Optimizing selection of restriction enzymes in the search for DNA variants.

Por Wijsman, E M
Publicado em 1984

Recurrence risk of a new dominant mutation in children of unaffected parents.

Por Wijsman, E M
Publicado em 1991

A deductive method of haplotype analysis in pedigrees.

Por Wijsman, E M
Publicado em 1987

Genome screens using linkage disequilibrium tests: optimal marker characteristics and feasibility.

Por Chapman, N H, Wijsman, E M
Publicado em 1998

Design and sample-size considerations in the detection of linkage disequilibrium with a disease locus.

Por Olson, J. M., Wijsman, E. M.
Publicado em 1994

Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees.

Por Daw, E W, Heath, S C, Wijsman, E M
Publicado em 1999

Influence of apolipoprotein E genotype on the transmission of Alzheimer disease in a community-based sample.

Por Jarvik, G., Larson, E. B., Goddard, K., Schellenberg, G. D., Wijsman, E. M.
Publicado em 1996

Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency.

Por Hokanson, J E, Brunzell, J D, Jarvik, G P, Wijsman, E M, Austin, M A
Publicado em 1999

Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Por Palmer, S. E., Scherer, S. W., Kukolich, M., Wijsman, E. M., Tsui, L. C., Stephens, K., Evans, J. P.
Publicado em 1994

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Por Goddard, K. A., Yu, C. E., Oshima, J., Miki, T., Nakura, J., Piussan, C., Martin, G. M., Schellenberg, G. D., Wijsman, E. M.
Publicado em 1996

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Por Yu, C E, Oshima, J, Wijsman, E M, Nakura, J, Miki, T, Piussan, C, Matthews, S, Fu, Y H, Mulligan, J, Martin, G M, Schellenberg, G D
Publicado em 1997

Identification of rare variants from exome sequence in a large pedigree with autism

Por Marchani, E. E., Chapman, N. H., Cheung, C. Y. K., Ankenman, K., Stanaway, I. B., Coon, H. H., Nickerson, D., Bernier, R., Brkanac, Z., Wijsman, E. M.
Publicado em 2013

Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.

Por Payami, H., Zareparsi, S., Montee, K. R., Sexton, G. J., Kaye, J. A., Bird, T. D., Yu, C. E., Wijsman, E. M., Heston, L. L., Litt, M., Schellenberg, G. D.
Publicado em 1996

Association of rare missense variants in the second intracellular loop of Na(V)1.7 sodium channels with familial autism

Por Rubinstein, M, Patowary, A, Stanaway, I B, McCord, E, Nesbitt, R R, Archer, M, Scheuer, T, Nickerson, D, Raskind, W H, Wijsman, E M, Bernier, R, Catterall, W A, Brkanac, Z
Publicado no Mol Psychiatry (2018)

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders

Por Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M. C., Adams, A. K., Nato, A. Q., Wijsman, E. M., Eicher, J. D., Gruen, J. R.
Publicado no Hum Genet (2016)