Common Variants in the 5′ Region of the Leptin Gene Are Associated with Body Mass Index in Men from the National Heart, Lung, and Blood Institute Family Heart Study by Jiang, Y., Wilk, J.B., Borecki, I., Williamson, S., DeStefano, A.L., Xu, G., Liu, J., Ellison, R.C., Province, M., Myers, R.H.

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Lettuce and rhizosphere microbiome responses to growth promoting Pseudomonas species under field conditions by Cipriano, Matheus A. P., Lupatini, Manoeli, Lopes-Santos, Lucilene, da Silva, Márcio J., Roesch, Luiz F. W., Destéfano, Suzete A. L., Freitas, Sueli S., Kuramae, Eiko E.

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The Alzheimer's Disease Sequencing Project: Study design and sample selection by Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G

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Correlation between CAG repeat length and clinical features in Machado-Joseph disease by MACIEL, P, GASPAR, C, NEZARATI, M. M, CORWIN, L. I, LOPES-CENDES, I, ROOKE, K, ROSENBERG, R, MACLEOD, P, FARRER, L. A, SEQUEIROS, J, ROULEAU, G. A, DESTEFANO, A. L, SILVEIRA, I, COUTINHO, P, RADVANY, J, DAWSON, D. M, SUDARSKY, L, GUIMARAES, J, LOUREIRO, J. E. L

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Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study by Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint-Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.

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Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17 by Baima, Jader, Nicolaou, Michael, Schwartz, Faina, DeStefano, Anita L, Manolis, Athanasios, Gavras, Irene, Laffer, Cheryl, Elijovich, Fernando, Farrer, Lindsay, Baldwin, Clinton T, Gavras, Haralambos

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Evidence for a Gene Influencing Blood Pressure on Chromosome 17: Genome Scan Linkage Results for Longitudinal Blood Pressure Phenotypes in Subjects From the Framingham Heart Study by Levy, Daniel, DeStefano, Anita L, Larson, Martin G, O’Donnell, Christopher J, Lifton, Richard P, Gavras, Haralambos, Cupples, L Adrienne, Myers, Richard H

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Maternal component in the familial aggregation of hypertension by DeStefano, AL, Gavras, H, Heard-Costa, N, Bursztyn, M, Manolis, A, Farrer, LA, Baldwin, CT, Gavras, I, Schwartz, F

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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3 by BONNE-TAMIR, B, DESTEFANO, A. L, BRIGGS, C. E, ADAIR, R, FRANKLYN, B, WEISS, S, KOROSTISHEVSKY, M, FRYDMAN, M, BALDWIN, C. T, FARRER, L. A

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Genetic predisposition to stroke in relatives of hypertensives by NICOLAOU, M, DESTEFANO, A. L, GAVRAS, I, CUPPLES, L. A, MANOLIS, A. J, BALDWIN, C. T, GAVRAS, H, FARRER, L. A

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Autosomal Dominant Orthostatic Hypotensive Disorder Maps to Chromosome 18q by DeStefano, Anita L., Baldwin, Clinton T., Burzstyn, Michael, Gavras, Irene, Handy, Diane E., Joost, Oscar, Martel, Timothy, Nicolaou, Michael, Schwartz, Faina, Streeten, David H.P., Farrer, Lindsay A., Gavras, Haralambos

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Bacterial leaf spot of coffee caused by Pseudomonas syringae pv. tabaci in Brazil by Destéfano, S.A.L, Rodrigues, L.M.R, Beriam, L.O.S, Patrício, F.R.A, Thomaziello, R.A, Rodrigues‐Neto, J

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A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease by DESTEFANO, A. L, CUPPLES, L. A, SEQUEIROS, J, ROULEAU, G. A, FARRER, L. A, MACIEL, P, GASPAR, C, RADVANY, J, DAWSON, D. M, SUDARSKY, L, CORWIN, L, COUTINHO, P, MACLEOD, P

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Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations by DESTEFANO, A. L, CUPPLES, L. A, LALWANI, A. K, MILUNSKY, A, NANCE, W. E, PANDYA, A, RAMESAR, R. S, READ, A. P, TASSABEJHI, M, WILCOX, E. R, FARRER, L. A, ARNOS, K. S, ASHER, J. H, BALDWIN, C. T, BLANTON, S, CAREY, M. L, DA SILVA, E. O, FRIEDMAN, T. B, GREENBERG, J

