Rachel E. Rodin

发表

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

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

Accurate detection of mosaic variants in sequencing data without matched controls

Peter J. Park, Minseok Kwon, Isidro Cortés-Ciriano, 2019, Nature Biotechnology.

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

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

Parallel RNA and DNA analysis after Deep-sequencing (PRDD-seq) reveals cell type specific lineage patterns in human brain

Trygve E Bakken, C. Walsh, Jeremy A. Miller, 2020, bioRxiv.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Michael E. Coulter, C. Walsh, S. Wiemann, 2017, Genome research.

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

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

Somatic Mutation in Pediatric Neurological Diseases.

C. Walsh, Rachel E. Rodin, 2018, Pediatric neurology.

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

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

MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutations

C. Walsh, Ryan N. Doan, A. Huang, 2021, BMC medical genomics.

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.

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

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

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.

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

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

Group II metabotropic glutamate receptor interactions with NHERF scaffold proteins: Implications for receptor localization in brain

Y. Smith, C. Yun, E. Weinman, 2017, Neuroscience.

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.

Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain

Trygve E Bakken, C. Walsh, Jeremy A. Miller, 2020, Proceedings of the National Academy of Sciences.

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.

Control-independent mosaic single nucleotide variant detection with DeepMosaic

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

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.

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

Minseok Kwon, Lovelace J Luquette, Isidro Cortés-Ciriano, 2019, Nature Genetics.

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

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2017, bioRxiv.