Jacques F. Banchereau - Nanotechnology

Author Information

Jacques F. Banchereau is a prominent researcher affiliated with The Jackson Laboratory for Genomic Medicine in Farmington, CT, United States. His research spans various aspects of immunology, cancer biology, and genomic medicine, contributing significantly to the understanding of immune system aging, cancer metastasis, and single-cell analysis techniques.

Research Contributions

Jacques F. Banchereau has made substantial contributions to the fields of immunology and cancer biology. His recent work includes studies on transcriptional signatures of metastatic triple-negative breast cancer, long-read isoform analysis for breast cancer, and the role of myeloid cells in melanoma metastasis. His research also covers innovative methods for detecting multiplets in single-nucleus ATAC-seq data and the activation of the AP-1 complex as a marker of immune system aging. Additionally, he has explored the implications of erythroid mitochondrial retention in triggering type I interferon responses in systemic lupus erythematosus (SLE).

Aliases

Jacques F. Banchereau is also known by several aliases, including Jacques Banchereau, J. Banchereau, J F Banchereau, and Jacques. Banchereau.

Publication and Citation Metrics

Metric	Value
H-index	147
Paper Count	731
Citation Count	104,273

Publications:

Abstract P5-01-05: Transcriptional signature of metastatic triple negative breast cancer in humanized mice

DOI: 10.1158/1538-7445.sabcs21-p5-01-05

Year: 2022

A comprehensive long-read isoform analysis platform and sequencing resource for breast cancer

DOI: 10.1126/sciadv.abg6711

Year: 2022

AP-1 complex activation is a conserved signature of immune system aging and a potential regulator of inflammaging in human and mice

DOI: 10.21203/rs.3.rs-1051151/v1

Year: 2021

AMULET: a novel read count-based method for effective multiplet detection from single nucleus ATAC-seq data

DOI: 10.1186/s13059-021-02469-x

Year: 2021

Abstract 1750: HumanKIT+myeloid cells facilitate visceral organ colonization by melanoma

DOI: 10.1158/1538-7445.AM2021-1750

Year: 2021

Human KIT+ myeloid cells facilitate visceral metastasis by melanoma

DOI: 10.1084/jem.20182163

Year: 2021

Erythroid mitochondrial retention triggers myeloid-dependent type I interferon in human SLE

DOI: 10.1016/j.cell.2021.07.021

Year: 2021

A read count-based method to detect multiplets and their cellular origins from snATAC-seq data

DOI: 10.1101/2021.01.04.425250

Year: 2021

Single Cell Analysis of Blood Mononuclear Cells Stimulated Through Either LPS or Anti-CD3 and Anti-CD28

DOI: 10.3389/fimmu.2021.636720

Year: 2021

Development of a fixed module repertoire for the analysis and interpretation of blood transcriptome data

DOI: 10.1038/s41467-021-24584-w

Year: 2021

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