HuGE Literature Finder
Records 1-8
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Effects of circadian clock genes and health-related behavior on metabolic syndrome in a Taiwanese population: Evidence from association and interaction analysis.
PloS one 2017 12 (3): e0173861. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Feng, Tsai Shih-J |
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Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease.
PloS one 2011 6 (1): e16542. Banasik Karina, Justesen Johanne M, Hornbak Malene, Krarup Nikolaj T, Gjesing Anette P, Sandholt Camilla H, Jensen Thomas S, Grarup Niels, Andersson Asa, Jørgensen Torben, Witte Daniel R, Sandbæk Annelli, Lauritzen Torsten, Thorens Bernard, Brunak Søren, Sørensen Thorkild I A, Pedersen Oluf, Hansen Torb |
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PER2 variantion is associated with depression vulnerability.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Mar 153B (2): 570-81. Lavebratt Catharina, Sjöholm Louise K, Partonen Timo, Schalling Martin, Forsell Yvon |
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Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance.
PloS one 2010 5 (2): e9259. Utge Siddheshwar J, Soronen Pia, Loukola Anu, Kronholm Erkki, Ollila Hanna M, Pirkola Sami, Porkka-Heiskanen Tarja, Partonen Timo, Paunio Tii |
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Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia.
Bipolar disorders 2009 Nov 11 (7): 701-10. Mansour Hader A, Talkowski Michael E, Wood Joel, Chowdari Kodavali V, McClain Lora, Prasad Konasale, Montrose Debra, Fagiolini Andrea, Friedman Edward S, Allen Michael H, Bowden Charles L, Calabrese Joseph, El-Mallakh Rif S, Escamilla Michael, Faraone Stephen V, Fossey Mark D, Gyulai Laszlo, Loftis Jennifer M, Hauser Peter, Ketter Terence A, Marangell Lauren B, Miklowitz David J, Nierenberg Andrew A, Patel Jayendra, Sachs Gary S, Sklar Pamela, Smoller Jordan W, Laird Nan, Keshavan Matcheri, Thase Michael E, Axelson David, Birmaher Boris, Lewis David, Monk Tim, Frank Ellen, Kupfer David J, Devlin Bernie, Nimgaonkar Vishwajit |
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A common variant in DRD3 receptor is associated with autism spectrum disorder.
Biological psychiatry 2009 Apr 65 (7): 625-30. de Krom Mariken, Staal Wouter G, Ophoff Roel A, Hendriks Judith, Buitelaar Jan, Franke Barbara, de Jonge Maretha V, Bolton Patrick, Collier David, Curran Sarah, van Engeland Herman, van Ree Jan |
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Dec 147B (8): 1355-8. Lasky-Su Jessica, Anney Richard J L, Neale Benjamin M, Franke Barbara, Zhou Kaixin, Maller Julian B, Vasquez Alejandro Arias, Chen Wai, Asherson Philip, Buitelaar Jan, Banaschewski Tobias, Ebstein Richard, Gill Michael, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Sonuga-Barke Edmund, Steinhausen Hans Christoph, Taylor Eric, Daly Mark, Laird Nan, Lange Christoph, Faraone Stephen |
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Molecular medicine (Cambridge, Mass.) 0 16 (7-8): 247-53. Rose Jed E, Behm Frédérique M, Drgon Tomas, Johnson Catherine, Uhl George |
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- Page last updated:Feb 20, 2020
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