Yatsenko SA - Search Results

1

Recurrent Xp22.31-Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three Families.

Daghsni M, Sheehan E, Madan-Khetarpal S, Aarabi M, Witchel SF, Rajkovic A, Yatsenko SA. Daghsni M, et al. Among authors: yatsenko sa. Am J Med Genet A. 2024 Oct 23:e63913. doi: 10.1002/ajmg.a.63913. Online ahead of print. Am J Med Genet A. 2024. PMID: 39440928

2

Partial 5p Deletion and Partial 5q Duplication in a Patient with Multiple Congenital Anomalies: A Two-Step Mechanism in Chromosomal Rearrangement Mediated by Non-Allelic Homologous Recombination.

Ou ZZ, Kochmar S, Yatsenko SA, Woerner AC, Acquaro R, Ortiz D, Surti U, Hu J. Ou ZZ, et al. Among authors: yatsenko sa. Cytogenet Genome Res. 2018;156(2):65-70. doi: 10.1159/000493381. Epub 2018 Oct 5. Cytogenet Genome Res. 2018. PMID: 30286452

3

Correction: High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions.

Chu T, Yeniterzi S, Yatsenko SA, Dunkel M, Shaw PA, Bunce KD, Peters DG. Chu T, et al. Among authors: yatsenko sa. PLoS One. 2016 Sep 20;11(9):e0163578. doi: 10.1371/journal.pone.0163578. eCollection 2016. PLoS One. 2016. PMID: 27648843 Free PMC article.

4

Therapy-related myeloid neoplasms with different latencies: a detailed clinicopathologic analysis.

Liu YC, Illar GM, Al Amri R, Canady BC, Rea B, Yatsenko SA, Geyer JT. Liu YC, et al. Among authors: yatsenko sa. Mod Pathol. 2022 May;35(5):625-631. doi: 10.1038/s41379-021-00958-9. Epub 2021 Dec 6. Mod Pathol. 2022. PMID: 34873304 Free article.

5

Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression.

Giorgio E, Rolyan H, Kropp L, Chakka AB, Yatsenko S, Di Gregorio E, Lacerenza D, Vaula G, Talarico F, Mandich P, Toro C, Pierre EE, Labauge P, Capellari S, Cortelli P, Vairo FP, Miguel D, Stubbolo D, Marques LC, Gahl W, Boespflug-Tanguy O, Melberg A, Hassin-Baer S, Cohen OS, Pjontek R, Grau A, Klopstock T, Fogel B, Meijer I, Rouleau G, Bouchard JP, Ganapathiraju M, Vanderver A, Dahl N, Hobson G, Brusco A, Brussino A, Padiath QS. Giorgio E, et al. Hum Mutat. 2013 Aug;34(8):1160-71. doi: 10.1002/humu.22348. Epub 2013 May 28. Hum Mutat. 2013. PMID: 23649844 Free PMC article.

6

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.

7

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

8

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

9

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

10

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.

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