Psychological changes in parents eight months after the loss of an infant from stillbirth, neonatal death, or sudden infant death syndrome : a longitudinal study von VANCE, J. C, NAJMAN, J. M, THEARLE, M. J, EMBELTON, G, FOSTER, W. J, BOYLE, F. M

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Demodex folliculorum and Demodex brevis in cutaneous biopsies von Aylesworth, Robert, Vance, J. Corwin

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A novel role for surfactant in the lung with implications for the sudden infant death syndrome von Hills, B.A., Masters, I.B., Vance, J.C.

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PFOS dominates PFAS composition in ambient fine particulate matter (PM) collected across North Carolina nearly 20 years after the end of its US production von Zhou, J, Baumann, K, Mead, R. N, Skrabal, S. A, Kieber, R. J, Avery, G. B, Shimizu, M, DeWitt, J. C, Sun, M, Vance, S. A, Bodnar, W, Zhang, Z, Collins, L. B, Surratt, J. D, Turpin, B. J

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Review: Modelling the pathology and behaviour of frontotemporal dementia von Solomon, D. A., Mitchell, J.C., Salcher‐Konrad, M.‐T., Vance, C.A., Mizielinska, S.

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Methicillin-Susceptible Staphylococcus aureus Endocarditis Isolates Are Associated With Clonal Complex 30 Genotype and a Distinct Repertoire of Enterotoxins and Adhesins von Nienaber, Juhsien J. C., Kuinkel, Batu K. Sharma, Clarke-Pearson, Michael, Lamlertthon, Supaporn, Park, Lawrence, Rude, Thomas H., Barriere, Steve, Woods, Christopher W., Chu, Vivian H., Marín, Mercedes, Bukovski, Suzana, Garcia, Patricia, Corey, G.Ralph, Korman, Tony, Doco-Lecompte, Thanh, Murdoch, David R., Reller, L. Barth, Fowler, Vance G.

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Plant viral synergism: the potyviral genome encodes a broad-range pathogenicity enhancer that transactivates replication of heterologous viruses von Pruss, G. (University of South Carolina, Columbia.), Ge, X, Shi, X.M, Carrington, J.C, Vance, V.B

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The Alzheimer's Disease Sequencing Project: Study design and sample selection von 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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Introduced trout sever trophic connections in watersheds: consequences for a declining amphibian von Finlay, J.C, Vredenburg, V.T

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Mutations in the Region Encoding the Central Domain of Helper Component-Proteinase (HC-Pro) Eliminate Potato Virus X/Potyviral Synergism von Shi, Xing Ming, Miller, Heather, Verchot, Jeanmarie, Carrington, James C., Vance, Vicki Bowman

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5′ Proximal potyviral sequences mediate potato virus X/potyviral synergistic disease in transgenic tobacco von Bowman Vance, Vicki, Berger, Philip H., Carrington, James C., Hunt, Arthur G., Ming Shi, Xing

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Longitudinal Effects of Classwide Peer Tutoring von Greenwood, Charles R, Delquadri, Joseph C, Hall, R. Vance

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Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene von Seizinger, B.R., Rouleau, G.A., Ozelius, L.J., Lane, A.H., Faryniarz, A.G., Chao, M.V., Huson, S., Korf, B.R., Parry, D.M., Pericak-Vance, M.A., Collins, F.S., Hobbs, W.J., Falcone, B.G., Iannazzi, J.A., Roy, J.C., St George-Hyslop, P.H., Tanzi, R.E., Bothwell, M.A., Upadhyaya, M., Harper, P., Goldstein, A.E., Hoover, D.L., Bader, J.L., Spence, M.A., Mulvihill, J.J., Aylsworth, A.S., Vance, J.M., Rossenwasser, G.O.D., Gaskell, P.C., Roses, A.D., Martuza, R.L., Breakefield, X.O., Gusella, J.F.

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Presenilin-1 polymorphism and Alzheimer's disease von Scott, WilliamK, Roses, AllenD, Haines, JonathanL, Pericak-Vance, MargaretA, Pérez-Tur, J., Wavrant-De Vrieze, F., Lambert, J.C., Chartier-Harlin, M-C., the Alzheimer's Study Group

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Harmonizing across environmental nanomaterial testing media for increased comparability of nanomaterial datasets von Geitner, N.K., Ogilvie Hendren, C., Cornelis, G., Kaegi, R., Lead, J.R., Lowry, G.V., Lynch, I., Nowack, B., Petersen, E., Bernhardt, E., Brown, S., Chen, W., Garidel-Thoron, C. de, Hanson, J., Harper, S., Jones, K., Kammer, F. von der, Kennedy, A., Kidd, J., Matson, C., Metcalfe, C.D., Pedersen, J., Peijnenburg, W.J.G.M., Quik, J.T.K., Rodrigues, S.M., Rose, J., Sayre, P., Simonin, M., Svendsen, C., Tanguay, R., Tefenkji, N., Teunenbroek, T. van, Thies, G., Tian, Y., Rice, J., Turner, A., Liu, J., Unrine, J., Vance, M., White, J.C., Wiesner, M.R.

