Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S, Allen, Mariet, Crook, Julia, Pankratz, V Shane, Carrasquillo, Minerva M, Rowley, Christopher N, Nair, Asha A, Middha, Sumit, Maharjan, Sooraj, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G, Palusak, Ryan, Lincoln, Sarah, Bisceglio, Gina, Georgescu, Constantin, Kouri, Naomi, Kolbert, Christopher P, Jen, Jin, Haines, Jonathan L, Mayeux, Richard, Pericak-Vance, Margaret A, Farrer, Lindsay A, Schellenberg, Gerard D, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer
Published in PLoS genetics (01.06.2012)
Published in PLoS genetics (01.06.2012)
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Novel Loci for Alzheimer Disease Identified by Genome Wide Association Study in Ashkenazi Jews
Li, Donghe, Farrell, John, Mez, Jesse B., Martin, Eden R., Bush, William S., Mayeux, Richard, Haines, Jonathan L., Pericak‐Vance, Margaret A., Wang, Li‐San, Schellenberg, Gerard D., Lunetta, Kathryn L., Farrer, Lindsay A.
Published in Alzheimer's & dementia (01.12.2022)
Published in Alzheimer's & dementia (01.12.2022)
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A large‐scale genome‐wide association study of early‐onset Alzheimer disease
Neupane, Achal, da Fonseca, Eder Lucio, Kurup, Jiji Thulaseedhara, Pericak‐Vance, Margaret A., Martin, Eden R., Schellenberg, Gerard D., Reitz, Christiane, Beecham, Gary W., Cruchaga, Carlos, Fernandez, Victoria
Published in Alzheimer's & dementia (01.12.2022)
Published in Alzheimer's & dementia (01.12.2022)
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Consequences of a Rare Complement Factor H Variant for Age-Related Macular Degeneration in the Amish
Waksmunski, Andrea R, Miskimen, Kristy, Song, Yeunjoo E, Grunin, Michelle, Laux, Renee, Fuzzell, Denise, Fuzzell, Sarada, Adams, Larry D, Caywood, Laura, Prough, Michael, Stambolian, Dwight, Scott, William K, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in Investigative ophthalmology & visual science (05.08.2022)
Published in Investigative ophthalmology & visual science (05.08.2022)
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Evidence for Polygenic Susceptibility to Multiple Sclerosis—The Shape of Things to Come
Bush, William S, Sawcer, Stephen J, de Jager, Philip L, Oksenberg, Jorge R, McCauley, Jacob L, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in American journal of human genetics (09.04.2010)
Published in American journal of human genetics (09.04.2010)
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Longitudinal Evaluation of the Distribution of Intraretinal Hyper-Reflective Foci in Eyes with Intermediate Age-Related Macular Degeneration
Verma, Aditya, Nittala, Muneeswar G, Corradetti, Giulia, Nassisi, Marco, Velaga, Swetha B, He, Ye, Haines, Jonathan L, Pericak-Vance, Margaret A, Stambolian, Dwight, Sadda, SriniVas R
Published in Current eye research (19.04.2024)
Published in Current eye research (19.04.2024)
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Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Kozol, Robert A, Cukier, Holly N, Zou, Bing, Mayo, Vera, De Rubeis, Silvia, Cai, Guiqing, Griswold, Anthony J, Whitehead, Patrice L, Haines, Jonathan L, Gilbert, John R, Cuccaro, Michael L, Martin, Eden R, Baker, James D, Buxbaum, Joseph D, Pericak-Vance, Margaret A, Dallman, Julia E
Published in Human molecular genetics (15.07.2015)
Published in Human molecular genetics (15.07.2015)
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An Alzheimer’s disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Cukier, Holly N., Duarte, Carolina L., Laverde-Paz, Mayra J., Simon, Shaina A., Van Booven, Derek J., Miyares, Amanda T., Whitehead, Patrice L., Hamilton-Nelson, Kara L., Adams, Larry D., Carney, Regina M., Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A., Griswold, Anthony J., Dykxhoorn, Derek M.
Published in Neurobiology of aging (01.11.2023)
Published in Neurobiology of aging (01.11.2023)
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Reproducibility of qualitative assessment of drusen volume in eyes with age related macular degeneration
Corvi, Federico, Srinivas, Sowmya, Nittala, Muneeswar Gupta, Corradetti, Giulia, Velaga, Swetha B., Stambolian, Dwight, Haines, Jonathan, Pericak-Vance, Margaret A., Sadda, SriniVas R.
Published in Eye (London) (01.09.2021)
Published in Eye (London) (01.09.2021)
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A Genome‐Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6
Cummings, Anna C., Lee, Stephen L., McCauley, Jacob L., Jiang, Lan, Crunk, Amy, McFarland, Lynne L., Gallins, Paul J., Fuzzell, Denise, Knebusch, Clare, Jackson, Charles E., Scott, William K., Pericak‐Vance, Margaret A., Haines, Jonathan L.
