Impact Factor
3.52
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
4.03
384 total citations
h5-index
26
h5 depth signal
Cited share
75.7%
78 of 103
Total citations
384
Citation footprint
Metric signal
3.94
External metric anchor
Self-citation
6.8%
26 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
233
Japan
144
Italy
87
Germany
69
France
69
Citing Fields of Research
Auto-Inflammatory Disorders
690
Cardiology
114
Neurodegenerative Disorders
70
Kidney Diseases
27
Hematology
25
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,882
Articles tracked across the journal lifetime
Indexed publication set
103
78 cited publications
Last 12 months
76
6.3 publications/month
Open access share
23.7%
18 OA publications in the last year
Leading citing country
United States
233 citing publications
Leading citing field
Auto-Inflammatory Disorders
690 citing publications
Latest tracked publication
15 October 2026
10 recent records available
Coverage & Indexing History
v5n1,Mar. 1998-
v5n1,Mar. 1998-
Active Coverage
Research Focus & Classification
Indexed Subjects
Auto-Inflammatory Disorders
Issuing & Sponsoring Bodies
Contributor
International Society of Amyloidosis
Broad Categories
Biochemistry
Auto-Inflammatory Disorders
MeSH Descriptors
Amyloid
Amyloidosis
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1080/13506129.2026.2747712
Open DOI
Full-length light chain sequencing refocuses attention on the constant domain in AL amyloidosis
02
DOI 10.1080/13506129.2026.2735580
Open DOI
Childhood onset, indolent progression, and risk of hepatic rupture: the natural history of hereditary lysozyme amyloidosis
03
04
DOI 10.1080/13506129.2026.2740737
Open DOI
Treatment of Waldenström macroglobulinemia associated with AL amyloidosis with teclistamab: a case report
AL amyloidosis is an uncommon complication of Waldenström Macroglobulinemia (WM), occurring in approximately 7.5% of WM patients [1]. AL amyloidosis patients with cardiac involvement confer a disma...
05
DOI 10.1080/13506129.2026.2738161
Open DOI
Cryo-EM reveals untwisted and non-periodic twist fibrils in ex vivo type B ATTRv-V30M fibrils
06
DOI 10.1080/13506129.2026.2729446
Open DOI
Frailty is a mortality risk factor in tafamidis-treated patients with transthyretin cardiac amyloidosis
07
DOI 10.1080/13506129.2026.2727117
Open DOI
Sodium-glucose cotransporter-2 inhibitor therapy and body composition analysis in transthyretin amyloid cardiomyopathy: a prospective, feasibility pilot study
To the EditorsSodium-glucose cotransporter-2 (SGLT2) inhibitors in transthyretin amyloid cardiomyopathy (ATTR-CM) are associated with a reduction in heart failure hospitalizations, cardiovascular a...
08
DOI 10.1080/13506129.2026.2725750
Open DOI
Liver stiffness in AL amyloidosis: interest in diagnosis and prognosis
Amyloidosis is a rare disease characterized by abnormal protein deposits, with a wide variety of clinical presentations and organ complications [1]. Several forms of amyloidosis exist, each with it...
09
DOI 10.1080/13506129.2026.2718204
Open DOI
Susceptibility and screening approaches in systemic amyloidosis: expert perspectives from the International Society of Amyloidosis (ISA)
1. Amyloidosis is a rare disease caused by the misfolding and aggregation of abnormal proteins [1–3]. At present, 42 precursor proteins have been identified that form amyloid deposits in multiple t...
10
DOI 10.1080/13506129.2026.2723933
Open DOI
Gastric amyloid pathology and mucosal denervation in ATTRv amyloidosis: insights from patients, mice, and gut microenvironment profiles
Hereditary ATTR amyloidosis with polyneuropathy (ATTRv-PN), caused by mutations in the transthyretin (TTR) gene, is a neurodegenerative disorder that affects mainly the peripheral nervous system, i...
Bibliographical & Catalog Notes
Vols. for <2001-> have subtitle: Journal of protein folding disorders.
Also issued online.