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DrArash Dehkordi

Healthcare Innovation Lead

A physician-scientist working across three disciplines that rarely meet in one person: medicine, pure mathematics and machine learning. Dr Dehkordi's research runs from the genetics of hypertrophic cardiomyopathy to RNA therapeutics for liver and pancreatic disease.

Dr Arash Dehkordi
Role at Apterna
Healthcare Innovation Lead
Imperial College London
Visiting Researcher, Department of Surgery & Cancer
University of Dundee
Honorary Fellow (Research), Faculty of Health
Qualifications
MD · Pure mathematics, University of Bath

01AN UNUSUAL COMBINATION

Three disciplines, one method.

Dr Dehkordi describes himself as a doctor of medicine, a pure mathematician and a computer scientist. The three are not separate interests but a single working method: clinical questions framed with mathematical precision and answered with computational tools.

His mathematics began at the University of Bath, in category theory and group theory — among the most abstract branches of the subject, concerned with the structure of relationships rather than with particular objects. He then read medicine, graduating from medical school in 2025, and was awarded his MD on 7 July that year.

That combination shapes what he works on. Where a clinician sees a patient cohort and a statistician sees a dataset, the questions he pursues tend to sit between the two: what does a genotype actually predict, and with what certainty.

02CARDIOVASCULAR RESEARCH

What a genotype does and does not tell you.

At the University of Dundee he is an Honorary Fellow (Research) in Neuroscience within the Faculty of Health, based at Ninewells Hospital and Medical School and working in the cardiovascular group in Molecular and Clinical Medicine alongside Dr Anna-Maria Choy and Professor Chim C. Lang.

His primary focus is hypertrophic cardiomyopathy and inherited cardiac conditions: genotype–phenotype correlation, phenotype conversion in family screening, and how disease progresses over time. These are questions about uncertainty as much as biology — a genotype-positive relative who has not yet developed the phenotype presents a problem of prediction, not diagnosis.

The work draws on the Tayside Inherited Cardiac Condition clinic cohort, and the methods are explicitly statistical: survival and mixed-effects modelling, Bayesian hierarchical methods, causal inference and machine learning applied to clinical cardiology data, alongside systematic reviews and meta-analyses conducted to PRISMA standards.

  • Hypertrophic cardiomyopathyGenotype–phenotype correlation
  • Family screeningPhenotype conversion in relatives
  • Heart failureCardio-hepatic axis

03RNA THERAPEUTICS

From the heart to the liver.

At Imperial College London he is a Visiting Researcher in the Department of Surgery & Cancer, working with Professor Nagy Habib on translational approaches to pancreatic and liver disease. His Imperial research keywords are gene and molecular therapy, artificial intelligence, bioinformatics and computational biology, and biomolecular modelling and design.

The work centres on pancreatic ductal adenocarcinoma, liver cancer and liver failure: gene therapy, RNA-based therapeutics, targeted delivery and precision medicine. He is also a co-author on work published in Molecular Therapy — Nucleic Acids on a GalNAc-conjugated siRNA targeting C/EBPβ in a murine model of metabolic dysfunction-associated steatotic liver disease.

The through-line from the cardiovascular work is the cardio-hepatic axis — the recognition that liver function and cardiac function are not independent problems, which is also the premise Apterna's programme rests on.

04METHOD AND TEACHING

Statistics as a clinical instrument.

A recurring theme is that the analysis should be as carefully constructed as the study. His methodological work spans Bayesian hierarchical modelling, causal inference, survival analysis and mixed-effects models, applied to the messy longitudinal data that clinical cohorts actually produce.

At Dundee he teaches medical statistics to junior doctors using SPSS and R, covering data handling, descriptive analysis, logistic regression and survival modelling, with an emphasis on reproducibility — the discipline of making an analysis one that someone else can run again and get the same answer.

  • ModellingSurvival, mixed-effects, Bayesian hierarchical
  • InferenceCausal inference and machine learning
  • Evidence synthesisSystematic review and meta-analysis, PRISMA
  • ToolingR · Python · SPSS

05AT APTERNA

Where the disciplines converge.

