Saller DN - Search Results

1

Copy number alterations involving 59 ACMG-recommended secondary findings genes.

Yatsenko SA, Aarabi M, Hu J, Surti U, Ortiz D, Madan-Khetarpal S, Saller DN, Bellissimo D, Rajkovic A. Yatsenko SA, et al. Among authors: saller dn. Clin Genet. 2020 Dec;98(6):577-588. doi: 10.1111/cge.13852. Epub 2020 Oct 10. Clin Genet. 2020. PMID: 33009833

2

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. Among authors: saller dn. 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.

3

Genotype-phenotype correlation and pregnancy outcomes of partial trisomy 14q: A systematic review.

Bregand-White J, Saller DN, Clemens M, Surti U, Yatsenko SA, Rajkovic A. Bregand-White J, et al. Among authors: saller dn. Am J Med Genet A. 2016 Sep;170(9):2365-71. doi: 10.1002/ajmg.a.37793. Epub 2016 Jun 10. Am J Med Genet A. 2016. PMID: 27286879 Review.

4

Importance of complete phenotyping in prenatal whole exome sequencing.

Aarabi M, Sniezek O, Jiang H, Saller DN, Bellissimo D, Yatsenko SA, Rajkovic A. Aarabi M, et al. Among authors: saller dn. Hum Genet. 2018 Feb;137(2):175-181. doi: 10.1007/s00439-017-1860-1. Epub 2018 Feb 1. Hum Genet. 2018. PMID: 29392406

5

Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype.

Marinescu PS, Saller DN, Parks WT, Yatsenko SA, Rajkovic A. Marinescu PS, et al. Among authors: saller dn. Clin Case Rep. 2015 Feb;3(2):92-5. doi: 10.1002/ccr3.162. Epub 2014 Oct 15. Clin Case Rep. 2015. PMID: 25767704 Free PMC article.

6

Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3.

Putra M, Surti U, Hu J, Steele D, Clemens M, Saller DN, Yatsenko SA, Rajkovic A. Putra M, et al. Among authors: saller dn. Am J Med Genet A. 2017 Dec;173(12):3153-3157. doi: 10.1002/ajmg.a.38497. Epub 2017 Oct 19. Am J Med Genet A. 2017. PMID: 29048729

7

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: saller dn. 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.

8

Expansion of phenotype and genotypic data in CRB2-related syndrome.

Lamont RE, Tan WH, Innes AM, Parboosingh JS, Schneidman-Duhovny D, Rajkovic A, Pappas J, Altschwager P, DeWard S, Fulton A, Gray KJ, Krall M, Mehta L, Rodan LH, Saller DN Jr, Steele D, Stein D, Yatsenko SA, Bernier FP, Slavotinek AM. Lamont RE, et al. Among authors: saller dn jr. Eur J Hum Genet. 2016 Oct;24(10):1436-44. doi: 10.1038/ejhg.2016.24. Epub 2016 Mar 23. Eur J Hum Genet. 2016. PMID: 27004616 Free PMC article. Review.

9

Cytogenetic signatures of recurrent pregnancy losses.

Yatsenko SA, Quesada-Candela C, Saller DN, Beck S, Jaffe R, Kostadinov S, Yanowitz J, Rajkovic A. Yatsenko SA, et al. Among authors: saller dn. Prenat Diagn. 2021 Jan;41(1):70-78. doi: 10.1002/pd.5838. Epub 2020 Oct 10. Prenat Diagn. 2021. PMID: 33015842 Free PMC article.

10

Prenatal whole-exome sequencing: parental attitudes.

Kalynchuk EJ, Althouse A, Parker LS, Saller DN Jr, Rajkovic A. Kalynchuk EJ, et al. Among authors: saller dn jr. Prenat Diagn. 2015 Oct;35(10):1030-6. doi: 10.1002/pd.4635. Epub 2015 Jul 6. Prenat Diagn. 2015. PMID: 26151551

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