Timothy J. Triche

University of Southern California — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

27h-index32.5kcitations115works3.12yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Epigenetics and DNA Methylation(29), Cancer Genomics and Diagnostics(24), Acute Myeloid Leukemia Research(20), RNA modifications and cancer(15), Protein Degradation and Inhibitors(15)

Publications107 total

Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity
Function·2025Open Access
IFN-α potentiates daratumumab response in multiple myeloma: A commpass study
Blood·2025Open Access
3128 – RECLASSIFICATION OF HIGH-RISK PEDIATRIC ACUTE MYELOID LEUKEMIA BASED ON MOLECULAR DRIVERS YIELDS NOVEL THERAPEUTIC STRATEGIES
Experimental Hematology·2025
Germline Variant Burden Warrants Universal Genetic Testing in Pediatric Myeloid Leukemia
2025Open Access
Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Nature Communications·2025· 4 citedOpen Access
Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglement
American Journal of Physiology-Cell Physiology·2025Open Access
BifurcatoR: A Framework for Revealing Clinically Actionable Signal in Variance Masquerading as Noise
2025Open Access
From castaways to discoveries: unveiling treasures in skin RNAseq using a novel multidimensional data processing workflow including infection-host dynamics
Physiological Genomics·2025· 1 citedOpen Access
TRIM28-dependent developmental heterogeneity determines cancer susceptibility through distinct epigenetic states
Nature Cancer·2025· 5 citedOpen Access
Referee report. For: A streamlined workflow for long-read DNA methylation analysis with NanoMethViz and Bioconductor [version 2; peer review: 2 approved]
Faculty of 1000 Research Ltd·2025Open Access
<i>bamSliceR</i> : a Bioconductor package for rapid, cross-cohort variant and allelic bias analysis
Bioinformatics Advances·2024· 1 citedOpen Access
Value-Compressed Sparse Column (VCSC): Sparse Matrix Storage for Single-cell Omics Data
2024· 1 cited
Long-read epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
2024· 1 citedOpen Access
Bone marrow microenvironment signatures associate with patient survival after guadecitabine and atezolizumab therapy in HMA-resistant MDS
2024Open Access
Multi-Cohort Meta-Analysis of Rnaseq Data to Determine Sex Bias in Pediatric Acute Myeloid Leukemia
Blood·2024
Germline Variant Burden Warrants Universal Genetic Testing in Pediatric AML
Blood·2024· 1 cited
Epigenomic Prognosis: Predicting fetal growth restriction beyond ultrasound markers
Placenta·2024Open Access
Value-Compressed Sparse Column (VCSC): Sparse Matrix Storage for Redundant Data
2024· 3 cited
BISCUIT: an efficient, standards-compliant tool suite for simultaneous genetic and epigenetic inference in bulk and single-cell studies
Nucleic Acids Research·2024· 39 citedOpen Access
Structural variants involving <i>MLLT10</i> fusion are associated with adverse outcomes in pediatric acute myeloid leukemia
Blood Advances·2024· 7 citedOpen Access
page 1 of 6Next →

Frequent Co-authors

Rhonda E. Ries(11), Todd A. Alonzo(9), E. Anders Kolb(9), Soheil Meshinchi(9), Jason E. Farrar(8), Alan S. Gamis(8), Jenny L. Smith(7), Amanda R. Leonti(7), Richard Aplenc(7), Benjamin K. Johnson(7), Xiaotu Ma(6), Lauren Harmon(5), Marco A. Marra(4), Richard A. Moore(4), Hui Shen(4), Robert B. Gerbing(4), Laura Pardo(4), Michael R. Loken(4), Timothy I. Shaw(4), Anthony Colombo(4)