Kong A - Search Results

1

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.

Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A. Cox NJ, et al. Among authors: kong a. Nat Genet. 1999 Feb;21(2):213-5. doi: 10.1038/6002. Nat Genet. 1999. PMID: 9988276

2

Allele-sharing models: LOD scores and accurate linkage tests.

Kong A, Cox NJ. Kong A, et al. Am J Hum Genet. 1997 Nov;61(5):1179-88. doi: 10.1086/301592. Am J Hum Genet. 1997. PMID: 9345087 Free PMC article.

3

Importance sampling. I. Computing multimodel p values in linkage analysis.

Kong A, Frigge M, Irwin M, Cox N. Kong A, et al. Am J Hum Genet. 1992 Dec;51(6):1413-29. Am J Hum Genet. 1992. PMID: 1463020 Free PMC article.

4

Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling.

Kong A, Frigge M, Cox N, Wong WH. Kong A, et al. Cytogenet Cell Genet. 1992;59(2-3):208-10. doi: 10.1159/000133248. Cytogenet Cell Genet. 1992. PMID: 1737503 No abstract available.

5

Sequential imputation and multipoint linkage analysis.

Kong A, Cox N, Frigge M, Irwin M. Kong A, et al. Genet Epidemiol. 1993;10(6):483-8. doi: 10.1002/gepi.1370100626. Genet Epidemiol. 1993. PMID: 8314048

6

Diabetes, dependence, asymptotics, selection and significance.

Kong A, Frigge M, Bell GI, Lander ES, Daly MJ, Cox NJ. Kong A, et al. Nat Genet. 1997 Oct;17(2):148. doi: 10.1038/ng1097-148. Nat Genet. 1997. PMID: 9326932 No abstract available.

7

A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.

Arngrímsson R, Sigurõardóttir S, Frigge ML, Bjarnadóttir RI, Jónsson T, Stefánsson H, Baldursdóttir A, Einarsdóttir AS, Palsson B, Snorradóttir S, Lachmeijer AM, Nicolae D, Kong A, Bragason BT, Gulcher JR, Geirsson RT, Stefánsson K. Arngrímsson R, et al. Among authors: kong a. Hum Mol Genet. 1999 Sep;8(9):1799-805. doi: 10.1093/hmg/8.9.1799. Hum Mol Genet. 1999. PMID: 10441346

8

Allegro, a new computer program for multipoint linkage analysis.

Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Gudbjartsson DF, et al. Among authors: kong a. Nat Genet. 2000 May;25(1):12-3. doi: 10.1038/75514. Nat Genet. 2000. PMID: 10802644 No abstract available.

9

A genome-wide scan for preeclampsia in the Netherlands.

Lachmeijer AM, Arngrímsson R, Bastiaans EJ, Frigge ML, Pals G, Sigurdardóttir S, Stéfansson H, Pálsson B, Nicolae D, Kong A, Aarnoudse JG, Gulcher JR, Dekker GA, ten Kate LP, Stéfansson K. Lachmeijer AM, et al. Among authors: kong a. Eur J Hum Genet. 2001 Oct;9(10):758-64. doi: 10.1038/sj.ejhg.5200706. Eur J Hum Genet. 2001. PMID: 11781687

10

Mapping of a familial essential tremor gene, FET1, to chromosome 3q13.

Gulcher JR, Jónsson P, Kong A, Kristjánsson K, Frigge ML, Kárason A, Einarsdóttir IE, Stefánsson H, Einarsdóttir AS, Sigurthoardóttir S, Baldursson S, Björnsdóttir S, Hrafnkelsdóttir SM, Jakobsson F, Benedickz J, Stefánsson K. Gulcher JR, et al. Among authors: kong a. Nat Genet. 1997 Sep;17(1):84-7. doi: 10.1038/ng0997-84. Nat Genet. 1997. PMID: 9288103

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