Site-specific Cu clustering and precipitation in laser powder-bed fusion 17–4 PH stainless steel von Haines, MP, Moyle, MS, Rielli, VV, Haghdadi, N, Primig, S

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Powder bed fusion additive manufacturing of Ni-based superalloys: a review of the main microstructural constituents and characterization techniques von Haines, MP, Rielli, VV, Primig, S, Haghdadi, N

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Grain Structure Evolution in Fe-6Si During Directed Energy Deposition von Plotkowski, A, Coleman, J, Fancher, CM, Haines, MP, Whetten, SR, Kustas, AB

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Effect of compositional variations on the heat treatment response in 17-4 PH stainless steel fabricated by laser powder bed fusion von Moyle, MS, Haghdadi, N, Theska, F, Haines, MP, Liao, XZ, Ringer, SP, Primig, S

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Experimental and computational analysis of site-specific formation of phases in laser powder bed fusion 17–4 precipitate hardened stainless steel von Haines, MP, Moyle, MS, Rielli, VV, Luzin, V, Haghdadi, N, Primig, S

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Role of scan strategies and heat treatment on grain structure evolution in Fe-Si soft magnetic alloys made by laser-powder bed fusion von Haines, MP, List, F., Carver, K., Leonard, DN, Plotkowski, A., Fancher, CM, Dehoff, RR, Babu, SS

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Site-specific Cu clustering and precipitation in laser powder-bed fusion 17–4 PH stainless steel von Haines, MP, Moyle, MS, Rielli, VV, Haghdadi, N, Primig, S, Vieira Rielli, Vitor

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Effect of compositional variations on the heat treatment response in 17-4 PH stainless steel fabricated by laser powder bed fusion von Moyle, MS, Haghdadi, N, Theska, F, Haines, MP, Liao, XZ, Ringer, SP, Primig, S

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Genome-wide association study of brain arteriolosclerosis von Shade, Lincoln MP, Katsumata, Yuriko, Hohman, Timothy J, Nho, Kwangsik, Saykin, Andrew J, Mukherjee, Shubhabrata, Boehme, Kevin L, Kauwe, John SK, Farrer, Lindsay A, Schellenberg, Gerard D, Haines, Jonathan L, Mayeux, Richard P, Schneider, Julie A, Nelson, Peter T, Fardo, David W

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Parkin mutations and susceptibility alleles in late-onset Parkinson's disease von Oliveira, Sofia A., Scott, William K., Martin, Eden R., Nance, Martha A., Watts, Ray L., Hubble, Jean P., Koller, William C., Pahwa, Rajesh, Stern, Matthew B., Hiner, Bradley C., Ondo, William G., Allen Jr, Fred H., Scott, Burton L., Goetz, Christopher G., Small, Gary W., Mastaglia, Frank, Stajich, Jeffrey M., Zhang, Fengyu, Booze, Michael W., Winn, Michelle P., Middleton, Lefkos T., Haines, Jonathan L., Pericak-Vance, Margaret A., Vance, Jeffery M.

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Bucindolol Decreases Atrial Fibrillation Burden in Patients With Heart Failure and the ADRB1 Arg389Arg Genotype von Piccini, Jonathan P., Dufton, Christopher, Carroll, Ian A., Healey, Jeff S., Abraham, William T., Khaykin, Yaariv, Aleong, Ryan, Krueger, Steven K., Sauer, William H., Wilton, Stephen B., Rienstra, Michiel, van Veldhuisen, Dirk J., Anand, Inder S., White, Michel, Camm, A. John, Ziegler, Paul D., Marshall, Debra, Bristow, Michael R., Connolly, Stuart J.

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Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34 von van Slegtenhorst, Marjon, de Hoogt, Ronald, Hermans, Caroline, Nellist, Mark, Janssen, Bart, Verhoef, Senno, Lindhout, Dick, Van den Ouweland, Ans, Halley, Dicky, Young, Janet, Burley, Mariwyn, Jeremiah, Steve, Woodward, Karen, Nahmias, Joseph, Fox, Margaret, Ekong, Rosemary, Osborne, John, Wolfe, Jonathan, Povey, Sue, Snell, Russell G., Cheadle, Jeremy P., Jones, Alistair C., Tachataki, Maria, Ravine, Dave, Sampson, Julian R., Reeve, Mary Pat, Richardson, Paul, Wilmer, Frierderike, Munro, Cheryl, Hawkins, Trevor L., Sepp, Tiina, Johari B. M. Ali, Ward, Susannah, Green, Andrew J., John R. W. Yates, Kwiatkowska, Jolanta, Elizabeth P. H enske, Short, M. Priscilla, Haines, Jonathan H., Jozwiak, Sergiusz, Kwiatkowski, David J.

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease von Sherrington, R, Rogaev, E I, Liang, Y, Rogaeva, E A, Levesque, G, Ikeda, M, Chi, H, Lin, C, Li, G, Holman, K, Tsuda, T, Mar, L, Foncin, J F, Bruni, A C, Montesi, M P, Sorbi, S, Rainero, I, Pinessi, L, Nee, L, Chumakov, I, Pollen, D, Brookes, A, Sanseau, P, Polinsky, R J, Wasco, W, Da Silva, H A, Haines, J L, Perkicak-Vance, M A, Tanzi, R E, Roses, A D, Fraser, P E, Rommens, J M, St George-Hyslop, P H

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease von Kandt, R. S, Haines, J. L, Smith, M, Northrup, H, Gardner, R. J. M, Short, M. P, Dumars, K, Roach, E. S, Steingold, S, Wall, S, Blanton, S. H, Flodman, P, Kwiatkowski, D. J, Jewell, A, Weber, J. L, Roses, A. D, Pericak-Vance, M. A

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Plasma insulin and cardiovascular mortality in non-diabetic European men and women: a meta-analysis of data from eleven prospective studies von Hu G, Qiao, Q, Tuomilehto, J, Eliasson, M, Feskens, E J, Pyorala, K, DECODE Insulin Study Group

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Hereditary Spastic Paraplegia: Advances in Genetic Research von Fink, J K, Heiman-Patterson, T, Bird, T, Cambi, F, Dube, M.-P, Figlewicz, D A, Fink, J K, Haines, J L, Hentati, A, Pericak-Vance, M A, Raskind, W, Rouleau, G A, Siddique, T

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Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene von FONTAINE, B, KHURANA, T. S, ROMANO, D, GUSELLA, J. F, BROWN, R. H, HOFFMAN, E. P, BRUNS, G. A. P, HAINES, J. L, TROFATTER, J. A, HANSON, M. P, RICH, J, MCFARLANE, H, YASEK, D. M

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High Incidence of Potential p53 Inactivation in Poor Outcome Childhood Acute Lymphoblastic Leukemia at Diagnosis von Marks, David I., Kurz, Benedikt W., Link, Michael P., Ng, Eliza, Shuster, Jonathan J., Lauer, Stephen J., Brodsky, Isadore, Haines, Dale S.

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Altered expression of p53 and mdm-2 proteins at diagnosis is associated with early treatment failure in childhood acute lymphoblastic leukemia von MARKS, D. I, KURZ, B. W, LINK, M. P, NG, E, SHUSTER, J. J, LAUER, S. J, CARROLL, D, BRODSKY, I, HAINES, D. S

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Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients von WILSON, P. J, VIJAYA RAMESH, KRISTIANSEN, A, BOVE, C, JOZWIAK, S, KWIATKOWSKI, D. J, SHORT, M. P, HAINES, J. L

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