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Published in Annals of neurology (01.09.2021)
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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
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The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
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Published in Autism research (01.12.2012)
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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
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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)
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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)
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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)
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Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease
Beecham, Gary W., Martin, Eden R., Li, Yi-Ju, Slifer, Michael A., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.
Published in American journal of human genetics (09.01.2009)
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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)
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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)
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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)
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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
GRISWOLD, Anthony J, DEQIONG MA, WRIGHT, Harry H, ABRAMSON, Ruth K, WILLIAMS, Scott M, MENON, Ramkumar, MARTIN, Eden R, HAINES, Jonathan L, GILBERT, John R, CUCCARO, Michael L, PERICAK-VANCE, Margaret A, CUKIER, Holly N, NATIONS, Laura D, SCHMIDT, Mike A, CHUNG, Ren-Hua, JAWORSKI, James M, SALYAKINA, Daria, KONIDARI, Loanna, WHITEHEAD, Patrice L
Published in Human molecular genetics (01.08.2012)
Published in Human molecular genetics (01.08.2012)
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Leveraging African American family connectors for Alzheimer's disease genomic studies
Byfield, Grace, Starks, Takiyah D., Luther, Ronqeiya, Edwards, Christopher L., Lloyd, Shawnta L., Caban‐Holt, Allison, Adams, Larry Deon, Vance, Jeffery M., Cuccaro, Michael, Haines, Jonathan L., Reitz, Christiane, Pericak‐Vance, Margaret A., Byrd, Goldie S.
Published in Alzheimer's & dementia (01.12.2023)
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Vitamin D from different sources is inversely associated with Parkinson disease
Wang, Liyong, Evatt, Marian L., Maldonado, Lizmarie G., Perry, William R., Ritchie, James C., Beecham, Gary W., Martin, Eden R., Haines, Jonathan L., Pericak-Vance, Margaret A., Vance, Jeffery M., Scott, William K.
Published in Movement disorders (01.04.2015)
Published in Movement disorders (01.04.2015)
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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
Vance, Jeffery M, Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael
Published in Nature genetics (01.05.2004)
Published in Nature genetics (01.05.2004)
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Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans
Logue, Mark W, Schu, Matthew, Vardarajan, Badri N, Farrell, John, Bennett, David A, Buxbaum, Joseph D, Byrd, Goldie S, Ertekin-Taner, Nilufer, Evans, Denis, Foroud, Tatiana, Goate, Alison, Graff-Radford, Neill R, Kamboh, M. Ilyas, Kukull, Walter A, Manly, Jennifer J
Published in Alzheimer's & dementia (01.11.2014)
Published in Alzheimer's & dementia (01.11.2014)
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PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation
Jun, Gyungah, Asai, Hirohide, Zeldich, Ella, Drapeau, Elodie, Chen, CiDi, Chung, Jaeyoon, Park, Jong-Ho, Kim, Sehwa, Haroutunian, Vahram, Foroud, Tatiana, Kuwano, Ryozo, Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Lunetta, Kathryn L., Kim, Jong-Won, Buxbaum, Joseph D., Mayeux, Richard, Ikezu, Tsuneya, Abraham, Carmela R., Farrer, Lindsay A.
Published in Annals of neurology (01.09.2014)
Published in Annals of neurology (01.09.2014)
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Independent Effects of Complement Factor H Y402H Polymorphism and Cigarette Smoking on Risk of Age-Related Macular Degeneration
Scott, William K., PhD, Schmidt, Silke, PhD, Hauser, Michael A., PhD, Gallins, Paul, MS, Schnetz-Boutaud, Nathalie, PhD, Spencer, Kylee L., BA, Gilbert, John R., PhD, Agarwal, Anita, MD, Postel, Eric A., MD, Haines, Jonathan L., PhD, Pericak-Vance, Margaret A., PhD
Published in Ophthalmology (Rochester, Minn.) (01.06.2007)
Published in Ophthalmology (Rochester, Minn.) (01.06.2007)
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