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Author Details
Full Name
Timo Lassmann
Affiliation
Telethon Kids Institute, University of Western Australia
ORCID
Career Start Year
2002
Papers
112
H Index
47
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36637208
SAMStat 2: quality control for next generation sequencing data.
Bioinformatics
2023
36637208
SAMStat 2: quality control for next generation sequencing data.
Bioinformatics
2023
35139903
CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency.
Stem Cell Res Ther
2022
35986006
Temporally restricted activation of IFNβ signaling underlies response to immune checkpoint therapy in mice.
Nat Commun
2022
36577370
CD4<sup>+</sup> T cells drive an inflammatory, TNF-α/IFN-rich tumor microenvironment responsive to chemotherapy.
Cell Rep
2022
35224813
An expanded phenotype centric benchmark of variant prioritisation tools.
Hum Mutat
2022
35139903
CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency.
Stem Cell Res Ther
2022
35176430
Functional validation of variants of unknown significance using CRISPR gene editing and transcriptomics: A Kleefstra syndrome case study.
Gene
2022
36577370
CD4<sup>+</sup> T cells drive an inflammatory, TNF-α/IFN-rich tumor microenvironment responsive to chemotherapy.
Cell Rep
2022
35986006
Temporally restricted activation of IFNβ signaling underlies response to immune checkpoint therapy in mice.
Nat Commun
2022
35224813
An expanded phenotype centric benchmark of variant prioritisation tools.
Hum Mutat
2022
35176430
Functional validation of variants of unknown significance using CRISPR gene editing and transcriptomics: A Kleefstra syndrome case study.
Gene
2022
32614431
Zika Virus Changes Methylation of Genes Involved in Immune Response and Neural Development in Brazilian Babies Born With Congenital Microcephaly.
J Infect Dis
2021
33693626
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clin Infect Dis
2021
32614431
Zika Virus Changes Methylation of Genes Involved in Immune Response and Neural Development in Brazilian Babies Born With Congenital Microcephaly.
J Infect Dis
2021
34526345
Searching for a technology-driven acute rheumatic fever test: the START study protocol.
BMJ Open
2021
33693626
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clin Infect Dis
2021
34526345
Searching for a technology-driven acute rheumatic fever test: the START study protocol.
BMJ Open
2021
32487174
Systematic assessment of tissue dissociation and storage biases in single-cell and single-nucleus RNA-seq workflows.
Genome Biol
2020
32350262
Reference exome data for Australian Aboriginal populations to support health-based research.
Sci Data
2020
32487174
Systematic assessment of tissue dissociation and storage biases in single-cell and single-nucleus RNA-seq workflows.
Genome Biol
2020
33154494
The bone marrow microenvironment of pre-B acute lymphoblastic leukemia at single-cell resolution.
Sci Rep
2020
32765492
Rhinovirus Infection Drives Complex Host Airway Molecular Responses in Children With Cystic Fibrosis.
Front Immunol
2020
33303739
A flexible computational pipeline for research analyses of unsolved clinical exome cases.
NPJ Genom Med
2020
33087711
Reference exome data for a Northern Brazilian population.
Sci Data
2020
33163002
Characteristics of TCR Repertoire Associated With Successful Immune Checkpoint Therapy Responses.
Front Immunol
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
33087711
Reference exome data for a Northern Brazilian population.
Sci Data
2020
33163002
Characteristics of TCR Repertoire Associated With Successful Immune Checkpoint Therapy Responses.
Front Immunol
2020
33303739
A flexible computational pipeline for research analyses of unsolved clinical exome cases.
NPJ Genom Med
2020
33154494
The bone marrow microenvironment of pre-B acute lymphoblastic leukemia at single-cell resolution.
Sci Rep
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
32718981
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
2020
32765492
Rhinovirus Infection Drives Complex Host Airway Molecular Responses in Children With Cystic Fibrosis.
Front Immunol
2020
32350262
Reference exome data for Australian Aboriginal populations to support health-based research.
Sci Data
2020
30610612
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Mol Neurobiol
2019
31665271
Kalign 3: multiple sequence alignment of large data sets.
Bioinformatics
2019
31754101
Personalised analytics for rare disease diagnostics.
Nat Commun
2019
30610612
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Mol Neurobiol
2019
31467181
Expression Levels of Therapeutic Targets as Indicators of Sensitivity to Targeted Therapeutics.
Mol Cancer Ther
2019
30664627
C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution.
Nat Commun
2019
31533632
Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis.
BMC Genomics
2019
31754101
Personalised analytics for rare disease diagnostics.
Nat Commun
2019
31665271
Kalign 3: multiple sequence alignment of large data sets.
Bioinformatics
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
30664627
C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution.
Nat Commun
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
1 - 50 of 224
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