Methods for comprehensive chromosome screening of oocytes and embryos: capabilities, limitations, and evidence of validity

por Treff, Nathan R., Scott, Richard T.
Publicado 2012

Editorial: Causes of Oocyte Aneuploidy and Infertility in Advanced Maternal Age and Emerging Therapeutic Approaches

por Bernstein, Lori R., Treff, Nathan R.
Publicado 2021

Isn’t it time to stop calling preimplantation embryos “mosaic”?

por Paulson, Richard J., Treff, Nathan R.
Publicado 2020

Preimplantation genetic testing for aneuploidy: A review of published blastocyst reanalysis concordance data

por Marin, Diego, Xu, Jia, Treff, Nathan R.
Publicado 2020

Telomere DNA Deficiency Is Associated with Development of Human Embryonic Aneuploidy

por Treff, Nathan R., Su, Jing, Taylor, Deanne, Scott, Richard T.
Publicado 2011

High-throughput real-time PCR-based genotyping without DNA purification

por Fedick, Anastasia, Su, Jing, Jalas, Chaim, Treff, Nathan R
Publicado 2012

Detecting mosaicism in trophectoderm biopsies: current challenges and future possibilities

por Capalbo, Antonio, Ubaldi, Filippo Maria, Rienzi, Laura, Scott, Richard, Treff, Nathan
Publicado 2017

Comprehensive chromosome screening and gene expression analysis from the same biopsy in human preimplantation embryos

por Marin, Diego, Wang, Yujue, Tao, Xin, Scott, Richard T., Treff, Nathan R.
Publicado 2017

Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses

por Treff, Nathan R., Su, Jing, Tao, Xin, Northrop, Lesley E., Scott, Richard T.
Publicado 2011

SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH

por Treff, Nathan R., Levy, Brynn, Su, Jing, Northrop, Lesley E., Tao, Xin, Scott, Richard T.
Publicado 2010

Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population

por Fedick, Anastasia M, Jalas, Chaim, Treff, Nathan R, Knowles, Michael R, Zariwala, Maimoona A
Publicado 2015

High-Throughput Carrier Screening Using TaqMan Allelic Discrimination

por Fedick, Anastasia, Su, Jing, Jalas, Chaim, Northrop, Lesley, Devkota, Batsal, Ekstein, Josef, Treff, Nathan R.
Publicado 2013

Expression and characterization of three Aurora kinase C splice variants found in human oocytes

por Fellmeth, Jessica E., Gordon, Derek, Robins, Christian E., Scott, Richard T., Treff, Nathan R., Schindler, Karen
Publicado 2015

Embryo Screening for Polygenic Disease Risk: Recent Advances and Ethical Considerations

por Tellier, Laurent C. A. M., Eccles, Jennifer, Treff, Nathan R., Lello, Louis, Fishel, Simon, Hsu, Stephen
Publicado 2021

Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocysts

por Treff, Nathan R., Forman, Eric J., Katz-Jaffe, Mandy G., Schoolcraft, William B., Levy, Brynn, Scott, Richard T.
Publicado 2013

Evaluation of comprehensive chromosome screening platforms for the detection of mosaic segmental aneuploidy

por Goodrich, David, Xing, Tongji, Tao, Xin, Lonczak, Agnieszka, Zhan, Yiping, Landis, Jessica, Zimmerman, Rebekah, Scott, Richard T., Treff, Nathan R.
Publicado 2017

Delivery of a chromosomally normal child from an oocyte with reciprocal aneuploid polar bodies

por Scott, Richard T., Treff, Nathan R., Stevens, John, Forman, Eric J., Hong, Kathleen H., Katz-Jaffe, Mandy G., Schoolcraft, William B.
Publicado 2012

A randomized and blinded comparison of qPCR and NGS-based detection of aneuploidy in a cell line mixture model of blastocyst biopsy mosaicism

por Goodrich, David, Tao, Xin, Bohrer, Chelsea, Lonczak, Agnieszka, Xing, Tongji, Zimmerman, Rebekah, Zhan, Yiping, Scott Jr, Richard T., Treff, Nathan R.
Publicado 2016

Levels of trophectoderm mitochondrial DNA do not predict the reproductive potential of sibling embryos

por Treff, Nathan R., Zhan, Yiping, Tao, Xin, Olcha, Meir, Han, Michael, Rajchel, Jessica, Morrison, Liza, Morin, Scott J., Scott, Richard T.
Publicado 2017

Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs

por Treff, Nathan R., Eccles, Jennifer, Marin, Diego, Messick, Edward, Lello, Louis, Gerber, Jessalyn, Xu, Jia, Tellier, Laurent C.A.M.
Publicado 2020