Last Posted: Jul 22, 2021
- Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).
Gregg Anthony R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 7
- Frequencies of Beta Thalassemia Mutations Show Different Pattern in Bannu Region than Other Parts of Pashtun Population in Khyber Pakhtunkhwa Province Pakistan.
Rehman Shoaib U et al. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2021 37(3) 479-483
- Frequency of carriers for rare recessive Mendelian diseases in a Brazilian cohort of 320 patients.
Quaio Caio Robledo D'Angioli Costa et al. American journal of medical genetics. Part C, Seminars in medical genetics 2021
- Interest in and uptake of genetic counseling for preconception carrier screening when offered to predominantly white reproductive-age persons seeking gynecologic care at a single U.S. academic medical center.
Nesbit Carleigh B et al. Journal of genetic counseling 2021
- Scope of practice distinctions based on primary work setting for genetic counselors in assisted reproductive technologies.
Snider Alyssa C et al. F&S reports 2021 2(1) 80-87
- Genetic landscape of recessive diseases in the Vietnamese population from large-scale clinical exome sequencing.
Tran Ngoc Hieu et al. Human mutation 2021
- Pathogenic gene variation spectrum and carrier screening for Wilson's disease in Qingdao area.
Qiao Lingyan et al. Molecular genetics & genomic medicine 2021 e1741
- Beyond the "Jewish panel": the importance of offering expanded carrier screening to the Ashkenazi Jewish population.
Dolitsky Shelley et al. F&S reports 2021 1(3) 294-298
- Knowledge and attitudes toward expanded carrier screening between the medical staff and general population in China.
Yang Jing et al. European journal of obstetrics, gynecology, and reproductive biology 2021 263198-204
- How genomics is changing the practice of prenatal testing.
Filges Isabel et al. Journal of perinatal medicine 2021
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Disclaimer: Articles listed in the Public Health Genomics and Precision Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.