Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses

por Barton, Alison R., Sherman, Maxwell A., Mukamel, Ronen E., Loh, Po-Ru
Publicado 2021

Genome-wide mapping of somatic mutation rates uncovers drivers of cancer

por Sherman, Maxwell A., Yaari, Adam U., Priebe, Oliver, Dietlein, Felix, Loh, Po-Ru, Berger, Bonnie
Publicado 2022

PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation

por Sherman, Maxwell A, Barton, Alison R, Lodato, Michael A, Vitzthum, Carl, Coulter, Michael E, Walsh, Christopher A, Park, Peter J
Publicado 2018

Hidden protein-altering variants influence diverse human phenotypes

por 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
Publicado 2023

Large mosaic copy number variations confer autism risk

por 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
Publicado 2021

Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritability

por 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.
Publicado 2021

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

por 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.
Publicado 2021

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

por Maury, Eduardo A., Sherman, Maxwell A., Genovese, Giulio, Gilgenast, Thomas G., Kamath, Tushar, Burris, S.J., Rajarajan, Prashanth, Flaherty, Erin, Akbarian, Schahram, Chess, Andrew, McCarroll, Steven A., Loh, Po-Ru, Phillips-Cremins, Jennifer E., Brennand, Kristen J., Macosko, Evan Z., Walters, James T.R., O’Donovan, Michael, Sullivan, Patrick, Sebat, Jonathan, Lee, Eunjung A., Walsh, Christopher A.
Publicado 2023

Comprehensive identification of somatic nucleotide variants in human brain tissue

por Wang, Yifan, Bae, Taejeong, Thorpe, Jeremy, Sherman, Maxwell A., Jones, Attila G., Cho, Sean, Daily, Kenneth, Dou, Yanmei, Ganz, Javier, Galor, Alon, Lobon, Irene, Pattni, Reenal, Rosenbluh, Chaggai, Tomasi, Simone, Tomasini, Livia, Yang, Xiaoxu, Zhou, Bo, Akbarian, Schahram, Ball, Laurel L., Bizzotto, Sara, Emery, Sarah B., Doan, Ryan, Fasching, Liana, Jang, Yeongjun, Juan, David, Lizano, Esther, Luquette, Lovelace J., Moldovan, John B., Narurkar, Rujuta, Oetjens, Matthew T., Rodin, Rachel E., Sekar, Shobana, Shin, Joo Heon, Soriano, Eduardo, Straub, Richard E., Zhou, Weichen, Chess, Andrew, Gleeson, Joseph G., Marquès-Bonet, Tomas, Park, Peter J., Peters, Mette A., Pevsner, Jonathan, Walsh, Christopher A., Weinberger, Daniel R., Vaccarino, Flora M., Moran, John V., Urban, Alexander E., Kidd, Jeffrey M., Mills, Ryan E., Abyzov, Alexej
Publicado 2021