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Items: 1 to 20 of 69

1.

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;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18.

PMID:
21333500
2.

Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.

Yang P, Shu BC, Hallmayer JF, Lung FW.

Neuropsychobiology. 2010;62(2):104-15. doi: 10.1159/000315441. Epub 2010 Jun 3.

PMID:
20523082
3.

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. doi: 10.1038/mp.2010.38. Epub 2010 Mar 30.

PMID:
20351714
4.

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.

Spine (Phila Pa 1976). 2010 Apr 20;35(9):983-8. doi: 10.1097/BRS.0b013e3181bc963c.

PMID:
20228709
5.

Association between the gamma-aminobutyric acid type B receptor 1 and 2 gene polymorphisms and mesial temporal lobe epilepsy in a Han Chinese population.

Wang X, Sun W, Zhu X, Li L, Wu X, Lin H, Zhu S, Liu A, Du T, Liu Y, Niu N, Wang Y, Liu Y.

Epilepsy Res. 2008 Oct;81(2-3):198-203. doi: 10.1016/j.eplepsyres.2008.06.001. Epub 2008 Jul 23.

PMID:
18653317
6.

[Variations within OLF1/EBF-associated zinc finger protein gene confer susceptibility to lupus nephritis in Chinese population].

Liang D, Huang XQ, Shen N, Mao HQ, Feng XB, Huang XF, Tang JP, Chen XX, Chen SL, Gu YY, Bao CD, Wang Y, Qian J.

Zhonghua Yi Xue Za Zhi. 2005 Apr 13;85(14):949-54. Chinese.

PMID:
16061000
7.

Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.

Heuser K, Nagelhus EA, Taubøll E, Indahl U, Berg PR, Lien S, Nakken S, Gjerstad L, Ottersen OP.

Epilepsy Res. 2010 Jan;88(1):55-64. doi: 10.1016/j.eplepsyres.2009.09.023. Epub 2009 Oct 28.

PMID:
19864112
8.

Association of specific haplotypes of D2 dopamine receptor gene with vulnerability to heroin dependence in 2 distinct populations.

Xu K, Lichtermann D, Lipsky RH, Franke P, Liu X, Hu Y, Cao L, Schwab SG, Wildenauer DB, Bau CH, Ferro E, Astor W, Finch T, Terry J, Taubman J, Maier W, Goldman D.

Arch Gen Psychiatry. 2004 Jun;61(6):597-606.

PMID:
15184239
9.

Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.

Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C.

Neurosci Lett. 2008 May 2;436(1):23-6. doi: 10.1016/j.neulet.2008.02.045. Epub 2008 Mar 4.

PMID:
18355961
10.

Estrogen receptor beta polymorphism is associated with prostate cancer risk.

Thellenberg-Karlsson C, Lindström S, Malmer B, Wiklund F, Augustsson-Bälter K, Adami HO, Stattin P, Nilsson M, Dahlman-Wright K, Gustafsson JA, Grönberg H.

Clin Cancer Res. 2006 Mar 15;12(6):1936-41.

11.

ADH4 intronic variations are associated with alcohol dependence: results from an Italian case-control association study.

Turchi C, Piva F, Solito G, Principato G, Buscemi L, Tagliabracci A.

Pharmacogenet Genomics. 2012 Feb;22(2):79-94. doi: 10.1097/FPC.0b013e32834d05c8.

PMID:
22044940
12.

Serotonin 1A receptor gene, schizophrenia and bipolar disorder: an association study and meta-analysis.

Kishi T, Okochi T, Tsunoka T, Okumura T, Kitajima T, Kawashima K, Yamanouchi Y, Kinoshita Y, Naitoh H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ujike H, Ozaki N, Iwata N.

Psychiatry Res. 2011 Jan 30;185(1-2):20-6. doi: 10.1016/j.psychres.2010.06.003. Epub 2010 Jul 1.

PMID:
20594600
13.

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans.

Zheng SL, Sun J, Cheng Y, Li G, Hsu FC, Zhu Y, Chang BL, Liu W, Kim JW, Turner AR, Gielzak M, Yan G, Isaacs SD, Wiley KE, Sauvageot J, Chen HS, Gurganus R, Mangold LA, Trock BJ, Gronberg H, Duggan D, Carpten JD, Partin AW, Walsh PC, Xu J, Isaacs WB.

J Natl Cancer Inst. 2007 Oct 17;99(20):1525-33. Epub 2007 Oct 9.

PMID:
17925536
14.

Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia.

Zhang F, St Clair D, Liu X, Sun X, Sham PC, Crombie C, Ma X, Wang Q, Meng H, Deng W, Yates P, Hu X, Walker N, Murray RM, Collier DA, Li T.

Genes Brain Behav. 2005 Oct;4(7):444-8.

15.

A polymorphism in CALHM1 is associated with temporal lobe epilepsy.

Lv RJ, He JS, Fu YH, Shao XQ, Wu LW, Lu Q, Jin LR, Liu H.

Epilepsy Behav. 2011 Apr;20(4):681-5. doi: 10.1016/j.yebeh.2011.02.007. Epub 2011 Mar 24.

PMID:
21439911
16.

A functional intronic variant in the tyrosine hydroxylase (TH) gene confers risk of essential hypertension in the Northern Chinese Han population.

Wang L, Li B, Lu X, Zhao Q, Li Y, Ge D, Li H, Zhang P, Chen S, Chen R, Qiang B, Gu D.

Clin Sci (Lond). 2008 Sep;115(5):151-8. doi: 10.1042/CS20070335.

PMID:
18208403
17.

The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.

Zhang H, Morrison MA, Dewan A, Adams S, Andreoli M, Huynh N, Regan M, Brown A, Miller JW, Kim IK, Hoh J, Deangelis MM.

BMC Med Genet. 2008 Jun 9;9:51. doi: 10.1186/1471-2350-9-51.

18.

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;150(6):1104-11.

PMID:
15214895
19.

Association of angiotensin-converting enzyme gene promoter single nucleotide polymorphisms and haplotype with major depression in a northeastern Thai population.

Angunsri R, Sritharathikhun T, Suttirat S, Tencomnao T.

J Renin Angiotensin Aldosterone Syst. 2009 Sep;10(3):179-84. doi: 10.1177/1470320309344151.

PMID:
19713413
20.

Single nucleotide polymorphisms in human Paneth cell defensin A5 may confer susceptibility to inflammatory bowel disease in a New Zealand Caucasian population.

Ferguson LR, Browning BL, Huebner C, Petermann I, Shelling AN, Demmers P, McCulloch A, Gearry RB, Barclay ML, Philpott M.

Dig Liver Dis. 2008 Sep;40(9):723-30. doi: 10.1016/j.dld.2008.02.011. Epub 2008 Apr 3.

PMID:
18394979

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