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Items: 1 to 20 of 72

1.

Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.

Toyota T, Yoshitsugu K, Ebihara M, Yamada K, Ohba H, Fukasawa M, Minabe Y, Nakamura K, Sekine Y, Takei N, Suzuki K, Itokawa M, Meerabux JM, Iwayama-Shigeno Y, Tomaru Y, Shimizu H, Hattori E, Mori N, Yoshikawa T.

Hum Mol Genet. 2004 Mar 1;13(5):551-61. Epub 2004 Jan 6.

PMID:
14709596
2.

[Schizophrenia and ocular misalignment: phenotypic and genetic association analysis].

Yoshikawa Y, Toyota T, Yoshitsugu K, Yamada K, Itokawa M, Minabe Y, Nakamura K, Tomaru Y, Takei N, Kumakura T, Mori N.

Seishin Shinkeigaku Zasshi. 2004;106(12):1585-92. Review. Japanese.

PMID:
15770961
3.

Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease.

Ide M, Yamada K, Toyota T, Iwayama Y, Ishitsuka Y, Minabe Y, Nakamura K, Hattori N, Asada T, Mizuno Y, Mori N, Yoshikawa T.

Hum Genet. 2005 Oct;117(6):520-7. Epub 2005 Jul 14.

PMID:
16021468
4.

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC.

Nat Genet. 2001 Nov;29(3):315-20.

PMID:
11600883
5.

Analysis of polymorphisms in AT-rich domains of neuregulin 1 gene in schizophrenia.

Lachman HM, Pedrosa E, Nolan KA, Glass M, Ye K, Saito T.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):102-9.

PMID:
16287046
6.

A family-based and case-control association study of SOX10 in schizophrenia.

Iwamoto K, Bundo M, Yamada K, Takao H, Iwayama Y, Yoshikawa T, Kato T.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141B(5):477-81.

PMID:
16741945
7.

Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder.

Smith KM, Bauer L, Fischer M, Barkley R, Navia BA.

Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):57-63.

PMID:
15635701
8.

Screening of the ARX gene in 682 retarded males.

Grønskov K, Hjalgrim H, Nielsen IM, Brøndum-Nielsen K.

Eur J Hum Genet. 2004 Sep;12(9):701-5.

9.
10.

HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg.

Kjaer KW, Hedeboe J, Bugge M, Hansen C, Friis-Henriksen K, Vestergaard MB, Tommerup N, Opitz JM.

Am J Med Genet. 2002 Jun 15;110(2):116-21.

PMID:
12116248
11.

In Vitro studies of non poly alanine PHOX2B mutations argue against a loss-of-function mechanism for congenital central hypoventilation.

Trochet D, Mathieu Y, Pontual Ld, Savarirayan R, Munnich A, Brunet JF, Lyonnet S, Goridis C, Amiel J.

Hum Mutat. 2009 Feb;30(2):E421-31. doi: 10.1002/humu.20923.

PMID:
19058226
12.

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.

PMID:
17621166
13.

No association found between 158 Val/Met polymorphism of the COMT gene and schizophrenia with minor physical anomalies.

Joo EJ, Jeong SH, Ahn YM, Lee KY, Chang Yoon S, Kim EJ, Kim SU, Cho SC, Sik Kim Y.

Psychiatry Res. 2005 Sep 15;136(2-3):83-91.

PMID:
16109444
14.

Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia.

Kockelkorn TT, Arai M, Matsumoto H, Fukuda N, Yamada K, Minabe Y, Toyota T, Ujike H, Sora I, Mori N, Yoshikawa T, Itokawa M.

Neurosci Lett. 2004 Sep 16;368(1):41-5.

PMID:
15342131
15.

Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history.

Toyosima M, Maekawa M, Toyota T, Iwayama Y, Arai M, Ichikawa T, Miyashita M, Arinami T, Itokawa M, Yoshikawa T.

Br J Psychiatry. 2011 Sep;199(3):245-6. doi: 10.1192/bjp.bp.111.093849.

16.

The human LMX1B gene: transcription unit, promoter, and pathogenic mutations.

Dunston JA, Hamlington JD, Zaveri J, Sweeney E, Sibbring J, Tran C, Malbroux M, O'Neill JP, Mountford R, McIntosh I.

Genomics. 2004 Sep;84(3):565-76.

PMID:
15498463
17.

Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE.

Hung CC, Su YN, Tsao PN, Chen PC, Lin SJ, Lin CH, Mu SC, Liu CA, Chang YC, Lin WL, Hsieh WS, Hsu SM.

Electrophoresis. 2007 Mar;28(6):894-9.

PMID:
17300129
18.

No association of CNR1 gene variations with susceptibility to schizophrenia.

Seifert J, Ossege S, Emrich HM, Schneider U, Stuhrmann M.

Neurosci Lett. 2007 Oct 9;426(1):29-33. Epub 2007 Aug 10.

PMID:
17881126
19.

Family-based association study of synapsin II and schizophrenia.

Chen Q, He G, Qin W, Chen QY, Zhao XZ, Duan SW, Liu XM, Feng GY, Xu YF, St Clair D, Li M, Wang JH, Xing YL, Shi JG, He L.

Am J Hum Genet. 2004 Nov;75(5):873-7. Epub 2004 Sep 24.

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