Yatsenko SA - Search Results

1

Reproductive outcomes in individuals with chromosomal reciprocal translocations.

Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Verdoni A, et al. Among authors: yatsenko sa. Genet Med. 2021 Sep;23(9):1753-1760. doi: 10.1038/s41436-021-01195-w. Epub 2021 May 10. Genet Med. 2021. PMID: 33972719 Free article.

2

AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.

Babcock M, Yatsenko S, Stankiewicz P, Lupski JR, Morrow BE. Babcock M, et al. Genome Res. 2007 Apr;17(4):451-60. doi: 10.1101/gr.5651507. Epub 2007 Feb 6. Genome Res. 2007. PMID: 17284672 Free PMC article.

3

Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis.

Shin YH, Choi Y, Erdin SU, Yatsenko SA, Kloc M, Yang F, Wang PJ, Meistrich ML, Rajkovic A. Shin YH, et al. Among authors: yatsenko sa. PLoS Genet. 2010 Nov 4;6(11):e1001190. doi: 10.1371/journal.pgen.1001190. PLoS Genet. 2010. PMID: 21079677 Free PMC article.

4

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.

Liao J, Sathanoori M, Yatsenko SA, Hu J, Kochmar SJ, Hoffner L, Hogge WA, Surti U. Liao J, et al. Among authors: yatsenko sa. Prenat Diagn. 2012 Dec;32(12):1166-9. doi: 10.1002/pd.3977. Epub 2012 Sep 26. Prenat Diagn. 2012. PMID: 23015528

5

Application of chromosomal microarray in the evaluation of abnormal prenatal findings.

Yatsenko SA, Davis S, Hendrix NW, Surti U, Emery S, Canavan T, Speer P, Hill L, Clemens M, Rajkovic A. Yatsenko SA, et al. Clin Genet. 2013 Jul;84(1):47-54. doi: 10.1111/cge.12027. Epub 2012 Nov 4. Clin Genet. 2013. PMID: 23020214

6

Familial microduplication of 17q23.1–q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females.

Peterson JF, Ghaloul-Gonzalez L, Madan-Khetarpal S, Hartman J, Surti U, Rajkovic A, Yatsenko SA. Peterson JF, et al. Among authors: yatsenko sa. Am J Med Genet A. 2014 Feb;164A(2):364-9. doi: 10.1002/ajmg.a.36238. Am J Med Genet A. 2014. PMID: 24592505

7

Interstitial 10p11.23-p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism.

Mroczkowski HJ, Arnold G, Schneck FX, Rajkovic A, Yatsenko SA. Mroczkowski HJ, et al. Among authors: yatsenko sa. Am J Med Genet A. 2014 Oct;164A(10):2623-6. doi: 10.1002/ajmg.a.36627. Epub 2014 Jul 29. Am J Med Genet A. 2014. PMID: 25073539

8

Recent advances of genomic testing in perinatal medicine.

Peters DG, Yatsenko SA, Surti U, Rajkovic A. Peters DG, et al. Among authors: yatsenko sa. Semin Perinatol. 2015 Feb;39(1):44-54. doi: 10.1053/j.semperi.2014.10.009. Epub 2014 Nov 28. Semin Perinatol. 2015. PMID: 25444417 Free PMC article. Review.

9

MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability.

Wood-Trageser MA, Gurbuz F, Yatsenko SA, Jeffries EP, Kotan LD, Surti U, Ketterer DM, Matic J, Chipkin J, Jiang H, Trakselis MA, Topaloglu AK, Rajkovic A. Wood-Trageser MA, et al. Among authors: yatsenko sa. Am J Hum Genet. 2014 Dec 4;95(6):754-62. doi: 10.1016/j.ajhg.2014.11.002. Am J Hum Genet. 2014. PMID: 25480036 Free PMC article.

10

Maternal cell-free DNA-based screening for fetal microdeletion and the importance of careful diagnostic follow-up.

Yatsenko SA, Peters DG, Saller DN, Chu T, Clemens M, Rajkovic A. Yatsenko SA, et al. Genet Med. 2015 Oct;17(10):836-8. doi: 10.1038/gim.2014.197. Epub 2015 Jan 8. Genet Med. 2015. PMID: 25569438 Free PMC article.

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