Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses von Barton, Alison R., Sherman, Maxwell A., Mukamel, Ronen E., Loh, Po-Ru

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An Activity-Mediated Transition in Transcription in Early Postnatal Neurons von Stroud, Hume, Yang, Marty G., Tsitohay, Yael N., Davis, Christopher P., Sherman, Maxwell A., Hrvatin, Sinisa, Ling, Emi, Greenberg, Michael E.

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Protein-coding repeat polymorphisms strongly shape diverse human phenotypes von Mukamel, Ronen E, Handsaker, Robert E, Sherman, Maxwell A, Barton, Alison R, Zheng, Yiming, McCarroll, Steven A, Loh, Po-Ru

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Neural mechanisms of transient neocortical beta rhythms: Converging evidence from humans, computational modeling, monkeys, and mice von Sherman, Maxwell A., Lee, Shane, Law, Robert, Haegens, Saskia, Thorn, Catherine A., Hämäläinen, Matti S., Moore, Christopher I., Jones, Stephanie R.

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Genome-wide mapping of somatic mutation rates uncovers drivers of cancer von Sherman, Maxwell A., Yaari, Adam U., Priebe, Oliver, Dietlein, Felix, Loh, Po-Ru, Berger, Bonnie

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Aging and neurodegeneration are associated with increased mutations in single human neurons von Lodato, Michael A, Rodin, Rachel E, Bohrson, Craig L, Coulter, Michael E, Barton, Alison R, Kwon, Minseok, Sherman, Maxwell A, Vitzthum, Carl M, Luquette, Lovelace J, Yandava, Chandri N, Yang, Pengwei, Chittenden, Thomas W, Hatem, Nicole E, Ryu, Steven C, Woodworth, Mollie B, Park, Peter J, Walsh, Christopher A

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A spectrum of recessiveness among Mendelian disease variants in UK Biobank von Barton, Alison R, Hujoel, Margaux L A, Mukamel, Ronen E, Sherman, Maxwell A, Loh, Po-Ru

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Paving the path toward genomic privacy with secure imputation von Sherman, Maxwell A.

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Influences of rare copy-number variation on human complex traits von Hujoel, Margaux L A, Sherman, Maxwell A, Barton, Alison R, Mukamel, Ronen E, Sankaran, Vijay G, Terao, Chikashi, Loh, Po-Ru

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Large mosaic copy number variations confer autism risk von Sherman, Maxwell A., Rodin, Rachel E., Genovese, Giulio, Dias, Caroline, Barton, Alison R., Mukamel, Ronen E., Berger, Bonnie, Park, Peter J., Walsh, Christopher A., Loh, Po-Ru

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Developmental dynamics of RNA translation in the human brain von Duffy, Erin E., Finander, Benjamin, Choi, GiHun, Carter, Ava C., Pritisanac, Iva, Alam, Aqsa, Luria, Victor, Karger, Amir, Phu, William, Sherman, Maxwell A., Assad, Elena G., Pajarillo, Naomi, Khitun, Alexandra, Crouch, Elizabeth E., Ganesh, Sanika, Chen, Jin, Berger, Bonnie, Sestan, Nenad, O’Donnell-Luria, Anne, Huang, Eric J., Griffith, Eric C., Forman-Kay, Julie D., Moses, Alan M., Kalish, Brian T., Greenberg, Michael E.

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Linked-read analysis identifies mutations in single-cell DNA-sequencing data von Bohrson, Craig L., Barton, Alison R., Lodato, Michael A., Rodin, Rachel E., Luquette, Lovelace J., Viswanadham, Vinay V., Gulhan, Doga C., Cortés-Ciriano, Isidro, Sherman, Maxwell A., Kwon, Minseok, Coulter, Michael E., Galor, Alon, Walsh, Christopher A., Park, Peter J.

