Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Cengiz, Cinnioglu"'
Autor:
Alyssa C. Snider, Ph.D., C.G.C., Tristan Darvin, M.S., Lauren Spor, B.S., Adedoyin Akinwole, M.P.H., Cengiz Cinnioglu, Ph.D., Refik Kayali, Ph.D.
Publikováno v:
F&S Reports, Vol 2, Iss 1, Pp 72-79 (2021)
Objective: To define criteria for determining when preimplantation genetic testing for aneuploidy (PGT-A) results are suggestive of a potential balanced chromosomal rearrangement in the egg or sperm source and warrant karyotyping. Design: Performance
Externí odkaz:
https://doaj.org/article/c23b3a8832684d49a819d594ce366672
Autor:
Shan Wei, Alexandre Djandji, Miriam T. Lattin, Odelia Nahum, Nataly Hoffman, Claudia Cujar, Refik Kayali, Cengiz Cinnioglu, Ronald Wapner, Mary D’Alton, Brynn Levy, Zev Williams
Publikováno v:
New England Journal of Medicine. 387:658-660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a74ffc06b108b98699c96e8c03037e
https://doi.org/10.1056/nejmc2201810
https://doi.org/10.1056/nejmc2201810
Autor:
Refik Kayali, Adedoyin Akinwole, Alyssa Snider, Lauren Spor, Cengiz Cinnioglu, Tristan Darvin
Publikováno v:
F&S Reports
F&S Reports, Vol 2, Iss 1, Pp 72-79 (2021)
F&S Reports, Vol 2, Iss 1, Pp 72-79 (2021)
Objective To define criteria for determining when preimplantation genetic testing for aneuploidy (PGT-A) results are suggestive of a potential balanced chromosomal rearrangement in the egg or sperm source and warrant karyotyping. Design Performance e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff944b98a16e518e3c03068b7e206480
http://europepmc.org/articles/PMC8244368
http://europepmc.org/articles/PMC8244368
Publikováno v:
J Assist Reprod Genet
PURPOSE: To compare a single-step medium with a sequential medium on human blastocyst development rates, aneuploidy rates, and clinical outcomes. METHODS: Retrospective cohort study of IVF cycles that used Sage advantage sequential medium (n = 347) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1758c7a9efaa658b65a0b4f6e8b224b
https://doi.org/10.1007/s10815-019-01621-8
https://doi.org/10.1007/s10815-019-01621-8
Publikováno v:
Fertility and Sterility. 118:e25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09b8d8f2dd341b8b29ad95038cf7ad1b
https://doi.org/10.1016/j.fertnstert.2022.09.259
https://doi.org/10.1016/j.fertnstert.2022.09.259
Autor:
Paloma Martinez-Redondo, Dongmei Ji, Taosheng Huang, Refik Kayali, David M. Lee, Karen Agaronyan, Shiyu Luo, Shoukhrat Mitalipov, Nuria Marti Gutierrez, Ying Li, Crystal Van Dyken, Diana Wu, Jeffrey T. Jensen, Hong Ma, Riffat Ahmed, Aida Platero-Luengo, Xinjian Wang, Rebecca Tippner-Hedges, David Battaglia, Dmitry Temiakov, Juan Carlos Izpisua Belmonte, Amy Koski, Jun Wu, Paula Amato, Eunju Kang, Susan B. Olson, Don P. Wolf, Cengiz Cinnioglu, Tomonari Hayama, Yeon-Mi Lee
Publikováno v:
Nature. 567:E5-E9
Change history In this Letter, there are several errors regarding the assignments of mtDNA haplotypes for a subset of egg donors from our study. These errors have not been corrected online.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26eda1536e74d63fd07a0b22aa627233
https://doi.org/10.1038/s41586-019-0876-1
https://doi.org/10.1038/s41586-019-0876-1
Publikováno v:
Fertility and Sterility. 107:1113-1119
The concept of embryos containing multiple cell lines (mosaicism) is not new, but much attention has been paid to this concept recently owing to recent advances in molecular techniques to analyze human embryos. Mosaicism in embryos has been known and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59733c99ac23905e8b03b9f540118b03
https://doi.org/10.1016/j.fertnstert.2017.03.016
https://doi.org/10.1016/j.fertnstert.2017.03.016
Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens
Autor:
Melissa K. Maisenbacher, Ruth B. Lathi, M. Shah, Ioanna A. Comstock, Cengiz Cinnioglu, Jonathan Kort
Publikováno v:
Fertility and Sterility. 107:1028-1033
Objective To compare chromosome testing of miscarriage specimens between traditional cytogenetic analysis and molecular karyotyping using single nucleotide polymorphism microarrays (SNP) and array comparative genomic hybridization (aCGH). Design Pros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fd1f1528de67268bb5aa15ca2fc2e5a
https://doi.org/10.1016/j.fertnstert.2017.01.022
https://doi.org/10.1016/j.fertnstert.2017.01.022
Autor:
Manoj Hariharan, Yeon-Mi Lee, David Battaglia, Don P. Wolf, Cengiz Cinnioglu, Amy Koski, Tomonari Hayama, Joseph R. Ecker, Diana H. Wu, Paula Amato, Joseph R. Nery, Ying Li, Hong Ma, Riffat Ahmed, Rebecca Tippner-Hedges, Zhuzhu Zhang, Susan B. Olson, Ryan C. O’Neil, Shoukhrat Mitalipov, Eunju Kang, Crystal Van Dyken, Nuria Marti Gutierrez, David M. Lee, Rosa Castanon, Refik Kayali, Yupeng He
Publikováno v:
Cell Stem Cell. 20:112-119
Oocyte defects lie at the heart of some forms of infertility and could potentially be addressed therapeutically by alternative routes for oocyte formation. Here, we describe the generation of functional human oocytes following nuclear transfer of fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470978e3e4c934dd9c07bba65967871d
https://doi.org/10.1016/j.stem.2016.10.001
https://doi.org/10.1016/j.stem.2016.10.001
Autor:
Rebecca Tippner-Hedges, Crystal Van Dyken, David Battaglia, David M. Lee, Eunju Kang, Paloma Martinez-Redondo, Karen Agaronyan, Shiyu Luo, Refik Kayali, Jun Wu, Paula Amato, Don P. Wolf, Cengiz Cinnioglu, Tomonari Hayama, Yeon-Mi Lee, Shoukhrat Mitalipov, Nuria Marti Gutierrez, Jeffrey T. Jensen, Diana Wu, Aida Platero-Luengo, Taosheng Huang, Xinjian Wang, Dmitry Temiakov, Dongmei Ji, Juan Carlos Izpisua Belmonte, Amy Koski, Susan B. Olson, Ying Li, Hong Ma, Riffat Ahmed
Publikováno v:
Nature. 540:270-275
Maternally inherited mitochondrial (mt)DNA mutations can cause fatal or severely debilitating syndromes in children, with disease severity dependent on the specific gene mutation and the ratio of mutant to wild-type mtDNA (heteroplasmy) in each cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b39e7f69164268e55ad8f5f09b2e5e9c
https://doi.org/10.1038/nature20592
https://doi.org/10.1038/nature20592