Noma
What's New
Last Posted: Jul 12, 2024
- Combined exercise training decreases blood pressure in OLDER women with NOS3 polymorphism providing changes in differentially methylated regions (DMRs).
Guilherme da Silva Rodrigues, et al. Epigenetics 2024 0 (1) 2375030 - Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models.
Otani Takahiro, et al. European journal of human genetics : EJHG 2018 0 (1) 140-149 - Distribution of the mutant allele of the DMRT3 gene associated with ambling gaits in Japanese native horse populations.
Chandra Paul Ripon, et al. Animal science journal = Nihon chikusan Gakkaiho 2020 0 (1) e13431 - Hepatic insulin clearance is increased in patients with high HbA1c type 2 diabetes: a preliminary report.
Okura Tsuyoshi, et al. BMJ open diabetes research & care 2020 0 (1) - Frequent allelic loss/imbalance on the short arm of chromosome 3 in tongue cancer.
Arai K, et al. The Bulletin of Tokyo Dental College 2002 0 (3) 151-7 - Machine learning prediction model of acute kidney injury after percutaneous coronary intervention.
Kuno Toshiki et al. Scientific reports 2022 12(1) 749 - Association of interleukin-17A rs2275913 polymorphism with rheumatoid arthritis susceptibility in Sudanese population.
Osman Rgda Mohamed, et al. SAGE open medicine 2021 0 20503121211020207 - Deep neural network-based machine learning reduces the screening workload for systematic review: Investigation based on recent clinical guidelines.
Yamada Tomohide et al. Journal of medical Internet research 2020 Nov - Empirical Bayes Estimation of Semi-parametric Hierarchical Mixture Models for Unbiased Characterization of Polygenic Disease Architectures.
Nishino Jo, et al. Frontiers in genetics 2018 0 115 - Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Takasaki Yuto, et al. Scientific reports 2016 0 33311
More
About Rare Diseases PHGKB
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
Content Summary
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
- Content source: