Dr. Truxal 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
700 Childrens Dr
Columbus, OH 43205Phone+1 614-722-3535Fax+1 614-722-3546
Summary
- Dr. Kristen Truxal is a medical geneticist in Columbus, OH and is affiliated with Nationwide Children's Hospital. She received her medical degree from Ohio State University College of Medicine and has been in practice 10 years. She specializes in clinical genetics, pediatrics, and clinical trials for patients with genetic conditions.
Education & Training
Nationwide Children's Hospital/Ohio State UniversityFellowship, Research, 2015 - 2016- Nationwide Children's Hospital/Ohio State UniversityResidency, Medical Genetics and Genomics, 2013 - 2015
Sidney Kimmel Medical College at Thomas Jefferson University/Nemours Children's Health, WilmingtonResidency, Pediatrics, 2009 - 2012
Ohio State University College of MedicineClass of 2009
Certifications & Licensure
OH State Medical License 2013 - 2025
DE State Medical License 2012 - 2015
PA State Medical License 2009 - 2012- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Novel truncating variant inassociated with cerebellar hypoplasia and velopharyngeal dysfunction.Nicolas J Abreu, Amy E Siemon, Adriane L Baylis, Richard E Kirschner, Ruthann B Pfau
Clinical Case Reports. 2022-02-01 - 3 citationsLongitudinal MRI brain volume changes over one year in children with mucopolysaccharidosis types IIIA and IIIB.Nicolas J. Abreu, Bhavani Selvaraj, Kristen V. Truxal, Melissa Moore-Clingenpeel, Nicholas Zumberge
Molecular Genetics and Metabolism. 2021-04-27 - 5 citationsFurther delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants.Sandra Whalen, Marie Shaw, Cyril Mignot, Delphine Héron, Sandra Chantot Bastaraud
European Journal of Human Genetics. 2021-02-18
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
