HuGE Literature Finder
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Records 1-8
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Abruptio Placentae Risk and Genetic Variations in Mitochondrial Biogenesis and Oxidative Phosphorylation: Replication of a Candidate Gene Association Study.
American journal of obstetrics and gynecology 2018 Sep . Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Thornton Timothy A, Tekola-Ayele Fasil, Sanchez Sixto E, Garcia Pedro J, Palomino Henry G, Hajat Anjum, Romero Roberto, Ananth Cande V, Williams Michelle |
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Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.
Psychiatry research 2015 Dec . Watanabe Yuichiro, Nunokawa Ayako, Shibuya Masako, Ikeda Masashi, Hishimoto Akitoyo, Kondo Kenji, Egawa Jun, Kaneko Naoshi, Muratake Tatsuyuki, Saito Takeo, Okazaki Satoshi, Shimasaki Ayu, Igeta Hirofumi, Inoue Emiko, Hoya Satoshi, Sugai Takuro, Sora Ichiro, Iwata Nakao, Someya Toshiyu |
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.
Annals of the rheumatic diseases 2014 Dec 73 (12): 2130-6. Evangelou Evangelos, Kerkhof Hanneke J, Styrkarsdottir Unnur, Ntzani Evangelia E, Bos Steffan D, Esko Tonu, Evans Daniel S, Metrustry Sarah, Panoutsopoulou Kalliope, Ramos Yolande F M, Thorleifsson Gudmar, Tsilidis Konstantinos K, , Arden Nigel, Aslam Nadim, Bellamy Nicholas, Birrell Fraser, Blanco Francisco J, Carr Andrew, Chapman Kay, Day-Williams Aaron G, Deloukas Panos, Doherty Michael, Engström Gunnar, Helgadottir Hafdis T, Hofman Albert, Ingvarsson Thorvaldur, Jonsson Helgi, Keis Aime, Keurentjes J Christiaan, Kloppenburg Margreet, Lind Penelope A, McCaskie Andrew, Martin Nicholas G, Milani Lili, Montgomery Grant W, Nelissen Rob G H H, Nevitt Michael C, Nilsson Peter M, Ollier William Er, Parimi Neeta, Rai Ashok, Ralston Stuart H, Reed Mike R, Riancho Jose A, Rivadeneira Fernando, Rodriguez-Fontenla Cristina, Southam Lorraine, Thorsteinsdottir Unnur, Tsezou Aspasia, Wallis Gillian A, Wilkinson J Mark, Gonzalez Antonio, Lane Nancy E, Lohmander L Stefan, Loughlin John, Metspalu Andres, Uitterlinden Andre G, Jonsdottir Ingileif, Stefansson Kari, Slagboom P Eline, Zeggini Eleftheria, Meulenbelt Ingrid, Ioannidis John Pa, Spector Tim D, van Meurs Joyce B J, Valdes Ana |
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Genome-wide and candidate gene association studies of placental abruption.
International journal of molecular epidemiology and genetics 2013 4 (3): 128-39. Workalemahu Tsegaselassie, Enquobahrie Daniel A, Moore Amy, Sanchez Sixto E, Ananth Cande V, Pacora Percy N, Liang Liming, Salazar Manuel, Williams Michelle |
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Genetic variability in the NMDA-dependent AMPA trafficking cascade is associated with alcohol dependence.
Addiction biology 2012 Jul 17 (4): 798-806. Karpyak Victor M, Geske Jennifer R, Colby Colin L, Mrazek David A, Biernacka Joanna |
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Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis.
European journal of human genetics : EJHG 2009 Jul 17 (7): 946-57. Need Anna C, Keefe Richard S E, Ge Dongliang, Grossman Iris, Dickson Sam, McEvoy Joseph P, Goldstein David |
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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 |
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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:Dec 12, 2019
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