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Nicholas J. Haradhvala

Center for Cancer Research · US
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Area of research
Cancer Research · Oncology
Research interest
Research interests include Cancer Genomics and Diagnostics, CAR-T cell therapy research, Multiple Myeloma Research and Treatments, and Monoclonal and Polyclonal Antibodies Research.
h-index
45
citations
18,881
works
173
NIH funding
primary concept
Biology
email

Recent publications

SWIFT-seq enables comprehensive single-cell transcriptomic profiling of circulating tumor cells in multiple myeloma and its precursors
Nature Cancer 2025cited by 6position: middledoi
On-target off-tumor toxicity of claudin18.2-directed CAR-T cells in preclinical models
Nature Communications 2025cited by 6position: middledoi
Comparative analysis of Bcl-2 family protein overexpression in CAR T cells alone and in combination with BH3 mimetics
Science Translational Medicine 2024cited by 25position: middledoi
Pan-cancer analysis of post-translational modifications reveals shared patterns of protein regulation
Cell 2023cited by 179position: middledoi
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Nature 2023cited by 12position: middledoi
Author Correction: The repertoire of mutational signatures in human cancer
Nature 2023cited by 9position: middledoi
CAR T cell killing requires the IFNγR pathway in solid but not liquid tumours
Nature 2022cited by 345position: middledoi
Distinct cellular dynamics associated with response to CAR-T therapy for refractory B cell lymphoma
Nature Medicine 2022cited by 250position: firstdoi
Designing sensitive viral diagnostics with machine learning
Nature Biotechnology 2022cited by 106position: middledoi
Single cell characterization of myeloma and its precursor conditions reveals transcriptional signatures of early tumorigenesis
Nature Communications 2022cited by 66position: middledoi
Immune biomarkers of response to immunotherapy in patients with high-risk smoldering myeloma
Cancer Cell 2022cited by 61position: middledoi
Author Correction: Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
Communications Biology 2022cited by 3position: middledoi
Author Correction: Pathway and network analysis of more than 2500 whole cancer genomes
Nature Communications 2022cited by 1position: middledoi
Author Correction: Integrative pathway enrichment analysis of multivariate omics data
Nature Communications 2022cited by 0position: middledoi
The repertoire of mutational signatures in human cancer
Nature 2020cited by 3,686position: middledoi
Single-cell RNA sequencing reveals compromised immune microenvironment in precursor stages of multiple myeloma
Nature Cancer 2020cited by 352position: middledoi
Integrative pathway enrichment analysis of multivariate omics data
Nature Communications 2020cited by 234position: middledoi
Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
Communications Biology 2020cited by 189position: middledoi
Pathway and network analysis of more than 2500 whole cancer genomes
Nature Communications 2020cited by 114position: middledoi
DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells
Cancer Discovery 2020cited by 84position: middledoi
Combined burden and functional impact tests for cancer driver discovery using DriverPower
Nature Communications 2020cited by 63position: middledoi
A post-transcriptional program of chemoresistance by AU-rich elements and TTP in quiescent leukemic cells
Genome biology 2020cited by 31position: middledoi
Designing viral diagnostics with model-based optimization
bioRxiv (Cold Spring Harbor Laboratory) 2020cited by 1position: middledoi
RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues
Science 2019cited by 513position: middledoi
Scaling computational genomics to millions of individuals with GPUs
Genome biology 2019cited by 303position: middledoi
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing
Cell 2018cited by 378position: middledoi
Quantification of somatic mutation flow across individual cell division events by lineage sequencing
Genome Research 2018cited by 31position: middledoi
Analysis of somatic microsatellite indels identifies driver events in human tumors
Nature Biotechnology 2017cited by 138position: middledoi
Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes
bioRxiv (Cold Spring Harbor Laboratory) 2017cited by 47position: middledoi
Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair
Cell 2016cited by 441position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Gad Getz · Broad Institute9 papers (2015–2025)Jaegil Kim · GlaxoSmithKline (United States)5 papers (2015–2019)Paz Polak · ID Genomics (United States)4 papers (2015–2019)Amnon Koren · Roswell Park Comprehensive Cancer Center3 papers (2016–2018)Michael S. Lawrence · Harvard University3 papers (2015–2017)Amanda A. Bouffard · Center for Cancer Research3 papers (2022–2025)François Aguet · Biopredic (France)3 papers (2019–2022)Yosef E. Maruvka · Technion – Israel Institute of Technology3 papers (2016–2018)Mark B. Leick · Harvard University3 papers (2022–2025)Paul C. Blainey · Broad Institute3 papers (2018–2022)Marcela V. Maus · Harvard University3 papers (2022–2025)Trisha R. Berger · Center for Cancer Research3 papers (2022–2025)Julian M. Hess · Broad Institute3 papers (2016–2019)Priya P. Pillai · Massachusetts Institute of Technology2 papers (2020–2022)Kent W. Mouw · Harvard University2 papers (2017–2018)Cheri M. Ackerman · Broad Institute2 papers (2020–2022)Stefanie R. Bailey · University of Virginia2 papers (2022–2024)Esther Rheinbay · Harvard University2 papers (2016–2017)David Yang · The University of Texas at Austin2 papers (2020–2022)Juliane Weller · Broad Institute2 papers (2020–2022)
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