المؤلفون: Conley, A. H., Overstreet, C. M., Hawn, S. E., Kendler, K. S., Dick, D. M., Amstadter, A. B.

المصدر: Journal of American College Health. 2017 65(1):41-49.

Peer Reviewed: Y

Sponsoring Agency: National Institute on Alcohol Abuse and Alcoholism (NIH)
National Center for Research Resources (NIH/DHHS)

Assessment and Survey Identifiers: NEO Five Factor Inventory

المؤلفون: Jami, E. S., Hammerschlag, A. R., Ip, H. F., Allegrini, A. G., Benyamin, B., Border, R., Diemer, E. W., Jiang, C., Karhunen, V., Lu, Y., Lu, Q., Mallard, T. T., Mishra, P. P., Nolte, I. M., Palviainen, T., Peterson, R. E., Sallis, H. M., Shabalin, A. A., Tate, A. E., Thiering, E., Vilor-Tejedor, N., Wang, C., Zhou, A., Adkins, D. E., Alemany, S., Ask, H., Chen, Q., Corley, R. P., Ehli, E. A., Evans, L. M., Havdahl, A., Hagenbeek, F. A., Hakulinen, C., Henders, A. K., Hottenga, J. J., Korhonen, T., Mamun, A., Marrington, S., Neumann, A., Rimfeld, K., Rivadeneira, F., Silberg, J. L., van Beijsterveldt, C. E., Vuoksimaa, E., Whipp, A. M., Tong, X. R., Andreassen, O. A., Boomsma, D. I., Brown, S. A., Burt, S. A., Copeland, W., Dick, D. M., Harden, K. P., Harris, K. M., Hartman, C. A., Heinrich, J., Hewitt, J. K., Hopfer, C., Hypponen, E., Jarvelin, M. R., Kaprio, J., Keltikangas-Jarvinen, L., Klump, K. L., Krauter, K., Kuja-Halkola, R., Larsson, H., Lehtimaki, T., Lichtenstein, P., Lundström, Sebastian, Maes, H. H., Magnus, P., Munafo, M. R., Najman, J. M., Njolstad, P. R., Oldehinkel, A. J., Pennell, C. E., Plomin, R., Reichborn-Kjennerud, T., Reynolds, C., Rose, R. J., Smolen, A., Snieder, H., Stallings, M., Standl, M., Sunyer, J., Tiemeier, H., Wadsworth, S. J., Wall, T. L., Whitehouse, A. J. O., Williams, G. M., Ystrom, E., Nivard, M. G., Bartels, M., Middeldorp, C. M.

المصدر: Journal of the American Academy of Child and Adolescent Psychiatry. 61(7):934-945

مصطلحات موضوعية: Psychiatry, Psykiatri, depression, anxiety, repeated measures, genetic epidemiology, molecular, genetics, major depressive disorder, behavioral-problems, mental-disorders, children, psychopathology, questionnaire, heritability, prevalence, risk, Psychology, Pediatrics

URL الوصول: https://gup.ub.gu.se/publication/319226

المؤلفون: Meyers, J L^{Aff1, IDmp2016239_cor1}, Zhang, J, Wang, J C, Su, J, Kuo, S I, Kapoor, M, Wetherill, L, Bertelsen, S, Lai, D, Salvatore, J E^{Aff3, Aff5}, Kamarajan, C, Chorlian, D, Agrawal, A, Almasy, L^{Aff7, Aff8}, Bauer, L, Bucholz, K K, Chan, G, Hesselbrock, V, Koganti, L, Kramer, J, Kuperman, S, Manz, N, Pandey, A, Seay, M, Scott, D, Taylor, R E, Dick, D M^{Aff3, Aff5}, Edenberg, H J^{Aff4, Aff13}, Goate, A^{Aff2, Aff14}, Foroud, T, Porjesz, B

