Wijsman EM - Search Results

1

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

Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM. Marchani EE, et al. Among authors: wijsman em. Hum Hered. 2012;74(3-4):153-64. doi: 10.1159/000346560. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594493 Free PMC article.

2

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.

Schellenberg GD, Pericak-Vance MA, Wijsman EM, Moore DK, Gaskell PC Jr, Yamaoka LA, Bebout JL, Anderson L, Welsh KA, Clark CM, et al. Schellenberg GD, et al. Among authors: wijsman em. Am J Hum Genet. 1991 Mar;48(3):563-83. Am J Hum Genet. 1991. PMID: 1998342 Free PMC article.

3

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

Palmer SE, Scherer SW, Kukolich M, Wijsman EM, Tsui LC, Stephens K, Evans JP. Palmer SE, et al. Among authors: wijsman em. Am J Hum Genet. 1994 Jul;55(1):21-6. Am J Hum Genet. 1994. PMID: 7912888 Free PMC article.

4

The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

Yu CE, Payami H, Olson JM, Boehnke M, Wijsman EM, Orr HT, Kukull WA, Goddard KA, Nemens E, White JA, et al. Yu CE, et al. Among authors: wijsman em. Am J Hum Genet. 1994 Apr;54(4):631-42. Am J Hum Genet. 1994. PMID: 8128960 Free PMC article.

5

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

6

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.

7

Achieving irreducibility of the Markov chain Monte Carlo method applied to pedigree data.

Lin S, Thompson E, Wijsman E. Lin S, et al. IMA J Math Appl Med Biol. 1993;10(1):1-17. doi: 10.1093/imammb/10.1.1. IMA J Math Appl Med Biol. 1993. PMID: 8409623

8

Pedigree analysis package vs. MIXD: fitting the mixed model on a large pedigree.

Olshen AB, Wijsman EM. Olshen AB, et al. Among authors: wijsman em. Genet Epidemiol. 1996;13(1):91-106. doi: 10.1002/(SICI)1098-2272(1996)13:1<91::AID-GEPI8>3.0.CO;2-9. Genet Epidemiol. 1996. PMID: 8647381

9

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.

Goddard KA, Yu CE, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, Schellenberg GD, Wijsman EM. Goddard KA, et al. Among authors: wijsman em. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

231 results

Search Page

Filters