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DR. JASON SEAN BRADFIELD M.D.
M.D.
Clinical Cardiac Electrophysiology Physician
NPI: 1760698237IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
A86969(CA)
Cardiovascular Disease Physician
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
A86969(CA)
Nuclear Cardiology Physician
Nuclear Medicine — Nuclear Cardiology
Code: 207UN0901X
A86969(CA)
Clinical Cardiac Electrophysiology PhysicianPrimary
Internal Medicine — Clinical Cardiac Electrophysiology
Code: 207RC0001X
A86969(CA)
Education
NORTHWESTERN UNIVERSITY FEINBERG MEDICAL SCHOOL
Class of 2002
Research & Publications (20)
Low referral rate for prophylactic implantation of cardioverter-defibrillators in a tertiary care medical center.
PMID 19250092·Pacing Clin Electrophysiol·2009
8-other
Aprotinin restores the adhesive capacity of dysfunctional platelets.
PMID 12757772·Thromb Res·2003
7-preclinical
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
PMID 19404256·Nature·2009
8-other
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
PMID 19592680·Genome Res·2009
8-other
17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry.
PMID 19660801·J Allergy Clin Immunol·2009
8-other
Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies.
PMID 19465406·J Med Genet·2009
8-other
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
PMID 19404257·Nature·2009
8-other
The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.
PMID 19478790·Obesity (Silver Spring)·2009
8-other
Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.
PMID 19592620·Diabetes·2009
8-other
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PMID 19557195·PLoS Genet·2009
8-other
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease.
PMID 19249008·Am J Hum Genet·2009
8-other
Effects of cage size and enrichment on reproductive performance and behavior in C57BL/6Tac mice.
PMID 19112447·Lab Anim (NY)·2009
7-preclinical
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
PMID 18840781·Diabetes·2009
8-other
A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.
PMID 19656524·J Pediatr·2009
8-other
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.
PMID 19412175·Nat Genet·2009
8-other
Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry.
PMID 19265794·Obesity (Silver Spring)·2009
8-other
Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.
PMID 18335027·PLoS One·2008
8-other
ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.
PMID 18760456·J Allergy Clin Immunol·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 100 UCLA MEDICAL PLZ STE 690
LOS ANGELES, CA 90024 - Phone
- (310) 206-2235
Quick Facts
- NPI
- 1760698237
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 3
- Years in Practice
- 24
- Publications
- 20
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