37873195 | Create Study | The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia risk. | bioRxiv : the preprint server for biology | Liang, Qiuman; Jiang, Yi; Shieh, Annie W; Zhou, Dan; Chen, Rui; Wang, Feiran; Xu, Meng; Niu, Mingming; Wang, Xusheng; Pinto, Dalila; Wang, Yue; Cheng, Lijun; Vadukapuram, Ramu; Zhang, Chunling; Grennan, Kay; Giase, Gina; PsychENCODE Consortium; White, Kevin P; Peng, Junming; Li, Bingshan; Liu, Chunyu; Chen, Chao; Wang, Sidney H | November 10, 2023 | Not Determined |
36993743 | Create Study | Evaluating performance and applications of sample-wise cell deconvolution methods on human brain transcriptomic data. | bioRxiv : the preprint server for biology | Dai, Rujia; Chu, Tianyao; Zhang, Ming; Wang, Xuan; Jourdon, Alexandre; Wu, Feinan; Mariani, Jessica; Vaccarino, Flora M; Lee, Donghoon; Fullard, John F; Hoffman, Gabriel E; Roussos, Panos; Wang, Yue; Wang, Xusheng; Pinto, Dalila; Wang, Sidney H; Zhang, Chunling; PsychENCODE consortium; Chen, Chao; Liu, Chunyu | March 15, 2023 | Not Determined |
36865150 | Create Study | Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. | medRxiv : the preprint server for health sciences | Epi25 Collaborative; Chen, Siwei; Neale, Benjamin M; Berkovic, Samuel F | February 24, 2023 | Not Determined |
36274170 | Create Study | High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy. | Acta neuropathologica communications | Pai, Balagopal; Tome-Garcia, Jessica; Cheng, Wan Sze; Nudelman, German; Beaumont, Kristin G; Ghatan, Saadi; Panov, Fedor; Caballero, Elodia; Sarpong, Kwadwo; Marcuse, Lara; Yoo, Jiyeoun; Jiang, Yan; Schaefer, Anne; Akbarian, Schahram; Sebra, Robert; Pinto, Dalila; Zaslavsky, Elena; Tsankova, Nadejda M | October 23, 2022 | Not Determined |
34758317 | Create Study | Sox6 expression distinguishes dorsally and ventrally biased dopamine neurons in the substantia nigra with distinctive properties and embryonic origins. | Cell reports | Pereira Luppi, Milagros; Azcorra, Maite; Caronia-Brown, Giuliana; Poulin, Jean-Francois; Gaertner, Zachary; Gatica, Serafin; Moreno-Ramos, Oscar Andrés; Nouri, Navid; Dubois, Marilyn; Ma, Yongchao C; Ramakrishnan, Charu; Fenno, Lief; Kim, Yoon Seok; Deisseroth, Karl; Cicchetti, Francesca; Dombeck, Daniel A; Awatramani, Rajeshwar | November 9, 2021 | Not Determined |
32522981 | Create Study | mTADA is a framework for identifying risk genes from de novo mutations in multiple traits. | Nature communications | Nguyen, Tan-Hoang; Dobbyn, Amanda; Brown, Ruth C; Riley, Brien P; Buxbaum, Joseph D; Pinto, Dalila; Purcell, Shaun M; Sullivan, Patrick F; He, Xin; Stahl, Eli A | June 2020 | Not Determined |
30545856 | Create Study | Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder. | Science (New York, N.Y.) | 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; PsychENCODE Consortium; Peters, Mette A; Gerstein, Mark; Liu, Chunyu; Iakoucheva, Lilia M; Pinto, Dalila; Geschwind, Daniel H | December 2018 | Not Determined |
29262854 | Create Study | Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders. | Genome medicine | Nguyen, Hoang T; Bryois, Julien; Kim, April; Dobbyn, Amanda; Huckins, Laura M; Munoz-Manchado, Ana B; Ruderfer, Douglas M; Genovese, Giulio; Fromer, Menachem; Xu, Xinyi; Pinto, Dalila; Linnarsson, Sten; Verhage, Matthijs; Smit, August B; Hjerling-Leffler, Jens; Buxbaum, Joseph D; Hultman, Christina; Sklar, Pamela; Purcell, Shaun M; Lage, Kasper; He, Xin; Sullivan, Patrick F; Stahl, Eli A | December 2017 | Not Determined |
29213072 | Create Study | Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects. | Scientific reports | de Jesús Ascencio-Montiel, Iván; Pinto, Dalila; Parra, Esteban J; Valladares-Salgado, Adán; Cruz, Miguel; Scherer, Stephen W | December 2017 | Not Determined |
28407363 | Create Study | De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome. | American journal of medical genetics. Part A | Sagar, Angela; Pinto, Dalila; Najjar, Fedra; Guter, Stephen J; Macmillan, Carol; Cook, Edwin H | June 2017 | Not Determined |
27668389 | Create Study | Gene expression elucidates functional impact of polygenic risk for schizophrenia. | Nature neuroscience | Fromer, Menachem; Roussos, Panos; Sieberts, Solveig K; Johnson, Jessica S; Kavanagh, David H; Perumal, Thanneer M; Ruderfer, Douglas M; Oh, Edwin C; Topol, Aaron; Shah, Hardik R; Klei, Lambertus L; Kramer, Robin; Pinto, Dalila; Gümüş, Zeynep H; Cicek, A Ercument; Dang, Kristen K; Browne, Andrew; Lu, Cong; Xie, Lu; Readhead, Ben; Stahl, Eli A; Xiao, Jianqiu; Parvizi, Mahsa; Hamamsy, Tymor; Fullard, John F; Wang, Ying-Chih; Mahajan, Milind C; Derry, Jonathan M J; Dudley, Joel T; Hemby, Scott E; Logsdon, Benjamin A; Talbot, Konrad; Raj, Towfique; Bennett, David A; De Jager, Philip L; Zhu, Jun; Zhang, Bin; Sullivan, Patrick F; Chess, Andrew; Purcell, Shaun M; Shinobu, Leslie A; Mangravite, Lara M; Toyoshiba, Hiroyoshi; Gur, Raquel E; Hahn, Chang-Gyu; Lewis, David A; Haroutunian, Vahram; Peters, Mette A; Lipska, Barbara K; Buxbaum, Joseph D; Schadt, Eric E; Hirai, Keisuke; Roeder, Kathryn; Brennand, Kristen J; Katsanis, Nicholas; Domenici, Enrico; Devlin, Bernie; Sklar, Pamela | November 2016 | Not Determined |