Search Results - "Treff, N"

Endometrial microbiome at the time of embryo transfer: next-generation sequencing of the 16S ribosomal subunit by Franasiak, J. M., Werner, M. D., Juneau, C. R., Tao, X., Landis, J., Zhan, Y., Treff, N. R., Scott, R. T.

“…Purpose Characterization of the human microbiome has become more precise with the application of powerful molecular tools utilizing the unique 16S ribosomal…”
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Single embryo transfer with comprehensive chromosome screening results in improved ongoing pregnancy rates and decreased miscarriage rates by Forman, E.J., Tao, X., Ferry, K.M., Taylor, D., Treff, N.R., Scott, R.T.

“…BACKGROUND Single embryo transfer (SET) provides the most certain means to reduce the risk of multiple gestation. Regrettably, prospective trials of SET have…”
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S18 Four hour 24 chromosome aneuploidy screening by Treff, N

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SNP microarray-based 24 chromosome aneuploidy screening demonstrates that cleavage-stage FISH poorly predicts aneuploidy in embryos that develop to morphologically normal blastocysts by Northrop, L.E., Treff, N.R., Levy, B., Scott, R.T.

“…Although selection of chromosomally normal embryos has the potential to improve outcomes for patients undergoing IVF, the clinical impact of aneuploidy…”
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AN INTERACTIVE EVACUATION TOOL TO IMPROVE THE PUBLIC FLOOD PERCEPTION by Li, W. L., Treff, N., Amann, F., Lehmen, J., Dehbi, Y., Haunert, J.-H.

“…The advancing climate change increases the danger of heavy rainfall events and devastating floods, which significantly threaten people’s lives and properties…”
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Preclinical validation of a targeted next generation sequencing-based comprehensive chromosome screening methodology in human blastocysts by Zimmerman, R S, Tao, X, Marin, D, Werner, M D, Hong, K H, Lonczak, A, Landis, J, Taylor, D, Zhan, Y, Scott, R T, Treff, N R

“…Abstract STUDY QUESTION Can a novel targeted next generation sequencing (tNGS) platform accurately detect whole chromosome aneuploidy in a trophectoderm biopsy…”
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Mitochondrial DNA content is increased in the aneuploid mouse blastocyst by Tao, X, Landis, J.N, Scott, R.T, Treff, N, Lonczak, A

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A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent by Fedick, A., Jalas, C., Treff, N.R.

“…Zellweger syndrome is known to be caused by numerous mutations that occur in at least 12 of the PEX genes. While phenotypes vary, many are severely…”
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Interaction of uterine natural killer cell immunoglobulin receptor (KIR) haplotype and trophoblastic HLA-C ligand influences risk of pregnancy loss: a retrospective analysis of direct embryo genotyping data by Morin, S.J, Han, M.M, Franasiak, J.M, Juneau, C.R, Treff, N, Scott, R.T

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Maternal whole exome sequencing reveals candidate pathways for embryonic aneuploidy risk by Marin, D, Bohrer, C, Zhang, Y, Zhan, Y, Scott, R.T, Xing, J, Treff, N

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Prospective randomized and blinded comparison of NGS CCS platforms by Zimmerman, R.S, Treff, N, Zhan, Y, Tao, X, Scott, R.T, Scott, K

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Embryos whose polar bodies contain isolated reciprocal chromosome aneuploidy are almost always euploid by Forman, E.J., Treff, N.R., Stevens, J.M., Garnsey, H.M., Katz-Jaffe, M.G., Scott, R.T., Schoolcraft, W.B.

“…STUDY QUESTION When a chromosome aneuploidy is detected in the first polar body and a reciprocal loss or gain of the same chromosome is detected in the second…”
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Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population by Fedick, A.M., Shi, L., Jalas, C., Treff, N.R., Ekstein, J., Kornreich, R., Edelmann, L., Mehta, L., Savage, S.A.

“…Hoyeraal–Hreidarsson syndrome (HH) is a clinically severe variant of dyskeratosis congenita (DC), characterized by cerebellar hypoplasia, microcephaly,…”
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Lactobacilli dominance on the embryo transfer catheter after euploid blastocyst transfer does not predict clinical outcomes by Franasiak, J, Juneau, C, Morin, S, Tao, X, Rajchel, J, Landis, J, Zhan, Y, Treff, N, Scott, R

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Polar body based aneuploidy screening is poorly predictive of embryo ploidy and reproductive potential by Salvaggio, C. N., Forman, E. J., Garnsey, H. M., Treff, N. R., Scott, R. T.

“…Purpose Polar body (polar body) biopsy represents one possible solution to performing comprehensive chromosome screening (CCS). This study adds to what is…”
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Special research presentation: gene variants in aurora kinase could be predictive of maternal oocyte aneuploidy by Schindler, K, Marin, D, Nguyen, A, Zhou, A, Wang, Y, Fedick, A, Taylor, D.M, Xing, J, Treff, N

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Reliable detection of segmental aneuploidy identified by next generation sequencing (NGS) by Juneau, C.R, Scott, K, Neal, S, Morin, S.J, Zhan, Y, Zimmerman, R.S, Treff, N, Franasiak, J.M, Scott, R.T

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Assessment of the embryo transfer catheter microbiome after euploid blastocyst transfer is not predictive of sustained implantation by Franasiak, J.M, Juneau, C.R, Morin, S.J, Tao, X, Rajchel, J, Landis, J.N, Zhan, Y, Treff, N, Scott, R.T

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Natural is not better: gonadotropin stimulation does not increase aneuploidy or diminish implantation rates of euploid embryos by Hong, K.H, Forman, E.J, Werner, M.D, Franasiak, J.M, Juneau, C.R, Morin, S.J, Whitehead, C, Treff, N, Scott, R.T

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Experiences in single gene disorder (SGD) preimplantation genetic diagnosis (PGD): a focus on indication for testing, family member availability and its influence on test design paradigms by Eccles, J.M, Iturriaga, A, Jalas, C, Behrens, A, Kleinman, E, Scott, R.T, Treff, N, Zimmerman, R

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