The Emerging Biology of Autism Spectrum Disorders
State, Matthew W., Šestan, Nenad
Published in Science (American Association for the Advancement of Science) (14.09.2012)
Published in Science (American Association for the Advancement of Science) (14.09.2012)
Get full text
Journal Article
The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders
Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Lehner, Thomas, Roeder, Kathryn, State, Matthew W.
Published in Neuron (20.12.2012)
Published in Neuron (20.12.2012)
Get full text
Journal Article
Conference Proceeding
Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice
Baldan, Lissandra Castellan, Williams, Kyle A, Gallezot, Jean-Dominique, Pogorelov, Vladimir, Rapanelli, Maximiliano, Crowley, Michael, Anderson, George M, Loring, Erin, Gorczyca, Roxanne, Billingslea, Eileen, Wasylink, Suzanne, Panza, Kaitlyn E, Ercan-Sencicek, A Gulhan, Krusong, Kuakarun, Leventhal, Bennett L, Ohtsu, Hiroshi, Bloch, Michael H, Hughes, Zoë A, Krystal, John H, Mayes, Linda, de Araujo, Ivan, Ding, Yu-Shin, State, Matthew W, Pittenger, Christopher
Published in Neuron (Cambridge, Mass.) (08.01.2014)
Published in Neuron (Cambridge, Mass.) (08.01.2014)
Get full text
Journal Article
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Markenscoff-Papadimitriou, Eirene, Whalen, Sean, Przytycki, Pawel, Thomas, Reuben, Binyameen, Fadya, Nowakowski, Tomasz J., Kriegstein, Arnold R., Sanders, Stephan J., State, Matthew W., Pollard, Katherine S., Rubenstein, John L.
Published in Cell (06.08.2020)
Published in Cell (06.08.2020)
Get full text
Journal Article
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Cotney, Justin, Muhle, Rebecca A., Sanders, Stephan J., Liu, Li, Willsey, A. Jeremy, Niu, Wei, Liu, Wenzhong, Klei, Lambertus, Lei, Jing, Yin, Jun, Reilly, Steven K., Tebbenkamp, Andrew T., Bichsel, Candace, Pletikos, Mihovil, Sestan, Nenad, Roeder, Kathryn, State, Matthew W., Devlin, Bernie, Noonan, James P.
Published in Nature communications (10.03.2015)
Published in Nature communications (10.03.2015)
Get full text
Journal Article
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
Willsey, A. Jeremy, Sanders, Stephan J., Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T., Muhle, Rebecca A., Reilly, Steven K., Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A., Murtha, Michael T., Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A. Gulhan, Gockley, Jake, Gupta, Abha R., Han, Wenqi, He, Xin, Hoffman, Ellen J., Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Ed S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Sestan, Nenad, State, Matthew W.
Published in Cell (21.11.2013)
Published in Cell (21.11.2013)
Get full text
Journal Article
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
Glessner, Joseph T, Bick, Alexander G, Ito, Kaoru, Homsy, Jason G, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R, Golhar, Ryan, Sanders, Stephan J, Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A Jeremy, State, Matthew W, Kaltman, Jonathan R, White, Peter S, Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D, Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K
Published in Circulation research (24.10.2014)
Published in Circulation research (24.10.2014)
Get full text
Journal Article
Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders
Luo, Rui, Sanders, Stephan J., Tian, Yuan, Voineagu, Irina, Huang, Ni, Chu, Su H., Klei, Lambertus, Cai, Chaochao, Ou, Jing, Lowe, Jennifer K., Hurles, Matthew E., Devlin, Bernie, State, Matthew W., Geschwind, Daniel H.
Published in American journal of human genetics (13.07.2012)
Published in American journal of human genetics (13.07.2012)
Get full text
Journal Article
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes
He, Xin, Sanders, Stephan J, Liu, Li, De Rubeis, Silvia, Lim, Elaine T, Sutcliffe, James S, Schellenberg, Gerard D, Gibbs, Richard A, Daly, Mark J, Buxbaum, Joseph D, State, Matthew W, Devlin, Bernie, Roeder, Kathryn
Published in PLoS genetics (01.08.2013)
Published in PLoS genetics (01.08.2013)
Get full text
Journal Article
Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
Markenscoff-Papadimitriou, Eirene, Binyameen, Fadya, Whalen, Sean, Price, James, Lim, Kenneth, Ypsilanti, Athena R., Catta-Preta, Rinaldo, Pai, Emily Ling-Lin, Mu, Xin, Xu, Duan, Pollard, Katherine S., Nord, Alex S., State, Matthew W., Rubenstein, John L.
Published in Cell reports (Cambridge) (07.12.2021)
Published in Cell reports (Cambridge) (07.12.2021)
Get full text
Journal Article
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex
Werling, Donna M., Pochareddy, Sirisha, Choi, Jinmyung, An, Joon-Yong, Sheppard, Brooke, Peng, Minshi, Li, Zhen, Dastmalchi, Claudia, Santpere, Gabriel, Sousa, André M.M., Tebbenkamp, Andrew T.N., Kaur, Navjot, Gulden, Forrest O., Breen, Michael S., Liang, Lindsay, Gilson, Michael C., Zhao, Xuefang, Dong, Shan, Klei, Lambertus, Cicek, A. Ercument, Buxbaum, Joseph D., Adle-Biassette, Homa, Thomas, Jean-Leon, Aldinger, Kimberly A., O’Day, Diana R., Glass, Ian A., Zaitlen, Noah A., Talkowski, Michael E., Roeder, Kathryn, State, Matthew W., Devlin, Bernie, Sanders, Stephan J., Sestan, Nenad
Published in Cell reports (Cambridge) (07.04.2020)
Published in Cell reports (Cambridge) (07.04.2020)
Get full text
Journal Article
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Chaste, Pauline, Klei, Lambertus, Sanders, Stephan J, Hus, Vanessa, Murtha, Michael T, Lowe, Jennifer K, Willsey, A. Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Mane, Shrikant M, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Sutcliffe, James S, Lese Martin, Christa, Beaudet, Arthur L, Lord, Catherine, State, Matthew W, Cook, Edwin H, Devlin, Bernie
Published in Biological psychiatry (1969) (01.05.2015)
Published in Biological psychiatry (1969) (01.05.2015)
Get full text
Journal Article
The genetics of autism: key issues, recent findings, and clinical implications
El-Fishawy, Paul, State, Matthew W
Published in The Psychiatric clinics of North America (01.03.2010)
Published in The Psychiatric clinics of North America (01.03.2010)
Get more information
Journal Article
L-Histidine Decarboxylase and Tourette's Syndrome
Ercan-Sencicek, A. Gulhan, Stillman, Althea A, Ghosh, Ananda K, Bilguvar, Kaya, O'Roak, Brian J, Mason, Christopher E, Abbott, Thomas, Gupta, Abha, King, Robert A, Pauls, David L, Tischfield, Jay A, Heiman, Gary A, Singer, Harvey S, Gilbert, Donald L, Hoekstra, Pieter J, Morgan, Thomas M, Loring, Erin, Yasuno, Katsuhito, Fernandez, Thomas, Sanders, Stephan, Louvi, Angeliki, Cho, Judy H, Mane, Shrikant, Colangelo, Christopher M, Biederer, Thomas, Lifton, Richard P, Gunel, Murat, State, Matthew W
Published in Nature reviews. Neuroscience (20.05.2010)
Published in Nature reviews. Neuroscience (20.05.2010)
Get full text
Journal Article