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Items: 7

1.

Integrated analysis supports ATXN1 as a schizophrenia risk gene.

Liu J, Su B.

Schizophr Res. 2018 May;195:298-305. doi: 10.1016/j.schres.2017.10.010. Epub 2017 Oct 19.

PMID:
29055568
2.

Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population.

Culjković B, Stojković O, Savić D, Zamurović N, Nesić M, Major T, Keckarevi D, Romac S, Zamurovi B, Vukosavić S.

Am J Med Genet. 2000 Dec 4;96(6):884-7. No abstract available.

PMID:
11121205
3.

No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects.

Li T, Breen G, Brown J, Liu X, Murray RM, Shaw DJ, Sham PC, St Clair D, Collier DA.

Psychiatr Genet. 1999 Sep;9(3):123-7.

PMID:
10551541
4.
5.

Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patients.

Pujana MA, Martorell L, Volpini V, Valero J, Labad A, Vilella E, Estivill X.

Hum Genet. 1997 Jun;99(6):772-5.

PMID:
9187671
6.

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.

Morris-Rosendahl DJ, Burgert E, Uyanik G, Mayerova A, Duval F, Macher JP, Crocq MA.

Am J Med Genet. 1997 May 31;74(3):324-30.

PMID:
9184318
7.

Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23.

Wang S, Detera-Wadleigh SD, Coon H, Sun CE, Goldin LR, Duffy DL, Byerley WF, Gershon ES, Diehl SR.

Am J Hum Genet. 1996 Sep;59(3):731-6. No abstract available.

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