المصدر: Molecular Psychiatry. 22(12):1767-1775

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Boraska, V^{Aff1, Aff2}, Franklin, C S, Floyd, J A B^{Aff1, Aff3}, Thornton, L M, Huckins, L M, Southam, L, Rayner, N W^{Aff1, Aff5, Aff6}, Tachmazidou, I, Klump, K L, Treasure, J, Lewis, C M, Schmidt, U, Tozzi, F, Kiezebrink, K, Hebebrand, J, Gorwood, P^{Aff12, Aff13}, Adan, R A H^{Aff14, Aff15}, Kas, M J H, Favaro, A, Santonastaso, P, Fernández-Aranda, F^{Aff17, Aff18}, Gratacos, M^{Aff19, Aff20, Aff21, Aff22}, Rybakowski, F, Dmitrzak-Weglarz, M, Kaprio, J^{Aff25, Aff26, Aff27}, Keski-Rahkonen, A, Raevuori, A^{Aff25, Aff28}, Van Furth, E F^{Aff29, Aff30}, Slof-Op 't Landt, M C T^{Aff29, Aff31}, Hudson, J I, Reichborn-Kjennerud, T^{Aff33, Aff34}, Knudsen, G P S, Monteleone, P^{Aff35, Aff36}, Kaplan, A S^{Aff37, Aff38}, Karwautz, A, Hakonarson, H^{Aff40, Aff41}, Berrettini, W H, Guo, Y, Li, D, Schork, N J, Komaki, G^{Aff44, Aff45}, Ando, T, Inoko, H, Esko, T, Fischer, K, Männik, K^{Aff48, Aff49}, Metspalu, A^{Aff47, Aff48}, Baker, J H, Cone, R D, Dackor, J, DeSocio, J E, Hilliard, C E, O'Toole, J K, Pantel, J, Szatkiewicz, J P, Taico, C, Zerwas, S, Trace, S E, Davis, O S P^{Aff9, Aff55}, Helder, S, Bühren, K, Burghardt, R, de Zwaan, M^{Aff58, Aff59}, Egberts, K, Ehrlich, S^{Aff61, Aff62}, Herpertz-Dahlmann, B, Herzog, W, Imgart, H, Scherag, A, Scherag, S, Zipfel, S, Boni, C, Ramoz, N, Versini, A, Brandys, M K^{Aff14, Aff15}, Danner, U N, de Kovel, C, Hendriks, J, Koeleman, B P C, Ophoff, R A^{Aff68, Aff69}, Strengman, E, van Elburg, A A^{Aff15, Aff70}, Bruson, A, Clementi, M, Degortes, D, Forzan, M, Tenconi, E, Docampo, E^{Aff19, Aff20, Aff21, Aff22}, Escaramís, G^{Aff19, Aff20, Aff21, Aff22}, Jiménez-Murcia, S^{Aff17, Aff18}, Lissowska, J, Rajewski, A, Szeszenia-Dabrowska, N, Slopien, A, Hauser, J, Karhunen, L, Meulenbelt, I, Slagboom, P E^{Aff31, Aff75}, Tortorella, A, Maj, M, Dedoussis, G, Dikeos, D, Gonidakis, F, Tziouvas, K, Tsitsika, A, Papezova, H, Slachtova, L, Martaskova, D, Kennedy, J L^{Aff37, Aff38}, Levitan, R D^{Aff37, Aff38}, Yilmaz, Z^{Aff4, Aff37}, Huemer, J, Koubek, D, Merl, E, Wagner, G, Lichtenstein, P, Breen, G, Cohen-Woods, S, Farmer, A, McGuffin, P, Cichon, S^{Aff83, Aff84, Aff85}, Giegling, I, Herms, S^{Aff83, Aff85}, Rujescu, D, Schreiber, S, Wichmann, H-E^{Aff88, Aff89}, Dina, C, Sladek, R, Gambaro, G, Soranzo, N, Julia, A, Marsal, S, Rabionet, R^{Aff19, Aff20, Aff21, Aff22}, Gaborieau, V, Dick, D M, Palotie, A^{Aff1, Aff96, Aff97}, Ripatti, S^{Aff96, Aff98}, Widén, E^{Aff96, Aff98}, Andreassen, O A, Espeseth, T^{Aff99, Aff100}, Lundervold, A^{Aff101, Aff102, Aff103}, Reinvang, I, Steen, V M^{Aff104, Aff105}, Le Hellard, S^{Aff104, Aff105}, Mattingsdal, M, Ntalla, I, Bencko, V, Foretova, L, Janout, V, Navratilova, M, Gallinger, S^{Aff109, Aff110}, Pinto, D, Scherer, S W, Aschauer, H, Carlberg, L, Schosser, A, Alfredsson, L, Ding, B, Klareskog, L, Padyukov, L, Courtet, P^{Aff116, Aff117}, Guillaume, S^{Aff116, Aff117}, Jaussent, I^{Aff116, Aff117}, Finan, C, Kalsi, G, Roberts, M, Logan, D W, Peltonen, L, Ritchie, G R S^{Aff1, Aff118}, Barrett, J C, Estivill, X^{Aff19, Aff20, Aff21, Aff22}, Hinney, A, Sullivan, P F^{Aff4, Aff51}, Collier, D A^{Aff9, Aff119}, Zeggini, E, Bulik, C M^{Aff4, Aff120, IDmp2013187_cor177}

