Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Boraska, V"'
Autor:
Bakija-Konsuo, A., Mulić, R., Boraska, V., Pehlic, M., Huffman, J.E., Hayward, C., Marlais, M., Zemunik, T., Rudan, I.
Publikováno v:
In European Journal of Medical Genetics 2011 54(6):e548-e552
Autor:
Boraska, V1, Franklin, C S2, Floyd, J A B3, Thornton, L M4, Huckins, L M2, Southam, L2, Rayner, N W5, Tachmazidou, I2, Klump, K L6, Treasure, J7, Lewis, C M8, Schmidt, U7, Tozzi, F4, Kiezebrink, K9, Hebebrand, J10, Gorwood, P11, Adan, R A H12, Kas, M J H13, Favaro, A14, Santonastaso, P14
Publikováno v:
Molecular Psychiatry. Oct2014, Vol. 19 Issue 10, p1085-1094. 10p.
Autor:
Fernandez-Cadenas, I, Prokopenko, I, Timpson, NJ, Boraska, V, Rayner, NW, Hattersley, AT, Frayling, TM, Zeggini, E, Lindgren, CM, McCarthy, MI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c6f58f086a39aec9750f7e00bd782ebe
https://ora.ox.ac.uk/objects/uuid:3ae4ad35-3cad-43c5-9e4e-334263ceb16b
https://ora.ox.ac.uk/objects/uuid:3ae4ad35-3cad-43c5-9e4e-334263ceb16b
Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial genome-wide association study (GWAS) have yielded significant and replicated results. We perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a6ec52621857d71a0faf2b366ea65038
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998851
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998851
Autor:
Huckins, Laura M, Boraska, Vesna, Southam, L, Karhunen, L, Meulenbelt, I, Slagboom, P E, Tortorella, A, Maj, M, Dedoussis, G, Dikeos, D, Gonidakis, F, Tziouvas, K, Tsitsika, A, Rayner, N William, Papezova, H, Slachtova, L, Martaskova, D, Kennedy, J L, Levitan, R D, Yilmaz, Z, Huemer, J, Koubek, D, Merl, E, Wagner, G, Tachmazidou, I, Lichtenstein, P, Breen, G, Cohen-Woods, S, Farmer, A, McGuffin, P, Cichon, Sven, Giegling, I, Herms, S, Rujescu, D, Schreiber, S, Klump, K L, Wichmann, H-E, Dina, C, Sladek, R, Gambaro, G, Soranzo, N, Julia, A, Marsal, S, Rabionet, R a, Gaborieau, V, Dick, D M, Treasure, J, Palotie, A, Ripatti, S, Widén, E, Andreassen, O A, Espeseth, T, Lundervold, A, Reinvang, I, Steen, V M, Hellard, S Le, Mattingsda, M, Lewis, C M, Ntalla, I, Bencko, V, Foretova, L, Janout, V, Navratilova, M, Gallinger, S, Pinto, D, Scherer, S W, Aschauer, H, Carlberg, L, Schmidt, U, Schosser, A, Alfredsson, L, Ding, B, Klareskog, L, Padyukov, L, Finan, C, Kalsi, G, Roberts, M, Logan, D W, Peltonen, L, Tozzi, F, Ritchie, G R S, Courtet, P, Guillame, S, Jaussent, I, Barrett, J C, Estivill, X, Hinney, A, Sullivan, P F, Collier, D A, Zeggini, E, Kiezebrink, K, Bulik, C M, Anderson, Carl A, Barrett, Jeffrey C, Floyd, James AB, Franklin, Christopher S, McGinnis, Ralph, Soranzo, Nicole, Zeggini, Eleftheria, Sambrook, Jennifer, Stephens, Jonathan, Hebebrand, J, Ouwehand, Willem H, McArdle, Wendy L, Ring, Susan M, Strachan, David P, Alexander, Graeme, Bulik, Cynthia M, Collier, David A, Conlon, Peter J, Dominiczak, Anna, Duncanson, Audrey, Gorwood, P, Hill, Adrian, Langford, Cordelia, Lord, Graham, Maxwell, Alexander P, Morgan, Linda, Peltonen, Leena, Sandford, Richard N, Sheerin, Neil, Vannberg, Fredrik O, Adan, R A H, Genotyping, D N A, Blackburn, Hannah, Chen, Wei-Min, Edkins, Sarah, Gillman, Mathew, Gray, Emma, Hunt, Sarah E, nengut-Gumuscu, Suna, Kas, M J H, Potter, Simon, Rich, Stephen S, Simpkin, Douglas, Whittaker, Pamela, Sullivan, Patrick F, Tyler-Smith, Chris, Tachmazidou, Ioanna, avaro, A F, Santonastaso, P, Fernández-Aranda, F, Gratacos, M, Rybakowski, F, Dmitrzak-Weglarz, M, Kaprio, J, Floyd, James A B, Keski-Rahkonen, A, Raevuori, A, Van Furth, E F, Slof-Op t Landt, M C T, Hudson, J I, Reichborn-Kjennerud, T, Knudsen, G P S, Monteleone, P, Kaplan, A S, Karwautz, A, Southam, Lorraine, Hakonarson, H, Berrettini, W