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Items: 9

1.

Familiality of novel factorial dimensions of schizophrenia.

McGrath JA, Avramopoulos D, Lasseter VK, Wolyniec PS, Fallin MD, Liang KY, Nestadt G, Thornquist MH, Luke JR, Chen PL, Valle D, Pulver AE.

Arch Gen Psychiatry. 2009 Jun;66(6):591-600. doi: 10.1001/archgenpsychiatry.2009.56.

PMID:
19487624
2.

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder.

Pisanté A, Bronstein M, Yakir B, Darvasi A.

Psychiatr Genet. 2009 Aug;19(4):212. doi: 10.1097/YPG.0b013e32832cebe6. No abstract available.

PMID:
19436241
3.

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.

Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A.

PLoS Genet. 2008 Feb;4(2):e28. doi: 10.1371/journal.pgen.0040028.

5.

Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

Fallin MD, Lasseter VK, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Liang KY, Pulver AE.

Am J Hum Genet. 2003 Sep;73(3):601-11. Epub 2003 Aug 15.

6.

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA.

Am J Hum Genet. 2002 Dec;71(6):1395-412. Epub 2002 Nov 26.

7.

A highly significant association between a COMT haplotype and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A.

Am J Hum Genet. 2002 Dec;71(6):1296-302. Epub 2002 Oct 25.

8.

Schizophrenia: diverse approaches to a complex disease.

Sawa A, Snyder SH.

Science. 2002 Apr 26;296(5568):692-5. Review.

PMID:
11976442
9.

A decrease of reelin expression as a putative vulnerability factor in schizophrenia.

Impagnatiello F, Guidotti AR, Pesold C, Dwivedi Y, Caruncho H, Pisu MG, Uzunov DP, Smalheiser NR, Davis JM, Pandey GN, Pappas GD, Tueting P, Sharma RP, Costa E.

Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15718-23.

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