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Cell Systems|October 21, 2021
Paving the path toward genomic privacy with secure imputationMaxwell A Sherman
Nature Genetics|July 6, 2021
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analysesAlison R Barton, Maxwell A Sherman, Ronen E Mukamel, et al.
Nature Biotechnology|June 21, 2022
Genome-wide mapping of somatic mutation rates uncovers drivers of cancerMaxwell A Sherman, Adam U Yaari, Oliver Priebe, et al.
American Journal of Human Genetics|June 1, 2022
A spectrum of recessiveness among Mendelian disease variants in UK BiobankAlison R Barton, Margaux L A Hujoel, Ronen E Mukamel, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Science (New York, N.Y.)|September 23, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.
Nucleic Acids Research|November 30, 2017
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimationMaxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Neuron|June 27, 2020
An Activity-Mediated Transition in Transcription in Early Postnatal NeuronsHume Stroud, Marty G Yang, Yael N Tsitohay, et al.
Cell|October 28, 2022
Influences of rare copy-number variation on human complex traitsMargaux L A Hujoel, Maxwell A Sherman, Alison R Barton, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 30, 2016
Neural mechanisms of transient neocortical beta rhythms: Converging evidence from humans, computational modeling, monkeys, and miceMaxwell A Sherman, Shane Lee, Robert Law, et al.
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