DNA from multiple viral species is associated with Alzheimer's disease risk
Tejeda, Marlene, Farrell, John, Zhu, Congcong, Wetzler, Lee, Lunetta, Kathryn L., Bush, William S., Martin, Eden R., Wang, Li‐San, Schellenberg, Gerard D., Pericak‐Vance, Margaret A., Haines, Jonathan L., Farrer, Lindsay A., Sherva, Richard
Published in Alzheimer's & dementia (01.01.2024)
Published in Alzheimer's & dementia (01.01.2024)
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One for all and all for One: Improving replication of genetic studies through network diffusion
Lancour, Daniel, Naj, Adam, Mayeux, Richard, Haines, Jonathan L, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Crovella, Mark, Farrer, Lindsay A, Kasif, Simon
Published in PLoS genetics (23.04.2018)
Published in PLoS genetics (23.04.2018)
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Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease
Archer, Derek B., Eissman, Jaclyn M., Mukherjee, Shubhabrata, Lee, Michael L., Choi, Seo‐Eun, Scollard, Phoebe, Trittschuh, Emily H., Mez, Jesse B., Bush, William S., Kunkle, Brian W., Naj, Adam C., Gifford, Katherine A., Cuccaro, Michael L., Pericak‐Vance, Margaret A., Farrer, Lindsay A., Wang, Li‐San, Schellenberg, Gerard D., Mayeux, Richard P., Haines, Jonathan L., Jefferson, Angela L., Kukull, Walter A., Keene, C. Dirk, Saykin, Andrew J., Thompson, Paul M., Martin, Eden R., Bennett, David A., Barnes, Lisa L., Schneider, Julie A., Crane, Paul K., Dumitrescu, Logan, Hohman, Timothy J.
Published in Alzheimer's & dementia (01.02.2024)
Published in Alzheimer's & dementia (01.02.2024)
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Sex‐specific genetic architecture of late‐life memory performance
Eissman, Jaclyn M., Archer, Derek B., Mukherjee, Shubhabrata, Lee, Michael L., Choi, Seo‐Eun, Scollard, Phoebe, Trittschuh, Emily H., Mez, Jesse B., Bush, William S., Kunkle, Brian W., Naj, Adam C., Gifford, Katherine A., Cuccaro, Michael L., Cruchaga, Carlos, Pericak‐Vance, Margaret A., Farrer, Lindsay A., Wang, Li‐San, Schellenberg, Gerard D., Mayeux, Richard P., Haines, Jonathan L., Jefferson, Angela L., Kukull, Walter A., Keene, C. Dirk, Saykin, Andrew J., Thompson, Paul M., Martin, Eden R., Bennett, David A., Barnes, Lisa L., Schneider, Julie A., Crane, Paul K., Hohman, Timothy J., Dumitrescu, Logan
Published in Alzheimer's & dementia (01.02.2024)
Published in Alzheimer's & dementia (01.02.2024)
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Factor Analysis of the Aberrant Behavior Checklist in Individuals with Autism Spectrum Disorders
Brinkley, Jason, Nations, Laura, Abramson, Ruth K, Hall, Alicia, Wright, Harry H, Gabriels, Robin, Gilbert, John R, Pericak-Vance, Margaret A. O, Cuccaro, Michael L
Published in Journal of autism and developmental disorders (01.11.2007)
Published in Journal of autism and developmental disorders (01.11.2007)
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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism
Hussman, John P, Chung, Ren-Hua, Griswold, Anthony J, Jaworski, James M, Salyakina, Daria, Ma, Deqiong, Konidari, Ioanna, Whitehead, Patrice L, Vance, Jeffery M, Martin, Eden R, Cuccaro, Michael L, Gilbert, John R, Haines, Jonathan L, Pericak-Vance, Margaret A
Published in Molecular autism (19.01.2011)
Published in Molecular autism (19.01.2011)
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Genomic convergence to identify candidate genes for Alzheimer Disease on chromosome 10
Liang, Xueying, Slifer, Michael, Martin, Eden R, Schnetz-Boutaud, Nathalie, Bartlett, Jackie, Anderson, Brent, Züchner, Stephan, Gwirtsman, Harry, Gilbert, John R, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in Human mutation (01.03.2009)
Published in Human mutation (01.03.2009)
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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Deng, Han-Xiang, Chen, Wenjie, Hong, Seong-Tshool, Boycott, Kym M., Gorrie, George H., Siddique, Nailah, Yang, Yi, Fecto, Faisal, Shi, Yong, Zhai, Hong, Jiang, Hujun, Hirano, Makito, Rampersaud, Evadnie, Jansen, Gerard H., Donkervoort, Sandra, Bigio, Eileen H., Brooks, Benjamin R., Ajroud, Kaouther, Sufit, Robert L., Haines, Jonathan L., Mugnaini, Enrico, Pericak-Vance, Margaret A., Siddique, Teepu
Published in Nature (London) (08.09.2011)
Published in Nature (London) (08.09.2011)
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Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration
Spencer, Kylee L, Olson, Lana M, Schnetz-Boutaud, Nathalie, Gallins, Paul, Agarwal, Anita, Iannaccone, Alessandro, Kritchevsky, Stephen B, Garcia, Melissa, Nalls, Michael A, Newman, Anne B, Scott, William K, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in PloS one (24.03.2011)
Published in PloS one (24.03.2011)
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Identification of TMEM230 mutations in familial Parkinson's disease
Deng, Han-Xiang, Shi, Yong, Yang, Yi, Ahmeti, Kreshnik B, Miller, Nimrod, Huang, Cao, Cheng, Lijun, Zhai, Hong, Deng, Sheng, Nuytemans, Karen, Corbett, Nicola J, Kim, Myung Jong, Deng, Hao, Tang, Beisha, Yang, Ziquang, Xu, Yanming, Chan, Piu, Huang, Bo, Gao, Xiao-Ping, Song, Zhi, Liu, Zhenhua, Fecto, Faisal, Siddique, Nailah, Foroud, Tatiana, Jankovic, Joseph, Ghetti, Bernardino, Nicholson, Daniel A, Krainc, Dimitri, Melen, Onur, Vance, Jeffery M, Pericak-Vance, Margaret A, Ma, Yong-Chao, Rajput, Ali H, Siddique, Teepu
Published in Nature genetics (01.07.2016)
Published in Nature genetics (01.07.2016)
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Neuropathological lesions and their contribution to dementia and cognitive impairment in a heterogeneous clinical population
Godrich, Dana, Martin, Eden R., Schellenberg, Gerard, Pericak‐Vance, Margaret A., Cuccaro, Michael, Scott, William K., Kukull, Walter, Montine, Thomas, Beecham, Gary W.
