VikasBhambhaniMD
Medical Genetics • Minneapolis, MNClinical Biochemical Genetics, Clinical Genetics, Medical Biochemical Genetics
Physician
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Office
2525 Chicago Ave
Minneapolis, MN 55404Phone+1 612-813-7240Fax+1 612-813-6360
Education & Training
National Institutes of Health Clinical CenterFellowship, Medical Biochemical Genetics, 2012 - 2013- National Institutes of Health Clinical CenterResidency, Medical Genetics and Genomics, 2010 - 2012
Westchester Medical CenterResidency, Pediatrics, 2007 - 2010
Maulana Azad Medical CollegeClass of 1999
Certifications & Licensure
MN State Medical License 2013 - 2025
IN State Medical License 2010 - 2013- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Mucopolysaccharidosis (MPS) I, II, and VI Screening in a High-Risk Population With Previous Surgical Repair or Presence of Inguinal and/or Umbilical Hernia in Combination With Pediatric ENT Surgery (The HATT Project) Start of enrollment: 2014 May 21
- A Study of ELAPRASE in Treatment-naïve Participants With Hunter Syndrome (Mucopolysaccharidosis [MPS] II) Start of enrollment: 2023 Feb 28
Roles: Principal Investigator
Publications & Presentations
PubMed
- Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.Juan Darío Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri
Movement Disorders. 2024-09-01 - 2 citationsParental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1.Kelly Schoch, Allyn McConkie-Rosell, Nicole Walley, Vikas Bhambhani, Timothy Feyma
Orphanet Journal of Rare Diseases. 2023-09-04 - 4 citationsThe clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.Afshin Saffari, Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad
Brain. 2023-08-01
Journal Articles
- SLC6A1 Variants Identified in Epilepsy Patients Reduce Γ‐Aminobutyric Acid TransportVikas Bhambhani, Bryan Philbrook, Epilepsia
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