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Journal Abstract Search
734 related items for PubMed ID: 20351714
1. Poor replication of candidate genes for major depressive disorder using genome-wide association data. Bosker FJ, Hartman CA, Nolte IM, Prins BP, Terpstra P, Posthuma D, van Veen T, Willemsen G, DeRijk RH, de Geus EJ, Hoogendijk WJ, Sullivan PF, Penninx BW, Boomsma DI, Snieder H, Nolen WA. Mol Psychiatry; 2011 May; 16(5):516-32. PubMed ID: 20351714 [Abstract] [Full Text] [Related]
2. ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples. Kloiber S, Czamara D, Karbalai N, Müller-Myhsok B, Hennings J, Holsboer F, Lucae S. J Psychiatr Res; 2012 Aug; 46(8):973-9. PubMed ID: 22647524 [Abstract] [Full Text] [Related]
3. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study. Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I. Int Clin Psychopharmacol; 2010 Jul; 25(4):218-27. PubMed ID: 20531207 [Abstract] [Full Text] [Related]
4. Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in recurrent major depressive disorder. Van Den Eede F, Venken T, Del-Favero J, Norrback KF, Souery D, Nilsson LG, Van den Bossche B, Hulstijn W, Sabbe BG, Cosyns P, Mendlewicz J, Adolfsson R, Van Broeckhoven C, Claes SJ. Psychiatry Res; 2007 Sep 30; 153(1):17-25. PubMed ID: 17599466 [Abstract] [Full Text] [Related]
6. Genetic association analysis of functional polymorphisms in neuronal nitric oxide synthase 1 gene (NOS1) and mood disorders and fluvoxamine response in major depressive disorder in the Japanese population. Okumura T, Kishi T, Okochi T, Ikeda M, Kitajima T, Yamanouchi Y, Kinoshita Y, Kawashima K, Tsunoka T, Inada T, Ozaki N, Iwata N. Neuropsychobiology; 2010 Sep 30; 61(2):57-63. PubMed ID: 20016223 [Abstract] [Full Text] [Related]
7. Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor. Thomson PA, Wray NR, Thomson AM, Dunbar DR, Grassie MA, Condie A, Walker MT, Smith DJ, Pulford DJ, Muir W, Blackwood DH, Porteous DJ. Mol Psychiatry; 2005 May 30; 10(5):470-8. PubMed ID: 15452587 [Abstract] [Full Text] [Related]
8. [Association of cyclic adenosine monophosphate response element-binding protein gene and major depressive disorder]. Liu XH, Xu YF, Cui DH, Jiang SD, Qian YP, Yu SY, Jiang KD. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun 30; 27(3):263-6. PubMed ID: 20533262 [Abstract] [Full Text] [Related]
9. Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects. Cousin E, Deleuze JF, Genin E. BMC Genet; 2006 Apr 05; 7():20. PubMed ID: 16597333 [Abstract] [Full Text] [Related]
10. Association of C/T polymorphism in intron 14 of the dopamine transporter gene (rs40184) with major depression in a northeastern Thai population. Pattarachotanant N, Sritharathikhun T, Suttirat S, Tencomnao T. Genet Mol Res; 2010 Mar 30; 9(1):565-72. PubMed ID: 20391341 [Abstract] [Full Text] [Related]
11. Association study of dopamine transporter gene and schizophrenia in Korean population using multiple single nucleotide polymorphism markers. Jeong SH, Joo EJ, Ahn YM, Kim YS. Prog Neuropsychopharmacol Biol Psychiatry; 2004 Sep 30; 28(6):975-83. PubMed ID: 15380858 [Abstract] [Full Text] [Related]
12. Association between norepinephrine transporter T-182C polymorphism and major depressive disorder: a meta-analysis. Zhou Y, Su H, Song J, Guo L, Sun Y. Neurosci Lett; 2014 Feb 21; 561():64-8. PubMed ID: 24374057 [Abstract] [Full Text] [Related]
13. Does refining the phenotype improve replication rates? A review and replication of candidate gene studies on Major Depressive Disorder and Chronic Major Depressive Disorder. Luo X, Stavrakakis N, Penninx BW, Bosker FJ, Nolen WA, Boomsma DI, de Geus EJ, Smit JH, Snieder H, Nolte IM, Hartman CA. Am J Med Genet B Neuropsychiatr Genet; 2016 Mar 21; 171B(2):215-36. PubMed ID: 26566975 [Abstract] [Full Text] [Related]
14. Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan. Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF. Br J Dermatol; 2004 Jun 21; 150(6):1104-11. PubMed ID: 15214895 [Abstract] [Full Text] [Related]
15. Association between major depressive disorder and a functional polymorphism of the 5-hydroxytryptamine (serotonin) transporter gene: a meta-analysis. Kiyohara C, Yoshimasu K. Psychiatr Genet; 2010 Apr 21; 20(2):49-58. PubMed ID: 20016401 [Abstract] [Full Text] [Related]
16. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R. Neurosci Lett; 2008 Aug 15; 441(1):56-60. PubMed ID: 18597938 [Abstract] [Full Text] [Related]
17. Support for association between the Ser205Leu polymorphism of p75(NTR) and major depressive disorder. Fujii T, Yamamoto N, Hori H, Hattori K, Sasayama D, Teraishi T, Hashikura M, Tatsumi M, Okamoto N, Higuchi T, Kunugi H. J Hum Genet; 2011 Nov 15; 56(11):806-9. PubMed ID: 21938001 [Abstract] [Full Text] [Related]
18. Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy. Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Epilepsy Res; 2011 Mar 15; 94(1-2):110-6. PubMed ID: 21333500 [Abstract] [Full Text] [Related]
19. TNF polymorphisms in psoriasis: association of psoriatic arthritis with the promoter polymorphism TNF*-857 independent of the PSORS1 risk allele. Reich K, Hüffmeier U, König IR, Lascorz J, Lohmann J, Wendler J, Traupe H, Mössner R, Reis A, Burkhardt H. Arthritis Rheum; 2007 Jun 15; 56(6):2056-64. PubMed ID: 17530646 [Abstract] [Full Text] [Related]
20. Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke. Matsushita T, Ashikawa K, Yonemoto K, Hirakawa Y, Hata J, Amitani H, Doi Y, Ninomiya T, Kitazono T, Ibayashi S, Iida M, Nakamura Y, Kiyohara Y, Kubo M. Hum Mol Genet; 2010 Mar 15; 19(6):1137-46. PubMed ID: 20042462 [Abstract] [Full Text] [Related] Page: [Next] [New Search]