A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25 von Bailey-Wilson, J.E., Amos, C.I., Pinney, S.M., Petersen, G.M., de Andrade, M., Wiest, J.S., Fain, P., Schwartz, A.G., You, M., Franklin, W., Klein, C., Gazdar, A., Rothschild, H., Mandal, D., Coons, T., Slusser, J., Lee, J., Gaba, C., Kupert, E., Perez, A., Zhou, X., Zeng, D., Liu, Q., Zhang, Q., Seminara, D., Minna, J., Anderson, M.W.

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Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease von Bilbao, J R, Calvo, B, Aransay, A M, Martin-Pagola, A, Perez de Nanclares, G, Aly, T A, Rica, I, Vitoria, J C, Gaztambide, S, Noble, J, Fain, P R, Awdeh, Z L, Alper, C A, Castaño, L

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X-Linked Syndrome of Polyendocrinopathy, Immune Dysfunction, and Diarrhea Maps to Xp11.23-Xq13.3 von Bennett, Craig L., Yoshioka, Ritsuko, Kiyosawa, Hidenori, Barker, David F., Fain, Pamela R., Shigeoka, Ann O., Chance, Phillip F.

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Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5 von Wang, Jen C., Cruchaga, Carlos, Saccone, Nancy L., Bertelsen, Sarah, Liu, Pengyuan, Budde, John P., Duan, Weimin, Fox, Louis, Grucza, Richard A., Kern, Jason, Mayo, Kevin, Reyes, Oliver, Rice, John, Saccone, Scott F., Spiegel, Noah, Steinbach, Joseph H., Stitzel, Jerry A., Anderson, Marshall W., You, Ming, Stevens, Victoria L., Bierut, Laura J., Goate, Alison M.

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A Genomewide Screen for Generalized Vitiligo: Confirmation of AIS1 on Chromosome 1p31 and Evidence for Additional Susceptibility Loci von Fain, Pamela R., Gowan, Katherine, LaBerge, Greggory S., Alkhateeb, Asem, Stetler, Gary L., Talbert, Janet, Bennett, Dorothy C., Spritz, Richard A.

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Children with early-onset inflammatory bowel disease (IBD): Analysis of a pediatric IBD consortium registry von Heyman, Melvin B., Kirschner, Barbara S., Gold, Benjamin D., Ferry, George, Baldassano, Robert, Cohen, Stanley A., Winter, Harland S., Fain, Patricia, King, Chris, Smith, Terry, El-Serag, Hashem B.

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Differential effects of DRB10301 and DQA10501-DQB10201 on the activation and progression of islet cell autoimmunity von Eller, E, Vardi, P, McFann, K K, Babu, S R, Yu, L, Bugawan, T L, Erlich, H A, Eisenbarth, G S, Fain, P R

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Influence of a Family History of Cancer Within and Across Multiple Sites on Patterns of Cancer Mortality Risk for Women von Poole, Carol A., Byers, Tim, Calle, Eugenia E., Bondy, Jessica, Fain, Pam, Rodriguez, Carmen

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A mutation causing alport syndrome with tardive hearing loss is common in the Western United States von BARKER, D. F, PRUCHNO, C. J, JIANG, X, ATKIN, C. L, STONE, E. M, DENISON, J. C, FAIN, P. R, GREGORY, M. C

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Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia von CAMBI, F, TANG, X.-M, CORDRAY, P, FAIN, P. R, KEPPEN, L. D, BARKER, D. F

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NALP1 in Vitiligo-Associated Multiple Autoimmune Disease von Jin, Ying, Mailloux, Christina M, Gowan, Katherine, Riccardi, Sheri L, LaBerge, Greggory, Bennett, Dorothy C, Fain, Pamela R, Spritz, Richard A

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Gene for Von Recklinghausen Neurofibromatosis is in the Pericentromeric Region of Chromosome 17 von Barker, D., Wright, E., Nguyen, K., Cannon, L., Fain, P., Goldgar, D., Bishop, D. T., Carey, J., Baty, B., Kivlin, J., Willard, H., Waye, J. S., Greig, G., Leinwand, L., Nakamura, Y., O'Connell, P., Leppert, M., J.-M. Lalouel, White, R., Skolnick, M.

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SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia von MCNAIR, William P, KU, Lisa, TAYLOR, Matthew R. G, FAIN, Pam R, DAO, Dmi, WOLFEL, Eugene, MESTRONI, Luisa

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Paternal origin of new mutations in Von Recklinghausen neurofibromatosis von Jadayel, D, Fain, P, Upadhyaya, M, Ponder, M. A, Huson, S. M, Carey, J, Fryer, A, Mathew, C. G. P, Barker, D. F, Ponder, B. A. J

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A High Resolution CEPH Crossover Mapping Panel and Integrated Map of Chromosome 11 von Fain, Pamela R., Kort, Edward N., Yousry, Cherine, James, Michael R., Litt, Michael

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Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family von Verge, C F, Vardi, P, Babu, S, Bao, F, Erlich, H A, Bugawan, T, Tiosano, D, Yu, L, Eisenbarth, G S, Fain, P R

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Processing and microstructural characterization of sputter-deposited Ni/Ni3Al multilayered thin films von Sperling, Evan A., Banerjee, Rajarshi, Thompson, Gregory B., Fain, Jason P., Anderson, Peter M., Fraser, Hamish L.

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Influence of crystallographic orientation and layer thickness on fracture behavior of Ni/Ni3Al multilayered thin films von BANERJEE, Rajarshi, FAIN, Jason P, ANDERSON, Peter M, FRASER, Hamish L

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A 2D crossover-based map of the human X chromosome as a model for map integration von Chance, Phillip F, Nguyen, Kim, Econs, Michael J, Kort, Edward N, Redd, Douglas F, Fain, Pamela R, Barker, David F

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Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22 von Barker, D.F., CIeverly, J., Fain, P.R.

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