Last Posted: Feb 17, 2021
- Gene-environment interactions between air pollution and biotransformation enzymes and risk of birth defects.
Padula Amy M, et al. Birth defects research 2021 2
- Genome-wide association studies of structural birth defects: A review and commentary.
Lupo Philip J et al. Birth defects research 2019 Oct
- Gene variants as risk factors for gastroschisis.
Padula Amy M, et al. American journal of medical genetics. Part A 2016 9
- Facts about Gastroschisis
- Increasing Prevalence of Gastroschisis 14 States, 19952012
MMWR, January 2016
- Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in Gastroschisis.
Makhmudi Akhmad, et al. Journal of investigative surgery : the official journal of the Academy of Surgical Research 2015 9 1-5
- Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Jenkins Mary M, et al. American journal of medical genetics. Part A 2014 6 (6) 1454-63
From NCATS Genetic and Rare Diseases Information Center
- Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis.
Torfs Claudine P, et al. Birth defects research. Part A, Clinical and molecular teratology 2006 10 (10) 723-30
- Genetic predispositions for thromboembolism as a possible etiology for gastroschisis.
Cardonick Elyce, et al. American journal of obstetrics and gynecology 2005 8 (2) 426-8
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public 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.