Yatsenko SA - Search Results

1

Duplication of Xq26.2-q27.1, including SOX3, in a mother and daughter with short stature and dyslalia.

Stankiewicz P, Thiele H, Schlicker M, Cseke-Friedrich A, Bartel-Friedrich S, Yatsenko SA, Lupski JR, Hansmann I. Stankiewicz P, et al. Among authors: yatsenko sa. Am J Med Genet A. 2005 Sep 15;138(1):11-7. doi: 10.1002/ajmg.a.30910. Am J Med Genet A. 2005. PMID: 16097007

2

Heterozygous TP63 pathogenic variants in isolated primary ovarian insufficiency.

Vanderschelden RK, Rodriguez-Escriba M, Chan SH, Berman AJ, Rajkovic A, Yatsenko SA. Vanderschelden RK, et al. Among authors: yatsenko sa. J Assist Reprod Genet. 2023 Sep;40(9):2211-2218. doi: 10.1007/s10815-023-02886-w. Epub 2023 Jul 15. J Assist Reprod Genet. 2023. PMID: 37453019 Free PMC article.

3

B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21.

Baloda V, Aggarwal N, Rosado FG, Mackey S, Felker J, Yatsenko SA. Baloda V, et al. Among authors: yatsenko sa. Cytogenet Genome Res. 2022;162(5):231-236. doi: 10.1159/000527025. Epub 2022 Dec 9. Cytogenet Genome Res. 2022. PMID: 36502796

4

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.

5

Prenatal and fetal diagnosis of trisomy 18 after low-risk cell-free fetal DNA screening: A report of four cases.

Sheehan E, Bacon V, Lascurain S, Stone J, Yatsenko S, Aarabi M, Skvarca LB, Clemens M, Saller D. Sheehan E, et al. Prenat Diagn. 2023 Jan;43(1):36-41. doi: 10.1002/pd.6273. Epub 2022 Nov 29. Prenat Diagn. 2023. PMID: 36426655 Review.

6

Omphalocele in trisomy 3q: further delineation of phenotype.

Yatsenko SA, Mendoza-Londono R, Belmont JW, Shaffer LG. Yatsenko SA, et al. Clin Genet. 2003 Nov;64(5):404-13. doi: 10.1034/j.1399-0004.2003.00159.x. Clin Genet. 2003. PMID: 14616763

7

Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].

Yatsenko SA, Sahoo T, Rosenkranz M, Mendoza-Londono R, Naeem R, Scaglia F. Yatsenko SA, et al. Am J Med Genet A. 2004 Jul 1;128A(1):72-7. doi: 10.1002/ajmg.a.30094. Am J Med Genet A. 2004. PMID: 15211662

8

Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.

Yatsenko SA, Yatsenko AN, Szigeti K, Craigen WJ, Stankiewicz P, Cheung SW, Lupski JR. Yatsenko SA, et al. Among authors: yatsenko an. Clin Genet. 2004 Aug;66(2):128-36. doi: 10.1111/j.1399-0004.2004.00290.x. Clin Genet. 2004. PMID: 15253763

9

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.

10

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

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