Shaw SH - Search Results

1

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

Francks C, DeLisi LE, Shaw SH, Fisher SE, Richardson AJ, Stein JF, Monaco AP. Francks C, et al. Among authors: shaw sh. Hum Mol Genet. 2003 Dec 15;12(24):3225-30. doi: 10.1093/hmg/ddg362. Epub 2003 Oct 28. Hum Mol Genet. 2003. PMID: 14583442

2

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.

Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lönnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoëga T, Helgason T. Lewis CM, et al. Among authors: shaw sh. Am J Hum Genet. 2003 Jul;73(1):34-48. doi: 10.1086/376549. Epub 2003 Jun 11. Am J Hum Genet. 2003. PMID: 12802786 Free PMC article.

3

Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome.

Laval SH, Dann JC, Butler RJ, Loftus J, Rue J, Leask SJ, Bass N, Comazzi M, Vita A, Nanko S, Shaw S, Peterson P, Shields G, Smith AB, Stewart J, DeLisi LE, Crow TJ. Laval SH, et al. Among authors: shaw s. Am J Med Genet. 1998 Sep 7;81(5):420-7. doi: 10.1002/(sici)1096-8628(19980907)81:5<420::aid-ajmg11>3.0.co;2-e. Am J Med Genet. 1998. PMID: 9754628

4

A genome-wide search for schizophrenia susceptibility genes.

Shaw SH, Kelly M, Smith AB, Shields G, Hopkins PJ, Loftus J, Laval SH, Vita A, De Hert M, Cardon LR, Crow TJ, Sherrington R, DeLisi LE. Shaw SH, et al. Am J Med Genet. 1998 Sep 7;81(5):364-76. doi: 10.1002/(sici)1096-8628(19980907)81:5<364::aid-ajmg4>3.0.co;2-t. Am J Med Genet. 1998. PMID: 9754621

5

Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder.

DeLisi LE, Shaw S, Sherrington R, Nanthakumar B, Shields G, Smith AB, Wellman N, Larach VW, Loftus J, Razi K, Stewart J, Comazzi M, Vita A, De Hert M, Crow TJ. DeLisi LE, et al. Am J Med Genet. 2000 Jun 12;96(3):335-41. doi: 10.1002/1096-8628(20000612)96:3<335::aid-ajmg20>3.0.co;2-e. Am J Med Genet. 2000. PMID: 10898911

6

Evaluation of linkage disequilibrium between chromosome 22q11 single nucleotide polymorphisms in a large outbred population.

Shaw SH, Hutchison D, Saiz R, Abel K, DeLisi LE, Schork NJ, Sherrington R. Shaw SH, et al. Am J Med Genet. 2002 Mar 8;114(2):205-13. doi: 10.1002/ajmg.10151. Am J Med Genet. 2002. PMID: 11857583

7

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.

DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R. DeLisi LE, et al. Among authors: shaw sh. Am J Psychiatry. 2002 May;159(5):803-12. doi: 10.1176/appi.ajp.159.5.803. Am J Psychiatry. 2002. PMID: 11986135 Free article.

8

Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder.

DeLisi LE, Shaw S, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nathankumar B, Razi K, Kushner M, Stewart J, Vita A, Comazzi M, Sherrington R. DeLisi LE, et al. Am J Med Genet. 2000 Apr 3;96(2):235-9. doi: 10.1002/(sici)1096-8628(20000403)96:2<235::aid-ajmg21>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10893503

9

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E. Lindholm E, et al. Am J Hum Genet. 2001 Jul;69(1):96-105. doi: 10.1086/321288. Epub 2001 May 25. Am J Hum Genet. 2001. PMID: 11389481 Free PMC article.

10

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.

Hampe J, Schreiber S, Shaw SH, Lau KF, Bridger S, Macpherson AJ, Cardon LR, Sakul H, Harris TJ, Buckler A, Hall J, Stokkers P, van Deventer SJ, Nürnberg P, Mirza MM, Lee JC, Lennard-Jones JE, Mathew CG, Curran ME. Hampe J, et al. Among authors: shaw sh. Am J Hum Genet. 1999 Mar;64(3):808-16. doi: 10.1086/302294. Am J Hum Genet. 1999. PMID: 10053016 Free PMC article.

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