97 related articles for article (PubMed ID: 11807409)
1. Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family.
Gross J; Grimm O; Ortega G; Teuber I; Lesch KP; Meyer J
Psychiatr Genet; 2001 Dec; 11(4):197-200. PubMed ID: 11807409
[TBL] [Abstract][Full Text] [Related]
2. Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.
Meyer J; Mai M; Ortega G; Mössner R; Lesch KP
Schizophr Res; 2002 Nov; 58(1):87-91. PubMed ID: 12363395
[TBL] [Abstract][Full Text] [Related]
3. Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.
Meyer J; Ortega G; Schraut K; Nürnberg G; Rüschendorf F; Saar K; Mössner R; Wienker TF; Reis A; Stöber G; Lesch KP
Mol Psychiatry; 2002; 7(2):220-3. PubMed ID: 11840317
[TBL] [Abstract][Full Text] [Related]
4. Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.
Stöber G; Kohlmann B; Iekiera M; Rubie C; Gawlik M; Möller-Ehrlich K; Meitinger T; Bettecken T
BMC Psychiatry; 2005 Oct; 5():36. PubMed ID: 16225677
[TBL] [Abstract][Full Text] [Related]
5. A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree.
Meyer J; Huberth A; Ortega G; Syagailo YV; Jatzke S; Mössner R; Strom TM; Ulzheimer-Teuber I; Stöber G; Schmitt A; Lesch KP
Mol Psychiatry; 2001 May; 6(3):302-6. PubMed ID: 11326298
[TBL] [Abstract][Full Text] [Related]
6. Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophrenia.
Georgieva L; Nikolov I; Poriazova N; Jones G; Toncheva D; Kirov G; Owen MJ
Psychiatr Genet; 2003 Jun; 13(2):103-6. PubMed ID: 12782967
[TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15.
Küry S; Rubie C; Moisan JP; Stöber G
J Neural Transm (Vienna); 2003 Nov; 110(11):1329-32. PubMed ID: 14628196
[TBL] [Abstract][Full Text] [Related]
8. Mutational analysis of the synapsin III gene on chromosome 22q12-q13 in schizophrenia.
Ohtsuki T; Ichiki R; Toru M; Arinami T
Psychiatry Res; 2000 Apr; 94(1):1-7. PubMed ID: 10788672
[TBL] [Abstract][Full Text] [Related]
9. Genomic organization and mutational analysis of the human UCP2 gene, a prime candidate gene for human obesity.
Lentes KU; Tu N; Chen H; Winnikes U; Reinert I; Marmann G; Pirke KM
J Recept Signal Transduct Res; 1999; 19(1-4):229-44. PubMed ID: 10071761
[TBL] [Abstract][Full Text] [Related]
10. Mutation analysis of SYNJ1: a possible candidate gene for chromosome 21q22-linked bipolar disorder.
Saito T; Guan F; Papolos DF; Lau S; Klein M; Fann CS; Lachman HM
Mol Psychiatry; 2001 Jul; 6(4):387-95. PubMed ID: 11443522
[TBL] [Abstract][Full Text] [Related]
11. Association of WKL1/MLC1 with catatonic schizophrenia.
Leegwater PA; Boor PK; Pronk JC; van der Knaap MS
Mol Psychiatry; 2002; 7(10):1037; author reply 1037-8. PubMed ID: 12476316
[No Abstract] [Full Text] [Related]
12. MLC1 gene is associated with schizophrenia and bipolar disorder in Southern India.
Verma R; Mukerji M; Grover D; B-Rao C; Das SK; Kubendran S; Jain S; Brahmachari SK
Biol Psychiatry; 2005 Jul; 58(1):16-22. PubMed ID: 15992519
[TBL] [Abstract][Full Text] [Related]
13. Polymorphism in SNAP29 gene promoter region associated with schizophrenia.
Saito T; Guan F; Papolos DF; Rajouria N; Fann CS; Lachman HM
Mol Psychiatry; 2001 Mar; 6(2):193-201. PubMed ID: 11317222
[TBL] [Abstract][Full Text] [Related]
14. Systematic search for mutations in the 14-3-3 eta chain gene on chromosome 22 in schizophrenics.
Hayakawa T; Ishiguro H; Toru M; Hamaguchi H; Arinami T
Psychiatr Genet; 1998; 8(1):33-6. PubMed ID: 9564686
[TBL] [Abstract][Full Text] [Related]
15. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
[TBL] [Abstract][Full Text] [Related]
16. A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia.
McQuillin A; Kalsi G; Moorey H; Lamb G; Mayet S; Quested D; Baker P; Curtis D; Gurling HM
Eur J Hum Genet; 2002 Aug; 10(8):491-4. PubMed ID: 12111645
[TBL] [Abstract][Full Text] [Related]
17. Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia.
Bengel D; Balling U; Stöber G; Heils A; Li SH; Ross CA; Jungkunz G; Franzek E; Beckmann H; Riederer P; Lesch KP
Eur Arch Psychiatry Clin Neurosci; 1998; 248(2):78-81. PubMed ID: 9684916
[TBL] [Abstract][Full Text] [Related]
18. Characterization of DNA polymorphisms in the E-cadherin gene (CDH1) promoter region.
Nakamura A; Shimazaki T; Kaneko K; Shibata M; Matsumura T; Nagai M; Makino R; Mitamura K
Mutat Res; 2002 May; 502(1-2):19-24. PubMed ID: 11996968
[TBL] [Abstract][Full Text] [Related]
19. Structure of the human N-cadherin gene: YAC analysis and fine chromosomal mapping to 18q11.2.
Wallis J; Fox MF; Walsh FS
Genomics; 1994 Jul; 22(1):172-9. PubMed ID: 7959764
[TBL] [Abstract][Full Text] [Related]
20. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.
Williams NM; Spurlock G; Norton N; Williams HJ; Hamshere ML; Krawczak M; Kirov G; Nikolov I; Georgieva L; Jones S; Cardno AG; O'Donovan MC; Owen MJ
Mol Psychiatry; 2002; 7(10):1092-100. PubMed ID: 12476324
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
