Amyloid-Journal of Protein Folding Disorders

Papers
(The TQCC of Amyloid-Journal of Protein Folding Disorders is 7. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-01-01 to 2026-01-01.)
ArticleCitations
Changes in the amyloid editorial board members and in editor positions287
A case of asymmetric insulin-derived localised amyloid deposition associated with long-acting insulin analog administration275
A second case of liraglutide-type localised amyloidosis107
Re-evaluation of Mayo 2004 and revised Mayo 2012 staging in patients with AL amyloidosis in the era of new therapies90
Impact of autonomic dysfunction in light chain amyloidosis patient with nephrotic syndrome and cardiac involvement76
Factors associated with financial toxicity in patients with transthyretin amyloidosis: results from Amyloidosis Research Consortium’s treatment affordability patient and caregiver survey36
Neurofilament light chain as a biomarker for hereditary ATTR amyloidosis − correlation between neurofilament light chain and nerve conduction study33
Comparison between tafamidis and liver transplantation as first-line therapy for hereditary transthyretin amyloidosis26
Commentary to revisiting the genetic epidemiology of ATTRv in Spain: the Balearic Islands as a high-prevalence founder focus25
Reduction of cardiac AL amyloid deposition after complete response visualised by PiB-PET imaging23
Real-world treatment patterns, costs, and outcomes in patients with AL amyloidosis: analysis of the Optum EHR and commercial claims databases23
A novel transthyretin variant p.Val114Glu (Val94Glu) in an Italian patient with mixed phenotype hereditary transthyretin amyloidosis22
Early cardiovascular autonomic failure in ATTRv predicts poor prognosis and may respond to disease-modifying therapy21
Characterising diflunisal as a transthyretin kinetic stabilizer at relevant concentrations in human plasma using subunit exchange19
Role of complementarity-determining regions 1 and 3 in pathologic amyloid formation by human immunoglobulin κ1 light chains19
Abnormal global longitudinal strain and reduced serum inflammatory markers in cardiac AL amyloidosis patients without significant amyloid fibril deposition18
Clinical impact of beta-blocker withdrawal in transthyretin amyloid cardiomyopathy18
Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study17
Human lysozyme inhibits the fibrillation of serum amyloid a protein from systemic AA amyloidosis15
Revisiting the genetic epidemiology of ATTRv in Spain: the Balearic Islands as a high-prevalence founder focus14
Patients with transthyretin amyloidosis enrolled in THAOS between 2018 and 2021 continue to experience substantial diagnostic delay14
Alterations in multi-layer strain in AL amyloidosis13
Hepatic involvement in light chain amyloidosis: analysis of 130 patients and predictors of hepatic response and survival13
Clinical profile and outcome of AA amyloidosis associated kidney disease in India13
Serum neurofilament light chain in hereditary transthyretin amyloidosis: validation in real-life practice12
Selective recognition of human small transthyretin aggregates by a novel monoclonal antibody12
Identification of epidermal growth factor-containing fibulin-like extracellular matrix protein 1-derived amyloid deposition in a rhesus macaque12
Natural course and determinants of short-term kidney function decline in hereditary transthyretin amyloidosis: a French observational study12
Mapping cellular response to destabilized transthyretin reveals cell- and amyloidogenic protein-specific signatures11
A natural history analysis of asymptomatic TTR gene carriers as they develop symptomatic transthyretin amyloidosis in the Transthyretin Amyloidosis Outcomes Survey (THAOS)11
Prevalence and prognostic role of nonsustained ventricular tachycardia in cardiac amyloidosis11
Whole tissue proteomic analyses of cardiac ATTR and AL unveil mechanisms of tissue damage11
Left atrioventricular coupling index assessed with three-dimensional echocardiography: a prognostic marker of short-term outcomes in light-chain cardiac amyloidosis11
Frontline Dara-CyBorD for AL amyloidosis: high response rates and cytogenetic insights from a real-world cohort11
Brain MRI in patients with V30M hereditary transthyretin amyloidosis11
Clinical and molecular insights into A97S variants in hereditary transthyretin amyloid polyneuropathy in South China11
Same same, but different? The neurological presentation of wildtype transthyretin (ATTRwt) amyloidosis11
Involvement of bile acid in diarrhoea and therapeutic effect of colestimide in hereditary ATTR amyloidosis10
Amyloid nomenclature 2024: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee10
A rare occurrence and near miss! Should a TTR gene test be routinely performed for suspected ATTR-cardiomyopathy?10
Refining prognostication in systemic AL amyloidosis: limited value of dFLC10
ALyzer3D.AI: a more generalizable deep learning predictor of light chain amyloidogenicity powered by structural and evolutionary Artificial Intelligence10
Correction9
Monitoring of cardiac transthyretin amyloid load by [99mTc]DPD scintigraphy: is it the end of the semi-quantitative evaluation?9
Predictors of cognitive dysfunction in hereditary transthyretin amyloidosis with liver transplant9
Change of guard at Amyloid – a tribute to outgoing Editor in Chief, Professor Per Westermark9
Possible transmission of leukocyte chemotactic factor 2 amyloidosis after interpopulational liver transplantation9
Cold pressor test and paradoxical blood pressure reduction in light chain amyloidosis9
AA amyloidosis as an adverse event of immune checkpoint inhibitor therapy: evidence from the FDA adverse event reporting system and a systematic review9
Complete remission after patisiran treatment in a patient with nephrotic syndrome secondary to hereditary transthyretin amyloidosis (ATTR)8
Prognostic impact of cardiac resynchronization therapy in wild-type transthyretin amyloid cardiomyopathy8
Treatment response and neurofilament light chain levels with long-term patisiran in hereditary transthyretin-mediated amyloidosis with polyneuropathy: 24-month results of an open-label extension study8
Longitudinal analysis of serum neurofilament light chain levels as marker for neuronal damage in hereditary transthyretin amyloidosis8
Epidemiology of hereditary transthyretin amyloidosis in the northernmost region of Sweden: a retrospective cohort study8
Bone marrow amyloid: a comprehensive analysis of 1,469 samples, including amyloid type, clinical features, and morphologic distribution8
Enhanced analytic methodology enables postmortem diagnosis of hereditary AApoAI amyloidosis8
Altered connectivity of central autonomic network: effects of dysautonomia in hereditary transthyretin amyloidosis with polyneuropathy7
Neuropathy progression in hereditary transthyretin amyloidosis (ATTRv) patients after liver transplantation7
Incidence and predictors of sudden death in patients with cardiac amyloidosis7
Heterogeneity in families with ATTRV30M amyloidosis: a historical and longitudinal Portuguese case study impact for genetic counselling7
Subtyping of cardiac amyloidosis by mass spectrometry-based proteomics of endomyocardial biopsies7
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