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Items: 1 to 20 of 189

1.

False discovery rate in linkage and association genome screens for complex disorders.

Sabatti C, Service S, Freimer N.

Genetics. 2003 Jun;164(2):829-33.

2.

Strategies for detecting susceptibility genes in a complex disease.

Babron MC, Barillot E, Margaritte-Jeannin P, Clerget-Darpoux F.

Genet Epidemiol. 1999;17 Suppl 1:S479-83.

PMID:
10597479
3.

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.

PMID:
17823922
4.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
5.

Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.

Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.

Eur J Hum Genet. 2006 Mar;14(3):340-8.

6.

Shared and specific susceptibility loci for schizophrenia and bipolar disorder: a dense genome scan in Eastern Quebec families.

Maziade M, Roy MA, Chagnon YC, Cliche D, Fournier JP, Montgrain N, Dion C, Lavallée JC, Garneau Y, Gingras N, Nicole L, Pirès A, Ponton AM, Potvin A, Wallot H, Mérette C.

Mol Psychiatry. 2005 May;10(5):486-99.

PMID:
15534619
7.

Controlling the proportion of false positives in multiple dependent tests.

Fernando RL, Nettleton D, Southey BR, Dekkers JC, Rothschild MF, Soller M.

Genetics. 2004 Jan;166(1):611-9.

8.

Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series.

Shaw SH, Mroczkowski-Parker Z, Shekhtman T, Alexander M, Remick RA, Sadovnick AD, McElroy SL, Keck PE Jr, Kelsoe JR.

Mol Psychiatry. 2003 May;8(5):558-64.

PMID:
12808435
9.

Interpretation of simultaneous linkage and family-based association tests in genome screens.

Chung RH, Hauser ER, Martin ER.

Genet Epidemiol. 2007 Feb;31(2):134-42.

PMID:
17123303
10.

Empirical Bayes screening of many p-values with applications to microarray studies.

Datta S, Datta S.

Bioinformatics. 2005 May 1;21(9):1987-94.

11.
12.

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.

Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, Varsani S, Skelding P, Hauser M, Vance J, Pericak-Vance M, Burns DK, Middleton LT, Brewster SR, Anderson WH, Riley JH.

Eur J Hum Genet. 2006 Mar;14(3):307-16. Erratum in: Eur J Hum Genet. 2007 Jun;15(6):714.

13.

False discoveries in genome scanning.

Drigalenko EI, Elston RC.

Genet Epidemiol. 1997;14(6):779-84.

PMID:
9433577
14.

Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy.

Fanous AH, Neale MC, Gardner CO, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS.

Mol Psychiatry. 2007 Oct;12(10):958-65.

PMID:
17440434
15.

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.

Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC.

Neurology. 2005 Jul 12;65(1):156-8.

PMID:
16009908
16.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696
17.

Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.

Lange EM, Ho LA, Beebe-Dimmer JL, Wang Y, Gillanders EM, Trent JM, Lange LA, Wood DP, Cooney KA.

Hum Genet. 2006 May;119(4):400-7.

PMID:
16508751
19.

A whole genome screen for linkage in Turkish multiple sclerosis.

Eraksoy M, Kurtuncu M, Akman-Demir G, Kilinc M, Gedizlioglu M, Mirza M, Anlar O, Kutlu C, Demirkiran M, Idrisoglu HA, Compston A, Sawcer S; Turkish Multiple Sclerosis Genetics Study Group..

J Neuroimmunol. 2003 Oct;143(1-2):17-24.

PMID:
14575909
20.

Issues in genomic screening: critical values, sample sizes, and the ability to detect linkage.

Rogus JJ, Cai T, Wei LJ.

Genet Epidemiol. 1999;17 Suppl 1:S697-701.

PMID:
10597516
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