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A novel Alzheimer disease locus located near the gene encoding tau protein by Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Tárraga, L, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Haines, J L, Psaty, B M, Van Broeckhoven, C, Holmans, P, Launer, L J, Mayeux, R, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation by Bis, Joshua C., Jian, Xueqiu, Kunkle, Brian W., Chen, Yuning, Hamilton-Nelson, Kara L., Bush, William S., Salerno, William J., Lancour, Daniel, Ma, Yiyi, Renton, Alan E., Marcora, Edoardo, Farrell, John J., Zhao, Yi, Qu, Liming, Ahmad, Shahzad, Amin, Najaf, Amouyel, Philippe, Beecham, Gary W., Below, Jennifer E., Campion, Dominique, Cantwell, Laura, Charbonnier, Camille, Chung, Jaeyoon, Crane, Paul K., Cruchaga, Carlos, Cupples, L. Adrienne, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Fulton, Lucinda, Gabriel, Stacey B., Genin, Emmanuelle, Gibbs, Richard A., Goate, Alison, Grenier-Boley, Benjamin, Gupta, Namrata, Haines, Jonathan L., Havulinna, Aki S., Helisalmi, Seppo, Hiltunen, Mikko, Howrigan, Daniel P., Ikram, M. Arfan, Kaprio, Jaakko, Konrad, Jan, Kuzma, Amanda, Lander, Eric S., Lathrop, Mark, Lehtimäki, Terho, Lin, Honghuang, Mattila, Kari, Mayeux, Richard, Muzny, Donna M., Nasser, Waleed, Neale, Benjamin, Nho, Kwangsik, Nicolas, Gaël, Patel, Devanshi, Pericak-Vance, Margaret A., Perola, Markus, Psaty, Bruce M., Quenez, Olivier, Rajabli, Farid, Redon, Richard, Reitz, Christiane, Remes, Anne M., Salomaa, Veikko, Sarnowski, Chloe, Schmidt, Helena, Schmidt, Michael, Schmidt, Reinhold, Soininen, Hilkka, Thornton, Timothy A., Tosto, Giuseppe, Tzourio, Christophe, van der Lee, Sven J., van Duijn, Cornelia M., Valladares, Otto, Vardarajan, Badri, Wang, Li-San, Wang, Weixin, Wijsman, Ellen, Wilson, Richard K., Witten, Daniela, Worley, Kim C., Zhang, Xiaoling, Bellenguez, Celine, Lambert, Jean-Charles, Kurki, Mitja I., Palotie, Aarno, Daly, Mark, Boerwinkle, Eric, Lunetta, Kathryn L., Destefano, Anita L., Dupuis, Josée, Martin, Eden R., Schellenberg, Gerard D., Seshadri, Sudha, Naj, Adam C., Fornage, Myriam, Farrer, Lindsay A.

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Utilization of Dominance Variance Through Mate Allocation Strategies by DeStefano, A.L., Hoeschele, I.

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Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study by Shearman, A M, Ordovas, J M, Cupples, L A, Schaefer, E J, Harmon, M D, Shao, Y, Keen, J D, DeStefano, A L, Joost, O, Wilson, P W, Housman, D E, Myers, R H

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Family‐Based Association Tests for Qualitative and Quantitative Traits Using Single‐Nucleotide Polymorphism and Microsatellite Data by Wilk, Jemma B., Volcjak, Jeannine S., Myers, Richard H., Maher, Nancy E., Knowlton, Beth A., Heard-Costa, Nancy L., Demissie, Serkalem, Cupples, L. Adrienne, DeStefano, Anita L.

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Linkage disequilibrium analysis in Machado-Joseph disease patients of different ethnic origins by GASPAR, C, LOPES-CENDES, I, DESTEFANO, A. L, MACIEL, P, SILVEIRA, I, COUTINHO, P, MACLEOD, P, SEQUEIROS, J, FARRER, L. A, ROULEAU, G. A

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