67 related articles for article (PubMed ID: 17557239)
1. [Association mapping of schizophrenia loci on chromosome 1 by use of pooled DNA genomic screening in eastern Shandong peninsula].
Chen G; Wen XY; Zhu HN; Wei R; Zhou P; Luan M; Gao CY; Zhu JP; Weng Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):288-92. PubMed ID: 17557239
[TBL] [Abstract][Full Text] [Related]
2. [Polymorphism of microsatellite markers D6S296, etc. in patients with schizophrenia].
Zhang X; Jiang S; Le Y; Qian Y; Wang D
Zhonghua Yi Xue Za Zhi; 2002 Mar; 82(5):334-7. PubMed ID: 11953193
[TBL] [Abstract][Full Text] [Related]
3. A genome-wide DNA microsatellite association screen to identify chromosomal regions harboring candidate genes in diabetic nephropathy.
McKnight AJ; Maxwell AP; Sawcer S; Compston A; Setakis E; Patterson CC; Brady HR; Savage DA
J Am Soc Nephrol; 2006 Mar; 17(3):831-6. PubMed ID: 16467450
[TBL] [Abstract][Full Text] [Related]
4. The microsatellite alleles on chromosome 1 associated with essential hypertension and blood pressure levels.
Nakayama T; Soma M; Kanmatsuse K; Kokubun S
J Hum Hypertens; 2004 Nov; 18(11):823-8. PubMed ID: 15190264
[TBL] [Abstract][Full Text] [Related]
5. Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.
Puri V; McQuillin A; Datta S; Choudhury K; Pimm J; Thirumalai S; Krasucki R; Lawrence J; Quested D; Bass N; Crombie C; Fraser G; Walker N; Moorey H; Ray MK; Sule A; Curtis D; St Clair D; Gurling H
Eur J Hum Genet; 2008 Oct; 16(10):1275-82. PubMed ID: 18414510
[TBL] [Abstract][Full Text] [Related]
6. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
Wang L; Lin H; Shen Y; Huang S; Gu J; Su H; Qi Y
Mol Vis; 2007 Aug; 13():1357-62. PubMed ID: 17768382
[TBL] [Abstract][Full Text] [Related]
7. Constitutive heterochromatin of chromosome 1 and Duffy blood group alleles in schizophrenia.
Kosower NS; Gerad L; Goldstein M; Parasol N; Zipser Y; Ragolsky M; Rozencwaig S; Elkabetz E; Abramovitch Y; Lerer B
Am J Med Genet; 1995 Apr; 60(2):133-8. PubMed ID: 7485247
[TBL] [Abstract][Full Text] [Related]
8. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
Holliday EG; McLean DE; Nyholt DR; Mowry BJ
Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696
[TBL] [Abstract][Full Text] [Related]
9. Microsatellite analysis of the GLC1B locus on chromosome 2 points to NCK2 as a new candidate gene for normal tension glaucoma.
Akiyama M; Yatsu K; Ota M; Katsuyama Y; Kashiwagi K; Mabuchi F; Iijima H; Kawase K; Yamamoto T; Nakamura M; Negi A; Sagara T; Kumagai N; Nishida T; Inatani M; Tanihara H; Ohno S; Inoko H; Mizuki N
Br J Ophthalmol; 2008 Sep; 92(9):1293-6. PubMed ID: 18723748
[TBL] [Abstract][Full Text] [Related]
10. Association of SOX10 with schizophrenia in the Japanese population.
Maeno N; Takahashi N; Saito S; Ji X; Ishihara R; Aoyama N; Branko A; Miura H; Ikeda M; Suzuki T; Kitajima T; Yamanouchi Y; Kinoshita Y; Iwata N; Inada T; Ozaki N
Psychiatr Genet; 2007 Aug; 17(4):227-31. PubMed ID: 17621166
[TBL] [Abstract][Full Text] [Related]
11. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.
Ohtsuki T; Horiuchi Y; Koga M; Ishiguro H; Inada T; Iwata N; Ozaki N; Ujike H; Watanabe Y; Someya T; Arinami T
Neurosci Lett; 2008 Apr; 435(3):194-7. PubMed ID: 18384956
[TBL] [Abstract][Full Text] [Related]
12. Number of STR repeats as a potential new quantitative genetic marker for complex diseases, illustrated by schizophrenia.
Liu H; Yu W; Wang X; Fang F; Yang G; Zhou J; Liang X; An W
Biochem Genet; 2007 Oct; 45(9-10):683-9. PubMed ID: 17690978
[TBL] [Abstract][Full Text] [Related]
13. Evidence of linkage and association with body fatness and abdominal fat on chromosome 15q26.
Bouchard L; Bouchard C; Chagnon YC; Perusse L
Obesity (Silver Spring); 2007 Aug; 15(8):2061-70. PubMed ID: 17712124
[TBL] [Abstract][Full Text] [Related]
14. Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18.
Tetens J; Ganter M; Müller G; Drögemüller C
Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3506-15. PubMed ID: 17652717
[TBL] [Abstract][Full Text] [Related]
15. A genome-wide scan maps a novel high myopia locus to 5p15.
Lam CY; Tam PO; Fan DS; Fan BJ; Wang DY; Lee CW; Pang CP; Lam DS
Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):3768-78. PubMed ID: 18421076
[TBL] [Abstract][Full Text] [Related]
16. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH
J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119
[TBL] [Abstract][Full Text] [Related]
17. Searching for a locus for schizophrenia within chromosome Xp11.
Wei J; Hemmings GP
Am J Med Genet; 2000 Feb; 96(1):4-7. PubMed ID: 10686543
[TBL] [Abstract][Full Text] [Related]
18. RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
Liu YL; Fann CS; Liu CM; Chen WJ; Wu JY; Hung SI; Chen CH; Jou YS; Liu SK; Hwang TJ; Hsieh MH; Chang CC; Yang WC; Lin JJ; Chou FH; Faraone SV; Tsuang MT; Hwu HG
Biol Psychiatry; 2008 Nov; 64(9):789-96. PubMed ID: 18571626
[TBL] [Abstract][Full Text] [Related]
19. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
Knight HM; Maclean A; Irfan M; Naeem F; Cass S; Pickard BS; Muir WJ; Blackwood DH; Ayub M
Eur J Hum Genet; 2008 Jun; 16(6):750-8. PubMed ID: 18322454
[TBL] [Abstract][Full Text] [Related]
20. [Progress in the studies on the molecular genetics of schizophrenia].
Deng H; Liu X; Sun X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Dec; 17(6):439-42. PubMed ID: 11110986
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