H, Guo, Y, Li, D, Schork, N J, Komaki, G, Ando, T, Inoko, H, Esko, T, Fischer, K, Boraska, V, Männik, K, Metspalu, A, Baker, J H, Cone, R D, Dackor, J, DeSocio, J E, Hilliard, C E, O'Toole, J K, Pantel, J, Szatkiewicz, J P, Franklin, C S, Taico, C, Zerwas, S, Trace, S E, Davis, O S P, Helder, S, Bühren, K, Burghardt, R, de Zwaan, M, Egberts, K, Ehrlich, S, Floyd, J A B, Herpertz-Dahlmann, B, Herzog, W, Imgart, H, Scherag, A, Scherag, S, Zipfel, S, Boni, C, Ramoz, N, Versini, A, Brandys, M K, Thornton, L M, Danner, U N, de Kove, C, Hendriks, J, Koeleman, B P C, Ophoff, R A, Strengman, E, van Elburg, A A, Bruson, A, Clementi, M, Degortes, D, Huckins, L M, Forzan, M, Tenconi, E, Docampo, E, Escaramís, G, Jiménez-Murcia, S, Lissowska, J, Rajewski, A, Szeszenia-Dabrowska, N, Slopien, A, Hauser, J
Publikováno v:
Huckins, L M, Boraska, V, Franklin, C S, Floyd, J A B, Southam, L, Sullivan, P F, Bulik, C M, Collier, D A, Tyler-smith, C, Zeggini, E, Tachmazidou, I & Lord, G 2014, ' Using ancestry-informative markers to identify fine structure across 15 populations of European origin ', European Journal of Human Genetics, vol. 22, no. 10, pp. 1190-1200 . https://doi.org/10.1038/ejhg.2014.1
European journal of human genetics : EJHG, vol 22, iss 10
European Journal of Human Genetics
European journal of human genetics 22, 1190–1200 (2014). doi:10.1038/ejhg.2014.1
European Journal of Human Genetics, 22(10), 1190. Nature Publishing Group
Eur. J. Hum. Genet. 22, 1190-1200 (2014)
GCAN, WTCCC3, Sullivan, P F, Bulik, C M, Collier, D A, Tyler-Smith, C, Zeggini, E & Tachmazidou, I 2014, ' Using ancestry-informative markers to identify fine structure across 15 populations of European origin ', European Journal of Human Genetics, vol. 22, pp. 1190-1200 . https://doi.org/10.1038/ejhg.2014.1
European journal of human genetics : EJHG, vol 22, iss 10
European Journal of Human Genetics
European journal of human genetics 22, 1190–1200 (2014). doi:10.1038/ejhg.2014.1
European Journal of Human Genetics, 22(10), 1190. Nature Publishing Group
Eur. J. Hum. Genet. 22, 1190-1200 (2014)
GCAN, WTCCC3, Sullivan, P F, Bulik, C M, Collier, D A, Tyler-Smith, C, Zeggini, E & Tachmazidou, I 2014, ' Using ancestry-informative markers to identify fine structure across 15 populations of European origin ', European Journal of Human Genetics, vol. 22, pp. 1190-1200 . https://doi.org/10.1038/ejhg.2014.1
The Wellcome Trust Case Control Consortium 3 anorexia nervosa genome-wide association scan includes 2907 cases from 15 different populations of European origin genotyped on the Illumina 670K chip. We compared methods for identifying population strati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3c6064fdc451b08d4633857f5d1cf5
https://www.bib.irb.hr/728015
https://www.bib.irb.hr/728015
The Wellcome Trust Case Control Consortium 3 anorexia nervosa genome-wide association scan includes 2907 cases from 15 different populations of European origin genotyped on the Illumina 670K chip. We compared methods for identifying population strati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::ce3aa5a1f9e2636da655b2a4f4d9e9dd
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088110
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088110
Autor:
Boraska V, Jerončić A, Colonna V, Southam L, Nyholt DR, Rayner NW, Perry JR, Toniolo D, Albrecht E, Ang W, Bandinelli S, Barbalic M, Barroso I, Beckmann JS, Biffar R, Boomsma D, Hottenga JJ, Vink JM, Willemsen G, de Geus E, Penninx BW, Schreiber S, Schunkert H, Spector TD, Stumvoll M, Uitterlinden AG, Ulivi S, van der Harst P, Vollenweider P, Vxf6lzke H, Wareham NJ, Wichmann HE, Wilson JF, Rudan I, Xue Y, Zeggini E
Publikováno v:
Human Molecular Genetics.
