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Publisher: Wolters Kluwer

Volume 27, Number 5, October 2017

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Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred
pp. 169-177(9)
Authors: Melhem, Nadine M.; Hamdan, Sami; Klei, Lambertus; Wood, Shawn; Zelazny, Jamie; Frisch, Amos; Weizman, Abraham; Carmel, Miri; Michaelovsky, Elena; Farbstein, Ilana; Wasserman, Danuta; El-Heib, Muhammad; Ferrell, Robert; Apter, Alan; Devlin, Bernie; Brent, David

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Genetic moderation of cocaine subjective effects by variation in the TPH1, TPH2, and SLC6A4 serotonin genes
pp. 178-186(9)
Authors: Patriquin, Michelle A.; Hamon, Sara C.; Harding, Mark J.; Nielsen, Ellen M.; Newton, Thomas F.; De La Garza, Richard; Nielsen, David A.

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Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist
pp. 187-196(10)
Authors: Martin, Jessica; Streit, Fabian; Treutlein, Jens; Lang, Maren; Frank, Josef; Forstner, Andreas J.; Degenhardt, Franziska; Witt, Stephanie H.; Schulze, Thomas G.; Cichon, Sven; Nöthen, Markus M.; Rietschel, Marcella; Strohmaier, Jana

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Lack of association between COMT Val158Met and ZDHHC8 rs175174 polymorphisms and susceptibility to schizophrenia in a Brazilian population
pp. 197-198(2)
Authors: Moraes, Leopoldo S.; Santos, Augusto C.C.; Ferreira-Fernandes, Hygor; Yoshioka, France K.N.; Teixeira, Silmar S.; GuimarĂ£es, Adriana C.; da Rocha, Carlos A.M.; Rey, Juan A.; Pinto, Giovanny R.; Burbano, Rommel R.

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