70 related articles for article (PubMed ID: 19125102)
1. Positive association of neuroligin-4 gene with nonspecific mental retardation in the Qinba Mountains Region of China.
Qi H; Xing L; Zhang K; Gao X; Zheng Z; Huang S; Guo Y; Zhang F
Psychiatr Genet; 2009 Feb; 19(1):1-5. PubMed ID: 19125102
[TBL] [Abstract][Full Text] [Related]
2. An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population.
Zhang K; Gao J; An C; Gao X; Zheng Z; Li R; Huang S; Zhang F
Neurosci Lett; 2007 May; 419(1):83-7. PubMed ID: 17442488
[TBL] [Abstract][Full Text] [Related]
3. No association between polymorphisms in the FACL4 (fatty acid-CoA ligase 4) gene and nonspecific mental retardation in Qin-Ba mountain region of China.
An C; Zhang K; Gao X; Zheng Z; Shi Z; Gong P; Guo Y; Huang S; Zhang F
Neurosci Lett; 2008 Aug; 441(2):197-200. PubMed ID: 18614287
[TBL] [Abstract][Full Text] [Related]
4. Mental retardation and Xq12-Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region.
Zhang K; Zhang J; Zheng Z; Gao X; Huang S; Li R; Chen C; Zhang F
Psychiatr Genet; 2009 Feb; 19(1):27-31. PubMed ID: 19125105
[TBL] [Abstract][Full Text] [Related]
5. Positive association of the DIO2 (deiodinase type 2) gene with mental retardation in the iodine-deficient areas of China.
Guo TW; Zhang FC; Yang MS; Gao XC; Bian L; Duan SW; Zheng ZJ; Gao JJ; Wang H; Li RL; Feng GY; St Clair D; He L
J Med Genet; 2004 Aug; 41(8):585-90. PubMed ID: 15286152
[TBL] [Abstract][Full Text] [Related]
6. Positive association between POU1F1 and mental retardation in young females in the Chinese Han population.
Sun Y; Zhang F; Gao J; Gao X; Guo T; Zhang K; Shi Y; Zheng Z; Tang W; Zheng Y; Li S; Li X; Feng G; Shen X; He L
Hum Mol Genet; 2006 Apr; 15(7):1237-43. PubMed ID: 16505001
[TBL] [Abstract][Full Text] [Related]
7. Gender differences in cognitive ability associated with genetic variants of NLGN4.
Zhang K; Gao X; Qi H; Li J; Zheng Z; Zhang F
Neuropsychobiology; 2010; 62(4):221-8. PubMed ID: 20714171
[TBL] [Abstract][Full Text] [Related]
8. Association between a functional COMT polymorphism, mental retardation and cognition in Qinba area children.
Zhang KJ; Gao XC; Li RL; Chen C; Zheng ZJ; Huang SP; Zhang FC
Yi Chuan Xue Bao; 2006 Jun; 33(6):495-500. PubMed ID: 16800379
[TBL] [Abstract][Full Text] [Related]
9. A common haplotype of the LBP gene predisposes to severe sepsis.
Flores C; Pérez-Méndez L; Maca-Meyer N; Muriel A; Espinosa E; Blanco J; Sangüesa R; Muros M; Garcia JG; Villar J;
Crit Care Med; 2009 Oct; 37(10):2759-66. PubMed ID: 19707138
[TBL] [Abstract][Full Text] [Related]
10. An association study of the SLC26A4 gene in children with mental retardation.
Li J; Zhang F; Gao J; Cai Z; Zhao Q; Xing Y; Xu J; Liu Y; Shao L; Che R; Wei Z; He L
Neurosci Lett; 2009 Jul; 457(3):155-8. PubMed ID: 19429184
[TBL] [Abstract][Full Text] [Related]
11. A family-based association study of DIO2 and children mental retardation in the Qinba region of China.
Zhang K; Xi H; Wang X; Guo Y; Huang S; Zheng Z; Zhang F; Gao X
J Hum Genet; 2012 Jan; 57(1):14-7. PubMed ID: 22048657
[TBL] [Abstract][Full Text] [Related]
12. PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden.
Kostulas K; Gretarsdottir S; Kostulas V; Manolescu A; Helgadottir A; Thorleifsson G; Gudmundsson LJ; Thorsteinsdottir U; Gulcher JR; Stefansson K; Hillert J
J Neurol Sci; 2007 Dec; 263(1-2):113-7. PubMed ID: 17655870
[TBL] [Abstract][Full Text] [Related]
13. A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China.
Zhang K; Zhang M; He H; Zhang J; Chi W; Guo Y; Huang S; Zheng Z; Zhang F; Gao X
Neurosci Lett; 2012 May; 516(1):1-4. PubMed ID: 22366260
[TBL] [Abstract][Full Text] [Related]
14. Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.
Liu CP; Li XG; Lou JT; Xue Y; Luo CF; Zhou XW; Chen F; Li X; Li M; Li JC
J Pediatr Surg; 2009 Sep; 44(9):1805-11. PubMed ID: 19735829
[TBL] [Abstract][Full Text] [Related]
15. Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.
Amre DK; Mack DR; Morgan K; Fujiwara M; Israel D; Deslandres C; Seidman EG; Lambrette P; Costea I; Krupoves A; Fegury H; Dong J; Grimard G; Levy E
Am J Gastroenterol; 2009 Nov; 104(11):2824-8. PubMed ID: 19623168
[TBL] [Abstract][Full Text] [Related]
16. Estrogen receptor polymorphisms and the risk of endometrial cancer.
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Gilbert M; Hamann U; Scott RJ
BJOG; 2009 Jul; 116(8):1053-61. PubMed ID: 19438492
[TBL] [Abstract][Full Text] [Related]
17. The association of CTLA-4 and CD28 gene polymorphisms with idiopathic ischemic stroke in the paediatric population.
Wang JJ; Jiang LQ; He B; Shi KL; Li JW; Zou LP
Int J Immunogenet; 2009 Apr; 36(2):113-8. PubMed ID: 19284445
[TBL] [Abstract][Full Text] [Related]
18. Single nucleotide polymorphisms and the haplotype in the DEFB1 gene are associated with atopic dermatitis in a Korean population.
Kim E; Lee JE; Namkung JH; Kim PS; Kim S; Shin ES; Cho EY; Yang JM
J Dermatol Sci; 2009 Apr; 54(1):25-30. PubMed ID: 19135873
[TBL] [Abstract][Full Text] [Related]
19. Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.
Polakova V; Pardini B; Naccarati A; Landi S; Slyskova J; Novotny J; Vodickova L; Bermejo JL; Hanova M; Smerhovsky Z; Tulupova E; Kumar R; Hemminki K; Vodicka P
Hum Mutat; 2009 Apr; 30(4):661-8. PubMed ID: 19224585
[TBL] [Abstract][Full Text] [Related]
20. Variants of the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene and risk of stroke: a HuGE gene-disease association review and meta-analysis.
Zintzaras E; Rodopoulou P; Sakellaridis N
Am J Epidemiol; 2009 Mar; 169(5):523-32. PubMed ID: 19126581
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
