Primary Biliary Cholangitis
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Last Posted: Aug 19, 2024
- Obstructive sleep apnea and 19 gastrointestinal diseases: a Mendelian randomization study.
Weiheng Yan, et al. Frontiers in psychiatry 2024 0 1256116 - Depressive symptom as a risk factor for cirrhosis in patients with primary biliary cholangitis: Analysis based on Lasso-logistic regression and decision tree models.
Simin Zhou, et al. Brain and behavior 2024 0 (8) e3639 - Causality of metabolites and metabolic pathways on cholestatic liver diseases: a Mendelian randomization study.
Zhengxiao Wei, et al. Frontiers in medicine 2024 0 1395526 - Cross-Phenotype GWAS Supports Shared Genetic Susceptibility to Systemic Sclerosis and Primary Biliary Cholangitis.
Yiming Luo, et al. medRxiv : the preprint server for health sciences 2024 0 - Primary biliary cholangitis and Sjogren's syndrome: bi-directional Mendelian randomization analysis.
N Wang, et al. European review for medical and pharmacological sciences 2024 0 (10) 3556-3565 - Causal association between systemic lupus erythematosus and primary biliary cholangitis: A bidirectional Mendelian randomization study.
Ying Wang, et al. Medicine 2024 0 (21) e38282 - Causal association of polyunsaturated fatty acids with biliary tract diseases: A Mendelian randomization study.
Xu Chen, et al. Clinical nutrition ESPEN 2024 0 37-45 - Association between diabetes mellitus and primary biliary cholangitis: a two-sample Mendelian randomization study.
Dan Lv, et al. Frontiers in endocrinology 2024 0 1362584 - Association between autoimmune liver diseases and chronic hepatitis B: A multivariable Mendelian randomization study in European population.
Wenhui Zhang, et al. Preventive medicine 2024 0 107984 - A genome-wide association study identified PTPN2 as a population-specific susceptibility gene locus for primary biliary cholangitis.
Yuki Hitomi, et al. Hepatology (Baltimore, Md.) 2024 0
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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
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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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