Search Results - "Benner, A.T"

The use of next-generation sequencing (NGS) for preimplantation genetic screening (PGS) and diagnosis (PGD) by Tobler, K.J, Ross, R, Benner, A.T, Du, L, Brezina, P.R, Kearns, W.G

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Comparative Genomic Hybridization Microarray (aCGH) Analysis of DNA Isolated from the Blastocoel Fluid from 26 Blastocysts by Tobler, K.J, Zhao, Y, Ross, R, Benner, A.T, Broman, K, Thrift, K, Kearns, W.G

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Preimplantation genetic screening (PGS) on day-5 blastocysts with a day-6 embryo transfer results in a clinical pregnancy rate of 71 by Tobler, K.J, Kaufmann, R, Ross, R, Dickey, R.P, Benner, A.T, Kearns, W.G

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The incidence of aneuploidy in differentiated blastocysts from patients with no prior first trimester spontaneous miscarriages or failed in vitro fertilization cycles by Tobler, K.J, Traub, M.L, Vaid, P, Benner, A.T, Boyd, B, Kearns, W.G

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Two different microarray technologies for preimplantation genetic diagnosis (PGD) and screening (PGS), due to reciprocal translocation imbalances, demonstrate equivalent clinical pregnancy rates by Tobler, K.J, Brezina, P.R, Benner, A.T, Xu, X, Du, L, Kearns, W.G

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Blastocoel fluid (BF) harbors embryonic DNA that may result from the marginalization of aneuploid cells during embryogenesis by Tobler, K.J, Zhao, Y, Ross, R, Benner, A.T, Xu, X, Du, L, Broman, K, Thrift, K, Brezina, P.R, Kearns, W.G

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The potential use of blastocoel fluid (BF) from expanded blastocysts as a less invasive form of embryo biopsy for preimplantation genetic testing by Tobler, K.J, Zhao, Y, Ross, R, Benner, A.T, Xu, X, Du, L, Broman, K, Thrift, K, Brezina, P.R, Kearns, W.G

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The majority of women undergoing preimplantation genetic screeining (PGS) using 23 chromosome single nucleotide polymorphism (SNP) microarrays will have euploid embryos available for uterine transfer by Brezina, P.R, Tobler, K.J, Benner, A.T, Du, L, Boyd, B, Kearns, W.G

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23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS) for recurrent pregnancy loss (RPL) in 687 in vitro fertilization (IVF) cycles and 5871 embryos by Tobler, K.J, Brezina, P.R, Benner, A.T, Du, L, Boyd, B, Kearns, W.G

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Evaluation of 571 In Vitro Fertilization (IVF) Cycels and 4,873 Embryos Using 23-Chromosome Single Nucleotide Polymorphism (SNP) Microarray Preimplantation Genetic Screening (PGS) by Brezina, P.R, Tobler, K, Benner, A.T, Du, L, Boyd, B, Kearns, W.G

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The Incidence of Aneuploidy Does not Significantly Increase With Advancing Paternal Age in Couples With A History of Recurrent Pregnancy Loss by Brezina, P.R, Tobler, K, Benner, A.T, Du, L, Boyd, B, Kearns, W.G

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The Incidence of Aneuploidy Significantly Increases After the Age of 40 in Women With a History of Recurrent Pregnancy Loss by Tobler, K, Brezina, P.R, Benner, A.T, Du, L, Boyd, B, Kearns, W.G

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All 23 Chromosomes have Significant Levels of Aneuploidy in Recurrent Pregnancy Loss Couples by Brezina, P.R, Tobler, K, Benner, A.T, Du, L, Xu, X, Kearns, W.G

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Dense Single Nucleotide Polymorphism (SNP) Microarrays for the Identification of Aneuploidy and Consanguinity in Preimplantation Embryos by Brezina, P.R, Benner, A.T, Garcia, J, Zhao, Y, Handyside, A, Kearns, W.G

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Chromosomal duplications (≥200 KILOBASES (KB)) are more common than deletions ≥200 KB in developing human embryos as identified by 23 chromosome single nucleotide polymorphism (SNP) microarray by Christianson, M.S, Brezina, P.R, Benner, A.T, Du, L, Siegel, A, Kearns, W.G

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23-chromosome single nucleotide polymorphism (SNP) microarray detects genomic aberrations that may be missed by comparative genomic hybridization (CGH) arrays in preimplantation genetic screening (PGS) by Siegel, A, Brezina, P.R, Benner, A.T, Du, L, Gunn, M, Kearns, W.G

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Deletions and duplications identified by 23 chromosome single nucleotide polymorphism (SNP) microarray are associated with aneuploidy by Chipko, C, Brezina, P.R, Benner, A.T, Du, L, Christianson, M.S, Kearns, W.G

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The rate of de novo and inherited aneuploidy as determined by 23-chromosome single nucleotide polymorphism microarray (SNP) in embryos generated from parents with known chromosomal translocations by Du, L, Brezina, P.R, Benner, A.T, Swelstad, B.B, Gunn, M, Kearns, W.G

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23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS) on blastocysts, versus day-3 embryos, results in significantly higher clinical pregnancy rates by Benner, A.T, Brezina, P.R, Du, L, Chipko, C, Gunn, M, Kearns, W.G

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The design and validation to amplify and detect the CCG repeats of the fragile X FMR1 gene by polymerase chain reaction of amplified embryonic DNA followed by fragment sizing on an applied biosystems Seq studio genetic analyzer by Benner, A.T., Pastore, L., Christianson, M.S., Segars, J.H., Dubey, A.K., Kearns, W.G.

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