Clinical Biochemistry

Papers
(The H4-Index of Clinical Biochemistry is 17. 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
Reply to Letter to the Editor “The importance of SII and FIB-4 scores in predicting mortality in idiopathic pulmonary fibrosis patients”96
Measuring copeptin, a surrogate for vasopressin in patients with hypertension – Can it identify those who are volume Responsive?83
The significance of PCSK-9′s level and polymorphism in premature coronary artery disease: Relation to risk and severity36
Editorial Board32
Serum levels of sonic hedgehog in patients with IgA nephropathy are closely associated with intrarenal arteriolar lesions30
Hydroxocobalamin does not interfere with high-sensitivity cardiac troponin T assay28
Comparison of two (data mining) indirect approaches for between-subject biological variation determination28
The biological diagnosis of Alzheimer’s disease using blood-based biomarkers: a Canadian prospective28
The pitfalls and significance of using ratios and calculated parameters in laboratory medicine26
Comparison of laboratory results and pain perception in self-sampled capillary blood versus venous blood sampling: a systematic review and meta-analysis25
Relationship between analytical imprecision and coefficient of determination (R2) of the calibration curve25
A circRNA-based ceRNA network shows its diagnostic value in non-small-cell lung cancer24
Association of phospholipid transfer protein (PLTP) and the effect of genetic variant rs5072 on hypertriglyceridemia and atherogenic dyslipidemia in children and adolescents from Southeastern Mexico23
Reducing AST orders by reviewing test panels21
Editorial Board20
Association of the C-terminal 42-peptide fragment of alpha-1 antitrypsin with the severity of ARDS: A pilot study20
Editorial Board19
Whole-exome sequencing reveals a novel frameshift mutation in a consanguineous family with a hereditary coagulation factor XII deficiency17
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