Impact Factor
4.98
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
13.55
22,603 total citations
h5-index
143
h5 depth signal
Cited share
93.1%
1,663 of 1,786
Total citations
22,603
Citation footprint
Metric signal
13.14
External metric anchor
Self-citation
1.4%
322 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
6,748
United States
1,676
Italy
654
Germany
586
United Kingdom
386
Citing Fields of Research
Cancer, Autophagy & Apoptosis
3,471
Cancer & Development
2,289
Immunology
1,667
Noncoding RNA
1,662
Cell Biology
1,209
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
12,384
Articles tracked across the journal lifetime
Indexed publication set
1,786
1,663 cited publications
Last 12 months
1,298
108.2 publications/month
Open access share
100.0%
1,298 OA publications in the last year
Leading citing country
China
6,748 citing publications
Leading citing field
Cancer, Autophagy & Apoptosis
3,471 citing publications
Latest tracked publication
18 October 2026
10 recent records available
Coverage & Indexing History
v1n1, Jan. 2010-
v1n1, Jan. 2010-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cancer, Autophagy & Apoptosis
Immunology
Cancer & Development
Noncoding RNA
Cell Biology
Oncology
Broad Categories
Cell Biology
Internal Medicine
Cancer, Autophagy & Apoptosis
Cancer & Development
Immunology
Noncoding RNA
Mitochondria
MeSH Descriptors
Cell Death
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1038/s41419-026-09365-x
Open DOI
TRIM2 negatively regulates antiviral immunity by degradation of MDA5 and STAT2 during influenza A virus infection
This study identifies TRIM2 as an interferon-stimulated gene (ISG) regulated by both type I and type II interferons. Contrary to the typical antiviral role of most ISGs, TRIM2 significantly enhances influenza A virus (IAV) replication bo...
02
DOI 10.1038/s41419-026-09344-2
Open DOI
SIL1 modulates Reelin signaling during cortical neuron migration
SIL1 , a nucleotide exchange factor for the endoplasmic reticulum chaperone BiP, primarily binds nascent polypeptides to facilitate proper protein folding. It is a causative gene of Marinesco-Sjögren syndrome (MSS). Previous studies have...
03
DOI 10.1038/s41419-026-09303-x
Open DOI
The long non-coding RNA FOXD2-AS1 promotes oral squamous cell carcinoma metastasis by recruiting the ADAR1-HuR complex to stabilize MYC mRNA
Metastasis remains a primary driver of poor outcomes in oral squamous cell carcinoma (OSCC), yet the underlying molecular mechanisms are incompletely understood. Here, we identify the long non-coding RNA FOXD2-AS1 as a critical regulator...
04
DOI 10.1038/s41419-026-09332-6
Open DOI
Intracellular C3 modulates senolytic responsiveness in senescent cells and aged tissues via AKT/S6K pro-survival signaling
Pathological accumulation of senescent cells (SnCs) across tissues drives aging and age-related diseases. Senolytic agents targeting senescent cell anti-apoptotic pathways (SCAPs) hold promise for treating age-related diseases, yet their...
05
DOI 10.1038/s41419-026-09345-1
Open DOI
Human iPSC-derived liver organoid model multicellular tissue responses and therapeutic rescue in Wolman disease
Wolman disease (WD), the severe infantile form of lysosomal acid lipase (LAL) deficiency, is a rare metabolic disorder caused by inactivating mutations in the LIPA gene. Although WD is characterized by profound hepatic dysfunction, exper...
06
DOI 10.1038/s41419-026-09294-9
Open DOI
Systems serology identifies differential pan-viral seroreactivity profiles associated with healthy aging and cancer
A viral exposure signature (VES) has previously been shown to predict the development of hepatocellular carcinoma (HCC) in at-risk individuals through comprehensive serological profiling using the VirScan platform. Whether cumulative ant...
07
DOI 10.1038/s41419-026-09346-0
Open DOI
Spatial multi-omics reveals that CXCL10 enhances the response to nICT in surgically resectable esophageal squamous cell carcinoma
Neoadjuvant immune-chemotherapy (nICT) has transformed the treatment strategy for esophageal squamous cell carcinoma (ESCC), yet the molecular mechanisms underlying treatment response remain incompletely understood. To investigate these ...
08
DOI 10.1038/s41419-026-09342-4
Open DOI
TMEM59 modulates TREM2-regulated microglial responses in ischemia and serves as a potential therapeutic target
Microglial responses mediated by the triggering receptor expressed on myeloid cells 2 (TREM2) play a crucial role in ischemia, but the underlying mechanism remains unclear. Herein, we found that TREM2 and its interacting protein, transme...
09
DOI 10.1038/s41419-026-09228-5
Open DOI
BRCAness in FLT3-ITD AML confers vulnerability to PARP inhibition
BReast CAncer ( BRCA1 and BRCA2 ) is a tumor suppressor gene that plays an important role in the repair of double strand DNA break (DSB) via error-free homologous recombination (HR). BRCA1 and BRCA2 mutations induce vulnerability to PARP...
10
DOI 10.1038/s41419-026-09324-6
Open DOI
ADA2high tumor cell-derived inosine induces an immunosuppressive microenvironment in gastric cancer by promoting macrophage M2 polarization
Metabolic alterations within the tumor microenvironment (TME) can reshape the polarization state of tumor-associated macrophages (TAMs) and weaken antitumor immunity, yet the underlying mechanisms remain unclear. In this study, we integr...
Bibliographical & Catalog Notes
Description based on: Vol. 1 (Jan. 2010); title from HTML header (publisher's Web site, viewed Feb. 4, 2010).
Latest issue consulted: Vol. 1 (Feb. 2010) (viewed Feb. 4, 2010).
Mode of access: World Wide Web.
Affiliated with: Cell death discovery 2058-7716 (DLC) 2015243428 (OCoLC)926100762 (DNLM)101665035.