Published in Annals of human genetics (01.05.2011)
Published in Annals of human genetics (01.05.2011)
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Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease
Liang, Xueying, Martin, Eden R, Schnetz-Boutaud, Nathalie, Bartlett, Jackie, Anderson, Brent, Züchner, Stephan, Gwirtsman, Harry, Schmechel, Don, Carney, Regina, Gilbert, John R, Pericak-Vance, Margaret A, Haines, Jonathan L
Published in Human mutation (01.11.2007)
Published in Human mutation (01.11.2007)
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A genome-wide linkage analysis of dementia in the Amish
Hahs, Daniel W., McCauley, Jacob L., Crunk, Amy E., McFarland, Lynne L., Gaskell, Perry C., Jiang, Lan, Slifer, Susan H., Vance, Jeffery M., Scott, William K., Welsh-Bohmer, Kathleen A., Johnson, Stephanie R., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2006)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2006)
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An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns
Jin, Bowen, Capra, John A, Benchek, Penelope, Wheeler, Nicholas, Naj, Adam C, Hamilton-Nelson, Kara L, Farrell, John J, Leung, Yuk Yee, Kunkle, Brian, Vadarajan, Badri, Schellenberg, Gerard D, Mayeux, Richard, Wang, Li-San, Farrer, Lindsay A, Pericak-Vance, Margaret A, Martin, Eden R, Haines, Jonathan L, Crawford, Dana C, Bush, William S
Published in Genome research (01.04.2022)
Published in Genome research (01.04.2022)
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Novel loci for Alzheimer's disease identified by a genome‐wide association study in Ashkenazi Jews
Li, Donghe, Farrell, John J., Mez, Jesse, Martin, Eden R., Bush, William S., Ruiz, Agustin, Boada, Mercè, Rojas, Itziar, Mayeux, Richard, Haines, Jonathan L., Vance, Margaret A. Pericak, Wang, Li‐San, Schellenberg, Gerard D., Lunetta, Kathryn L., Farrer, Lindsay A.
Published in Alzheimer's & dementia (01.12.2023)
Published in Alzheimer's & dementia (01.12.2023)
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African Ancestry Individuals with Higher Educational Attainment Are Resilient to Alzheimer’s Disease Measured by pTau181
Rajabli, Farid, Seixas, Azizi A., Akgun, Bilcag, Adams, Larry D., Inciute, Jovita, Hamilton, Kara L., Whithead, Patrice G., Konidari, Ioanna, Gu, Tianjie, Arvizu, Jamie, Golightly, Charles G., Starks, Takiyah D., Laux, Renee, Byrd, Goldie S., Haines, Jonathan L., Beecham, Gary W., Griswold, Anthony J., Vance, Jeffery M., Cuccaro, Michael L., Pericak-Vance, Margaret A.
Published in Journal of Alzheimer's disease (05.03.2024)
Published in Journal of Alzheimer's disease (05.03.2024)
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Outreach and recruitment of African Americans for Alzheimer’s disease studies during the COVID‐19 pandemic
Starks, Takiyah D, Caban‐Holt, Allison M, Williams, Kelvin, Adams, Larry D, Haines, Johnathan L, Beecham, Gary W, Reitz, Christiane, Cuccaro, Michael L, Vance, Jeffery M, Pericak‐Vance, Margaret A, Byrd, Goldie S
Published in Alzheimer's & dementia (01.12.2021)
Published in Alzheimer's & dementia (01.12.2021)
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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport
Kunkle, Brian W, Vardarajan, Badri N, Naj, Adam C, Whitehead, Patrice L, Rolati, Sophie, Slifer, Susan, Carney, Regina M, Cuccaro, Michael L, Vance, Jeffery M, Gilbert, John R, Wang, Li-San, Farrer, Lindsay A, Reitz, Christiane, Haines, Jonathan L, Beecham, Gary W, Martin, Eden R, Schellenberg, Gerard D, Mayeux, Richard P, Pericak-Vance, Margaret A
Published in JAMA neurology (01.09.2017)
Published in JAMA neurology (01.09.2017)
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Genetic architecture of RNA editing regulation in Alzheimer’s disease across diverse ancestral populations
Gardner, Olivia K, Van Booven, Derek, Wang, Lily, Gu, Tianjie, Hofmann, Natalia K, Whitehead, Patrice L, Nuytemans, Karen, Hamilton-Nelson, Kara L, Adams, Larry D, Starks, Takiyah D, Cuccaro, Michael L, Martin, Eden R, Vance, Jeffery M, Bush, William S, Byrd, Goldie S, Haines, Jonathan L, Beecham, Gary W, Pericak-Vance, Margaret A, Griswold, Anthony J
Published in Human molecular genetics (25.08.2022)
Published in Human molecular genetics (25.08.2022)
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Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
Winn, Michelle P, Conlon, Peter J, Lynn, Kelvin L, Farrington, Merry Kay, Creazzo, Tony, Hawkins, April F, Daskalakis, Nikki, Kwan, Shu Ying, Ebersviller, Seth, Burchette, James L, Pericak-Vance, Margaret A, Howell, David N, Vance, Jeffery M, Rosenberg, Paul B
Published in Science (American Association for the Advancement of Science) (17.06.2005)
Published in Science (American Association for the Advancement of Science) (17.06.2005)
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Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
Cukier, Holly N, Dueker, Nicole D, Slifer, Susan H, Lee, Joycelyn M, Whitehead, Patrice L, Lalanne, Eminisha, Leyva, Natalia, Konidari, Ioanna, Gentry, Ryan C, Hulme, William F, Booven, Derek Van, Mayo, Vera, Hofmann, Natalia K, Schmidt, Michael A, Martin, Eden R, Haines, Jonathan L, Cuccaro, Michael L, Gilbert, John R, Pericak-Vance, Margaret A
Published in Molecular autism (10.01.2014)
Published in Molecular autism (10.01.2014)
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