Yatsenko SA - Search Results

1

Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.

Liao J, Coffman KA, Locker J, Padiath QS, Nmezi B, Filipink RA, Hu J, Sathanoori M, Madan-Khetarpal S, McGuire M, Schreiber A, Moran R, Friedman N, Hoffner L, Rajkovic A, Yatsenko SA, Surti U. Liao J, et al. Among authors: yatsenko sa. Mol Genet Genomic Med. 2021 Apr;9(4):e1647. doi: 10.1002/mgg3.1647. Epub 2021 Mar 5. Mol Genet Genomic Med. 2021. PMID: 33666368 Free PMC article.

2

Identification of critical regions for clinical features of distal 10q deletion syndrome.

Yatsenko SA, Kruer MC, Bader PI, Corzo D, Schuette J, Keegan CE, Nowakowska B, Peacock S, Cai WW, Peiffer DA, Gunderson KL, Ou Z, Chinault AC, Cheung SW. Yatsenko SA, et al. Clin Genet. 2009 Jul;76(1):54-62. doi: 10.1111/j.1399-0004.2008.01115.x. Epub 2009 Jun 22. Clin Genet. 2009. PMID: 19558528 Free article.

3

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.

Peters D, Chu T, Yatsenko SA, Hendrix N, Hogge WA, Surti U, Bunce K, Dunkel M, Shaw P, Rajkovic A. Peters D, et al. Among authors: yatsenko sa. N Engl J Med. 2011 Nov 10;365(19):1847-8. doi: 10.1056/NEJMc1106975. N Engl J Med. 2011. PMID: 22070496 Free PMC article. No abstract available.

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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