Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis

Apolipoprotein E ε-4 as a genetic determinant of Alzheimer's disease heterogeneity.

Degenerative neurological and neuromuscular disease·2020

Familial hypercholesterolaemia workshop for leveraging point-of-care testing and personalised medicine in association with the Lipid and Atherosclerosis Society of Southern Africa.

Cardiovascular journal of Africa·2019

Pharmacogenetics of Aromatase Inhibitors in Endocrine Responsive Breast Cancer: Lessons Learnt from Tamoxifen and CYP2D6 Genotyping.

Anti-cancer agents in medicinal chemistry·2017

Pathogenic Mechanisms Underlying Iron Deficiency and Iron Overload: New Insights for Clinical Application.

EJIFCC·2016

Postmenopausal Breast Cancer, Aromatase Inhibitors, and Bone Health: What the Surgeon Should Know.

World journal of surgery·2016

Apolipoprotein E genotyping and questionnaire-based assessment of lifestyle risk factors in dyslipidemic patients with a family history of Alzheimer's disease: test development for clinical application.

Metabolic brain disease·2015

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

Human genetics·2026

Central nervous system involvement of hantaviruses: clinical presentations, neuroimaging findings, and current implications.

Reviews in the neurosciences·2026

Antitumor activity of high-density lipoproteins and their use for targeted drug delivery.

Biomeditsinskaia khimiia·2026

Non-contrast CT Markers of Hematoma Expansion and Andexanet Response in Factor Xa Inhibitor-Associated Intracerebral Hemorrhage: An Analysis from ANNEXa-I Trial.

Annals of neurology·2026

Emergency Cholecystectomy for Gangrenous Acute Cholecystitis with Profound Thrombocytopenia: Immune Thrombocytopenia Diagnosed Postoperatively.

Surgical case reports·2026

Vascular adventitial cells and vascular remodeling: when a harp of thousand strings does not keep in tune so long.

Frontiers in physiology·2026

Early Reperfusion in Basilar Artery Occlusion Stroke Managed With Tenecteplase Versus Alteplase Before Endovascular Treatment.

Stroke (Hoboken, N.J.)·2026

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Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis

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Apolipoprotein E ε-4 as a genetic determinant of Alzheimer's disease heterogeneity.

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Pharmacogenetics of Aromatase Inhibitors in Endocrine Responsive Breast Cancer: Lessons Learnt from Tamoxifen and CYP2D6 Genotyping.

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Apolipoprotein E genotyping and questionnaire-based assessment of lifestyle risk factors in dyslipidemic patients with a family history of Alzheimer's disease: test development for clinical application.

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