Yatsenko SA - Search Results

1

A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.

Landis BJ, Helvaty LR, Geddes GC, Lin JI, Yatsenko SA, Lo CW, Border WL, Wechsler SB, Murali CN, Azamian MS, Lalani SR, Hinton RB, Garg V, McBride KL, Hodge JC, Ware SM. Landis BJ, et al. Among authors: yatsenko sa. J Am Heart Assoc. 2023 Sep 19;12(18):e029340. doi: 10.1161/JAHA.123.029340. Epub 2023 Sep 8. J Am Heart Assoc. 2023. PMID: 37681527 Free PMC article.

2

Dermatofibrosarcoma protuberans with fibrosarcomatous transformation: our experience, molecular evaluation of selected cases, and short literature review.

Lopez LV, Yatsenko SA, Burgess M, Schoedel K, Rao UNM. Lopez LV, et al. Among authors: yatsenko sa. Int J Dermatol. 2019 Nov;58(11):1246-1252. doi: 10.1111/ijd.14462. Epub 2019 Apr 10. Int J Dermatol. 2019. PMID: 30968395 Review.

3

Reproductive aging and MCM8/9.

Yatsenko SA, Rajkovic A. Yatsenko SA, et al. Oncotarget. 2015 Jun 30;6(18):15750-1. doi: 10.18632/oncotarget.4589. Oncotarget. 2015. PMID: 26119146 Free PMC article. No abstract available.

4

Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome.

Babcock M, Yatsenko S, Hopkins J, Brenton M, Cao Q, de Jong P, Stankiewicz P, Lupski JR, Sikela JM, Morrow BE. Babcock M, et al. Hum Mol Genet. 2007 Nov 1;16(21):2560-71. doi: 10.1093/hmg/ddm197. Epub 2007 Aug 3. Hum Mol Genet. 2007. PMID: 17675367

5

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.

6

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilization.

Yatsenko SA, Hixson P, Roney EK, Scott DA, Schaaf CP, Ng YT, Palmer R, Fisher RB, Patel A, Cheung SW, Lupski JR. Yatsenko SA, et al. Hum Genet. 2012 Dec;131(12):1895-910. doi: 10.1007/s00439-012-1216-9. Epub 2012 Aug 14. Hum Genet. 2012. PMID: 22890305 Free PMC article.

7

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly.

Yatsenko SA, Cheung SW, Scott DA, Nowaczyk MJ, Tarnopolsky M, Naidu S, Bibat G, Patel A, Leroy JG, Scaglia F, Stankiewicz P, Lupski JR. Yatsenko SA, et al. J Med Genet. 2005 Apr;42(4):328-35. doi: 10.1136/jmg.2004.028258. J Med Genet. 2005. PMID: 15805160 Free PMC article. No abstract available.

8

A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.

Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT. Posmyk R, et al. Among authors: yatsenko sa. Genet Couns. 2005;16(1):17-25. Genet Couns. 2005. PMID: 15844774

9

Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.

Leipoldt M, Erdel M, Bien-Willner GA, Smyk M, Theurl M, Yatsenko SA, Lupski JR, Lane AH, Shanske AL, Stankiewicz P, Scherer G. Leipoldt M, et al. Among authors: yatsenko sa. Clin Genet. 2007 Jan;71(1):67-75. doi: 10.1111/j.1399-0004.2007.00736.x. Clin Genet. 2007. PMID: 17204049

10

De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.

Purandare SM, Mendoza-Londono R, Yatsenko SA, Napierala D, Scott DA, Sibai T, Casas K, Wilson P, Lee J, Muneer R, Leonard JC, Ramji FG, Lachman R, Li S, Stankiewicz P, Lee B, Mulvihill JJ. Purandare SM, et al. Among authors: yatsenko sa. Am J Med Genet A. 2008 Feb 15;146A(4):453-8. doi: 10.1002/ajmg.a.31750. Am J Med Genet A. 2008. PMID: 18203189 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

116 results

Search Page