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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene von Nicolas, A., Kenna, K.P., Chia, R., Dominov, J.A., Kenna, B.J., Nalls, M.A., Keagle, P., Rheenen, W. van, Murphy, N.A., Pliner, H.A., Topp, S.D., Mora, G., Calvo, A., Mazzini, L., Riva, N., Mandrioli, J., Bella, V. la, Conforti, F.L., Borghero, G., Salvi, F., Corrado, L., Ferrucci, L., Kamalakaran, S., Musunuri, R.L., Abhyankar, A., Eyk, J.E. van, Berry, J.D., Miller, T.M., Baxi, E., Taylor, J.P., Rampersaud, E., Wu, G., Verde, F., Fogh, I., Tiloca, C., Soraru, G., Cereda, C., Myllykangas, L., Jansson, L., Ealing, J., Rollinson, S., Pickering-Brown, S., Sidle, K.C., Asress, S., Al-Sarraj, S., King, A., Belleroche, J. de, Baas, F., Hernandez, D.G., Ding, J.H., Floeter, M.K., Landi, F., Bowser, R., Ravits, J.M., MacGowan, D.J.L., Kirby, J., Pamphlett, R., Broach, J., Gerhard, G., Brady, C.B., Lumbroso, S., Heiman-Patterson, T.D., Kamel, F., Baloh, R.H., Strom, T.M., Meitinger, T., Eijk, K.R. van, Moisse, M., McLaughlin, R.L., Es, M.A. van, Weber, M., Boylan, K.B., Mora, J.S., Shaw, P.J., Turner, M.R., Talbot, K., Hardiman, O., Nicholson, G.A., Blair, I.P., Rouleau, G.A., Esteban-Perez, J., Garcia-Redondo, A., Zinman, L., Ostrow, L.W., Simmons, Z., Ratti, A., Fratta, P., Sabatelli, M., Lunetta, C., Weishaupt, J.H., Camu, W., Brown, R.H., Berg, L.H. van den, Veldink, J.H., Glass, J.D., Silani, V., Chio, A., Shaw, C.E., Traynor, B.J., Landers, J.E.

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis von Smith, B.N, Topp, S.D, Fallini, C, Shibata, H, Chen, H.J, Troakes, C, King, A, Ticozzi, N, Kenna, K.P, Soragia-Gkazi, A, Miller, J.W, Sato, A, Dias, D.M, Jeon, M, Vance, C, Wong, C.H, de Majo, M, Kattuah, W, Mitchell, J.C, Scotter, E.L, Parkin, N.W, Sapp, P.C, Nolan, M, Nestor, P.J, Simpson, M, Weale, M, Lek, M, Baas, F, Vianney de Jong, J.M, ten Asbroek, A.L.M.A, Redondo, A.G, Esteban-Pérez, J, Tiloca, C, Verde, F, Duga, S, Leigh, N, Pall, H, Morrison, K.E, Al-Chalabi, A, Shaw, P.J, Kirby, J, Turner, M.R, Talbot, K, Hardiman, O, Glass, J.D, De Belleroche, J, Maki, M, Moss, S.E, Miller, C, Gellera, C, Ratti, A, Al-Sarraj, S, Brown, R.H, Silani, V, Landers, J.E, Shaw, C.E

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Supplementary Material for: Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer’s Disease Sequencing Project von Blue, E.E., Bis, J.C., Dorschner, M.O., Tsuang, D.W., Barral, S.M., Beecham, G., Below, J.E., Bush, W.S., Butkiewicz, M., Cruchaga, C., DeStefano, A., Farrer, L.A., Goate, A., Haines, J., Jaworski, J., Jun, G., Kunkle, B., Kuzma, A., Lee, J.J., Lunetta, K.L., Ma, Y., Martin, E., Naj, A., Nato, A.Q., Navas, P., Nguyen, H., Reitz, C., Reyes, D., Salerno, W., Schellenberg, G.D., Seshadri, S., Sohi, H., Thornton, T.A., Valadares, O., Van Duijn, C., Vardarajan, B.N., Wang, L.-S., Boerwinkle, E., Dupuis, J., Pericak-Vance, M.A., Mayeux, R., Wijsman, E.M., Project, On Behalf Of The Alzheimer’s Disease Sequencing

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Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17 von Seizinger, B.R., Rouleau, G.A., Lane, A.H., Farmer, G., Ozelius, L.J., Haines, J.L., Parry, D.M., Korf, B.R., Pericak-Vance, M.A., Faryniarz, A.G., Hobbs, W.J., Iannazzi, J.A., Roy, J.C., Menon, A., Bader, J.L., Spence, M.A., Chao, M.V., Mulvihill, J.J., Roses, A.D., Martuza, R.L., Breakefield, X.O., Conneally, P.M., Gusella, J.F.

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CHANGES IN CANINE MYOCARDIAL BLOOD FLOW AND OXYGEN CONSUMPTION IN RESPONSE TO HALOTHANE von SMITH, G., MCMILLAN, J.C., VANCE, J.P., BROWN, D.M.

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