المصدر: Molecular Psychiatry. 19(10):1085-1094

المؤلفون: Chan, T W S^{Aff1, IDijo2013123_cor1}, Bates, J E, Lansford, J E, Dodge, K A, Pettit, G S, Dick, D M, Latendresse, S J

المصدر: International Journal of Obesity. 38(3):404-410

المؤلفون: Savage, J. E., Jansen, P. R., Stringer, S., Watanabe, K., Bryois, J., De Leeuw, C. A., Nagel, M., Awasthi, S., Barr, P. B., Coleman, J. R. I., Grasby, K. L., Hammerschlag, A. R., Kaminski, J. A., Karlsson, R., Krapohl, E., Lam, M., Nygaard, M., Reynolds, C. A., Trampush, J. W., Young, H., Zabaneh, D., Hägg, S., Hansell, N. K., Karlsson, Ida K., Linnarsson, S., Montgomery, G. W., Muñoz-Manchado, A. B., Quinlan, E. B., Schumann, G., Skene, N. G., Webb, B. T., White, T., Arking, D. E., Avramopoulos, D., Bilder, R. M., Bitsios, P., Burdick, K. E., Cannon, T. D., Chiba-Falek, O., Christoforou, A., Cirulli, E. T., Congdon, E., Corvin, A., Davies, G., Deary, I. J., Derosse, P., Dickinson, D., Djurovic, S., Donohoe, G., Conley, E. D., Eriksson, J. G., Espeseth, T., Freimer, N. A., Giakoumaki, S., Giegling, I., Gill, M., Glahn, D. C., Hariri, A. R., Hatzimanolis, A., Keller, M. C., Knowles, E., Koltai, D., Konte, B., Lahti, J., Le Hellard, S., Lencz, T., Liewald, D. C., London, E., Lundervold, A. J., Malhotra, A. K., Melle, I., Morris, D., Need, A. C., Ollier, W., Palotie, A., Payton, A., Pendleton, N., Poldrack, R. A., Räikkönen, K., Reinvang, I., Roussos, P., Rujescu, D., Sabb, F. W., Scult, M. A., Smeland, O. B., Smyrnis, N., Starr, J. M., Steen, V. M., Stefanis, N. C., Straub, R. E., Sundet, K., Tiemeier, H., Voineskos, A. N., Weinberger, D. R., Widen, E., Yu, J., Abecasis, G., Andreassen, O. A., Breen, G., Christiansen, L., Debrabant, B., Dick, D. M., Heinz, A., Hjerling-Leffler, J., Ikram, M. A., Kendler, K. S., Martin, N. G., Medland, S. E., Pedersen, N. L., Plomin, R., Polderman, T. J. C., Ripke, S., Van Der Sluis, S., Sullivan, P. F., Vrieze, S. I., Wright, M. J., Posthuma, D.

