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Trust score 97/100
Accepting new patients
Dr
Dr Ehsan Karimiani
Clinical Genetics
English
Persian
3,658+
Patients seen
7
Years in practice
6
Publications
2
Languages spoken
About
Dr Ehsan Karimiani is a UK-based Clinical Geneticist at Kensington International Clinic (KIC) in London, specialising in precision genomic medicine, rare disease diagnostics, and personalised patient care. With over a decade of combined clinical and academic experience, he integrates advanced genomic technologies with a highly individualised, patient-centred approach.
His practice spans hereditary cancer genetics, where he provides comprehensive risk assessment for conditions including breast and ovarian cancer, Lynch syndrome, and familial colorectal cancer. He offers tumour–germline interpretation, cascade testing, and tailored surveillance strategies aligned with international guidelines, supporting both prevention and treatment decision-making.
Dr Karimiani has a strong focus on reproductive genomics and preconception medicine. He supports individuals and couples through expanded carrier screening, preimplantation genetic testing (PGT-M and PGT-A), and prenatal genomic assessment. He works closely with leading fertility specialists to deliver integrated, evidence-based care within assisted reproduction pathways.
A key area of his expertise is neurogenetics and rare inherited disorders, particularly complex and undiagnosed conditions. He provides advanced genomic evaluation—including exome and whole genome sequencing—combined with deep phenotyping and multidisciplinary input. He is actively involved in research and reanalysis pipelines for unresolved cases, including collaboration with academic centres.
Dr Karimiani also has established expertise in audiogenetics, offering comprehensive genomic evaluation for congenital, progressive, and familial hearing loss. His approach combines audiological phenotyping with genomic technologies to inform diagnosis, prognosis, and eligibility for emerging therapies and clinical trials.
His broader clinical services include genomic assessment for:
• Developmental delay and intellectual disability
• Autism spectrum conditions
• Inherited cardiac, ophthalmic, and multisystem genetic disorders
• Pharmacogenetics for personalised prescribing
• Expanded carrier screening across hundreds of genetic conditions
Dr Karimiani has particular expertise in working with patients from diverse and international backgrounds, including populations with higher rates of consanguinity. He is highly experienced in identifying rare recessive disorders and founder mutations, and provides culturally sensitive, tailored genetic counselling.
He is an Honorary Lecturer in Medical Genetics at University College London and is actively involved in clinical research, teaching, and international collaborations in genomic medicine. His work includes contributions to large-scale genomic studies and rare disease gene discovery, with a focus on translating research findings into clinical care.
Through his private practice and the London Genetics platform, Dr Karimiani delivers a highly personalised, consultant-led service, often coordinating multidisciplinary input across specialties. His approach emphasises clarity, precision, and continuity of care—from initial consultation through to diagnosis, management, and long-term follow-up.
His practice spans hereditary cancer genetics, where he provides comprehensive risk assessment for conditions including breast and ovarian cancer, Lynch syndrome, and familial colorectal cancer. He offers tumour–germline interpretation, cascade testing, and tailored surveillance strategies aligned with international guidelines, supporting both prevention and treatment decision-making.
Dr Karimiani has a strong focus on reproductive genomics and preconception medicine. He supports individuals and couples through expanded carrier screening, preimplantation genetic testing (PGT-M and PGT-A), and prenatal genomic assessment. He works closely with leading fertility specialists to deliver integrated, evidence-based care within assisted reproduction pathways.
A key area of his expertise is neurogenetics and rare inherited disorders, particularly complex and undiagnosed conditions. He provides advanced genomic evaluation—including exome and whole genome sequencing—combined with deep phenotyping and multidisciplinary input. He is actively involved in research and reanalysis pipelines for unresolved cases, including collaboration with academic centres.
Dr Karimiani also has established expertise in audiogenetics, offering comprehensive genomic evaluation for congenital, progressive, and familial hearing loss. His approach combines audiological phenotyping with genomic technologies to inform diagnosis, prognosis, and eligibility for emerging therapies and clinical trials.
His broader clinical services include genomic assessment for:
• Developmental delay and intellectual disability
• Autism spectrum conditions
• Inherited cardiac, ophthalmic, and multisystem genetic disorders
• Pharmacogenetics for personalised prescribing
• Expanded carrier screening across hundreds of genetic conditions
Dr Karimiani has particular expertise in working with patients from diverse and international backgrounds, including populations with higher rates of consanguinity. He is highly experienced in identifying rare recessive disorders and founder mutations, and provides culturally sensitive, tailored genetic counselling.
