Pavel N. Pichurin MD
Clinical Genetics
Assistant Professor, Medical Genetics, Mayo Medical School
Join to View Full Profile
200 1st St SwRochester, MN 55905
Phone+1 507-284-2511
Dr. Pichurin 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.
Summary
- Dr. Pavel Pichurin is a medical geneticist in Rochester, MN and is affiliated with Mayo Clinic Hospital - Rochester. He received his medical degree from Ural State Medical Academy and has been in practice 23 years. He specializes in clinical genetics.
Education & Training
University of Texas Southwestern Medical CenterResidency, Medical Genetics and Genomics, 2009 - 2011
Cedars-Sinai Medical CenterResidency, Surgery, 2006 - 2008
Ural State Medical AcademyClass of 1994
Certifications & Licensure
CA State Medical License 2011 - Present
AZ State Medical License 2016 - 2025
MN State Medical License 2012 - 2025
FL State Medical License 2016 - 2024
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Mucopolysaccharidosis Type IIIA Presenting as Hypertrophic Cardiomyopathy.Filippo Pinto E Vairo, Jeffrey B Geske, Ravinder J Singh, Roy B Dyer, Konstantinos C Siontis
Circulation. Heart Failure. 2025-03-31 - 1 citationsMayo Clinic Tapestry Study: A Large-Scale Decentralized Whole Exome Sequencing Study for Clinical Practice, Research Discovery, and Genomic Education.Lorelei A Bandel, Robert A Vierkant, Teresa M Kruisselbrink, Michelle L Bublitz, Tammy A Wilson
Mayo Clinic Proceedings. 2024-11-05 - 4 citationsLoss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio
Annals of Neurology. 2024-09-20
Journal Articles
- Extension of the Mutational and Clinical Spectrum of SOX2 Related Disorders: Description of Six New Cases and a Novel Association with Suprasellar TeratomaElizabeth J Bhoj, Rachael A Vaubel, Joseph E Parisi, Pavel N Pichurin, American Journal of Medical Genetics Part A
Press Mentions
Genetic Sleuths Dig Deep to Identify a Young Boy’s Rare ConditionFebruary 13th, 2018
Next Generation Sequencing – a Game ChangerMarch 28th, 2017
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
