Wijsman EM - Search Results

1

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. Among authors: wijsman em. Mol Psychiatry. 2005 Jul;10(7):699-711. doi: 10.1038/sj.mp.4001657. Mol Psychiatry. 2005. PMID: 15753956 Clinical Trial.

2

X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.

Raskind WH, Wijsman E, Pagon RA, Cox TC, Bawden MJ, May BK, Bird TD. Raskind WH, et al. Am J Hum Genet. 1991 Feb;48(2):335-41. Am J Hum Genet. 1991. PMID: 1671320 Free PMC article.

3

A familial Alzheimer's disease locus on chromosome 1.

Levy-Lahad E, Wijsman EM, Nemens E, Anderson L, Goddard KA, Weber JL, Bird TD, Schellenberg GD. Levy-Lahad E, et al. Among authors: wijsman em. Science. 1995 Aug 18;269(5226):970-3. doi: 10.1126/science.7638621. Science. 1995. PMID: 7638621

4

Monte Carlo analysis on a large pedigree.

Thompson EA, Lin S, Olshen AB, Wijsman EM. Thompson EA, et al. Among authors: wijsman em. Genet Epidemiol. 1993;10(6):677-82. doi: 10.1002/gepi.1370100658. Genet Epidemiol. 1993. PMID: 8314080

5

Chromosome 14 and late-onset familial Alzheimer disease (FAD).

Schellenberg GD, Payami H, Wijsman EM, Orr HT, Goddard KA, Anderson L, Nemens E, White JA, Alonso ME, Ball MJ, et al. Schellenberg GD, et al. Among authors: wijsman em. Am J Hum Genet. 1993 Sep;53(3):619-28. Am J Hum Genet. 1993. PMID: 8352272 Free PMC article.

6

Differences in Lp[a] concentrations and apo[a] polymorphs between black and white Americans.

Marcovina SM, Albers JJ, Wijsman E, Zhang Z, Chapman NH, Kennedy H. Marcovina SM, et al. J Lipid Res. 1996 Dec;37(12):2569-85. J Lipid Res. 1996. PMID: 9017509 Free article.

7

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. Among authors: wijsman em. 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

8

MCMC segregation and linkage analysis.

Heath SC, Snow GL, Thompson EA, Tseng C, Wijsman EM. Heath SC, et al. Among authors: wijsman em. Genet Epidemiol. 1997;14(6):1011-6. doi: 10.1002/(SICI)1098-2272(1997)14:6<1011::AID-GEPI75>3.0.CO;2-L. Genet Epidemiol. 1997. PMID: 9433616

9

Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.

Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS. Wijsman EM, et al. Arterioscler Thromb Vasc Biol. 1998 Feb;18(2):215-26. doi: 10.1161/01.atv.18.2.215. Arterioscler Thromb Vasc Biol. 1998. PMID: 9484986

10

Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.

Raskind WH, Conrad EU 3rd, Matsushita M, Wijsman EM, Wells DE, Chapman N, Sandell LJ, Wagner M, Houck J. Raskind WH, et al. Among authors: wijsman em. Hum Mutat. 1998;11(3):231-9. doi: 10.1002/(SICI)1098-1004(1998)11:3<231::AID-HUMU8>3.0.CO;2-K. Hum Mutat. 1998. PMID: 9521425

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