scholarly journals COMPARISON OF FRESH AND FROZEN EJACULATED SPERM IN DONOR OOCYTE RECIPIENT CYCLES: A PAIRED ANALYSIS UTILIZING SIBLING OOCYTES

2020 ◽  
Vol 114 (3) ◽  
pp. e57-e58
Author(s):  
Kelly McCarter ◽  
Robert Setton ◽  
Alice Chung ◽  
Zev Rosenwaks ◽  
Steven Spandorfer
2020 ◽  
Vol 114 (3) ◽  
pp. e94-e95
Author(s):  
Kelly McCarter ◽  
Robert Setton ◽  
Alice Chung ◽  
Zev Rosenwaks ◽  
Steven Spandorfer

F&S Reports ◽  
2020 ◽  
Vol 1 (1) ◽  
pp. 25-29 ◽  
Author(s):  
Robert Setton ◽  
Alice Chung ◽  
Lilli Zimmerman ◽  
Alexis Melnick ◽  
Zev Rosenwaks ◽  
...  

2020 ◽  
Vol 114 (3) ◽  
pp. e244-e245
Author(s):  
Kelly McCarter ◽  
Robert Setton ◽  
Alice Chung ◽  
Zev Rosenwaks ◽  
Steven Spandorfer

2021 ◽  
Vol 116 (3) ◽  
pp. e244
Author(s):  
Jonah D. Bardos ◽  
Samantha Kodama ◽  
Jaclyn M. Kwal ◽  
Samad Jahandideh ◽  
Micah J. Hill ◽  
...  
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sandra Monfort ◽  
Carmen Orellana ◽  
Silvestre Oltra ◽  
Mónica Rosello ◽  
Alfonso Caro-Llopis ◽  
...  

AbstractDevelopment of assisted reproductive technologies to address infertility has favored the birth of many children in the last years. The majority of children born with these treatments are healthy, but some concerns remain on the safety of these medical procedures. We have retrospectively analyzed both the fertilization method and the microarray results in all those children born between 2010 and 2019 with multiple congenital anomalies, developmental delay and/or autistic spectrum disorder (n = 486) referred for array study in our center. This analysis showed a significant excess of pathogenic copy number variants among those patients conceived after in vitro fertilization with donor oocyte with respect to those patients conceived by natural fertilization (p = 0.0001). On the other hand, no significant excess of pathogenic copy number variants was observed among patients born by autologous oocyte in vitro fertilization. Further studies are necessary to confirm these results and in order to identify the factors that may contribute to an increased risk of genomic rearrangements, as well as consider the screening for genomic alterations after oocyte donation in prenatal diagnosis.


2020 ◽  
Vol 30 (6) ◽  
pp. 525-526
Author(s):  
John Quigley ◽  
Deirdre Sweetman ◽  
Cathy Allen ◽  
Mary F. Higgins ◽  
Carol Cantwell ◽  
...  
Keyword(s):  

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