Feingold E - Search Results

1

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL. Oliver TR, et al. Among authors: feingold e. Hum Genet. 2012 Jul;131(7):1039-46. doi: 10.1007/s00439-011-1121-7. Epub 2011 Dec 9. Hum Genet. 2012. PMID: 22160426 Free PMC article.

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

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.

8

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

9

Testing for contributions of mitochondrial DNA mutations to complex diseases.

Sun F, Ashley-Koch AE, Durham LK, Feingold E, Halloran ME, Manatunga AK, Sherman SL. Sun F, et al. Among authors: feingold e. Genet Epidemiol. 1998;15(5):451-69. doi: 10.1002/(SICI)1098-2272(1998)15:5<451::AID-GEPI2>3.0.CO;2-3. Genet Epidemiol. 1998. PMID: 9728889

10

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).

Estop AM, Cieply KM, Munne S, Feingold E. Estop AM, et al. Among authors: feingold e. Hum Genet. 1999 May;104(5):412-7. doi: 10.1007/s004390050977. Hum Genet. 1999. PMID: 10394934

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