Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations von Rajabli, Farid, Feliciano, Briseida E, Celis, Katrina, Hamilton-Nelson, Kara L, Whitehead, Patrice L, Adams, Larry D, Bussies, Parker L, Manrique, Clara P, Rodriguez, Alejandra, Rodriguez, Vanessa, Starks, Takiyah, Byfield, Grace E, Sierra Lopez, Carolina B, McCauley, Jacob L, Acosta, Heriberto, Chinea, Angel, Kunkle, Brian W, Reitz, Christiane, Farrer, Lindsay A, Schellenberg, Gerard D, Vardarajan, Badri N, Vance, Jeffery M, Cuccaro, Michael L, Martin, Eden R, Haines, Jonathan L, Byrd, Goldie S, Beecham, Gary W, Pericak-Vance, Margaret A

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia von 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

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Recurrent tissue-specific mtDNA mutations are common in humans von Samuels, David C, Li, Chun, Li, Bingshan, Song, Zhuo, Torstenson, Eric, Boyd Clay, Hayley, Rokas, Antonis, Thornton-Wells, Tricia A, Moore, Jason H, Hughes, Tia M, Hoffman, Robert D, Haines, Jonathan L, Murdock, Deborah G, Mortlock, Douglas P, Williams, Scott M

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The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future von Gottesman, Omri, Kuivaniemi, Helena, Tromp, Gerard, Faucett, W. Andrew, Li, Rongling, Manolio, Teri A., Sanderson, Saskia C., Kannry, Joseph, Zinberg, Randi, Basford, Melissa A., Brilliant, Murray, Carey, David J., Chisholm, Rex L., Chute, Christopher G., Connolly, John J., Crosslin, David, Denny, Joshua C., Gallego, Carlos J., Haines, Jonathan L., Hakonarson, Hakon, Harley, John, Jarvik, Gail P., Kohane, Isaac, Kullo, Iftikhar J., Larson, Eric B., McCarty, Catherine, Ritchie, Marylyn D., Roden, Dan M., Smith, Maureen E., Böttinger, Erwin P., Williams, Marc S.

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Finding the missing heritability of complex diseases von Haines, Jonathan L, Guttmacher, Alan E, Ramos, Erin M, Eichler, Evan E, Valle, David, McCarthy, Mark I, Slatkin, Montgomery, Kruglyak, Leonid, Cardon, Lon R, Cho, Judy H, Gibson, Greg, Mackay, Trudy F. C, Clark, Andrew G, Whittemore, Alice S, Chakravarti, Aravinda, Goldstein, David B, Mardis, Elaine, Cox, Nancy J, Kong, Augustine, Boehnke, Michael, Collins, Francis S, Hindorff, Lucia A, Hunter, David J, Visscher, Peter M, Manolio, Teri A, Rotimi, Charles N, McCarroll, Steven A

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Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1 von Zheng, Wei, Li, Chun, Fair, Alecia Malin, Lu, Wei, Levy, Shawn, Wen, Wanqing, Long, Jirong, Zheng, Ying, Deming, Sandra L, Cai, Qiuyin, Xiang, Yong-Bin, Shu, Xiao-Ou, Gao, Yu-Tang, Haines, Jonathan L, Gu, Kai

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Meta-analysis of genome scans and replication identify CD6 , IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci von Baranzini, Sergio E, McCauley, Jacob L, Oksenberg, Jorge R, Jia, Xiaoming, Matthews, Paul M, Naeglin, Yvonne, Romano, Susan, Hauser, Stephen L, Hafler, David A, Briskin, Rebeccah, Pericak-Vance, Margaret A, Aggarwal, Neelum T, Wang, Joanne, Ottoboni, Linda, Daly, Mark J, Tran, Dong, Raychaudhuri, Soumya, Sawcer, Stephen J, Piccio, Laura, Strachan, David P, Kappos, Ludwig, Evans, Denis, Weiner, Howard L, Haines, Jonathan L, Compston, Alastair, Polman, Chris, Uitdehaag, Bernard, Gibson, Rachel A, de Bakker, Paul I W, Aubin, Cristin, Cross, Anne H, De Jager, Philip L, McArdle, Wendy L

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One for all and all for One: Improving replication of genetic studies through network diffusion von Lancour, Daniel, Naj, Adam, Mayeux, Richard, Haines, Jonathan L, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Crovella, Mark, Farrer, Lindsay A, Kasif, Simon

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Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration von 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

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Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease von Beecham, Gary W., Martin, Eden R., Li, Yi-Ju, Slifer, Michael A., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.

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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record von Ritchie, Marylyn D., Denny, Joshua C., Crawford, Dana C., Ramirez, Andrea H., Weiner, Justin B., Pulley, Jill M., Basford, Melissa A., Brown-Gentry, Kristin, Balser, Jeffrey R., Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.

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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways von 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

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Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma von Kuchtey, John, Olson, Lana M, Rinkoski, Tommy, Mackay, Edward O, Iverson, T M, Gelatt, Kirk N, Haines, Jonathan L, Kuchtey, Rachel W

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Imputation and quality control steps for combining multiple genome-wide datasets von Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants von Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R, Boyle, Evan A, Martin, Beth K, Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo, Scherer, Martin, Farrer, Lindsay A, Haines, Jonathan L, Pericak-Vance, Margaret A, Raskind, Wendy H, Cruchaga, Carlos, Schellenberg, Gerard D, Joseph, Bertrand, Brkanac, Zoran

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Two novel loci, COBL and SLC10A2 , for Alzheimer's disease in African Americans von Mez, Jesse, Chung, Jaeyoon, Jun, Gyungah, Kriegel, Joshua, Bourlas, Alexandra P, Sherva, Richard, Logue, Mark W, Barnes, Lisa L, Bennett, David A, Buxbaum, Joseph D, Byrd, Goldie S, Crane, Paul K, Ertekin-Taner, Nilüfer, Evans, Denis, Fallin, M. Daniele, Foroud, Tatiana, Goate, Alison, Graff-Radford, Neill R, Hall, Kathleen S, Kamboh, M. Ilyas, Kukull, Walter A, Larson, Eric B, Manly, Jennifer J, Haines, Jonathan L, Mayeux, Richard, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Lunetta, Kathryn L, Farrer, Lindsay A

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Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration von Schmidt, Silke, Hauser, Michael A., Scott, William K., Postel, Eric A., Agarwal, Anita, Gallins, Paul, Wong, Frank, Chen, Yu Sarah, Spencer, Kylee, Schnetz-Boutaud, Nathalie, Haines, Jonathan L., Pericak-Vance, Margaret A.

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Correcting Away the Hidden Heritability von Williams, Scott M., Haines, Jonathan L.

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Genetics, statistics and human disease: analytical retooling for complexity von Thornton-Wells, Tricia A., Moore, Jason H., Haines, Jonathan L.

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Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities von Naj, Adam C, Beecham, Gary W, Martin, Eden R, Gallins, Paul J, Powell, Eric H, Konidari, Ioanna, Whitehead, Patrice L, Cai, Guiqing, Haroutunian, Vahram, Scott, William K, Vance, Jeffery M, Slifer, Michael A, Gwirtsman, Harry E, Gilbert, John R, Haines, Jonathan L, Buxbaum, Joseph D, Pericak-Vance, Margaret A

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