As Healthcare Innovation Lead, Dr Dehkordi's brief sits where his three disciplines meet: RNA delivery and aptamer chemistry on one side, computational and statistical method on the other, and the clinical question of restoring liver function running between them.

It is the same problem his cardiovascular work approaches from the opposite direction. Apterna's programme asks whether liver function can be restored where it currently limits treatment; his research asks how confidently a genetic finding predicts what a patient will experience. Both are questions about turning a molecular fact into a clinical decision.

Apterna's lead programme, REGEN001, is preclinical. Nothing on this page describes an approved treatment or a demonstrated clinical outcome.

06SELECTED PUBLICATIONS

Published work.

Thirteen publications are listed on his ResearchGate profile, spanning RNA therapeutics, inherited cardiac disease, haematology and clinical audit. A selection follows; the full list is linked in the references below.

  1. GalNAc-conjugated siRNA targeting C/EBPβ reverses metabolic dysfunction and restores liver homeostasis in a murine MASLD modelMolecular Therapy — Nucleic Acids · 2026
  2. Age-related decline in lymphocyte counts: establishing age-specific reference intervals for clinical practiceAmerican Journal of Hematology · 2025
  3. Acute myocardial infarction and antiphospholipid syndrome: an updated systematic review and meta-analysisAnnals of Medicine and Surgery · 2025
  4. Genotypic influence on phenotypic expression and clinical outcomes in hypertrophic cardiomyopathy: insights from a regional HCM cohort registryHeart · 2025
  5. Phenotype conversion and disease progression in relatives of hypertrophic cardiomyopathy probands: a stratified analysis by genotype statusConference paper · 2025
  6. Clinical profile and outcomes in hypertrophic cardiomyopathy: findings from the Tayside Inherited Cardiac Condition clinic studyPoster · 2024
  7. Serial reticulocyte monitoring after primary spontaneous intracerebral haemorrhage: a novel and scalable window into early erythropoietic failurePresentation · 2026

07SELECTED CHRONOLOGY

A record, in order.

  1. 2018Begins medical school
  2. 2024Joins the cardiovascular group at the University of Dundee
  3. 2024Cardiovascular and molecular genetic research, Imperial College London
  4. 2025Awarded MD
  5. 2026Visiting Researcher, Department of Surgery & Cancer, Imperial
  6. 2026C/EBPβ siRNA work published in Molecular Therapy — Nucleic Acids

08REFERENCES

Where this comes from.

This profile is compiled from published sources. Each is listed below so any statement on this page can be checked against it.

A CLEARER UNDERSTANDING

Questions about Dr Dehkordi.

Who is Dr Arash Dehkordi?

Dr Arash Dehkordi is a physician-scientist and Apterna's Healthcare Innovation Lead. He is a Visiting Researcher in the Department of Surgery & Cancer at Imperial College London and an Honorary Fellow (Research) at the University of Dundee, and holds an MD alongside a background in pure mathematics from the University of Bath.

What does Arash Dehkordi research?

His research spans two areas. In cardiovascular medicine he studies hypertrophic cardiomyopathy and inherited cardiac conditions, including genotype–phenotype correlation and phenotype conversion in family screening. In molecular oncology he works on RNA-based therapeutics, gene therapy and targeted delivery for liver and pancreatic disease. Both use statistical and machine learning methods applied to clinical data.

Where is Arash Dehkordi based?

He works with Apterna in London, with Imperial College London's Department of Surgery & Cancer, and with the cardiovascular group in Molecular and Clinical Medicine at the University of Dundee, based at Ninewells Hospital and Medical School.

What has Arash Dehkordi published?

Thirteen publications are listed on his ResearchGate profile. They include work in Molecular Therapy — Nucleic Acids on a GalNAc-conjugated siRNA targeting C/EBPβ in a murine MASLD model, a systematic review and meta-analysis of acute myocardial infarction in antiphospholipid syndrome in Annals of Medicine and Surgery, and studies of hypertrophic cardiomyopathy genotype and outcomes in Heart. His ORCID is 0009-0002-1754-2271.