Hassold TJ - Search Results

1

A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.

Chernus JM, Allen EG, Zeng Z, Hoffman ER, Hassold TJ, Feingold E, Sherman SL. Chernus JM, et al. Among authors: hassold tj. PLoS Genet. 2019 Dec 12;15(12):e1008414. doi: 10.1371/journal.pgen.1008414. eCollection 2019 Dec. PLoS Genet. 2019. PMID: 31830031 Free PMC article.

2

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. Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391. Hum Mol Genet. 1997. PMID: 9285774

3

The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.

Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. Hall HE, et al. Am J Med Genet A. 2007 Oct 1;143A(19):2249-55. doi: 10.1002/ajmg.a.31918. Am J Med Genet A. 2007. PMID: 17705154

4

Down syndrome: genetic recombination and the origin of the extra chromosome 21.

Hassold T, Sherman S. Hassold T, et al. Clin Genet. 2000 Feb;57(2):95-100. doi: 10.1034/j.1399-0004.2000.570201.x. Clin Genet. 2000. PMID: 10735628 Review.

5

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. Hassold TJ, et al. Am J Hum Genet. 1991 Aug;49(2):253-60. Am J Hum Genet. 1991. PMID: 1867189 Free PMC article.

6

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.

Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. Sherman SL, et al. Among authors: hassold tj. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907

7

Paternal nondisjunction in trisomy 21: excess of male patients.

Petersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D, Mikkelsen M. Petersen MB, et al. Among authors: hassold tj. Hum Mol Genet. 1993 Oct;2(10):1691-5. doi: 10.1093/hmg/2.10.1691. Hum Mol Genet. 1993. PMID: 8268923

8

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.

Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, Sherman SL. Lamb NE, et al. Among authors: hassold tj. Nat Genet. 1996 Dec;14(4):400-5. doi: 10.1038/ng1296-400. Nat Genet. 1996. PMID: 8944019

9

Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome.

Shen JJ, Sherman SL, Hassold TJ. Shen JJ, et al. Among authors: hassold tj. Chromosoma. 1998 Jun;107(3):166-72. doi: 10.1007/s004120050293. Chromosoma. 1998. PMID: 9639654

10

Effect of meiotic recombination on the production of aneuploid gametes in humans.

Lamb NE, Sherman SL, Hassold TJ. Lamb NE, et al. Among authors: hassold tj. Cytogenet Genome Res. 2005;111(3-4):250-5. doi: 10.1159/000086896. Cytogenet Genome Res. 2005. PMID: 16192701 Review.

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