Sharp AJ - Search Results

1

Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction.

Borel C, Cheung F, Stewart H, Koolen DA, Phillips C, Thomas NS, Jacobs PA, Eliez S, Sharp AJ. Borel C, et al. Among authors: sharp aj. Hum Genet. 2012 Sep;131(9):1519-24. doi: 10.1007/s00439-012-1180-4. Epub 2012 May 30. Hum Genet. 2012. PMID: 22643917

2

Evidence for a cryptic 46,XX cell line in a 45,X/46,X,psu idic(Xq) patient with normal reproduction.

James RS, Sharp AJ, Cockwell AE, Coppin B, Jacobs PA. James RS, et al. Among authors: sharp aj. J Med Genet. 1997 Dec;34(12):1030-2. doi: 10.1136/jmg.34.12.1030. J Med Genet. 1997. PMID: 9429151 Free PMC article.

3

A study of females with deletions of the short arm of the X chromosome.

James RS, Coppin B, Dalton P, Dennis NR, Mitchell C, Sharp AJ, Skuse DH, Thomas NS, Jacobs PA. James RS, et al. Among authors: sharp aj. Hum Genet. 1998 May;102(5):507-16. doi: 10.1007/s004390050733. Hum Genet. 1998. PMID: 9654198

4

Xp deletions associated with autism in three females.

Thomas NS, Sharp AJ, Browne CE, Skuse D, Hardie C, Dennis NR. Thomas NS, et al. Among authors: sharp aj. Hum Genet. 1999 Jan;104(1):43-8. doi: 10.1007/s004390050908. Hum Genet. 1999. PMID: 10071191

5

Age- and tissue-specific variation of X chromosome inactivation ratios in normal women.

Sharp A, Robinson D, Jacobs P. Sharp A, et al. Hum Genet. 2000 Oct;107(4):343-9. doi: 10.1007/s004390000382. Hum Genet. 2000. PMID: 11129333

6

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.

Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA. Thomas NS, et al. Among authors: sharp aj. Hum Mol Genet. 2001 Feb 1;10(3):243-50. doi: 10.1093/hmg/10.3.243. Hum Mol Genet. 2001. PMID: 11159943

7

Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation.

Sharp A, Robinson DO, Jacobs P. Sharp A, et al. Hum Genet. 2001 Sep;109(3):295-302. doi: 10.1007/s004390100578. Hum Genet. 2001. PMID: 11702210

8

Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocations.

Sharp AJ, Spotswood HT, Robinson DO, Turner BM, Jacobs PA. Sharp AJ, et al. Hum Mol Genet. 2002 Dec 1;11(25):3145-56. doi: 10.1093/hmg/11.25.3145. Hum Mol Genet. 2002. PMID: 12444099

9

Segmental duplications and copy-number variation in the human genome.

Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, Vallente RU, Pertz LM, Clark RA, Schwartz S, Segraves R, Oseroff VV, Albertson DG, Pinkel D, Eichler EE. Sharp AJ, et al. Am J Hum Genet. 2005 Jul;77(1):78-88. doi: 10.1086/431652. Epub 2005 May 25. Am J Hum Genet. 2005. PMID: 15918152 Free PMC article.

10

Structural variation of the human genome.

Sharp AJ, Cheng Z, Eichler EE. Sharp AJ, et al. Annu Rev Genomics Hum Genet. 2006;7:407-42. doi: 10.1146/annurev.genom.7.080505.115618. Annu Rev Genomics Hum Genet. 2006. PMID: 16780417 Review.

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