Sinsheimer JS - Search Results

1

Effect of Rhesus D incompatibility on schizophrenia depends on offspring sex.

Palmer CG, Mallery E, Turunen JA, Hsieh HJ, Peltonen L, Lonnqvist J, Woodward JA, Sinsheimer JS. Palmer CG, et al. Among authors: sinsheimer js. Schizophr Res. 2008 Sep;104(1-3):135-45. doi: 10.1016/j.schres.2008.06.022. Epub 2008 Aug 9. Schizophr Res. 2008. PMID: 18692992 Free PMC article.

2

No evidence of linkage or linkage disequilibrium between DAT1 and attention deficit hyperactivity disorder in a large sample.

Palmer CG, Bailey JN, Ramsey C, Cantwell D, Sinsheimer JS, Del'Homme M, McGough J, Woodward JA, Asarnow R, Asarnow J, Nelson S, Smalley SL. Palmer CG, et al. Among authors: sinsheimer js. Psychiatr Genet. 1999 Sep;9(3):157-60. doi: 10.1097/00041444-199909000-00009. Psychiatr Genet. 1999. PMID: 10551548 No abstract available.

3

Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.

Pajukanta P, Bodnar JS, Sallinen R, Chu M, Airaksinen T, Xiao Q, Castellani LW, Sheth SS, Wessman M, Palotie A, Sinsheimer JS, Demant P, Lusis AJ, Peltonen L. Pajukanta P, et al. Among authors: sinsheimer js. Mamm Genome. 2001 Mar;12(3):238-45. doi: 10.1007/s003350010265. Mamm Genome. 2001. PMID: 11252174

4

Chromosome 1 loci in Finnish schizophrenia families.

Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajärvi R, Partonen T, Suvisaari J, Lönnqvist J, Meyer J, Peltonen L. Ekelund J, et al. Among authors: sinsheimer js. Hum Mol Genet. 2001 Jul 15;10(15):1611-7. doi: 10.1093/hmg/10.15.1611. Hum Mol Genet. 2001. PMID: 11468279

5

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.

Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I. Auranen M, et al. Among authors: sinsheimer js. Am J Hum Genet. 2002 Oct;71(4):777-90. doi: 10.1086/342720. Epub 2002 Aug 21. Am J Hum Genet. 2002. PMID: 12192642 Free PMC article.

6

RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility.

Palmer CG, Turunen JA, Sinsheimer JS, Minassian S, Paunio T, Lönnqvist J, Peltonen L, Woodward JA. Palmer CG, et al. Among authors: sinsheimer js. Am J Hum Genet. 2002 Dec;71(6):1312-9. doi: 10.1086/344659. Epub 2002 Nov 18. Am J Hum Genet. 2002. PMID: 12439825 Free PMC article.

7

Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test.

Sinsheimer JS, Palmer CG, Woodward JA. Sinsheimer JS, et al. Genet Epidemiol. 2003 Jan;24(1):1-13. doi: 10.1002/gepi.10211. Genet Epidemiol. 2003. PMID: 12508251

8

RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order.

Kraft P, Palmer CG, Woodward AJ, Turunen JA, Minassian S, Paunio T, Lönnqvist J, Peltonen L, Sinsheimer JS. Kraft P, et al. Among authors: sinsheimer js. Eur J Hum Genet. 2004 Mar;12(3):192-8. doi: 10.1038/sj.ejhg.5201129. Eur J Hum Genet. 2004. PMID: 14735156

9

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

Pajukanta P, Lilja HE, Sinsheimer JS, Cantor RM, Lusis AJ, Gentile M, Duan XJ, Soro-Paavonen A, Naukkarinen J, Saarela J, Laakso M, Ehnholm C, Taskinen MR, Peltonen L. Pajukanta P, et al. Among authors: sinsheimer js. Nat Genet. 2004 Apr;36(4):371-6. doi: 10.1038/ng1320. Epub 2004 Feb 29. Nat Genet. 2004. PMID: 14991056 Free article.

10

An exact maternal-fetal genotype incompatibility (MFG) test.

Minassian SL, Palmer CG, Sinsheimer JS. Minassian SL, et al. Among authors: sinsheimer js. Genet Epidemiol. 2005 Jan;28(1):83-95. doi: 10.1002/gepi.20027. Genet Epidemiol. 2005. PMID: 15368616

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