Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
dc.contributor.author | Huckins, L M | |
dc.contributor.author | Hatzikotoulas, K | |
dc.contributor.author | Southam, L | |
dc.contributor.author | Thornton, L M | |
dc.contributor.author | Steinberg, J | |
dc.contributor.author | Aguilera-McKay, F | |
dc.contributor.author | Treasure, J | |
dc.contributor.author | Schmidt, U | |
dc.contributor.author | Gunasinghe, C | |
dc.contributor.author | Romero, A | |
dc.contributor.author | Curtis, C | |
dc.contributor.author | Rhodes, D | |
dc.contributor.author | Moens, J | |
dc.contributor.author | Kalsi, G | |
dc.contributor.author | Dempster, D | |
dc.contributor.author | Leung, R | |
dc.contributor.author | Keohane, A | |
dc.contributor.author | Burghardt, R | |
dc.contributor.author | Ehrlich, S | |
dc.contributor.author | Hebebrand, J | |
dc.contributor.author | Hinney, A | |
dc.contributor.author | Ludolph, A | |
dc.contributor.author | Walton, E | |
dc.contributor.author | Deloukas, P | |
dc.contributor.author | Hofman, A | |
dc.contributor.author | Palotie, A | |
dc.contributor.author | Palta, P | |
dc.contributor.author | van Rooij, F J A | |
dc.contributor.author | Stirrups, K | |
dc.contributor.author | Adan, R | |
dc.contributor.author | Boni, C | |
dc.contributor.author | Cone, R | |
dc.contributor.author | Dedoussis, G | |
dc.contributor.author | van Furth, E | |
dc.contributor.author | Gonidakis, F | |
dc.contributor.author | Gorwood, P | |
dc.contributor.author | Hudson, J | |
dc.contributor.author | Kaprio, J | |
dc.contributor.author | Kas, M | |
dc.contributor.author | Keski-Rahonen, A | |
dc.contributor.author | Kiezebrink, K | |
dc.contributor.author | Knudsen, Gun Peggy | |
dc.contributor.author | Slof-Op ’t Landt, M C T | |
dc.contributor.author | Maj, M | |
dc.contributor.author | Monteleone, A | |
dc.contributor.author | Monteleone, P | |
dc.contributor.author | Raevuori, A | |
dc.contributor.author | Reichborn-Kjennerud, Ted | |
dc.contributor.author | Tozzi, F | |
dc.contributor.author | Tsitsika, A | |
dc.contributor.author | Van Elburg, A | |
dc.contributor.author | Collier, D A | |
dc.contributor.author | Sullivan, P F | |
dc.contributor.author | Breen, G | |
dc.contributor.author | Bulik, C M | |
dc.contributor.author | Zeggini, E | |
dc.date.accessioned | 2017-12-13T13:57:21Z | |
dc.date.available | 2017-12-13T13:57:21Z | |
dc.date.created | 2017-12-06T14:00:50Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 1359-4184 | |
dc.identifier.uri | http://hdl.handle.net/11250/2471307 | |
dc.language.iso | eng | |
dc.relation.uri | https://www.nature.com/articles/mp201788.pdf | |
dc.title | Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa | |
dc.type | Peer reviewed | |
dc.type | Journal article | |
dc.description.version | publishedVersion | |
dc.source.journal | Molecular Psychiatry | |
dc.identifier.cristin | 1523613 | |
cristin.unitcode | 7502,5,0,0 | |
cristin.unitcode | 7502,3,12,0 | |
cristin.unitname | Helsedata og digitalisering | |
cristin.unitname | Psykiske lidelser | |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 2 |
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