M. Sherman

发表

Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

Ronen E. Mukamel, R. Handsaker, S. Mccarroll, 2021, bioRxiv.

An Activity-Mediated Transition in Transcription in Early Postnatal Neurons

Christopher P. Davis, Sinisa Hrvatin, M. Greenberg, 2020, Neuron.

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

Ronen E. Mukamel, Po-Ru Loh, R. Mukamel, 2020, medRxiv.

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

Po-Ru Loh, F. Dietlein, M. Sherman, 2022, Nature Biotechnology.

Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2022, Science.

Repeat polymorphisms in non-coding DNA underlie top genetic risk loci for glaucoma and colorectal cancer.

Ronen E. Mukamel, R. Handsaker, Po-Ru Loh, 2022, medRxiv.

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

Ryan E. Mills, J. V. Moran, Jennifer A. Erwin, 2017, Science.

Influences of rare copy number variation on human complex traits

Ronen E. Mukamel, Po-Ru Loh, M. Hujoel, 2021, bioRxiv.

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

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2021, Nature Neuroscience.

The Landscape of Mutational Mosaicism in Autistic and Normal Human Cerebral Cortex

Lovelace J. Luquette, C. Walsh, P. Park, 2020, bioRxiv.

Large mosaic copy number variations confer autism risk

Ronen E. Mukamel, B. Berger, C. Walsh, 2020, Nature Neuroscience.

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

Eric C. Griffith, Sinisa Hrvatin, M. Greenberg, 2021, Nature Neuroscience.

Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

R. Handsaker, S. Mccarroll, R. Mukamel, 2021, Science.

Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance

Lovelace J Luquette, Peter J Park, Lovelace J. Luquette, 2019, Nature Communications.

Linked-read analysis identifies mutations in single-cell DNA-sequencing data

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2019, Nature Genetics.

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017, Science.

Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

J. V. Moran, Michael E. Coulter, Laurel L. Ball, 2019, bioRxiv.

Paving the path toward genomic privacy with secure imputation.

M. Sherman, 2021, Cell systems.

Learning the mutational landscape of the cancer genome

Po-Ru Loh, F. Dietlein, M. Sherman, 2021, bioRxiv.

Developmental Dynamics of RNA Translation in the Human Brain

Alan M. Moses, Eric C. Griffith, Ava C. Carter, 2021, bioRxiv.

Comprehensive identification of somatic nucleotide variants in human brain tissue

Peter J. Park, Jonathan Pevsner, Eduardo Soriano, 2020, bioRxiv.

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Sara B. Linker, Ryan E. Mills, Kiely N. James, 2023, Nature Genetics.

A spectrum of recessiveness among Mendelian disease variants in UK Biobank

Ronen E. Mukamel, Po-Ru Loh, M. Hujoel, 2021, medRxiv.

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Thomas G. Gilgenast, Jennifer E. Phillips-Cremins, J. Sebat, 2022, medRxiv.

Multi-resolution modeling of a discrete stochastic process identifies causes of cancer

Andrei Barbu, Boris Katz, Po-Ru Loh, 2021, ICLR.

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

Michael E. Coulter, C. Walsh, P. Park, 2017, bioRxiv.

Comprehensive identification of somatic nucleotide variants in human brain tissue

J. V. Moran, Lovelace J. Luquette, Laurel L. Ball, 2021, Genome Biology.

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

Lovelace J. Luquette, C. Walsh, P. Park, 2021, Nature neuroscience.

Hidden protein-altering variants influence diverse human phenotypes

Ronen E. Mukamel, R. Handsaker, S. Mccarroll, 2023, bioRxiv.

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

Sara B. Linker, Evan Z. Macosko, Thomas G. Gilgenast, 2023, Cell genomics.

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal 1 contribution to risk and recurrent, isoform-specific NRXN1 disruptions 2

Thomas G. Gilgenast, Jennifer E. Phillips-Cremins, J. Sebat, 2021 .

Control-independent mosaic single nucleotide variant detection with DeepMosaic

Ryan E. Mills, J. V. Moran, Michael E. Coulter, 2023, Nature Biotechnology.

Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer

Ronen E. Mukamel, R. Handsaker, S. Mccarroll, 2023, Cell.

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal 1 contribution to risk and recurrent, isoform-specific NRXN1 disruptions 2

Thomas G. Gilgenast, Jennifer E. Phillips-Cremins, J. Sebat, 2021 .

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal 1 contribution to risk and recurrent, isoform-specific NRXN1 disruptions 2

Thomas G. Gilgenast, Jennifer E. Phillips-Cremins, J. Sebat, 2021 .

Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2021, Nature Neuroscience.