Associate Professor of Neurology and Associate Professor of Neuroscience, Mayo Clinic College of Medicine
Neurology
Dr. Nilufer Taner, MD
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Nilufer Taner is an expert in the field of Neurology. She received 2 awards: "Health Care Hero" and "Basic Science Research Award". Doctor Nilufer Taner, MD is a published doctor and has 60 publications published. The lastest was: 'Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.' Doctor Nilufer Taner, MD accepts Medicare payments and is listed with Medicare.gov.
Publications
- Role for the microtubule-associated protein tau variant p.A152T in risk of alpha-synucleinopathies.
- Global and local ancestry in African-Americans: Implications for Alzheimer's Disease risk.
- Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.
- Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study.
- Genome-wide association study of corticobasal degeneration identifies risk variants shared with Progressive supranuclear palsy.
- TREM2 is associated with increased risk for Alzheimer's Disease in African Americans.
- A novel Alzheimer Disease locus located near the gene encoding tau protein.
- Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States.
- Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's Disease.
- Two rare AKAP9 variants are associated with Alzheimer's Disease in African Americans.
- Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease: A Genome-Wide Association Study.
- Association of MAPT haplotypes with Alzheimer's Disease risk and MAPT brain gene expression levels.
- Genome-wide association interaction analysis for Alzheimer's Disease.
- Alzheimer's Disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci.
- ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family.
- Late-onset Alzheimer Disease genetic variants in posterior cortical atrophy and posterior AD.
- ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's Disease.
- Two phase 3 trials of bapineuzumab in mild-to-moderate Alzheimer's Disease.
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's Disease.
- Alzheimer's Disease: analyzing the missing heritability.
- TREM2 and neurodegenerative Disease.
- Gene-based GWAS and biological pathway analysis of the resilience of executive functioning.
- TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal Dementia.
- Alzheimer Disease: the quest for Alzheimer Disease genes--focus on CSF tau.
- TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's Disease.
- LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's Disease (LOAD).
- Evaluation of memory endophenotypes for association with CLU, CR1, and PICALM variants in black and white subjects.
- Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ?4,and the risk of late-onset Alzheimer Disease in African Americans.
- SORL1 is genetically associated with late-onset Alzheimer's Disease in Japanese, Koreans and Caucasians.
- Alternative Approaches in Gene Discovery and Characterization in Alzheimer's Disease.
- DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with Dementia and hearing loss.
- Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci.
- Comprehensive search for Alzheimer Disease susceptibility loci in the APOE region.
- Genetic architecture of resilience of executive functioning.
- Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
- Novel late-onset Alzheimer Disease loci variants associate with brain gene expression.
- Glutathione S-transferase omega genes in Alzheimer and Parkinson Disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implic...
- Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus.
- Brain expression genome-wide association study (eGWAS) identifies human Disease-associated variants.
- Association and heterogeneity at the GAPDH locus in Alzheimer's Disease.
- Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS.
- Gene expression endophenotypes: a novel approach for gene discovery in Alzheimer's Disease.
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's Disease.
- Association of common KIBRA variants with episodic memory and AD risk.
- Meta-analysis confirms CR1, CLU, and PICALM as alzheimer Disease risk loci and reveals interactions with APOE genotypes.
- Genetics of Alzheimer Disease in the pre- and post-GWAS era.
- Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer Disease.
- Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's Disease.
- Development of monoclonal antibodies and quantitative ELISAs targeting insulin-degrading enzyme.
- Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's Disease.
- Plasma amyloid beta protein is elevated in late-onset Alzheimer Disease families.
- Genetics of Alzheimer's Disease: a centennial review.
- Elevated amyloid beta protein (Abeta42) and late onset Alzheimer''s Disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activ...
- Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Abeta42 levels and risk for Alzheimer Disease.
- Live discussion: Amyloid-beta degradation: the forgotten half of Alzheimer's Disease. 12 September 2002.
- Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.
- Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer''s Disease pedigrees.
- Heritability of plasma amyloid beta in typical late-onset Alzheimer's Disease pedigrees.
- Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's Disease pedigrees.
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
Conditions Treated
- Alzheimer's Disease
- Ataxia
- Autonomic Disorders
- Brain Aneurysm
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Doctors Specialties
- Neurology
Accepted Insurances
Awards
- Health Care Hero
- Basic Science Research Award
Education
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Mayo School of Graduate Medical Education
Hospital
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Mayo Clinic - Jacksonville, Florida
Drug Facts
| NPI NUMBER | 1992777676 | |
| NPPES Provider LastName | TANER | |
| NPPES Provider FirstName | NILUFER | |
| NPPES Provider ZIPCode | 322241865 | |
| NPPES Provider State | FL | |
| Specialty Description | Neurology | |
| Total Claim Count | 214.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1992777676 |
| Last Name Of The Provider | TANER |
| First Name Of The Provider | NILUFER |
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