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Author Details

Hsin-Ta Wu
2006
23
15
PMIDPaper TitleJournal TitlePublished Year
37601688Molecular residual disease detection in resected, muscle-invasive urothelial cancer with a tissue-based comprehensive genomic profiling-informed personalized monitoring assay.2023
36253484A phase II study of talazoparib monotherapy in patients with wild-type BRCA1 and BRCA2 with a mutation in other homologous recombination genes.Nat Cancer2022
36232827Comprehensive Genomic Profiling (CGP)-Informed Personalized Molecular Residual Disease (MRD) Detection: An Exploratory Analysis from the PREDATOR Study of Metastatic Colorectal Cancer (mCRC) Patients Undergoing Surgical Resection.International Journal of Molecular Sciences2022
36170624Circulating Tumor DNA After Neoadjuvant Chemotherapy in Breast Cancer Is Associated With Disease Relapse.JCO Precision Oncology2022
36117009Circulating tumor DNA monitoring for early recurrence detection in epithelial ovarian cancer.Gynecol Oncol2022
30992300Personalized Detection of Circulating Tumor DNA Antedates Breast Cancer Metastatic Recurrence.Clin Cancer Res2019
31070691Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer.JAMA Oncology2019
31059311Early Detection of Metastatic Relapse and Monitoring of Therapeutic Efficacy by Ultra-Deep Sequencing of Plasma Cell-Free DNA in Patients With Urothelial Bladder Carcinoma.Journal of Clinical Oncology2019
29112732Identifying structural variants using linked-read sequencing data.Bioinformatics2018
28241635Optimization of PAM-4 transmitters based on lumped silicon photonic MZMs for high-speed short-reach optical links.Optics Express2017
27505681Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma.Cancer Cell2016
27165744Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma.Cancer Cell2016
27485716Erratum to: CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer.Genome Biol2016
26813760Reply: Co-occurrence of MYC amplification and TP53 mutations in human cancer.Nat Genet2016
26020500MAGI: visualization and collaborative annotation of genomic aberrations.Nat Methods2015
25501392Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes.Nat Genet2015
26253137CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer.Genome Biol2015
24732363Expression profiling of primary and metastatic ovarian tumors reveals differences indicative of aggressive disease.PLoS One2014
24931984Detecting independent and recurrent copy number aberrations using interval graphs.Bioinformatics2014
23554878Identification of ovarian cancer metastatic miRNAs.PLoS One2013
23634996Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.N Engl J Med2013
22452995An integrative probabilistic model for identification of structural variation in sequencing data.Genome Biol2012
16644790An online literature mining tool for protein phosphorylation.Bioinformatics2006
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Princeton University
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University of Padova
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Present address: Dxige Research Inc.
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Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill
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Broad Institute
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Baylor College of Medicine
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Stanford University
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Dana-Farber Cancer Institute
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Stanford University School of Medicine
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McDonnell Genome Institute, Washington University in St. Louis
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Allen Institute for Cell Science
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Johns Hopkins University School of Medicine
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McDonnell Genome Institute, Washington University School of Medicine
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University of California Santa Cruz Genomics Institute
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University of British Columbia
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Bloomberg-Kimmel Immunotherapy Institute, Johns Hopkins University School of Medicine
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University of Michigan ann arbor
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Broad Institute of the Massachusetts Institute of Technology and Harvard
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Yale School of Medicine
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University of Michigan ann arbor
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Harvard Medical School
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University of Lausanne (UNIL)
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Stony Brook University, and Stony Brook Cancer Center
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Washington University School of Medicine.
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