Evidence for an important role of perilipin in the regulation of human adipocyte lipolysis von MOTTAGUI-TABAR, S, RYDEN, M, LÖFGREN, P, FAULDS, G, HOFFSTEDT, J, BROOKES, A. J, ANDERSSON, I, ARNER, P

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Validation, Deployment, and Real-World Implementation of a Modular Toolbox for Alzheimer’s Disease Detection and Dementia Risk Reduction: The AD-RIDDLE Project von Malzbender, K., Barbarino, P., Ferrell, P. Barkman, Bradshaw, A., Brookes, A. J., Díaz, C., van der Flier, W. M., Georges, J., Hansson, O., Hartmanis, M., Jönsson, L., Krishnan, R., MacLeod, T., Mangialasche, F., Mecocci, P., Minguillon, C., Middleton, L., Pla, S., Sardi, S. P., Schöll, M., Suárez-Calvet, M., Weidner, W., Visser, P. J., Zetterberg, H., Bose, N., Solomon, A., Kivipelto, Miia

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Targeted enrichment of genomic DNA regions for next-generation sequencing von Mertes, Florian, ElSharawy, Abdou, Sauer, Sascha, van Helvoort, Joop M.L.M., van der Zaag, P.J., Franke, Andre, Nilsson, Mats, Lehrach, Hans, Brookes, Anthony J.

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The essence of SNPs von Brookes, Anthony J.

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HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources von Fredman, D, Siegfried, M, Yuan, Y P, Bork, P, Lehväslaiho, H, Brookes, A J

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HGBASE: a database of SNPs and other variations in and around human genes von Brookes, A J, Lehväslaiho, H, Siegfried, M, Boehm, J G, Yuan, Y P, Sarkar, C M, Bork, P, Ortigao, F

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Dynamic contrast enhanced MRI of the axilla in women with breast cancer: comparison with pathology of excised nodes von MURRAY, A. D, STAFF, R. T, REDPATH, T. W, GILBERT, F. J, AH-SEE, A. K, BROOKES, J. A, MILLER, I. D, PAYNE, S

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HGVbase: a curated resource describing human DNA variation and phenotype relationships von Fredman, D., Munns, G., Rios, D., Sjöholm, F., Siegfried, M., Lenhard, B., Lehväslaiho, H., Brookes, A. J.

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Toward a roadmap in global biobanking for health von HARRIS, Jennifer R, BURTON, Paul, FORTIER, Isabel, HAINAUT, Pierre, HEWITT, Robert, KAYE, Jane, LITTON, Jan-Eric, METSPALU, Andres, OLLIER, Bill, PALMER, Lyle J, PALOTIE, Aarno, PASTERK, Markus, KNOPPERS, Bartha Maria, PEROLA, Markus, RIEGMAN, Peter Hj, OMMEN, Gert-Janvan, YUILLE, Martin, ZATLOUKAL, Kurt, LINDPAINTNER, Klaus, BLEDSOE, Marianna, BROOKES, Anthony J, BUDIN-LJØSNE, Isabelle, CHISHOLM, Rex, COX, David, DESCHENES, Mylène

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Improving data and knowledge management to better integrate health care and research von Cases, M., Furlong, L. I., Albanell, J., Altman, R. B., Bellazzi, R., Boyer, S., Brand, A., Brookes, A. J., Brunak, S., Clark, T. W., Gea, J., Ghazal, P., Graf, N., Guigó, R., Klein, T. E., López‐Bigas, N., Maojo, V., Mons, B., Musen, M., Oliveira, J. L., Rowe, A., Ruch, P., Shabo, A., Shortliffe, E. H., Valencia, A., Lei, J., Mayer, M. A., Sanz, F.

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A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans von Alcocer-Varela, Jorge, Castillejo-López, Casimiro, Sturfelt, Gunnar, Gunnarsson, Iva, Alarcón-Riquelme, Marta E, Bolstad, Anne Isine, Svenungsson, Elisabet, Lundberg, Ingrid, Prokunina, Ludmila, Kristjansdóttir, Helga, Gröndal, Gerdur, Harley, John B, Lima, Guadalupe, Berg, Louise, Truedsson, Lennart, Tentler, Dmitry, Jönssen, Andreas, Jonsson, Roland, Magnusson, Veronica, Steinsson, Kristján, Öberg, Fredrik, Brookes, Anthony J, Gyllensten, Ulf B, Alarcón-Segovia, Donato

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DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applications von Fredman, David, Jobs, M., Strömqvist, L., Brookes, A.J.

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No association between the α2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression von BLENNOW, K, RICKSTEN, A, NÄGGA, K, WALLIN, A, REGLAND, B, OLOFSSON, H, HESSE, C, DAVIDSSON, P, MINTHON, L, JANSSON, A, PALMQVIST, L, RYMO, L, PRINCE, J. A, BROOKES, A. J, EMAHAZION, T, WASSLAVIK, C, BOGDANOVIC, N, ANDREASEN, N, BATSMAN, S, MARCUSSON, J

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Recommendations for locus-specific databases and their curation von Cotton, R.G.H, Auerbach, A.D, Beckmann, J.S, Blumenfeld, O.O, Brookes, A.J, Brown, A.F, Carrera, P, Cox, D.W, Gottlieb, B, Greenblatt, M.S, Hilbert, P, Lehvaslaiho, H, Liang, P, Marsh, S, Nebert, D.W, Povey, S, Rossetti, S, Scriver, C.R, Summar, M, Tolan, D.R, Verma, I.C, Vihinen, M, den Dunnen, J.T

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Presenilin-I, presenilin-II, and VLDL-R associations in early onset Alzheimer's disease von Brookes, Anthony J, Howell, W Mathias, Woodburn, Kirsty, Johnstone, Eve C, Carothers, Andrew

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Dynamic allele-specific hybridization. A new method for scoring single nucleotide polymorphisms von Howell, W M, Jobs, M, Gyllensten, U, Brookes, A J

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HGBASE – a unified human SNP database von Brookes, A.J.

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Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to β-amyloid metabolism von Katzov, Hagit, Chalmers, Katy, Palmgren, Juni, Andreasen, Niels, Johansson, Boo, Cairns, Nigel J., Gatz, Margaret, Wilcock, Gordon K., Love, Seth, Pedersen, Nancy L., Brookes, Anthony J., Blennow, Kaj, Kehoe, Patrick G., Prince, Jonathan A.

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Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation von Prince, J A, Feuk, L, Howell, W M, Jobs, M, Emahazion, T, Blennow, K, Brookes, A J

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DNA, diseases and databases: disastrously deficient von Patrinos, George P., Brookes, Anthony J.

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