Associate Professor, Neurology, University of Virginia School of Medicine
Neurology
Dr. Bradford B. Worrall, MD
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Bradford B. Worrall, MD practices Neurology. He researched medicine at Emory University School of Medicine. Emory University School of Medicine is ranked 23/42 in Research/PrimaryCare. He received 1 awards: "CMS Meaningful Use Stage 1 Certification". Bradford Worrall is a published doctor. He has 88 publications published. The most current publication "Anterior ischemic optic neuropathy and activated protein C resistance. A case report and review of the literature." He accepts all Medicare patients.
Publications
- Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
- Incontinence and gait disturbance after intraventricular extension of intracerebral hemorrhage.
- Evolution of brain lesions in a patient with TREX1 cerebroretinal vasculopathy.
- Endovascular vs medical management of acute ischemic stroke.
- Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection.
- Etiologic stroke subtypes: updated definition and efficient workup strategies.
- Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network.
- Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
- Genome-Wide Association Study of Intracranial Aneurysm Identifies a New Association on Chromosome 7.
- Agreement between TOAST and CCS ischemic stroke classification: The NINDS SiGN Study.
- Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage.
- Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
- Effect of Long-Chain Ï-3 Fatty Acids and Luteinâ+âZeaxanthin Supplements on Cardiovascular Outcomes: Results of the Age-Related Eye Disease Study 2 (AREDS2) Randomized...
- Genome-Wide Meta-Analysis of Homocysteine and Methionine Metabolism Identifies Five One Carbon Metabolism Loci and a Novel Association of ALDH1L1 with Ischemic Stroke.
- Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2.
- Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2.
- Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes.
- The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study Protocol.
- NINDS stroke genetics network (SiGN) experience with the causative classification system.
- Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage.
- Shared associations of nonatherosclerotic, large-vessel, cerebrovascular arteriopathies: considering intracranial aneurysms, cervical artery dissection, moyamoya disea...
- Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).
- Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage.
- Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.
- Genome-wide association analysis of ischemic stroke in young adults.
- Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.
- Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci.
- Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and rando...
- Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.
- APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study.
- Genetic susceptibility to ischemic stroke.
- Common mitochondrial sequence variants in ischemic stroke.
- Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis.
- Variants at APOE influence risk of deep and lobar intracerebral hemorrhage.
- White matter hyperintensity volume is increased in small vessel stroke subtypes.
- The Causative Classification of Stroke system: an international reliability and optimization study.
- Health Heritage© a web-based tool for the collection and assessment of family health history: initial user experience and analytic validity.
- Candidate gene polymorphisms for ischemic stroke.
- Prestroke physical activity and early functional status after stroke.
- Joint Commission primary stroke center certification does not affect proband enrollment: the siblings with ischemic stroke study.
- SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
- Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms.
- Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices.
- Structural genomic variation in ischemic stroke.
- Impact of restricting enrollment in stroke genetics research to adults able to provide informed consent.
- Association of integrin alpha2 gene variants with ischemic stroke.
- Is anti-inflammatory therapy for type 2 diabetes mellitus ready for routine clinical practice?
- Sex and stroke: are they really different in midlife?
- Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review.
- Sex differences in stroke evaluations in the Ischemic Stroke Genetics Study.
- Sex differences in stroke severity, symptoms, and deficits after first-ever ischemic stroke.
- Advancing stroke therapeutics through genetic understanding.
- A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
- IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations.
- Coma reversal after basilar artery thrombolysis.
- Family history of stroke and severity of neurologic deficit after stroke.
- Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson''s disease.
- PDE4D and stroke: a real advance or a case of the Emperor''s new clothes?
- Intraplaque dissection of the basilar artery.
- The Siblings With Ischemic Stroke Study (SWISS): a progress report.
- Practice-based clinical research and ethical decision making--Part II: deciding whether to host a particular research study in your practice.
- Practice-based clinical research and ethical decision making--Part I: deciding whether to incorporate practice-based research into your clinical practice.
- Stroke acute management and recovery.
- Herbal energy drinks, phenylpropanoid compounds, and cerebral vasculopathy.
- Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke.
- Should thrombolysis be given to a stroke patient refusing therapy due to profound anosognosia?
- A survey of the SWISS researchers on the impact of sibling privacy protections on pedigree recruitment.
- The impact of privacy protections on recruitment in a multicenter stroke genetics study.
- New advances in identifying genetic anomalies in stroke-prone probands.
- Teleradiology Assessment of Computerized Tomographs Online Reliability Study (TRACTORS) for acute stroke evaluation.
- The Ischemic Stroke Genetics Study (ISGS) Protocol.
- Spouses and unrelated friends of probands as controls for stroke genetics studies.
- Interleukin-1 receptor antagonist gene polymorphisms in carotid atherosclerosis.
- The genetics of cerebrovascular atherosclerosis.
- Stroke risk factor profiles in African American women: an interim report from the African-American Antiplatelet Stroke Prevention Study.
- Ethical and methodological issues in pedigree stroke research.
- Correlation of aphasia and/or neglect with cortical infarction in a subpopulation of RANTTAS.
- Propofol and midazolam in the treatment of refractory status epilepticus.
- Antiplatelet therapy in secondary stroke prevention.
- Amyotrophy in prion diseases.
- Update on therapies for acute ischemic stroke.
- Antiplatelet agents, carotid endarterectomy, and perioperative complications.
- Mother with amyotrophic lateral sclerosis and daughter with Creutzfeldt-Jakob disease.
- Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.
- Anterior ischemic optic neuropathy and activated protein C resistance. A case report and review of the literature.
- Pairing neuropathology with genetics: a new tool for parsing cerebrovascular disease.
- NOTCH3 Variants and Risk of Ischemic Stroke.
Schools
Emory University School Of Medicine
Emory University Affiliated Hospitals
Columbia Presbyterian Med Center The Neurological Institute Of New York
University Of Virginia
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
Doctors Specialties
- Neurology
- Vascular Neurology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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New York Presbyterian Hospital - Columbia Campus -
Emory University School of Medicine
Hospital
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Novant Health Prince William Medical Center
Drug Facts
| NPI NUMBER | 1821167461 | |
| NPPES Provider LastName | WORRALL | |
| NPPES Provider FirstName | BRADFORD | |
| NPPES Provider ZIPCode | 229080001 | |
| NPPES Provider State | VA | |
| Specialty Description | Neurology | |
| Total Claim Count | 23.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1821167461 |
| Last Name Of The Provider | WORRALL |
| First Name Of The Provider | BRADFORD |
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