Overview
Maarten Knapen practices in Rotterdam, Netherlands. Mr. Knapen is rated as an Advanced expert by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Mosaicism, and Micrognathia.
His clinical research consists of co-authoring 37 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 3 articles in the study of Chromosome 13q Duplication.
Locations
Rotterdam, ZH, Netherlands
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Chromosome 13q DuplicationMr. Knapen isAdvanced. Learn about Chromosome 13q Duplication.
- MicrognathiaMr. Knapen isAdvanced. Learn about Micrognathia.
- MosaicismMr. Knapen isAdvanced. Learn about Mosaicism.
- Trisomy 13Mr. Knapen isAdvanced. Learn about Trisomy 13.
- Trisomy 18Mr. Knapen isAdvanced. Learn about Trisomy 18.
- Experienced
- Acromesomelic DysplasiaMr. Knapen isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeMr. Knapen isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Brachydactyly Mononen TypeMr. Knapen isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMr. Knapen isExperienced. Learn about Chondrodystrophy.