المصدر: Nature Genetics. 50(7):912-919

مصطلحات موضوعية: Alzheimer disease, Article, attention deficit disorder, chromatin, conserved sequence, corpus striatum, exon, expression quantitative trait locus, gene expression, gene location, gene locus, gene mapping, genetic association, genetic correlation, genetic variability, genome-wide association study, heredity, hippocampus, human, intelligence, medium spiny neuron, Mendelian randomization analysis, nervous system development, pleiotropy, priority journal, pyramidal nerve cell, schizophrenia, synapse

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-41590

المؤلفون: Boraska, Vesna, Franklin, Christopher S., Floyd, James A. B., Thornton, Laura M., Huckins, Laura M., Southam, Lorraine, Rayner, Nigel William, Tachmazidou, Ioanna, Klump, Kelly L., Treasure, Janet, Lewis, Cathryn M., Dedoussis, G., Dikeos, D., Gonidakis, F., Tziouvas, K., Tsitsika, A., Papezova, H., Slachtova, L., Martaskova, D., Kennedy, J. L., Levitan, R. D., Schmidt, U., Yilmaz-Ergül, Zeynep, Huemer, J., Koubek, D., Merl, E., Wagner, G., Lichtenstein, P., Breen, G., Cohen-Woods, S., Farmer, A., McGuffin, P., Tozzi, F., Cichon, S., Giegling, I., Herms, S., Rujescu, D., Schreiber, S., Wichmann, H.-E., Dina, C., Sladek, R., Gambaro, G., Soranzo, N., Kiezebrink, K., Julia, A., Marsal, S., Rabionet, R., Gaborieau, V., Dick, D. M., Palotie, A., Ripatti, S., Widen, E., Andreassen, O. A., Espeseth, T., Hebebrand, J., Lundervold, A., Reinvang, I., Steen, V. M., Le Hellard, S., Mattingsdal, M., Ntalla, I., Bencko, V., Foretova, L., Janout, V., Navratilova, M., Gorwood, P., Gallinger, S., Pinto, D., Scherer, S. W., Aschauer, H., Carlberg, L., Schosser, A., Alfredsson, L., Ding, B., Klareskog, L., Padyukov, L., Adan, R. A. H., Courtet, P., Guillaume, S., Jaussent, I., Finan, C., Kalsi, G., Roberts, M., Logan, D. W., Peltonen, L., Ritchie, G. R. S., Barrett, J. C., Kas, M. J. H., Estivill, X., Hinney, A., Sullivan, P. F., Collier, D. A., Zeggini, E., Bulik, C. M., Favaro, A., Santonastaso, P., Fernandez-Aranda, F., Gratacos, M., Rybakowski, F., Dmitrzak-Weglarz, M., Kaprio, J., 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., Hakonarson, H., Berrettini, W. H., Guo, Y., Li, D., Schork, N. J., Komaki, G., Ando, T., Inoko, H., Esko, T., Fischer, K., Mannik, Katrin, 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., Taico, C., Zerwas, S., Trace, S. E., Davis, O. S. P., Helder, S., Buhren, K., Burghardt, R., de Zwaan, M., Egberts, K., Ehrlich, S., Herpertz-Dahlmann, B., Herzog, W., Imgart, H., Scherag, A., Scherag, S., Zipfel, S., Boni, C., Ramoz, N., Versini, A., Brandys, M. K., Danner, U. N., de Kovel, C., Hendriks, J., Koeleman, B. P. C., Ophoff, R. A., Strengman, E., van Elburg, Anne-Marie A., Bruson, Alice, Clementi, Maurizio, Degortes, Daniela, Forzan, Monica, Tenconi, Elodie, Docampo Martinez, Elisa, Escaramis, Geòrgia, Jimenez-Murcia, Susana, Lissowska, Jolanta, Rajewski, Andrzej, Szeszenia-Dabrowska, Neonila, Slopien, Agnieszka, Hauser, Joanna, Karhunen, Leila, Meulenbelt, Ingrid, Slagboom, P. E., Tortorella, Alfonso, Maj, Mario

المصدر: Molecular Psychiatry, 19 (10), 1085-94 (2014)

مصطلحات موضوعية: Anorexia Nervosa/genetics, Asian Continental Ancestry Group/genetics, Calcineurin/genetics, Carrier Proteins/genetics, Case-Control Studies, Cullin Proteins/genetics, European Continental Ancestry Group/genetics, Female, Genome-Wide Association Study, Guanine Nucleotide Exchange Factors/genetics, Humans, Japan, Male, Meta-Analysis as Topic, Nuclear Proteins/genetics, Polymorphism, Single Nucleotide, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques

