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Ertekin‐Taner, Nilüfer

https://orcid.org/0000-0003-4436-8889

Mayo Clinic

Mayo Clinic

Citations 221

P3‐257: Investigation of established Alzheimer's disease–risk SNPs for association with Alzheimer's disease in an African‐American case control series
Allen, Mariet , Pedraza, Otto , Nguyen, Thuy , Bisceglio, Gina, Flingai, Seleeke, Miles, Richard J., Hirpa, Meron, Malphrus, Kimberly G., Petersen, Ronald C. , Graff‐Radford, Neill R. , Younkin, Steven G., Ertekin‐Taner, Nilüfer , Ma, Li

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_15 | Pages: No page available

10.1016/j.jalz.2012.05.1480 Get It

P4‐126: Genome‐wide exploration of DNA methylation in the aging brain and its relation to Alzheimer's disease
Jager, Philip L. De , Srivastava, Gyan , Eaton, Matthew L. , Zou, Fangeng, Song, High, Younkin, Curtis, Younkin, Steven G., Ertekin‐Taner, Nilüfer , Bernstein, B, Meissner, Alexander , Chibnik, Lori Beth , Keenan, Brendan T , Kellis, Manolis , Bennett, David A.

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_18 | Pages: No page available

10.1016/j.jalz.2012.05.1829 Get It

P4‐123: The genetics of cognitively healthy aging
Bisceglio, Gina, Graff‐Radford, Neill R. , Talisha, Hunter, Ertekin‐Taner, Nilüfer , Younkin, Steven G. , Carrasquillo, Minerva M. , Carrasquillo, Minerva M.

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_18 | Pages: No page available

10.1016/j.jalz.2012.05.1826 Get It

O1‐09‐01: CTNNA3, CAPRIN2 and SPG20 are significantly associated with Alzheimer's disease in preliminary analyses of a genome‐wide association study in African‐Americans
Reitz, Christiane , Hall, Kathleen, Evans, Denis A., Ertekin‐Taner, Nilüfer , Fallin, Danielle, Pericak‐Vance, Margaret A. , Haines, Jonathan L. , Mayeux, Richard , Schellenberg, Gerard D. , Manly, Jennifer J. , Bennett, David A. , Buxbaum, Joseph D. , Kamboh, M. Ilyas , Foroud, Tatiana , Goate, Alison , Farrer, Lindsay A.

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_3 | Pages: No page available

10.1016/j.jalz.2012.05.251 Get It

Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS
DeJesus‐Hernandez, Mariely, Desaro, Pamela , Johnston, Amelia, Ross, Owen A. , Ertekin‐Taner, Nilüfer , Graff-Radford, N. R., Rademakers, Rosa , Wszołek, Zbigniew K. , Boylan, Khrista , Ross, Owen A

Neurology | September 1, 2011 | Volume: 77 | Issue: 11 | Pages: 1102-1103

10.1212/wnl.0b013e31822e563c Get It