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Matthew Rabinowitz

Showing results (11-20 of 50) with videos related to

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Journal of Translational Medicine|June 10, 2023
Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinicStephanie U Greer, Jacquelin Botello, Donna Hongo, et al.
Fertility and Sterility|June 18, 2018
Pregnancy outcomes from more than 1,800 in vitro fertilization cycles with the use of 24-chromosome single-nucleotide polymorphism-based preimplantation genetic testing for aneuploidyAlexander L Simon, Michelle Kiehl, Erin Fischer, et al.
Fertility and Sterility|December 27, 2011
Origins and rates of aneuploidy in human blastomeresMatthew Rabinowitz, Allison Ryan, George Gemelos, et al.
Science (New York, N.Y.)|April 11, 2015
Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryosRajiv C McCoy, Zachary Demko, Allison Ryan, et al.
Obstetrics and Gynecology|July 9, 2014
Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysisBrynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, et al.
NPJ Cardiovascular Health|March 3, 2026
Polygenic risk scores improve CAD risk prediction in individuals at borderline and intermediate clinical riskDariusz Ratman, Placede Tshiaba, Michael Levin, et al.
American Journal of Obstetrics and Gynecology|December 3, 2014
Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal testKirsten J Curnow, Louise Wilkins-Haug, Allison Ryan, et al.
Prenatal Diagnosis|October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociBernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Prenatal Diagnosis|May 29, 2013
SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracyCarole Samango-Sprouse, Milena Banjevic, Allison Ryan, et al.
JCO Precision Oncology|February 22, 2023
Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk StratificationPlacede T Tshiaba, Dariusz K Ratman, Jiayi M Sun, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Journal of Translational Medicine|June 10, 2023
Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinicStephanie U Greer, Jacquelin Botello, Donna Hongo, et al.
Fertility and Sterility|June 18, 2018
Pregnancy outcomes from more than 1,800 in vitro fertilization cycles with the use of 24-chromosome single-nucleotide polymorphism-based preimplantation genetic testing for aneuploidyAlexander L Simon, Michelle Kiehl, Erin Fischer, et al.
Fertility and Sterility|December 27, 2011
Origins and rates of aneuploidy in human blastomeresMatthew Rabinowitz, Allison Ryan, George Gemelos, et al.
Science (New York, N.Y.)|April 11, 2015
Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryosRajiv C McCoy, Zachary Demko, Allison Ryan, et al.
Obstetrics and Gynecology|July 9, 2014
Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysisBrynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, et al.
NPJ Cardiovascular Health|March 3, 2026
Polygenic risk scores improve CAD risk prediction in individuals at borderline and intermediate clinical riskDariusz Ratman, Placede Tshiaba, Michael Levin, et al.
American Journal of Obstetrics and Gynecology|December 3, 2014
Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal testKirsten J Curnow, Louise Wilkins-Haug, Allison Ryan, et al.
Prenatal Diagnosis|October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociBernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Prenatal Diagnosis|May 29, 2013
SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracyCarole Samango-Sprouse, Milena Banjevic, Allison Ryan, et al.
JCO Precision Oncology|February 22, 2023
Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk StratificationPlacede T Tshiaba, Dariusz K Ratman, Jiayi M Sun, et al.
Pageof 5