Impact Factor
4.64
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
56.21
13,282 total citations
h5-index
148
h5 depth signal
Cited share
69.9%
174 of 249
Total citations
13,282
Citation footprint
Metric signal
55.48
External metric anchor
Self-citation
0.3%
36 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
459
United Kingdom
135
Germany
124
China
67
France
55
Citing Fields of Research
Cell Biology
450
Genetics & Genomics
335
Noncoding RNA
180
DNA Damage
148
Cancer, Autophagy & Apoptosis
142
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
5,041
Articles tracked across the journal lifetime
Indexed publication set
249
174 cited publications
Last 12 months
127
10.6 publications/month
Open access share
2.4%
3 OA publications in the last year
Leading citing country
United States
459 citing publications
Leading citing field
Cell Biology
450 citing publications
Latest tracked publication
14 October 2026
10 recent records available
Coverage & Indexing History
v1n1, Oct. 2000-
v1n1, Oct. 2000-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cell Biology
Genetics & Genomics
Noncoding RNA
Stem Cell Biology
Nucleic Acids Chemistry
Cancer, Autophagy & Apoptosis
Broad Categories
Molecular Biology
Genetics & Genomics
Cell Biology
Nucleic Acids Chemistry
DNA Damage
Cancer, Autophagy & Apoptosis
Cancer & Development
MeSH Descriptors
Cells
Molecular Biology
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1038/s41580-026-01040-5
Open DOI
Revealing the invisible transcriptome
02
DOI 10.1038/s41580-026-01030-7
Open DOI
Atomic, structural and molecular insights into GPCR ligand binding and signalling
G-protein-coupled receptors (GPCRs) are the largest group of human membrane proteins, comprising over 800 members, and represent the most common target of therapeutics. GPCRs orchestrate context-dependent functions and have diverse physi...
03
DOI 10.1038/s41580-026-01043-2
Open DOI
Ubiquitin phosphorylation opens a hatch to a code still largely undeciphered
04
DOI 10.1038/s41580-026-01044-1
Open DOI
Scaling up measurements of the interactions that build condensates
05
DOI 10.1038/s41580-026-01021-8
Open DOI
Towards a systematic understanding of the diverse subtypes, biogenesis and functions of large extracellular vesicles
Large extracellular vesicles (lEVs) are heterogeneous structures with sizes that exceed 200 nm. Unlike small extracellular vesicles, which originate from either the endosomal system or the plasma membrane, most lEVs stem directly from th...
06
DOI 10.1038/s41580-026-01036-1
Open DOI
Engineering synthetic proteins to toggle function in response to kinase signals
07
DOI 10.1038/s41580-026-01023-6
Open DOI
Chaperone-mediated autophagy in physiological homeostasis, disease and ageing
Chaperone-mediated autophagy (CMA), the first-described selective lysosomal degradation pathway, is distinguished from other degradative pathways by the unique mechanism by which substrates reach the lysosomal lumen: CMA relies on a cyto...
08
DOI 10.1038/s41580-026-01032-5
Open DOI
Neutrality as the null hypothesis of biological evolution
09
DOI 10.1038/s41580-026-01033-4
Open DOI
HoT self-blinking probes for chromatin imaging
10
DOI 10.1038/s41580-026-01034-3
Open DOI
Technological prominence alone does not justify leadership in SynCell governance
Bibliographical & Catalog Notes
Also available online to subscribers.
v. 1, no. 1 (Oct. 2000)20010321 Notice published Printed on acid-free paper