Genomic variation in educational attainment modifies Alzheimer disease risk

por Raghavan, Neha S., Vardarajan, Badri, Mayeux, Richard
Publicado 2019

Reliability and Validity of Self-Reported Vascular Risk Factors: Hypertension, Diabetes, and Heart Disease, in a Multi-Ethnic Community Based Study of Aging and Dementia

por Lee, Annie J., Sanchez, Didi, Reyes-Dumeyer, Dolly, Brickman, Adam M., Lantigua, Rafael A., Vardarajan, Badri N., Mayeux, Richard
Publicado 2023

Behavioral Variant Frontotemporal Lobar Degeneration with Amyotrophic Lateral Sclerosis with a Chromosome 9p21 Hexanucleotide Repeat

por Friedland, Robert P., Shah, Jignesh J., Farrer, Lindsay A., Vardarajan, Badri, Rebolledo-Mendez, Jovan D., Mok, Kin, Hardy, John
Publicado 2012

Differences in plasma metabolites related to Alzheimer's disease, APOE ε4 status, and ethnicity

por Vardarajan, Badri, Kalia, Vrinda, Manly, Jennifer, Brickman, Adam, Reyes‐Dumeyer, Dolly, Lantigua, Rafael, Ionita‐Laza, Iuliana, Jones, Dean P., Miller, Gary W., Mayeux, Richard
Publicado 2020

Disease-related mutations among Caribbean Hispanics with familial dementia

por Lee, Joseph H, Kahn, Amanda, Cheng, Rong, Reitz, Christiane, Vardarajan, Badri, Lantigua, Rafael, Medrano, Martin, Jiménez-Velázquez, Ivonne Z, Williamson, Jennifer, Nagy, Peter, Mayeux, Richard
Publicado 2014

Lysophosphatidylcholines are associated with P-tau181 levels in early stages of Alzheimer’s Disease

por Kalia, Vrinda, Reyes-Dumeyer, Dolly, Dubey, Saurabh, Nandakumar, Renu, Lee, Annie J., Lantigua, Rafael, Medrano, Martin, Rivera, Diones, Honig, Lawrence S., Mayeux, Richard, Miller, Gary W., Vardarajan, Badri N.
Publicado 2023

The APOE ε4 allele is associated with a reduction in FEV(1)/FVC in women: A cross-sectional analysis of the Long Life Family Study

por Kulminski, Alexander M., Barochia, Amisha V., Loika, Yury, Raghavachari, Nalini, Arbeev, Konstantin G., Wojczynski, Mary K., Thyagarajan, Bharat, Vardarajan, Badri N., Christensen, Kaare, Yashin, Anatoliy I., Levine, Stewart J.
Publicado 2018

Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools

por Sariya, Sanjeev, Lee, Joseph H., Mayeux, Richard, Vardarajan, Badri N., Reyes-Dumeyer, Dolly, Manly, Jennifer J., Brickman, Adam M., Lantigua, Rafael, Medrano, Martin, Jimenez-Velazquez, Ivonne Z., Tosto, Giuseppe
Publicado 2019

Synonymous variants associated with Alzheimer disease in multiplex families

por Tang, Min, Alaniz, Maria Eugenia, Felsky, Daniel, Vardarajan, Badri, Reyes-Dumeyer, Dolly, Lantigua, Rafael, Medrano, Martin, Bennett, David A., de Jager, Philip L., Mayeux, Richard, Santa-Maria, Ismael, Reitz, Christiane
Publicado 2020

Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease

por Chen, Jacinda, Soni, Rajesh Kumar, Xu, Yimeng, Simoes, Sabrina, Liang, Feng-Xia, DeFreitas, Laura, Hwang, Robert, Montesinos, Jorge, Lee, Joseph H., Area-Gomez, Estela, Nandakumar, Renu, Vardarajan, Badri, Marquer, Catherine
Publicado 2023

Risk of Alzheimer’s Disease is Associated with Longitudinal Changes in Plasma Biomarkers in the Multiethnic Washington Heights, Inwood Columbia Aging Project Cohort

por Gu, Yian, Honig, Lawrence S., Kang, Min Suk, Bahl, Aanya, Sanchez, Danurys, Reyes-Dumeyer, Dolly, Manly, Jennifer J., Lantigua, Rafael A., Dage, Jeffrey L., Brickman, Adam M., Vardarajan, Badri N, Mayeux, Richard
Publicado 2023

Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

por Raghavan, Neha S., Brickman, Adam M., Andrews, Howard, Manly, Jennifer J., Schupf, Nicole, Lantigua, Rafael, Wolock, Charles J., Kamalakaran, Sitharthan, Petrovski, Slave, Tosto, Giuseppe, Vardarajan, Badri N., Goldstein, David B., Mayeux, Richard
Publicado 2018

SORL1 mutations in early- and late-onset Alzheimer disease

por Cuccaro, Michael L., Carney, Regina M., Zhang, Yalun, Bohm, Christopher, Kunkle, Brian W., Vardarajan, Badri N., Whitehead, Patrice L., Cukier, Holly N., Mayeux, Richard, St. George-Hyslop, Peter, Pericak-Vance, Margaret A.
Publicado 2016

Admixture Mapping of Alzheimer’s disease in Caribbean Hispanics identifies a new locus on 22q13.1

por Kizil, Caghan, Sariya, Sanjeev, Kim, Yoon A., Rajabli, Farid, Martin, Eden, Reyes-Dumeyer, Dolly, Vardarajan, Badri, Maldonado, Aleyda, Haines, Jonathan L., Mayeux, Richard, Jiménez-Velázquez, Ivonne Z., Santa-Maria, Ismael, Tosto, Giuseppe
Publicado 2022

Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer’s Diseases Sequencing Project Subjects

por Lee, Wan-Ping, Wang, Hui, Dombroski, Beth, Cheng, Po-Liang, Tucci, Albert, Si, Ya-qin, Farrell, John, Tzeng, Jung-Ying, Leung, Yuk Yee, Malamon, John, Wang, Li-San, Vardarajan, Badri, Farrer, Lindsay, Schellenberg, Gerard
Publicado 2023

Episodic memory performance in a multi-ethnic longitudinal study of 13,037 elderly

por Lee, Seonjoo, Zhou, Xingtao, Gao, Yizhe, Vardarajan, Badri, Reyes-Dumeyer, Dolly, Rajan, Kumar B., Wilson, Robert S., Evans, Denis A., Besser, Lilah M., Kukull, Walter A., Bennett, David A., Brickman, Adam M., Schupf, Nicole, Mayeux, Richard, Barral, Sandra
Publicado 2018

Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer’s Diseases Sequencing Project Subjects

por Wang, Hui, Dombroski, Beth A, Cheng, Po-Liang, Tucci, Albert, Si, Ya-Qin, Farrell, John J, Tzeng, Jung-Ying, Leung, Yuk Yee, Malamon, John S, Wang, Li-San, Vardarajan, Badri N, Farrer, Lindsay A, Schellenberg, Gerard D, Lee, Wan-Ping
Publicado 2023

Rare coding mutations identified by sequencing of Alzheimer disease genome‐wide association studies loci

por Vardarajan, Badri N., Ghani, Mahdi, Kahn, Amanda, Sheikh, Stephanie, Sato, Christine, Barral, Sandra, Lee, Joseph H., Cheng, Rong, Reitz, Christiane, Lantigua, Rafael, Reyes‐Dumeyer, Dolly, Medrano, Martin, Jimenez‐Velazquez, Ivonne Z., Rogaeva, Ekaterina, St George‐Hyslop, Peter, Mayeux, Richard
Publicado 2015

The National Institute on Aging Late‐Onset Alzheimer's Disease Family Based Study: A resource for genetic discovery

por Reyes‐Dumeyer, Dolly, Faber, Kelley, Vardarajan, Badri, Goate, Alison, Renton, Alan, Chao, Michael, Boeve, Brad, Cruchaga, Carlos, Pericak‐Vance, Margaret, Haines, Jonathan L., Rosenberg, Roger, Tsuang, Debby, Sweet, Robert A., Bennett, David A., Wilson, Robert S., Foroud, Tatiana, Mayeux, Richard
Publicado 2022

Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease

por Vardarajan, Badri N., Tosto, Giuseppe, Lefort, Roger, Yu, Lei, Bennett, David A., De Jager, Philip L., Barral, Sandra, Reyes-Dumeyer, Dolly, Nagy, Peter L., Lee, Joseph H., Cheng, Rong, Medrano, Martin, Lantigua, Rafael, Rogaeva, Ekaterina, St George-Hyslop, Peter, Mayeux, Richard
Publicado 2017