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Trust score 8/100
Accepting new patients
Dr
Dr David Mowat
Clinical Genetics
English
1,602+
Patients seen
16
Years in practice
10
Publications
1
Languages spoken
About
Dr David Mowat is a clinician and researcher with a primary interest in diagnosing the genetic causes of rare diseases and syndromes. Their work focuses on translational medicine to improve clinical outcomes for patients. Dr Mowat is involved in genomic projects across various disease cohorts, including rare Mendelian disorders, intellectual disability, and adult and paediatric neuromuscular disorders. They are recognised for identifying an important syndromal cause of intellectual disability ��� Mowat-Wilson syndrome ��� and has contributed to the discovery of a number of novel disease-causing genes.
Dr Mowat has been an active member of several professional organisations, NIH grant study sections, and editorial boards of journals. They have conducted extramurally funded research on Prader-Willi syndrome and obesity-related disorders, alcoholism, the genetics of autism and intellectual disabilities, and the delineation of rare and uncommon genetic disorders such as Mowat-Wilson syndrome. Dr Mowat has an active medical practice in clinical genetics. Their groundbreaking work has revealed how interactions between multiple genetic mutations converge to produce the observed clinical phenotype in patients.
Currently, their lab focuses on uncovering the complex genetic and cellular interactions underlying disorders that affect both the central and enteric nervous systems. This includes research on Mowat-Wilson Syndrome, where their team aims to dissect the genetic and mechanistic pathways that contribute to the spectrum of symptoms in these patients. Ultimately, their research seeks to inform therapeutic strategies for managing these challenging conditions.
Dr Mowat has been an active member of several professional organisations, NIH grant study sections, and editorial boards of journals. They have conducted extramurally funded research on Prader-Willi syndrome and obesity-related disorders, alcoholism, the genetics of autism and intellectual disabilities, and the delineation of rare and uncommon genetic disorders such as Mowat-Wilson syndrome. Dr Mowat has an active medical practice in clinical genetics. Their groundbreaking work has revealed how interactions between multiple genetic mutations converge to produce the observed clinical phenotype in patients.
Currently, their lab focuses on uncovering the complex genetic and cellular interactions underlying disorders that affect both the central and enteric nervous systems. This includes research on Mowat-Wilson Syndrome, where their team aims to dissect the genetic and mechanistic pathways that contribute to the spectrum of symptoms in these patients. Ultimately, their research seeks to inform therapeutic strategies for managing these challenging conditions.
“Evidence-based care tailored to each patient — taking the time to explain options and shared decisions.”
— Dr David Mowat
Education & training
-
2000–2006 MD · Medicine and Surgery
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2006–2010 Residency · Clinical Genetics
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2010–2011 Fellowship · Subspecialty training
Career & appointments
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2010-09–2011-08 Junior consultant
Licenses & insurance
Medical licenses
— Organización Médica Colegial de España (OMC)
Board certifications
European Board of Clinical Genetics
Malpractice insurance:
AmTrust Europe · 3,000,000 EUR coverage
· No claims on file
Procedures performed
| Procedure | Code | Lifetime count |
|---|---|---|
| GP consultation | 99213 | 1,511 |
| Annual physical exam | 99395 | 113 |
| Vaccination administration | 90471 | 1,833 |
| Minor procedure (skin) | 17110 | 1,302 |
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 | 90 min | in_clinic | 540.00 EUR |
| Minor procedure (skin) | 60 min | in_clinic | 810.00 EUR |
Office, team & in practice
Videos
Research & publications
h-index: 7 · i10: 8
-
Outcomes of Clinical Genetics in adults — a multi-centre cohort
DOI: 10.9522/euroclin.2025.0 · PMID: 31537045 · cited by 95
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European registry analysis of Clinical Genetics outcomes
DOI: 10.1180/euroclin.2024.1 · PMID: 39268835 · cited by 93
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Outcomes of Clinical Genetics in adults — a multi-centre cohort
DOI: 10.6146/euroclin.2023.2 · PMID: 31883597 · cited by 91
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European registry analysis of Clinical Genetics outcomes
DOI: 10.4762/euroclin.2022.3 · PMID: 34438163 · cited by 65
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
Society memberships
- WONCA Europe — Family Doctors — Member · since 2011
- national college of family doctors — Member · since 2011
- European Union of Medical Specialists (UEMS) — Member · since 2011
Patient reviews
- Bedside Manner
- 0.05
- Knowledge
- 0.08
- Wait Time
- 3.80
- Staff Friendliness
- 0.02
- Ease Of Appointment
- 4.00
- Value For Money
- 4.10
- Would Recommend Pct
- 4
-
★ 5 verified visit
“Very thorough first visit — explained every step. Booking was easy and the staff were welcoming.”
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★ 5 verified visit
“Took time to listen and reviewed all my previous results. I would absolutely recommend.”
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★ 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 · david.mowat@euroclinics.example
