The multiphase and magnetized neutral hydrogen seen by LOFAR von Bracco, A., Jelic, Marchal, A., Turic, L., Erceg, A., Miville-Deschenes, M-A, Bellomi, E.

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Associating LOFAR Galactic Faraday structures with the warm neutral medium von Boulanger, F., Gry, C., Jenkins, E. B., Bracco, A., Erceg, A., Jelić, V., Turić, L.

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Associating LOFAR Galactic Faraday structures with the warm neutral medium von Boulanger, F, Gry, C, Jenkins, E B, Bracco, A, Erceg, A, Jelić, V, Turić, L

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First look at the multiphase interstellar medium with synthetic observations of low-frequency Faraday tomography von Bracco, A, Ntormousi, E, Jelić, V, Padovani, M, Šiljeg, B, Erceg, A, Turić, L, Ceraj, L, Šnidarić, I

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LOFAR deep fields: probing faint galactic polarised emission in ELAIS-N1 von Šnidarić, I., Jelić, V., Mevius, M., Brentjens, M., Erceg, A., Shimwell, T.W., Piras, S., Horellou, C., Sabater, J., Best, P.N., Bracco, A., Ceraj, L., Haverkorn, M., O'Sullivan, S.P., Turić, L., Vacca, V.

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Faraday tomography of LoTSS-DR2 data: I. Faraday moments in the high-latitude outer Galaxy and revealing Loop III in polarisation von Erceg, A., Jelić, V., Haverkorn, M., Bracco, A., Shimwell, T.W., Tasse, C., Dickey, J.M., Ceraj, L., Drabent, A., Hardcastle, M.J., Turić, L.

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LOFAR Deep Fields: Probing faint Galactic polarised emission in ELAIS-N1 von Šnidarić, Iva, Jelić, Vibor, Mevius, Maaijke, Brentjens, Michiel, Erceg, Ana, Shimwell, Timothy W., Piras, Sara, Horellou, Cathy, Sabater, Jose, Best, Philip N., Bracco, Andrea, Ceraj, Lana, Haverkorn, Marijke, O’Sullivan, Shane P., Turić, Luka, Vacca, Valentina

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A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability von PLOMIN, R, TURIC, D. M, HILL, L, TURIC, D. E, STEPHENS, M, WILLIAMS, J, OWEN, M. J, O'DONOVAN, M. C

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Umrichtersystem mit höherem Grundschwingungsgehalt für die Drehstromtraktion von Alexa, D, Turic, L, Stiurcă, D

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Extending the duration of treatment with progesterone and equine chorionic gonadotropin improves fertility in suckled beef cows with low body condition score subjected to timed art... von Bilbao, M.G., Massara, N., Ramos, S., Zapata, L.O., Farcey, M.F., Pesoa, J., Turic, E., Vázquez, M.I., Bartolome, J.A.

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Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease von Morgan, A.R., Hamilton, G., Turic, D., Jehu, L., Harold, D., Abraham, R., Hollingworth, P., Moskvina, V., Brayne, C., Rubinsztein, D.C., Lynch, A., Lawlor, B., Gill, M., O'Donovan, M., Powell, J., Lovestone, S., Williams, J., Owen, M.J.

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Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior von Langley, K, Turic, D, Rice, F, Holmans, P, van den Bree, M B M, Craddock, N, Kent, L, Owen, M J, O'Donovan, M C, Thapar, A

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Concentrations of danofloxacin 18% solution in plasma, milk and tissues after subcutaneous injection in dairy cows von Mestorino, N., Marchetti, M.L., Turic, E., Pesoa, J., Errecalde, J.

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Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 273 nuclear families from a multi-centre sa... von HAWI, Z, DRING, M, LAWSON, D, PAY, H, TURIC, D, LANGLEY, K, OWEN, M, O'DONOVAN, M, THAPAR, A, FITZGERALD, M, GILL, M, KIRLEY, A, FOLEY, D, KENT, L, CRADDOCK, N, ASHERSON, P, CURRAN, S, GOULD, A, RICHARDS, S

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Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder von Lawson, Deborah C., Turic, Darko, Langley, Kate, Pay, Helen M., Govan, Catherine F., Norton, Nadine, Hamshere, Marian L., Owen, Michael J., O'Donovan, Michael C., Thapar, Anita

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Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD von TURIC, D, LANGLEY, K, OWEN, M, O'DONOVAN, M, THAPAR, A, MILLS, S, STEPHENS, M, LAWSON, D, GOVAN, C, WILLIAMS, N, VAN DEN BREE, M, CRADDOCK, N, KENT, L

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Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease von Morgan, A.R., Turic, D., Jehu, L., Hamilton, G., Hollingworth, P., Moskvina, V., Jones, L., Lovestone, S., Brayne, C., Rubinsztein, D.C., Lawlor, B., Gill, M., O'Donovan, M.C., Owen, M.J., Williams, J.

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DNA Pooling Identifies QTLs on Chromosome 4 for General Cognitive Ability in Children von Fisher, Paul J., Turic, Dragana, Williams, Nigel M., McGuffin, Peter, Asherson, Philip, Ball, David, Craig, Ian, Eley, Thalia, Hill, Linzy, Chorney, Karen, Chorney, Michael J., Benbow, Camilla P., Lubinski, David, Plomin, Robert, Owen, Michael J.

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Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22 von TURIC, D, ROBINSON, L, GRIERSON, A, EASTON, M, WILLIAMS, N, VAN DEN BREE, M, CHOWDHURY, R, GRUEN, J, STEVENSON, J, KRAWCZAK, M, OWEN, M. J, O'DONOVAN, M. C, DUKE, M, WILLIAMS, J, MORRIS, D. W, WEBB, V, HAMSHERE, M, MILHAM, C, HOPKIN, E, POUND, K, FERNANDO, S

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Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease von ABRAHAM, Richard, MYERS, Amanda, KWON, Jennifer M, PETERSEN, Ronald C, TANGALOS, Eric, NORTON, Joanne, MORRIS, John C, BULLOCK, Roger, LIOLITSA, Danae, LOVESTONE, Simon, HARDY, John, GOATE, Alison, WAVRANT-DEVRIEZE, Fabienne, O'DONOVAN, Michael, WILLIAMS, Julie, OWEN, Michael J, JONES, Lesley, HAMSHERE, Marian L, THOMAS, Hollie V, MARSHALL, Helen, COMPTON, Danielle, SPURLOCK, Gillian, TURIC, Dragana, HOOGENDOORN, Bastiaan

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