fore, Ruby, Jungius, James, Kvist, Tuomas, Lent, Samantha, Miles, Harriet E., Salas, Lucas A., Rifas-Shiman, Sheryl, Starling, Anne P., Yousefi, Paul, Ladd-Acosta, Christine, Baccarelli, Andrea, Binder, Elisabeth B., Chatzi, Vaia Lida, Czamara, Darina, Dabelea, Dana, DeMeo, Dawn L., Ghantous, Akram, Herceg, Zdenko, Kajantie, Eero, Lahti, Jari M.T., Lawlor, Debbie A., Litonjua, Augusto, Nawrot, Tim S., Nohr, Ellen A., Oken, Emily, Pizzi, Costanza, Plusquin, Michelle, Räikkönen, Katri, Relton, Caroline L., Sharp, Gemma C., Sørensen, Thorkild I.A., Sunyer, Jordi, Vrijheid, Martine, Zhang, Weiming, Hivert, Marie-France, Breton, Carrie V.
Published in Diabetes care (01.01.2020)
Published in Diabetes care (01.01.2020)
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Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS
Ross, P. Joel, Zhang, Wen-Bo, Mok, Rebecca S.F., Zaslavsky, Kirill, Deneault, Eric, D’Abate, Lia, Rodrigues, Deivid C., Yuen, Ryan K.C., Faheem, Muhammad, Mufteev, Marat, Piekna, Alina, Wei, Wei, Pasceri, Peter, Landa, Rebecca J., Nagy, Andras, Varga, Balazs, Salter, Michael W., Scherer, Stephen W., Ellis, James
Published in Biological psychiatry (1969) (15.01.2020)
Published in Biological psychiatry (1969) (15.01.2020)
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SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons
Zaslavsky, Kirill, Zhang, Wen-Bo, McCready, Fraser P., Rodrigues, Deivid C., Deneault, Eric, Loo, Caitlin, Zhao, Melody, Ross, P. Joel, El Hajjar, Joelle, Romm, Asli, Thompson, Tadeo, Piekna, Alina, Wei, Wei, Wang, Zhuozhi, Khattak, Shahryar, Mufteev, Marat, Pasceri, Peter, Scherer, Stephen W., Salter, Michael W., Ellis, James
Published in Nature neuroscience (01.04.2019)
Published in Nature neuroscience (01.04.2019)
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Gabrb3 is required for the functional integration of pyramidal neuron subtypes in the somatosensory cortex
Babij, Rachel, Ferrer, Camilo, Donatelle, Alexander, Wacks, Sam, Buch, Amanda M., Niemeyer, James E., Ma, Hongtao, Duan, Zhe Ran S., Fetcho, Robert N., Che, Alicia, Otsuka, Takumi, Schwartz, Theodore H., Huang, Ben S., Liston, Conor, De Marco García, Natalia V.
Published in Neuron (Cambridge, Mass.) (18.01.2023)
Published in Neuron (Cambridge, Mass.) (18.01.2023)
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Polygenic Risk of Mental Disorders and Subject-Specific School Grades
Jefsen, Oskar Hougaard, Holde, Katrine, McGrath, John J., Rajagopal, Veera Manikandan, Albiñana, Clara, Vilhjálmsson, Bjarni Jóhann, Grove, Jakob, Agerbo, Esben, Yilmaz, Zeynep, Plana-Ripoll, Oleguer, Munk-Olsen, Trine, Demontis, Ditte, Børglum, Anders, Mors, Ole, Bulik, Cynthia M., Mortensen, Preben Bo, Petersen, Liselotte Vogdrup
Published in Biological psychiatry (1969) (01.08.2024)
Published in Biological psychiatry (1969) (01.08.2024)
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Multi-angle meta-analysis of the gut microbiome in Autism Spectrum Disorder: a step toward understanding patient subgroups
West, Kiana A., Yin, Xiaochen, Rutherford, Erica M., Wee, Brendan, Choi, Jinlyung, Chrisman, Brianna S., Dunlap, Kaiti L., Hannibal, Roberta L., Hartono, Wiputra, Lin, Michelle, Raack, Edward, Sabino, Kayleen, Wu, Yonggan, Wall, Dennis P., David, Maude M., Dabbagh, Karim, DeSantis, Todd Z., Iwai, Shoko
Published in Scientific reports (11.10.2022)
Published in Scientific reports (11.10.2022)
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Potassium channels and autism spectrum disorder: An overview
Cheng, Peipei, Qiu, Zilong, Du, Yasong
Published in International journal of developmental neuroscience (01.10.2021)
Published in International journal of developmental neuroscience (01.10.2021)
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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome
Bassett, Anne S, Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C, van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E, Swillen, Ann, Van den Bree, Marianne, Murphy, Clodagh, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E, Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M, Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zackai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris R, Owen, Michael, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J, Scherer, Stephen W, Emanuel, Beverly S, Guo, Tingwei, Morrow, Bernice E, Marshall, Christian R
Published in American Journal of Psychiatry (01.11.2017)
Published in American Journal of Psychiatry (01.11.2017)
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Dysregulation of Cortical Neuron DNA Methylation Profile in Autism Spectrum Disorder
Nardone, Stefano, Sams, Dev Sharan, Zito, Antonino, Reuveni, Eli, Elliott, Evan
Published in Cerebral cortex (New York, N.Y. 1991) (01.12.2017)
Published in Cerebral cortex (New York, N.Y. 1991) (01.12.2017)
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Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder
Lin, Amy, Vajdi, Ariana, Kushan-Wells, Leila, Helleman, Gerhard, Hansen, Laura Pacheco, Jonas, Rachel K., Jalbrzikowski, Maria, Kingsbury, Lyle, Raznahan, Armin, Bearden, Carrie E.