Relation: urn:issn:1359-4184; urn:issn:1476-5578

URL الوصول: https://orbi.uliege.be/handle/2268/194209

المؤلفون: Dick, D M^{Aff1, IDmp201073_cor1}, Aliev, F, Krueger, R F, Edwards, A, Agrawal, A, Lynskey, M, Lin, P, Schuckit, M, Hesselbrock, V, Nurnberger, Jr, J, Almasy, L, Porjesz, B, Edenberg, H J, Bucholz, K, Kramer, J, Kuperman, S, Bierut, L

المصدر: Molecular Psychiatry. 16(8):800-808

المؤلفون: Ip, H. F., van der Laan, C. M., Krapohl, E. M. L., Brikell, I., Sanchez-Mora, C., Nolte, I. M., St Pourcain, B., Bolhuis, K., Palviainen, T., Zafarmand, H., Colodro-Conde, L., Gordon, S., Zayats, T., Aliev, F., Jiang, C., Wang, C. R. A., Saunders, G., Karhunen, V., Hammerschlag, A. R., Adkins, D. E., Border, R., Peterson, R. E., Prinz, J. A., Thiering, E., Seppala, I., Vilor-Tejedor, N., Ahluwalia, T. S., Day, F. R., Hottenga, J. J., Allegrini, A. G., Rimfeld, K., Chen, Q., Lu, Y., Martin, J., Artigas, M. S., Rovira, P., Bosch, R., Espanol, G., Quiroga, J. A. R., Neumann, A., Ensink, J., Grasby, K., Morosoli, J. J., Tong, X. R., Marrington, S., Middeldorp, C., Scott, J. G., Vinkhuyzen, A., Shabalin, A. A., Corley, R., Evans, L. M., Sugden, K., Alemany, S., Sass, L., Vinding, R., Ruth, K., Tyrrell, J., Davies, G. E., Ehli, E. A., Hagenbeek, F. A., De Zeeuw, E., Van Beijsterveldt, Tcem, Larsson, H., Snieder, H., Verhulst, F. C., Amin, N., Whipp, A. M., Korhonen, T., Vuoksimaa, E., Rose, R. J., Uitterlinden, A. G., Heath, A. C., Madden, P., Haavik, J., Harris, J. R., Helgeland, O., Johansson, S., Knudsen, G. P. S., Njolstad, P. R., Lu, Q., Rodriguez, A., Henders, A. K., Mamun, A., Najman, J. M., Brown, S., Hopfer, C., Krauter, K., Reynolds, C., Smolen, A., Stallings, M., Wadsworth, S., Wall, T. L., Silberg, J. L., Miller, A., Keltikangas-Jarvinen, L., Hakulinen, C., Pulkki-Raback, L., Havdahl, A., Magnus, P., Raitakari, O. T., Perry, J. R. B., Llop, S., Lopez-Espinosa, M. J., Bonnelykke, K., Bisgaard, H., Sunyer, J., Lehtimaki, T., Arseneault, L., Standl, M., Heinrich, J., Boden, J., Pearson, J., Horwood, L. J., Kennedy, M., Poulton, R., Eaves, L. J., Maes, H. H., Hewitt, J., Copeland, W. E., Costello, E. J., Williams, G. M., Wray, N., Jarvelin, M. R., McGue, M., Iacono, W., Caspi, A., Moffitt, T. E., Whitehouse, A., Pennell, C. E., Klump, K. L., Burt, S. A., Dick, D. M., Reichborn-Kjennerud, T., Martin, N. G., Medland, S. E., Vrijkotte, T., Kaprio, J., Tiemeier, H., Smith, G. D., Hartman, C. A., Oldehinkel, A. J., Casas, M., Ribases, M., Lichtenstein, P., Lundström, Sebastian, Plomin, R., Bartels, M., Nivard, M. G., Boomsma, D. I.

المصدر: Translational Psychiatry. 11(1)

مصطلحات موضوعية: Psychiatry, Psykiatri, genome-wide association, trajectories, heritability, adolescence, disorder, behavior, origins

URL الوصول: https://gup.ub.gu.se/publication/307427