Rudd MK - Search Results

1

Elevated rates of sister chromatid exchange at chromosome ends.

Rudd MK, Friedman C, Parghi SS, Linardopoulou EV, Hsu L, Trask BJ. Rudd MK, et al. PLoS Genet. 2007 Feb 23;3(2):e32. doi: 10.1371/journal.pgen.0030032. PLoS Genet. 2007. PMID: 17319749 Free PMC article.

2

Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event.

Rudd MK, Endicott RM, Friedman C, Walker M, Young JM, Osoegawa K; NISC Comparative Sequencing Program; de Jong PJ, Green ED, Trask BJ. Rudd MK, et al. Genome Res. 2009 Jan;19(1):33-41. doi: 10.1101/gr.083170.108. Epub 2008 Oct 24. Genome Res. 2009. PMID: 18952852 Free PMC article.

3

Large inverted duplications in the human genome form via a fold-back mechanism.

Hermetz KE, Newman S, Conneely KN, Martin CL, Ballif BC, Shaffer LG, Cody JD, Rudd MK. Hermetz KE, et al. Among authors: rudd mk. PLoS Genet. 2014 Jan 30;10(1):e1004139. doi: 10.1371/journal.pgen.1004139. eCollection 2014 Jan. PLoS Genet. 2014. PMID: 24497845 Free PMC article.

4

A 360-kb interchromosomal duplication of the human HYDIN locus.

Doggett NA, Xie G, Meincke LJ, Sutherland RD, Mundt MO, Berbari NS, Davy BE, Robinson ML, Rudd MK, Weber JL, Stallings RL, Han C. Doggett NA, et al. Among authors: rudd mk. Genomics. 2006 Dec;88(6):762-771. doi: 10.1016/j.ygeno.2006.07.012. Epub 2006 Aug 30. Genomics. 2006. PMID: 16938426 Free article.

5

Tandem repeats and G-rich sequences are enriched at human CNV breakpoints.

Bose P, Hermetz KE, Conneely KN, Rudd MK. Bose P, et al. Among authors: rudd mk. PLoS One. 2014 Jul 1;9(7):e101607. doi: 10.1371/journal.pone.0101607. eCollection 2014. PLoS One. 2014. PMID: 24983241 Free PMC article.

6

Integrating 5-hydroxymethylcytosine into the epigenomic landscape of human embryonic stem cells.

Szulwach KE, Li X, Li Y, Song CX, Han JW, Kim S, Namburi S, Hermetz K, Kim JJ, Rudd MK, Yoon YS, Ren B, He C, Jin P. Szulwach KE, et al. Among authors: rudd mk. PLoS Genet. 2011 Jun;7(6):e1002154. doi: 10.1371/journal.pgen.1002154. Epub 2011 Jun 23. PLoS Genet. 2011. PMID: 21731508 Free PMC article.

7

Structural variation in subtelomeres.

Rudd MK. Rudd MK. Methods Mol Biol. 2012;838:137-49. doi: 10.1007/978-1-61779-507-7_6. Methods Mol Biol. 2012. PMID: 22228010

8

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Luo Y, Hermetz KE, Jackson JM, Mulle JG, Dodd A, Tsuchiya KD, Ballif BC, Shaffer LG, Cody JD, Ledbetter DH, Martin CL, Rudd MK. Luo Y, et al. Among authors: rudd mk. Hum Mol Genet. 2011 Oct 1;20(19):3769-78. doi: 10.1093/hmg/ddr293. Epub 2011 Jul 4. Hum Mol Genet. 2011. PMID: 21729882 Free PMC article.

9

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.

Tsuchiya KD, Shaffer LG, Aradhya S, Gastier-Foster JM, Patel A, Rudd MK, Biggerstaff JS, Sanger WG, Schwartz S, Tepperberg JH, Thorland EC, Torchia BA, Brothman AR. Tsuchiya KD, et al. Among authors: rudd mk. Genet Med. 2009 Dec;11(12):866-73. doi: 10.1097/GIM.0b013e3181c0c3b0. Genet Med. 2009. PMID: 19904209 Free article.

10

Segmental duplications mediate novel, clinically relevant chromosome rearrangements.

Rudd MK, Keene J, Bunke B, Kaminsky EB, Adam MP, Mulle JG, Ledbetter DH, Martin CL. Rudd MK, et al. Hum Mol Genet. 2009 Aug 15;18(16):2957-62. doi: 10.1093/hmg/ddp233. Epub 2009 May 14. Hum Mol Genet. 2009. PMID: 19443486 Free PMC article.

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