Rational design of materials with extreme negative compressibility: selective soft-mode frustration in KMn[Ag(CN)2]3 by Cairns, A, Thompson, A, Tucker, M, Haines, J, Goodwin, A

Rational design of materials with extreme negative compressibility: selective soft-mode frustration in KMn[Ag(CN)2]3. by Cairns, AB, Thompson, A, Tucker, MG, Haines, J, Goodwin, A

DNA linkage analysis of X chromosome-linked chronic granulomatous disease. by Baehner, R, Kunkel, L, Monaco, A, Haines, J, Conneally, P, Palmer, C, Heerema, N, Orkin, S

Flexibility windows and compression of monoclinic and orthorhombic silicalites by Sartbaeva, A, Haines, J, Cambon, O, Santoro, M, Gorelli, F, Levelut, C, Garbarino, G, Wells, SA

Vibrational and Thermal Properties of Ag-3[Co(CN)(6)] from FirstPrinciples Calculations and Infrared Spectroscopy by Hermet, P, Catafesta, J, Bantignies, J, Levelut, C, Maurin, D, Cairns, AB, Goodwin, A, Haines, J

Five quantitative trait loci control radiation-induced adenoma multiplicity in Mom1R Apc Min/+ mice. by Elahi, E, Suraweera, N, Volikos, E, Haines, J, Brown, N, Davidson, G, Churchman, M, Ilyas, M, Tomlinson, I, Silver, A

Five quantitative trait loci control radiation-induced adenoma multiplicity in Mom 1R ApcMin/+ mice by Elahi, E, Suraweera, N, Volikos, E, Haines, J, Brown, N, Davidson, G, Churchman, M, Ilyas, M, Tomlinson, I, Silver, A

Giant negative linear compressibility in zinc dicyanoaurate by Cairns, A, Catafesta, J, Levelut, C, Rouquette, J, van der Lee, A, Peters, L, Thompson, A, Dmitriev, V, Haines, J, Goodwin, A

Giant negative linear compressibility in zinc dicyanoaurate. by Cairns, AB, Catafesta, J, Levelut, C, Rouquette, J, van der Lee, A, Peters, L, Thompson, A, Dmitriev, V, Haines, J, Goodwin, A

Giant negative linear compressibility in zinc dicyanoaurate by Cairns, AB, Catafesta, J, Levelut, C, Rouquette, J, van der Lee, A, Peters, L, Thompson, A, Dmitriev, V, Haines, J, Goodwin, A

Homologous critical behavior in the molecular frameworks Zn(CN)(2) and Cd(imidazolate)(2) by Collings, I, Cairns, A, Thompson, A, Parker, J, Tang, C, Tucker, M, Catafesta, J, Levelut, C, Haines, J, Dmitriev, V, Pattison, P, Goodwin, A

Homologous critical behavior in the molecular frameworks Zn(CN)2 and Cd(imidazolate)2. by Collings, I, Cairns, AB, Thompson, A, Parker, J, Tang, C, Tucker, MG, Catafesta, J, Levelut, C, Haines, J, Dmitriev, V, Pattison, P, Goodwin, A

Genetic determinants modulate susceptibility to pregnancy-associated tumourigenesis in a recombinant line of Min mice. by Suraweera, N, Haines, J, McCart, A, Rogers, P, Latchford, A, Coster, M, Polanco-Echeverry, G, Guenther, T, Wang, J, Sieber, O, Tomlinson, I, Silver, A

Effect of extra-framework cations on negative linear compressibility and high-pressure phase transitions: A study of KCd[Ag(CN)2]3 by Cairns, AB, Catafesta, J, Hermet, P, Rouquette, J, Levelut, C, Maurin, D, van der Lee, A, Dmitriev, V, Bantignies, J-L, Goodwin, AL, Haines, J

Genetic basis of variation in adenoma multiplicity in ApcMin/+ Mom1S mice. by Haines, J, Johnson, V, Pack, K, Suraweera, N, Slijepcevic, P, Cabuy, E, Coster, M, Ilyas, M, Wilding, J, Sieber, O, Bodmer, W, Tomlinson, I, Silver, A

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease by Zhang, X, Zhu, C, Beecham, G, Vardarajan, B, Ma, Y, Lancour, D, Farrell, J, Chung, J, Project, A, Mayeux, R, Haines, J, Schellenberg, G, Pericak-Vance, M, Lunetta, K, Farrer, L

A meta-analysis of genomic screens in multiple sclerosis. The Transatlantic Multiple Sclerosis Genetics Cooperative. by Pericak-Vance, M, Rimmler, J, Saunders, A, Martin, E, Haines, J, Garcia, M, Oksenberg, JR, Barcellos, L, Lincoln, R, Goodkin, D, Hauser, S, Compston, D, Sawcer, S, Clayton, D, Jones, H, Walker, N, Goodfellow, P, Bulman, D, Sadovnick, D, Ebers, G, Dyment, D, Willer, C, Risch, N, Transatlantic, MSG

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers. by Burwick, R, Ramsay, P, Haines, J, Hauser, S, Oksenberg, JR, Pericak-Vance, M, Schmidt, S, Compston, A, Sawcer, S, Cittadella, R, Savettieri, G, Quattrone, A, Polman, C, Uitdehaag, B, Zwemmer, J, Hawkins, C, Ollier, W, Weatherby, S, Enzinger, C, Fazekas, F, Schmidt, H, Schmidt, R, Hillert, J, Masterman, T, Hogh, P

Finding the missing heritability of complex diseases. by Manolio, T, Collins, F, Cox, N, Goldstein, D, Hindorff, L, Hunter, D, McCarthy, M, Ramos, E, Cardon, L, Chakravarti, A, Cho, J, Guttmacher, A, Kong, A, Kruglyak, L, Mardis, E, Rotimi, C, Slatkin, M, Valle, D, Whittemore, A, Boehnke, M, Clark, A, Eichler, E, Gibson, G, Haines, J, Mackay, T

Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease by Gusareva, E, Twizere, J, Sleegers, K, Dourlen, P, Abisambra, J, Meier, S, Cloyd, R, Weiss, B, Dermaut, B, Bessonov, K, Van Der Lee, S, Carrasquillo, M, Katsumata, Y, Cherkaoui, M, Asselbergh, B, Ikram, M, Mayeux, R, Farrer, L, Haines, J, Pericak-Vance, M, Schellenberg, G, Genetic And Environmental Risk In Alzheimer'S Disease 1 Consortium (GERAD1), Alzheimer'S Disease Genetics Consortium (ADGC), European Alzheimer Disease Initiative Investigators (EADI1 Consortium), Sims, R, Williams, J, Amouyel, P, Van Duijn, C, Ertekin-Taner, N, Van Broeckhoven, C, Dequiedt, F, Fardo, D, Lambert, J, Van Steen, K