He is an Honorary Lecturer in Medical Genetics at University College London and is actively involved in clinical research, teaching, and international collaborations in genomic medicine. His work includes contributions to large-scale genomic studies and rare disease gene discovery, with a focus on translating research findings into clinical care.
Through his private practice and the London Genetics platform, Dr Karimiani delivers a highly personalised, consultant-led service, often coordinating multidisciplinary input across specialties. His approach emphasises clarity, precision, and continuity of care—from initial consultation through to diagnosis, management, and long-term follow-up.
“Evidence-based care tailored to each patient — taking the time to explain options and shared decisions.”
— Dr Ehsan Karimiani
Education & training
-
2009–2015 MD · Medicine and Surgery
-
2015–2019 Residency · Clinical Genetics
Career & appointments
-
2019-09–2020-08 Junior consultant
Licenses & insurance
Medical licenses
GB — Organización Médica Colegial de España (OMC)
Board certifications
European Board of Clinical Genetics
Malpractice insurance:
AXA Healthcare Liability · 2,000,000 EUR coverage
· No claims on file
Procedures performed
| Procedure | Code | Lifetime count |
|---|---|---|
| GP consultation | 99213 | 1,894 |
| Annual physical exam | 99395 | 832 |
| Vaccination administration | 90471 | 712 |
| Minor procedure (skin) | 17110 | 1,735 |
Services & pricing
| Service | Duration | Modality | Price |
|---|---|---|---|
| New patient consultation (60m) | 60 min | in_clinic|telemed | 180.00 EUR |
| Follow-up consultation (30m) | 30 min | in_clinic|telemed|phone | 90.00 EUR |
| Vaccination administration | 30 min | in_clinic | 720.00 EUR |
| Minor procedure (skin) | 120 min | in_clinic | 630.00 EUR |
Office, team & in practice
Videos
Research & publications
h-index: 9 · i10: 13
-
Validation of clinical scoring in Clinical Genetics
DOI: 10.6732/euroclin.2026.0 · PMID: 31962646 · cited by 94
-
Long-term follow-up of Clinical Genetics across GB
DOI: 10.7717/euroclin.2025.1 · PMID: 36747220 · cited by 68
-
Validation of clinical scoring in Clinical Genetics
DOI: 10.5518/euroclin.2024.2 · PMID: 39648134 · cited by 26
-
Long-term follow-up of Clinical Genetics across GB
DOI: 10.6182/euroclin.2023.3 · PMID: 34577643 · cited by 136
Invited talks
- Practical updates in Clinical Genetics European Annual Congress (Clinical Genetics) · Vienna · 2024 · invited
- Single-centre experience in Clinical Genetics National Society Meeting · · 2023 · oral abstract
Awards & memberships
Awards
- 🏆 Top-rated Clinical Genetics — · EuroClinics Patient Choice · 2025 · regional
- 🏆 Excellence in Patient Care · National Society · 2024 · national
- 🏆 Young Investigator Award · European Society · 2023 · international
Society memberships
- WONCA Europe — Family Doctors — Member · since 2020
- national college of family doctors — Member · since 2020
- European Union of Medical Specialists (UEMS) — Member · since 2020
Patient reviews
- Bedside Manner
- 5.00
- Knowledge
- 5.00
- Wait Time
- 4.72
- Staff Friendliness
- 4.99
- Ease Of Appointment
- 4.87
- Value For Money
- 4.89
- Would Recommend Pct
- 98
-
★ 5 verified visit
“Very thorough first visit — explained every step. Booking was easy and the staff were welcoming.”
-
★ 5 verified visit
“Took time to listen and reviewed all my previous results. I would absolutely recommend.”
-
★ 4 verified visit
“Professional and knowledgeable. Wait on the day was a bit long, otherwise excellent.”
Articles by this doctor
- Patient education Patient guide to Clinical Genetics
- Awareness When should you see a clinical genetics?
For international patients
- Coordinator
- Patient liaison · ehsan.ghayoor.karimiani@euroclinics.example
- Accepted intl insurance
- Allianz Worldwide · AXA Global · BUPA Global · Cigna Global