Published in Alzheimer's & dementia (01.12.2022)
Published in Alzheimer's & dementia (01.12.2022)
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KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers
Murdock, Deborah G, Bradford, Yuki, Schnetz-Boutaud, Nathalie, Mayo, Ping, Allen, Melissa J, D'Aoust, Laura N, Liang, Xueying, Mitchell, Sabrina L, Zuchner, Stephan, Small, Gary W, Gilbert, John R, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in PloS one (12.12.2013)
Published in PloS one (12.12.2013)
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Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons
DeRosa, Brooke A., El Hokayem, Jimmy, Artimovich, Elena, Garcia-Serje, Catherine, Phillips, Andre W., Van Booven, Derek, Nestor, Jonathan E., Wang, Lily, Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A., Cukier, Holly N., Nestor, Michael W., Dykxhoorn, Derek M.
Published in Scientific reports (30.05.2018)
Published in Scientific reports (30.05.2018)
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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Published in BMC medicine (22.10.2009)
Published in BMC medicine (22.10.2009)
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Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets
Nuytemans, Karen, Lipkin Vasquez, Marina, Wang, Liyong, Van Booven, Derek, Griswold, Antony J., Rajabli, Farid, Celis, Katrina, Oron, Oded, Hofmann, Natalia, Rolati, Sophie, Garcia‐Serje, Catherine, Zhang, Shanshan, Jin, Fulai, Argenziano, Mariana, Grant, Struan F.A., Chesi, Alessandra, Brown, Christopher D., Young, Juan I., Dykxhoorn, Derek M., Pericak‐Vance, Margaret A., Vance, Jeffery M.
Published in Alzheimer's & dementia (01.10.2022)
Published in Alzheimer's & dementia (01.10.2022)
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Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease
Zhang, Xiaoling, Farrell, John J., Tong, Tong, Hu, Junming, Zhu, Congcong, Wang, Li‐San, Mayeux, Richard, Haines, Jonathan L., Pericak‐Vance, Margaret A., Schellenberg, Gerard D., Lunetta, Kathryn L., Farrer, Lindsay A.
Published in Alzheimer's & dementia (01.02.2022)
Published in Alzheimer's & dementia (01.02.2022)
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Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration
Haines, Jonathan L, Hauser, Michael A, Schmidt, Silke, Scott, William K, Olson, Lana M, Gallins, Paul, Spencer, Kylee L, Kwan, Shu Ying, Noureddine, Maher, Gilbert, John R, Schnetz-Boutaud, Nathalie, Agarwal, Anita, Postel, Eric A, Pericak-Vance, Margaret A
Published in Science (American Association for the Advancement of Science) (15.04.2005)
Published in Science (American Association for the Advancement of Science) (15.04.2005)
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Genome‐wide association and multi‐omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women
Chung, Jaeyoon, Das, Anjali, Sun, Xinyu, Sobreira, Débora R., Leung, Yuk Yee, Igartua, Catherine, Mozaffari, Sahar, Chou, Yi‐Fan, Thiagalingam, Sam, Mez, Jesse, Zhang, Xiaoling, Jun, Gyungah R., Stein, Thor D., Kunkle, Brian W., Martin, Eden R., Pericak‐Vance, Margaret A., Mayeux, Richard, Haines, Jonathan L., Schellenberg, Gerard D., Nobrega, Marcelo A., Lunetta, Kathryn L., Pinto, Jayant M., Wang, Li‐San, Ober, Carole, Farrer, Lindsay A.
Published in Alzheimer's & dementia (01.03.2023)
Published in Alzheimer's & dementia (01.03.2023)
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Increased APOE ε4 expression is associated with the difference in Alzheimer's disease risk from diverse ancestral backgrounds
Griswold, Anthony J., Celis, Katrina, Bussies, Parker L., Rajabli, Farid, Whitehead, Patrice L., Hamilton‐Nelson, Kara L., Beecham, Gary W., Dykxhoorn, Derek M., Nuytemans, Karen, Wang, Liyong, Gardner, Olivia K., Dorfsman, Daniel A., Bigio, Eileen H., Mesulam, Marek Marsel, Weintraub, Sandra, Geula, Changiz, Gearing, Marla, McGrath‐Martinez, Elisa, Dalgard, Clifton L., Scott, William K., Haines, Jonathan L., Pericak‐Vance, Margaret A., Young, Juan I., Vance, Jeffery M.
Published in Alzheimer's & dementia (01.07.2021)
Published in Alzheimer's & dementia (01.07.2021)
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