Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
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Published in Nature (London) (08.09.2011)
Published in Nature (London) (08.09.2011)
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Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations
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
Published in PLoS genetics (01.12.2018)
Published in PLoS genetics (01.12.2018)
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Finding the missing heritability of complex diseases
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
Published in Nature (London) (08.10.2009)
Published in Nature (London) (08.10.2009)
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The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
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.
Published in Genetics in medicine (01.10.2013)
Published in Genetics in medicine (01.10.2013)
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Recurrent tissue-specific mtDNA mutations are common in humans
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
Published in PLoS genetics (01.11.2013)
Published in PLoS genetics (01.11.2013)
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Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
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
Published in Nature genetics (01.03.2009)
Published in Nature genetics (01.03.2009)
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Meta-analysis of genome scans and replication identify CD6 , IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
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
Published in Nature genetics (01.07.2009)
Published in Nature genetics (01.07.2009)
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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)
Published in American journal of human genetics (09.01.2009)
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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record
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.
Published in American journal of human genetics (09.04.2010)
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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)
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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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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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Imputation and quality control steps for combining multiple genome-wide datasets
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
Published in Frontiers in genetics (11.12.2014)
Published in Frontiers in genetics (11.12.2014)
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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
Kuchtey, John, Olson, Lana M, Rinkoski, Tommy, Mackay, Edward O, Iverson, T M, Gelatt, Kirk N, Haines, Jonathan L, Kuchtey, Rachel W
Published in PLoS genetics (01.02.2011)
Published in PLoS genetics (01.02.2011)
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Two novel loci, COBL and SLC10A2 , for Alzheimer's disease in African Americans
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
Published in Alzheimer's & dementia (01.02.2017)
Published in Alzheimer's & dementia (01.02.2017)
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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants
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
Published in PloS one (06.10.2017)
Published in PloS one (06.10.2017)
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Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites
Tong, Tong, Zhu, Congcong, Farrell, John J, Khurshid, Zainab, Martin, Eden R, Pericak-Vance, Margaret A, Wang, Li-San, Bush, William S, Schellenberg, Gerard D, Haines, Jonathan L, Qiu, Wei Qiao, Lunetta, Kathryn L, Farrer, Lindsay A, Zhang, Xiaoling
Published in Alzheimer's research & therapy (23.10.2024)
Published in Alzheimer's research & therapy (23.10.2024)
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Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer’s disease carrying an ABCA7 deletion (p.Arg578Alafs)
Cukier, Holly N., Simon, Shaina A., Tang, Eugene, Golightly, Charles G., Laverde-Paz, Mayra Juliana, Adams, Larry Deon, Starks, Takiyah D., Vance, Jeffery M., Cuccaro, Michael L., Haines, Jonathan L., Byrd, Goldie S., Pericak-Vance, Margaret A., Dykxhoorn, Derek M.
Published in Stem cell research (01.04.2024)
Published in Stem cell research (01.04.2024)
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Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration
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.
Published in American journal of human genetics (01.05.2006)
Published in American journal of human genetics (01.05.2006)
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