Published in Biological psychiatry (1969) (01.08.2020)
Published in Biological psychiatry (1969) (01.08.2020)
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Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum Disorder
Brownstein, Catherine A., Douard, Elise, Mollon, Josephine, Smith, Richard, Hojlo, Margaret A., Das, Ananth, Goldman, Maria, Garvey, Emily, Cabral, Kristin, Li, Jianqiao, Bowen, Joshua, Rao, Abhijit S., Genetti, Casie, Carroll, Devon, Knowles, Emma E. M., Deaso, Emma, Agrawal, Pankaj B., Beggs, Alan H., D’Angelo, Eugene, Almasy, Laura, Alexander-Bloch, Aaron, Saci, Zohra, Moreau, Clara A., Huguet, Guillaume, Deo, Anthony J., Jacquemont, Sébastien, Glahn, David C., Gonzalez-Heydrich, Joseph
Published in The American journal of psychiatry (01.11.2022)
Published in The American journal of psychiatry (01.11.2022)
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Pathogenic Yield of Genetic Testing in Autism Spectrum Disorder
Harris, Holly K., Sideridis, Georgios D., Barbaresi, William J., Harstad, Elizabeth
Published in Pediatrics (Evanston) (01.10.2020)
Published in Pediatrics (Evanston) (01.10.2020)
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Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
Sanchez Russo, Rossana, Gambello, Michael J., Murphy, Melissa M., Aberizk, Katrina, Black, Emily, Burrell, T. Lindsey, Carlock, Grace, Cubells, Joseph F., Epstein, Michael T., Espana, Roberto, Goines, Katrina, Guest, Ryan M., Klaiman, Cheryl, Koh, Sookyong, Leslie, Elizabeth J., Li, Longchuan, Novacek, Derek M., Saulnier, Celine A., Sefik, Esra, Shultz, Sarah, Walker, Elaine, White, Stormi Pulver, Mulle, Jennifer Gladys
Published in Genetics in medicine (01.05.2021)
Published in Genetics in medicine (01.05.2021)
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Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Marcogliese, Paul C., Deal, Samantha L., Andrews, Jonathan, Harnish, J. Michael, Bhavana, V. Hemanjani, Graves, Hillary K., Jangam, Sharayu, Luo, Xi, Liu, Ning, Bei, Danqing, Chao, Yu-Hsin, Hull, Brooke, Lee, Pei-Tseng, Pan, Hongling, Bhadane, Pradnya, Huang, Mei-Chu, Longley, Colleen M., Chao, Hsiao-Tuan, Chung, Hyung-lok, Haelterman, Nele A., Kanca, Oguz, Manivannan, Sathiya N., Rossetti, Linda Z., German, Ryan J., Gerard, Amanda, Schwaibold, Eva Maria Christina, Fehr, Sarah, Guerrini, Renzo, Vetro, Annalisa, England, Eleina, Murali, Chaya N., Barakat, Tahsin Stefan, van Dooren, Marieke F., Wilke, Martina, van Slegtenhorst, Marjon, Lesca, Gaetan, Sabatier, Isabelle, Chatron, Nicolas, Brownstein, Catherine A., Madden, Jill A., Agrawal, Pankaj B., Keren, Boris, Courtin, Thomas, Perrin, Laurence, Brugger, Melanie, Roser, Timo, Leiz, Steffen, Mau-Them, Frederic Tran, Delanne, Julian, Sukarova-Angelovska, Elena, Trajkova, Slavica, Rosenhahn, Erik, Strehlow, Vincent, Platzer, Konrad, Keller, Roberto, Pavinato, Lisa, Brusco, Alfredo, Rosenfeld, Jill A., Marom, Ronit, Wangler, Michael F., Yamamoto, Shinya
Published in Cell reports (Cambridge) (15.03.2022)
Published in Cell reports (Cambridge) (15.03.2022)
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