Genetic analysis of complex diseases / by Haines, Jonathan L., 1957-, Pericak-Vance, Margaret Ann

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures by Sutcliffe James S, Abou-Khalil Bassel, Ma Shaochun, Haines Jonathan L, Hedera Peter

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Examination of <it>NRCAM</it>, <it>LRRN3</it>, KIAA0716, and <it>LAMB1 </it>as autism candidate genes by Santangelo Susan L, Folstein Susan E, Bradford Yuki, Olson Lana M, Hutcheson Holli B, Sutcliffe James S, Haines Jonathan L

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A comparative analysis of the information content in long and short SAGE libraries by Haines Jonathan L, Hulette Christine M, Schmechel Donald E, Qin Xuejun, Xu Puting, Li Yi-Ju, Pericak-Vance Margaret A, Gilbert John R

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates by Folstein Susan E, Gainer Kimberly, Crockett Genea, Olson Lana M, Jiang Lan, Li Chun, McCauley Jacob L, Haines Jonathan L, Sutcliffe James S

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Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish by Vance Jeffery M, Jackson Charles E, Welsh-Bohmer Kathleen A, Scott William K, Jiang Lan, Hahs Daniel W, McCauley Jacob L, Pericak-Vance Margaret A, Haines Jonathan L

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DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity by Miller Joan W, del Bono Elizabeth, Kim Ivana, DeAngelis Margaret M, Chen Teresa, Rhee Douglas, Grosskreutz Cynthia L, Pasquale Louis, Fan Bao, Li Tiansen, Haines Jonathan L, Wiggs Janey L

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Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12 by Weeks Daniel E, Gilbert John R, De La Paz Monica A, Hauser Elizabeth R, Agarwal Anita, Postel Eric A, Scott William K, Schmidt Silke, Gorin Michael B, Haines Jonathan L, Pericak-Vance Margaret A

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An X chromosome-wide association study in autism families identifies <it>TBL1X </it>as a novel autism spectrum disorder candidate gene in males by Chung Ren-Hua, Ma Deqiong, Wang Kai, Hedges Dale J, Jaworski James M, Gilbert John R, Cuccaro Michael L, Wright Harry H, Abramson Ruth K, Konidari Ioanna, Whitehead Patrice L, Schellenberg Gerard D, Hakonarson Hakon, Haines Jonathan L, Pericak-Vance Margaret A, Martin Eden R

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Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer’s disease by Posthuma, Danielle, Andreassen, Ole A., Karch, Celeste M., Desikan, Rahul S., Broce, Iris J., Tan, Chin Hong, Fan, Chun Chieh, Jansen, Iris, Savage, Jeanne E., Witoelar, Aree, Wen, Natalie, Hess, Christopher P., Dillon, William P., Glastonbury, Christine M., Glymour, Maria, Yokoyama, Jennifer S., Elahi, Fanny M., Rabinovici, Gil D., Miller, Bruce L., Mormino, Elizabeth C., Sperling, Reisa A., Bennett, David A., McEvoy, Linda K., Brewer, James B., Feldman, Howard H., Hyman, Bradley T., Pericak-Vance, Margaret, Haines, Jonathan L., Farrer, Lindsay A., Mayeux, Richard, Schellenberg, Gerard D., Yaffe, Kristine, Sugrue, Leo P., Dale, Anders M.

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The role of the CD[subscript 5]8 locus in multiple sclerosis by De Jager, Philip L., Baecher-Allan, Clare, Maier, Lisa M., Arthur, Ariel T., Ottoboni, Linda, Barcellos, Lisa F., McCauley, Jacob L., Sawcer, Stephen, Goris, An, Saarela, Janna, Yelensky, Roman, Price, Alkes, Leppa, Virpi, Patterson, Nick, de Bakker, Paul I. W., Tran, Dong, Aubin, Cristin, Pobywajlo, Susan, Rossin, Elizabeth, Hu, Xinli, Ashley, Charles W., Choy, Edwin, Rioux, John D., Pericak-Vance, Margaret A., Ivinson, Adrian, Booth, David R., Stewart, Graeme J., Palotie, Aarno, Peltonen, Leena, Dubois, Benedicte, Haines, Jonathan L., Weiner, Howard L., Compston, Alastair, Hauser, Stephen L., Daly, Mark J., Reich, David, Oksenberg, Jorge R., Hafler, David A.

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