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Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer von Mukamel, Ronen E, Handsaker, Robert E, Sherman, Maxwell A, Barton, Alison R, Hujoel, Margaux L A, McCarroll, Steven A, Loh, Po-Ru

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Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritability von Boulting, Gabriella L., Durresi, Ershela, Ataman, Bulent, Sherman, Maxwell A., Mei, Kevin, Harmin, David A., Carter, Ava C., Hochbaum, Daniel R., Granger, Adam J., Engreitz, Jesse M., Hrvatin, Sinisa, Blanchard, Michael R., Yang, Marty G., Griffith, Eric C., Greenberg, Michael E.

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Protein-altering variants at copy number-variable regions influence diverse human phenotypes von Hujoel, Margaux L. A., Handsaker, Robert E., Sherman, Maxwell A., Kamitaki, Nolan, Barton, Alison R., Mukamel, Ronen E., Terao, Chikashi, McCarroll, Steven A., Loh, Po-Ru

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PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation von Sherman, Maxwell A, Barton, Alison R, Lodato, Michael A, Vitzthum, Carl, Coulter, Michael E, Walsh, Christopher A, Park, Peter J

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The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing von Rodin, Rachel E., Dou, Yanmei, Kwon, Minseok, Sherman, Maxwell A., D’Gama, Alissa M., Doan, Ryan N., Rento, Lariza M., Girskis, Kelly M., Bohrson, Craig L., Kim, Sonia N., Nadig, Ajay, Luquette, Lovelace J., Gulhan, Doga C., Park, Peter J., Walsh, Christopher A.

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Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development von Chung, Changuk, Yang, Xiaoxu, Bae, Taejeong, Vong, Keng Ioi, Mittal, Swapnil, Donkels, Catharina, Westley Phillips, H., Li, Zhen, Marsh, Ashley P. L., Breuss, Martin W., Ball, Laurel L., Garcia, Camila Araújo Bernardino, George, Renee D., Gu, Jing, Xu, Mingchu, Barrows, Chelsea, James, Kiely N., Stanley, Valentina, Nidhiry, Anna S., Khoury, Sami, Howe, Gabrielle, Riley, Emily, Xu, Xin, Copeland, Brett, Wang, Yifan, Kim, Se Hoon, Kang, Hoon-Chul, Schulze-Bonhage, Andreas, Haas, Carola A., Urbach, Horst, Prinz, Marco, Limbrick, David D., Gurnett, Christina A., Smyth, Matthew D., Sattar, Shifteh, Nespeca, Mark, Gonda, David D., Imai, Katsumi, Takahashi, Yukitoshi, Chen, Hsin-Hung, Tsai, Jin-Wu, Conti, Valerio, Guerrini, Renzo, Devinsky, Orrin, Silva, Wilson A., Machado, Helio R., Mathern, Gary W., Abyzov, Alexej, Baldassari, Sara, Baulac, Stéphanie, Gleeson, Joseph G.

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Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability von Bae, Taejeong, Fasching, Liana, Wang, Yifan, Shin, Joo Heon, Suvakov, Milovan, Jang, Yeongjun, Norton, Scott, Dias, Caroline, Mariani, Jessica, Jourdon, Alexandre, Wu, Feinan, Panda, Arijit, Pattni, Reenal, Chahine, Yasmine, Yeh, Rebecca, Roberts, Rosalinda C, Huttner, Anita, Kleinman, Joel E, Hyde, Thomas M, Straub, Richard E, Walsh, Christopher A, Urban, Alexander E, Leckman, James F, Weinberger, Daniel R, Vaccarino, Flora M, Abyzov, Alexej

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Somatic mosaicism reveals clonal distributions of neocortical development von Breuss, Martin W., Yang, Xiaoxu, Schlachetzki, Johannes C. M., Antaki, Danny, Lana, Addison J., Xu, Xin, Chung, Changuk, Chai, Guoliang, Stanley, Valentina, Song, Qiong, Newmeyer, Traci F., Nguyen, An, O’Brien, Sydney, Hoeksema, Marten A., Cao, Beibei, Nott, Alexi, McEvoy-Venneri, Jennifer, Pasillas, Martina P., Barton, Scott T., Copeland, Brett R., Nahas, Shareef, Van Der Kraan, Lucitia, Ding, Yan, Glass, Christopher K., Gleeson, Joseph G.

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