Work

Identifying risk variants for embryo aneuploidy using ultra-low coverage whole-genome sequencing from preimplantation genetic testing

Year: 2023

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2023.11.002

Authors: Siqi Sun, Mansour Aboelenain, Daniel Ariad, Mary E. Haywood, Charles R. Wageman, Marlena Duke, Aishee Bag, Manuel Viotti, Mandy Katz-Jaffe, Rajiv C. McCoy, Karen Schindler, Jinchuan Xing

Institutions: Rutgers, The State University of New Jersey, Mansoura University, Johns Hopkins University, Foundation for Reproductive Medicine

Language: English

Topic: Prenatal Screening and Diagnostics

Subfield: Pediatrics, Perinatology and Child Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute on Drug Abuse, National Human Genome Research Institute, NIH Office of the Director, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Common Fund

Awards: G2450216003, G469708262, G9000088201, Understanding genetic risk for aneuploid conception

OpenAlex ID: W4389101136

FWCI: 5.598

Cites: 70

Cited by: 17

Related to: 10