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Introduction: linkage analyses in the Hutterites.
Chapman NH, Wijsman EM. Chapman NH, et al. Genet Epidemiol. 2001;21 Suppl 1:S222-3. doi: 10.1002/gepi.2001.21.s1.s222. Genet Epidemiol. 2001. PMID: 11858132 No abstract available.
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.
Raskind WH, Igo RP, Chapman NH, Berninger VW, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Brown M, Wijsman EM. Raskind WH, et al. Mol Psychiatry. 2005 Jul;10(7):699-711. doi: 10.1038/ Mol Psychiatry. 2005. PMID: 15753956 Clinical Trial.
The importance of connections: joining components of the Hutterite pedigree.
Chapman NH, Leutenegger AL, Badzioch MD, Bogdan M, Conlon EM, Daw EW, Gagnon F, Li N, Maia JM, Wijsman EM, Thompson EA. Chapman NH, et al. Genet Epidemiol. 2001;21 Suppl 1:S230-5. doi: 10.1002/gepi.2001.21.s1.s230. Genet Epidemiol. 2001. PMID: 11793674
Evaluation of genetic and environmental effects using GEE and APM methods.
Bull SB, Chapman NH, Greenwood CM, Darlington GA. Bull SB, et al. Genet Epidemiol. 1995;12(6):729-34. doi: 10.1002/gepi.1370120633. Genet Epidemiol. 1995. PMID: 8788000
Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees.
Graham J, Chapman NH, Goddard KA, Goode EL, Wijsman EM, Jarvik GP. Graham J, et al. Genet Epidemiol. 1997;14(6):999-1004. doi: 10.1002/(SICI)1098-2272(1997)14:6<999::AID-GEPI73>3.0.CO;2-F. Genet Epidemiol. 1997. PMID: 9433614
Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.
Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH. Chapman NH, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):67-75. doi: 10.1002/ajmg.b.30018. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389770
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