Autor:
Zeggini, E., Panoutsopoulou, K., Southam, L., Rayner, N.W., Day-Williams, A.G., Lopes, M.C., Boraska, V., Esko, T., Evangelou, E., Hofman, A., Houwing-Duistermaat, J.J., Ingvarsson, T., Jonsdottir, I., Jonsson, H., Kerkhof, H.J.M., Kloppenburg, M., Bos, S.D., Mangino, M., Metrustry, S., Slagboom, P.E., Thorleifsson, G., Raine, E.V.A., Ratnayake, M., Ricketts, M., Beazley, C., Blackburn, H., Bumpstead, S., Elliott, K.S., Hunt, S.E., Potter, S.C., Shin, S.Y., Yadav, V.K., Zhai, G.J., Sherburn, K., Dixon, K., Arden, E., Aslam, N., Battley, P.K., Carluke, I., Doherty, S., Gordon, A., Joseph, J., Keen, R., Koller, N.C., Mitchell, S., O'Neill, F., Paling, E., Reed, M.R., Rivadeneira, F., Swift, D., Walker, K., Watkins, B., Wheeler, M., Birrell, F., Ioannidis, J.P.A., Meulenbelt, I., Metspalu, A., Rai, A., Salter, D., Stefansson, K., Styrkarsdottir, U., Uitterlinden, A.G., Meurs, J.B.J. van, Chapman, K., Deloukas, P., Ollier, W.E.R., Wallis, G.A., Arden, N., Carr, A., Doherty, M., McCaskie, A., Wilkinson, J.M., Ralston, S.H., Valdes, A.M., Spector, T.D., Loughlin, J., arcOGEN Consortium & arcOGEN Colla
Publikováno v:
Lancet, 380(9844), 815-823
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5dce68dc7cbfc888297764fdc675dea6
https://hdl.handle.net/1887/106407
https://hdl.handle.net/1887/106407
Autor:
Boraska, V, Day-Williams, A, Franklin, CS, Elliott, KS, Panoutsopoulou, K, Tachmazidou, I, Albrecht, E, Bandinelli, S, Beilin, L, Bochud, M, Cadby, G, Ernst, F, Evans, David M., Hayward, C, Hicks, AA, Huffman, Jennifer, Huth, C, James, AL, Klopp, N, Kolcic, I, Kutalik, Z, Lawlor, Debbie A., Musk, AW, Pehlic, M, Pennell, CE, Perry, JRB, Peters, Annette, Polasek, O, St Pourcain, B, Ring, SM, Salvi, E, Schipf, S, Staessen, JA, Teumer, A, Timpson, N, Vitart, V, Warrington, NM, Yaghootkar, H, Zemunik, T, Zgaga, L, An, P, Anttila, V, Borecki, IB, Holmen, Jostein, Ntalla, I, Palotie, A, Pietilainen, KH, Wedenoja, J, Winsvold, Bendik Kristoffer Slagsvold, Dedoussis, GV, Kaprio, J, Province, MA, Zwart, John-Anker, Burnier, M, Campbell, H, Cusi, D, Smith, GD, Frayling, TM, Gieger, C, Palmer, LJ, Pramstaller, PP, Rudan, I, Volzke, H, Wichmann, HE, Wright, AF, Zeggini, E
Externí odkaz:
http://hdl.handle.net/11250/2365399
Autor:
Zemunik, T., Boban, M., Lauc, G., Jankovic, S., Rotim, K., Vatavuk, Z., Bencic, G., Dogas, Z., Boraska, V., Torlak, V., Susac, J., Zobic, I., Rudan, D., Pulanic, D., Modun, D., Mudnic, I., Gunjaca, G., Budimir, D., Hayward, C., Vitart, V., Wright, Alan, Campbell, Harry, Rudan, I.
Publikováno v:
Zemunik, T, Boban, M, Lauc, G, Jankovic, S, Rotim, K, Vatavuk, Z, Bencic, G, Dogas, Z, Boraska, V, Torlak, V, Susac, J, Zobic, I, Rudan, D, Pulanic, D, Modun, D, Mudnic, I, Gunjaca, G, Budimir, D, Hayward, C, Vitart, V, Wright, A, Campbell, H & Rudan, I 2009, ' Genome-wide association study of biochemical traits in Korcula Island, Croatia 8 ', Croatian Medical Journal, vol. 50, no. 1, pp. 7-16 . https://doi.org/10.3325/cmj.2009.50.23
AIM:To identify genetic variants underlying biochemical traits--total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides, uric acid, albumin, and fibrinogen, in a genome-wide association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3094::98e34ac2833edae8d1cc8a7b4d5449b4
https://hdl.handle.net/20.500.11820/32505583-f0f1-453f-aabe-f0deabf6c24e
https://hdl.handle.net/20.500.11820/32505583-f0f1-453f-aabe-f0deabf6c24e