Journal profile

Biochemical Society transactions

Publisher: Portland Press On The Behalf Of The Biochemical Society
ISSN0300-5127 | 1470-8752 FormatPrint StatusCurrently indexed

Journal Citation Impact

Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.

Impact Factor
4.31
Citation rate 6.54 2,333 total citations
h5-index 53 h5 depth signal
Cited share 90.3% 346 of 383
Total citations 2,333 Citation footprint
Metric signal 6.43 External metric anchor
Self-citation 0.3% 8 self-citations

Citations Trend

Monthly Publications Cadence

Citing Geographic Demographics

United Kingdom 584
United States 496
Australia 168
Germany 130
China 80

Citing Fields of Research

Cell Biology 610
Genetics & Genomics 365
Cellular Membrane Transporters & Receptors 189
Cancer, Autophagy & Apoptosis 181
Immunology 157

Publishing Activity & Reach

Volume, recency, access pattern, and citing-community signals from the journal analytics record.

All-time article footprint 30,735 Articles tracked across the journal lifetime
Indexed publication set 383 346 cited publications
Last 12 months 126 10.5 publications/month
Open access share 99.2% 125 OA publications in the last year
Leading citing country United Kingdom 584 citing publications
Leading citing field Cell Biology 610 citing publications
Latest tracked publication 13 October 2026 10 recent records available

Coverage & Indexing History

MEDLINE
v1n4, Jul. 1973-
PubMed
v1n4, Jul. 1973-
Index medicus
Active Coverage

Research Focus & Classification

Indexed Subjects

Cell Biology Genetics & Genomics Bacteriology Cancer, Autophagy & Apoptosis Immunology DNA Damage

Issuing & Sponsoring Bodies

Contributor
Biochemical Society (Great Britain)

Broad Categories

Biochemistry Cell Biology Genetics & Genomics DNA Damage Cancer, Autophagy & Apoptosis Mitochondria Cancer & Development Neurodegenerative Disorders

MeSH Descriptors

Biochemistry

Latest Publications

Recent article records with DOI-first linking and condensed abstracts.

01
Sanjna Singh, Timothy J. Sargeant
Autophagy is the cell’s recycling system; it removes unwanted or dysfunctional cellular material, thereby preventing damage. Importantly, it is a key pro-survival pathway during periods of stress, for instance, during nutrient scarcity. ...
02
Thu Uyen Tran, Quan Thinh Le, Tuong-Khanh My Tu et al.
Plasma membrane rupture (PMR) is a terminal event in many forms of lytic cell death, yet was long regarded as a passive consequence of osmotic swelling and mechanical membrane failure. The identification of ninjurin-1 (NINJ1) as a key me...
03
Jiamin Guo, Qinyu Han, Kyogo Nagashima et al.
A substantial portion of the proteome consists of intrinsically disordered regions (IDRs) that do not fold into well-defined structures. IDRs often comprise low-complexity domains (LCDs), whose repetitive, compositionally biased sequence...
04
Grant Steiner, Chloe Wilke, Colin Gates
Photosystem II is a highly conserved protein complex found across all oxygenic phototrophs and the source of almost all biologically available electrons and atmospheric oxygen. This large, membrane-bound complex is at continuous risk of ...
05
Ester Díaz-Mora, Ana Risco, Ana Cuenda
The p38γ and p38δ mitogen-activated protein kinases (MAPKs) are members of the p38 family that have emerged as important regulators of inflammatory signaling. Initially considered minor or alternative isoforms, accumulating evidence has ...
06
Julia S. Scott, Catrin Lutz, Stefan Prekovic
Cellular plasticity is a central feature of malignant progression, allowing tumour cells to change identity during tumour evolution, therapeutic adaptation, and metastatic dissemination. This issue is especially acute in lung cancer, whe...
07
Madison Bandini, Nathan M. Sherer
Many viruses manipulate the host cell cycle to enhance viral replication and promote their evasion of host immune defenses. Human immunodeficiency virus type 1 (HIV-1) is no exception and triggers cell cycle arrest during its infection o...
10
Prasanna Suresh, Yu P. Zhang, Clare Bryant et al.
Innate immune signalling is uniquely driven through the formation of supramolecular organising centres (SMOCs), which couple receptor activation with downstream effector recruitment. The adaptor protein TRIF coordinates interferon, infla...

Bibliographical & Catalog Notes

Also issued online.

Vol. 11, no. 1 (1983)19920824 Notice not published Printed on acid-free paper