Biliary Atresia
What's New
Last Posted: Oct 21, 2023
- Contribution of ADD3 and the HLA Genes to Biliary Atresia Risk in Chinese.
Meng-Meng Cui, et al. International journal of molecular sciences 2023 0 (19) - Rare sequence variants associated with the risk of non-syndromic biliary atresia.
Satoshi Tamaoka, et al. Hepatology research : the official journal of the Japan Society of Hepatology 2023 0 - The association of immune-related genes and the potential role of IL10 with biliary atresia.
Zefeng Lin, et al. Pediatric research 2023 0 - Association analysis and functional follow-up identified common variants of JAG1 accounting for risk to biliary atresia.
Mei-Rong Bai, et al. Frontiers in genetics 2023 0 1186882 - The Impact of Thrombophilic Factors on Disease Progression in Children with Biliary Atresia-A Single-Centre Cohort Study.
Ohlendorf Johanna, et al. Journal of clinical medicine 2023 0 (6) - Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants.
Sok Pagna, et al. American journal of medical genetics. Part A 2023 0 - MiR-100 rs1834306 A>G Increases Biliary Atresia Risk in Southern Han Chinese Children.
Chang Jiaming, et al. BioMed research international 2023 0 4835839 - Cytotoxic T lymphocyte-associated antigen-4 gene polymorphisms and biliary atresia susceptibility in Chinese children.
Liu Jia, et al. International journal of clinical and experimental pathology 2020 0 (5) 2846-2851 - Correlation between hepatic oxidative damage and clinical severity and mitochondrial gene sequencing results in biliary atresia.
Wang Junfeng, et al. Hepatology research : the official journal of the Japan Society of Hepatology 2019 0 (6) 695-704 - MicroRNA-499 rs3746444 polymorphism in Egyptian children with biliary atresia.
Gawish Eman, et al. Clinical and experimental hepatology 2020 0 (3) 263-269
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch 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.
- Page last reviewed:Feb 1, 2024
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