Feingold E - Search Results

1

Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21.

Brown AS, Feingold E, Broman KW, Sherman SL. Brown AS, et al. Among authors: feingold e. Hum Mol Genet. 2000 Mar 1;9(4):515-23. doi: 10.1093/hmg/9.4.515. Hum Mol Genet. 2000. PMID: 10699174

2

Methods for genetic linkage analysis using trisomies.

Feingold E, Lamb NE, Sherman SL. Feingold E, et al. Am J Hum Genet. 1995 Feb;56(2):475-83. Am J Hum Genet. 1995. PMID: 7847384 Free PMC article.

3

Statistical models for trisomic phenotypes.

Lamb NE, Feingold E, Sherman SL. Lamb NE, et al. Among authors: feingold e. Am J Hum Genet. 1996 Jan;58(1):201-12. Am J Hum Genet. 1996. PMID: 8554057 Free PMC article.

4

Non-disjunction in human sperm: evidence for an effect of increasing paternal age.

Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ. Griffin DK, et al. Among authors: feingold e. Hum Mol Genet. 1995 Dec;4(12):2227-32. doi: 10.1093/hmg/4.12.2227. Hum Mol Genet. 1995. PMID: 8634691

5

Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome.

Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. Griffin DK, et al. Among authors: feingold e. Am J Hum Genet. 1996 Nov;59(5):1108-13. Am J Hum Genet. 1996. PMID: 8900240 Free PMC article.

6

Familial transmission of the FMR1 CGG repeat.

Nolin SL, Lewis FA 3rd, Ye LL, Houck GE Jr, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Brown WT. Nolin SL, et al. Among authors: feingold e. Am J Hum Genet. 1996 Dec;59(6):1252-61. Am J Hum Genet. 1996. PMID: 8940270 Free PMC article.

7

Strategies for mapping heterogeneous recessive traits by allele-sharing methods.

Feingold E, Siegmund DO. Feingold E, et al. Am J Hum Genet. 1997 Apr;60(4):965-78. Am J Hum Genet. 1997. PMID: 9106544 Free PMC article.

8

Estimating meiotic exchange patterns from recombination data: an application to humans.

Lamb NE, Feingold E, Sherman SL. Lamb NE, et al. Among authors: feingold e. Genetics. 1997 Jul;146(3):1011-7. doi: 10.1093/genetics/146.3.1011. Genetics. 1997. PMID: 9215904 Free PMC article.

9

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL. Lamb NE, et al. Among authors: feingold e. Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391. Hum Mol Genet. 1997. PMID: 9285774

10

Genome scanning for segments shared identical by descent among distant relatives in isolated populations.

Durham LK, Feingold E. Durham LK, et al. Among authors: feingold e. Am J Hum Genet. 1997 Oct;61(4):830-42. doi: 10.1086/514891. Am J Hum Genet. 1997. PMID: 9382093 Free PMC article.

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