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Author Details
Full Name
Alistair R R Forrest
Affiliation
RIKEN Center for Integrative Medical Sciences
ORCID
Career Start Year
1994
Papers
147
H Index
56
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36700121
Characterization of the humanized FRG mouse model and development of an AAV-LK03 variant with improved liver lobular biodistribution.
Mol Ther Methods Clin Dev
2023
36700121
Characterization of the humanized FRG mouse model and development of an AAV-LK03 variant with improved liver lobular biodistribution.
Mol Ther Methods Clin Dev
2023
36318921
Human prefrontal cortex gene regulatory dynamics from gestation to adulthood at single-cell resolution.
Cell
2022
35961773
Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs.
Genome Res
2022
35749574
MaxHiC: A robust background correction model to identify biologically relevant chromatin interactions in Hi-C and capture Hi-C experiments.
PLoS Comput Biol
2022
35986006
Temporally restricted activation of IFNβ signaling underlies response to immune checkpoint therapy in mice.
Nat Commun
2022
36318921
Human prefrontal cortex gene regulatory dynamics from gestation to adulthood at single-cell resolution.
Cell
2022
35749574
MaxHiC: A robust background correction model to identify biologically relevant chromatin interactions in Hi-C and capture Hi-C experiments.
PLoS Comput Biol
2022
35961773
Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs.
Genome Res
2022
35986006
Temporally restricted activation of IFNβ signaling underlies response to immune checkpoint therapy in mice.
Nat Commun
2022
34551826
Improved CRISPR/Cas9 gene editing in primary human myoblasts using low confluency cultures on Matrigel.
Skelet Muscle
2021
34551826
Improved CRISPR/Cas9 gene editing in primary human myoblasts using low confluency cultures on Matrigel.
Skelet Muscle
2021
34470851
Intra- and intertumoral heterogeneity of liver metastases in a patient with uveal melanoma revealed by single-cell RNA sequencing.
Cold Spring Harb Mol Case Stud
2021
34470851
Intra- and intertumoral heterogeneity of liver metastases in a patient with uveal melanoma revealed by single-cell RNA sequencing.
Cold Spring Harb Mol Case Stud
2021
32161175
Comprehensive Characterization of Transcriptional Activity during Influenza A Virus Infection Reveals Biases in Cap-Snatching of Host RNA Sequences.
J Virol
2020
31992766
CANCERSIGN: a user-friendly and robust tool for identification and classification of mutational signatures and patterns in cancer genomes.
Sci Rep
2020
32161175
Comprehensive Characterization of Transcriptional Activity during Influenza A Virus Infection Reveals Biases in Cap-Snatching of Host RNA Sequences.
J Virol
2020
32487174
Systematic assessment of tissue dissociation and storage biases in single-cell and single-nucleus RNA-seq workflows.
Genome Biol
2020
32641116
Human genetics and genomics meetings going virtual: practical lessons learned from two international meetings in early 2020.
Hum Genomics
2020
33024107
Predicting cell-to-cell communication networks using NATMI.
Nat Commun
2020
33072063
Molecular Insights Into Regulatory T-Cell Adaptation to Self, Environment, and Host Tissues: Plasticity or Loss of Function in Autoimmune Disease.
Front Immunol
2020
32790115
Stromal cell diversity associated with immune evasion in human triple-negative breast cancer.
EMBO J
2020
33113368
Brain-Enriched Coding and Long Non-coding RNA Genes Are Overrepresented in Recurrent Neurodevelopmental Disorder CNVs.
Cell Rep
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
31992766
CANCERSIGN: a user-friendly and robust tool for identification and classification of mutational signatures and patterns in cancer genomes.
Sci Rep
2020
33113368
Brain-Enriched Coding and Long Non-coding RNA Genes Are Overrepresented in Recurrent Neurodevelopmental Disorder CNVs.
Cell Rep
2020
33072063
Molecular Insights Into Regulatory T-Cell Adaptation to Self, Environment, and Host Tissues: Plasticity or Loss of Function in Autoimmune Disease.
Front Immunol
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
32790115
Stromal cell diversity associated with immune evasion in human triple-negative breast cancer.
EMBO J
2020
33024107
Predicting cell-to-cell communication networks using NATMI.
Nat Commun
2020
32641116
Human genetics and genomics meetings going virtual: practical lessons learned from two international meetings in early 2020.
Hum Genomics
2020
32487174
Systematic assessment of tissue dissociation and storage biases in single-cell and single-nucleus RNA-seq workflows.
Genome Biol
2020
30610612
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Mol Neurobiol
2019
30610612
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Mol Neurobiol
2019
31028376
scMatch: a single-cell gene expression profile annotation tool using reference datasets.
Bioinformatics
2019
30918256
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.
Nat Commun
2019
31467181
Expression Levels of Therapeutic Targets as Indicators of Sensitivity to Targeted Therapeutics.
Mol Cancer Ther
2019
31533632
Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis.
BMC Genomics
2019
31533632
Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis.
BMC Genomics
2019
31467181
Expression Levels of Therapeutic Targets as Indicators of Sensitivity to Targeted Therapeutics.
Mol Cancer Ther
2019
30918256
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.
Nat Commun
2019
31028376
scMatch: a single-cell gene expression profile annotation tool using reference datasets.
Bioinformatics
2019
29325522
Correction to: Relatively frequent switching of transcription start sites during cerebellar development.
BMC Genomics
2018
30407537
Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity.
Nucleic Acids Res
2018
30215711
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Hum Mol Genet
2018
30538238
Author Correction: Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system.
Sci Data
2018
30089658
Conserved temporal ordering of promoter activation implicates common mechanisms governing the immediate early response across cell types and stimuli.
Open Biol
2018
29307116
Discovery of Transcription Factors Novel to Mouse Cerebellar Granule Cell Development Through Laser-Capture Microdissection.
Cerebellum
2018
29712924
Transcriptional landscape of Mycobacterium tuberculosis infection in macrophages.
Sci Rep
2018
29325522
Correction to: Relatively frequent switching of transcription start sites during cerebellar development.
BMC Genomics
2018
1 - 50 of 294
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RIKEN Center for Integrative Medical Sciences
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Hideya Kawaji
RIKEN Center for Integrative Medical Sciences
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Co-authored papers
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28
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Co-authored papers
27
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Mater Research Institute-UQ, Translational Research Institute
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The University of Melbourne
Co-authored papers
23
Jun Kawai
RIKEN Center for Integrative Medical Sciences
Co-authored papers
22
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20
Dave S B Hoon
Saint John's Cancer Institute at Saint John's Health Center
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20
Jessica Severin
Center for Integrative Medical Sciences
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Albin Sandelin
University of Copenhagen
Co-authored papers
19
Nicolas Bertin
University Bordeaux, CNRS
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15
Mutsumi Kanamori-Katayama
Karolinska Institutet
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15
Christine A Wells
The University of Melbourne
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University of Copenhagen
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13
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