DavidB.FlanneryMD
Medical Genetics • Cleveland, OHClinical Genetics
Director of Telegenetics and Digital Genetics Cleveland Clinic
Dr. Flannery is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
9500 Euclid Avenue
R 4
Cleveland, OH 44195Phone+1 216-444-0744
Summary
- Dr. David Flannery is a medical geneticist in Cleveland, OH. He received his medical degree from Emory University School of Medicine and has been in practice 41 years. He specializes in clinical genetics and is experienced in telemedicine.
Education & Training
Virginia Commonwealth University Health SystemFellowship, Medical Genetics and Genomics, 1981 - 1983
University of Virginia Medical CenterResidency, Pediatrics, 1978 - 1979
Emory University School of MedicineResidency, Pediatrics, 1977 - 1978- Emory University School of MedicineInternship, Pediatrics, 1976 - 1977
- Emory University School of MedicineClass of 1976
Certifications & Licensure
GA State Medical License 1984 - 2025
OH State Medical License 2018 - 2025
MD State Medical License 2015 - 2018- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Pediatrics Pediatrics
Awards, Honors, & Recognition
- Regional Top Doctor Castle Connolly, 2014
Publications & Presentations
PubMed
- 13 citationsAmino acids in amniotic fluid in the second trimester of gestation.W Christine Mesavage, Sharon F. Suchy, Debra L. Weiner, Carol S. Nance, David B. Flannery
Pediatric Research. 1985-10-01 - 201 citationsVerification of the fetal valproate syndrome phenotype.Holly H Ardinger, Joan F. Atkin, R D Blackston, Louis J. Elsas, Sterling K. Clarren
American Journal of Medical Genetics. 1988-01-01 - 42 citationsRecurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.Pawel Stankiewicz, Shashikant Kulkarni, Avinash V. Dharmadhikari, Srirangan Sampath, Samarth Bhatt
Human Mutation. 2012-01-01
Press Mentions
Virginia Beach Pastor Returns Home from COVID-19 Hot SpotApril 26th, 2020
Healthcare Symposium Concludes on Genetics and AddictionMay 23rd, 2019
The ACMG Foundation Announces Recipient of the ACMG Foundation Carolyn Mills Lovell AwardApril 4th, 2019- Join now to see all
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
